-
1
-
-
0035936780
-
Molecular mechanisms of human hypertension
-
Lifton R.P., Gharavi A.G., Geller D.S. Molecular mechanisms of human hypertension. Cell 2001, 104:545-556.
-
(2001)
Cell
, vol.104
, pp. 545-556
-
-
Lifton, R.P.1
Gharavi, A.G.2
Geller, D.S.3
-
3
-
-
0014029230
-
Hypertension, increased aldosterone secretion and low plasma renin activity relieved by dexamethasone
-
Sutherland D.J., Ruse J.L., Laidlaw J.C. Hypertension, increased aldosterone secretion and low plasma renin activity relieved by dexamethasone. Can Med Assoc J 1966, 95:1109-1119.
-
(1966)
Can Med Assoc J
, vol.95
, pp. 1109-1119
-
-
Sutherland, D.J.1
Ruse, J.L.2
Laidlaw, J.C.3
-
4
-
-
0031605731
-
Intracranial aneurysm and hemorrhagic stroke in glucocorticoid-remediable aldosteronism
-
Litchfield W.R., Anderson B.F., Weiss R.J., Lifton R.P., Dluhy R.G. Intracranial aneurysm and hemorrhagic stroke in glucocorticoid-remediable aldosteronism. Hypertension 1998, 31:445-450.
-
(1998)
Hypertension
, vol.31
, pp. 445-450
-
-
Litchfield, W.R.1
Anderson, B.F.2
Weiss, R.J.3
Lifton, R.P.4
Dluhy, R.G.5
-
5
-
-
0027052962
-
Glucocorticoid-remediable aldosteronism in a large kindred: clinical spectrum and diagnosis using a characteristic biochemical phenotype
-
Rich G.M., Ulick S., Cook S., Wang J.Z., Lifton R.P., Dluhy R.G. Glucocorticoid-remediable aldosteronism in a large kindred: clinical spectrum and diagnosis using a characteristic biochemical phenotype. Ann Intern Med 1992, 116:813-820.
-
(1992)
Ann Intern Med
, vol.116
, pp. 813-820
-
-
Rich, G.M.1
Ulick, S.2
Cook, S.3
Wang, J.Z.4
Lifton, R.P.5
Dluhy, R.G.6
-
6
-
-
0030966560
-
Impaired potassium-stimulated aldosterone production: a possible explanation for normokalemic glucocorticoid-remediable aldosteronism
-
Litchfield W.R., Coolidge C., Silva P., Lifton R.P., Fallo F., Williams G.H., et al. Impaired potassium-stimulated aldosterone production: a possible explanation for normokalemic glucocorticoid-remediable aldosteronism. J Clin Endocrinol Metab 1997, 82:1507-1510.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 1507-1510
-
-
Litchfield, W.R.1
Coolidge, C.2
Silva, P.3
Lifton, R.P.4
Fallo, F.5
Williams, G.H.6
-
7
-
-
0020321013
-
Isolation and identification of 18-hydroxycortisol from the urine of patients with primary aldosteronism
-
Chu M.D., Ulick S. Isolation and identification of 18-hydroxycortisol from the urine of patients with primary aldosteronism. J Biol Chem 1982, 257:2218-2224.
-
(1982)
J Biol Chem
, vol.257
, pp. 2218-2224
-
-
Chu, M.D.1
Ulick, S.2
-
8
-
-
0020541134
-
Biosynthesis of 18-oxocortisol by aldosterone-producing adrenal tissue
-
Ulick S., Chu M.D., Land M. Biosynthesis of 18-oxocortisol by aldosterone-producing adrenal tissue. J Biol Chem 1983, 258:5498-5502.
-
(1983)
J Biol Chem
, vol.258
, pp. 5498-5502
-
-
Ulick, S.1
Chu, M.D.2
Land, M.3
-
9
-
-
0026580019
-
A chimaeric 11 beta-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension
-
Lifton R.P., Dluhy R.G., Powers M., Rich G.M., Cook S., Ulick S., et al. A chimaeric 11 beta-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension. Nature 1992, 355:262-265.
-
(1992)
Nature
, vol.355
, pp. 262-265
-
-
Lifton, R.P.1
Dluhy, R.G.2
Powers, M.3
Rich, G.M.4
Cook, S.5
Ulick, S.6
-
10
-
-
0026919361
-
Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase
-
Lifton R.P., Dluhy R.G., Powers M., Rich G.M., Gutkin M., Fallo F., et al. Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase. Nat Genet 1992, 2:66-74.
-
(1992)
Nat Genet
, vol.2
, pp. 66-74
-
-
Lifton, R.P.1
Dluhy, R.G.2
Powers, M.3
Rich, G.M.4
Gutkin, M.5
Fallo, F.6
-
11
-
-
0033331027
-
Mutations in CYP11B1 gene converting 11beta-hydroxylase into an aldosterone-producing enzyme are not present in aldosterone-producing adenomas
-
Pilon C., Mulatero P., Barzon L., Veglio F., Garrone C., Boscaro M., et al. Mutations in CYP11B1 gene converting 11beta-hydroxylase into an aldosterone-producing enzyme are not present in aldosterone-producing adenomas. J Clin Endocrinol Metab 1999, 84:4228-4231.
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 4228-4231
-
-
Pilon, C.1
Mulatero, P.2
Barzon, L.3
Veglio, F.4
Garrone, C.5
Boscaro, M.6
-
12
-
-
0028890480
-
A new genetic test for familial hyperaldosteronism type I aids in the detection of curable hypertension
-
Jonsson J.R., Klemm S.A., Tunny T.J., Stowasser M., Gordon R.D. A new genetic test for familial hyperaldosteronism type I aids in the detection of curable hypertension. Biochem Biophys Res Commun 1995, 207:565-571.
-
(1995)
Biochem Biophys Res Commun
, vol.207
, pp. 565-571
-
-
Jonsson, J.R.1
Klemm, S.A.2
Tunny, T.J.3
Stowasser, M.4
Gordon, R.D.5
-
13
-
-
51749083776
-
Case detection, diagnosis, and treatment of patients with primary aldosteronism: an endocrine society clinical practice guideline
-
Funder J.W., Carey R.M., Fardella C., Gomez-Sanchez C.E., Mantero F., Stowasser M., et al. Case detection, diagnosis, and treatment of patients with primary aldosteronism: an endocrine society clinical practice guideline. J Clin Endocrinol Metab 2008, 93:3266-3281.
-
(2008)
J Clin Endocrinol Metab
, vol.93
, pp. 3266-3281
-
-
Funder, J.W.1
Carey, R.M.2
Fardella, C.3
Gomez-Sanchez, C.E.4
Mantero, F.5
Stowasser, M.6
-
14
-
-
0842308015
-
Coexistence of different phenotypes in a family with glucocorticoid-remediable aldosteronism
-
Fallo F., Pilon C., Williams T.A., Sonino N., Morra Di Cella S., Veglio F., et al. Coexistence of different phenotypes in a family with glucocorticoid-remediable aldosteronism. J Hum Hypertens 2004, 18:47-51.
-
(2004)
J Hum Hypertens
, vol.18
, pp. 47-51
-
-
Fallo, F.1
Pilon, C.2
Williams, T.A.3
Sonino, N.4
Morra Di Cella, S.5
Veglio, F.6
-
15
-
-
80053907554
-
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
-
Ehret G.B., Munroe P.B., Rice K.M., Bochud M., Johnson A.D., Chasman D.I., et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 2011, 478:103-109.
-
(2011)
Nature
, vol.478
, pp. 103-109
-
-
Ehret, G.B.1
Munroe, P.B.2
Rice, K.M.3
Bochud, M.4
Johnson, A.D.5
Chasman, D.I.6
-
16
-
-
12244307553
-
Primary aldosteronism: a new clinical entity
-
discussion, 231-213
-
Conn J.W., Louis L.H. Primary aldosteronism: a new clinical entity. Trans Assoc Am Physicians 1955, 68:215-231. discussion, 231-213.
-
(1955)
Trans Assoc Am Physicians
, vol.68
, pp. 215-231
-
-
Conn, J.W.1
Louis, L.H.2
-
17
-
-
33748132658
-
A prospective study of the prevalence of primary aldosteronism in 1,125 hypertensive patients
-
Rossi G.P., Bernini G., Caliumi C., Desideri G., Fabris B., Ferri C., et al. A prospective study of the prevalence of primary aldosteronism in 1,125 hypertensive patients. J Am Coll Cardiol 2006, 48:2293-2300.
-
(2006)
J Am Coll Cardiol
, vol.48
, pp. 2293-2300
-
-
Rossi, G.P.1
Bernini, G.2
Caliumi, C.3
Desideri, G.4
Fabris, B.5
Ferri, C.6
-
22
-
-
0036188942
-
TASK-3 dominates the background potassium conductance in rat adrenal glomerulosa cells
-
Czirjak G., Enyedi P. TASK-3 dominates the background potassium conductance in rat adrenal glomerulosa cells. Mol Endocrinol 2002, 16:621-629.
-
(2002)
Mol Endocrinol
, vol.16
, pp. 621-629
-
-
Czirjak, G.1
Enyedi, P.2
-
23
-
-
0030953265
-
+ conductance in rat adrenal glomerulosa cells
-
+ conductance in rat adrenal glomerulosa cells. J Membr Biol 1997, 156:261-277.
-
(1997)
J Membr Biol
, vol.156
, pp. 261-277
-
-
Lotshaw, D.P.1
-
24
-
-
0025730965
-
ANG II blocks potassium currents in zona glomerulosa cells from rat, bovine, and human adrenals
-
Brauneis U., Vassilev P.M., Quinn S.J., Williams G.H., Tillotson D.L. ANG II blocks potassium currents in zona glomerulosa cells from rat, bovine, and human adrenals. Am J Physiol 1991, 260:E772-E779.
-
(1991)
Am J Physiol
, vol.260
-
-
Brauneis, U.1
Vassilev, P.M.2
Quinn, S.J.3
Williams, G.H.4
Tillotson, D.L.5
-
25
-
-
84861799719
-
Zona glomerulosa cells of the mouse adrenal cortex are intrinsic electrical oscillators
-
Hu C., Rusin C.G., Tan Z., Guagliardo N.A., Barrett P.Q. Zona glomerulosa cells of the mouse adrenal cortex are intrinsic electrical oscillators. J Clin Invest 2012, 122(6):2046-2053.
-
(2012)
J Clin Invest
, vol.122
, Issue.6
, pp. 2046-2053
-
-
Hu, C.1
Rusin, C.G.2
Tan, Z.3
Guagliardo, N.A.4
Barrett, P.Q.5
-
26
-
-
18844464024
-
Control of aldosterone secretion: a model for convergence in cellular signaling pathways
-
Spat A., Hunyady L. Control of aldosterone secretion: a model for convergence in cellular signaling pathways. Physiol Rev 2004, 84:489-539.
-
(2004)
Physiol Rev
, vol.84
, pp. 489-539
-
-
Spat, A.1
Hunyady, L.2
-
27
-
-
84864612057
-
-
Akerström T, Crona J, Delgado Verdugo A, Starker LF, Cupisti K, Willenberg HS, et al. Comprehensive Re-Sequencing of Adrenal Aldosterone Producing Lesions Reveal Three Somatic Mutations near the KCNJ5 Potassium Channel Selectivity Filter. PLoS One 2012;7:e41926.
-
Akerström T, Crona J, Delgado Verdugo A, Starker LF, Cupisti K, Willenberg HS, et al. Comprehensive Re-Sequencing of Adrenal Aldosterone Producing Lesions Reveal Three Somatic Mutations near the KCNJ5 Potassium Channel Selectivity Filter. PLoS One 2012;7:e41926.
-
-
-
-
28
-
-
84857623168
-
Prevalence, clinical, and molecular correlates of KCNJ5 mutations in primary aldosteronism
-
Boulkroun S., Beuschlein F., Rossi G.P., Golib-Dzib J.F., Fischer E., Amar L., et al. Prevalence, clinical, and molecular correlates of KCNJ5 mutations in primary aldosteronism. Hypertension 2012, 59:592-598.
-
(2012)
Hypertension
, vol.59
, pp. 592-598
-
-
Boulkroun, S.1
Beuschlein, F.2
Rossi, G.P.3
Golib-Dzib, J.F.4
Fischer, E.5
Amar, L.6
-
29
-
-
49249091443
-
A novel form of human Mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism
-
Geller D.S., Zhang J., Wisgerhof M.V., Shackleton C., Kashgarian M., Lifton R.P. A novel form of human Mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism. J Clin Endocrinol Metab 2008, 93:3117-3123.
-
(2008)
J Clin Endocrinol Metab
, vol.93
, pp. 3117-3123
-
-
Geller, D.S.1
Zhang, J.2
Wisgerhof, M.V.3
Shackleton, C.4
Kashgarian, M.5
Lifton, R.P.6
-
30
-
-
84863115868
-
Hypertension with or without adrenal hyperplasia due to different inherited mutations in the potassium channel KCNJ5
-
Scholl U.I., Nelson-Williams C., Yue P., Grekin R., Wyatt R.J., Dillon M.J., et al. Hypertension with or without adrenal hyperplasia due to different inherited mutations in the potassium channel KCNJ5. Proc Natl Acad Sci USA 2012, 109:2533-2538.
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, pp. 2533-2538
-
-
Scholl, U.I.1
Nelson-Williams, C.2
Yue, P.3
Grekin, R.4
Wyatt, R.J.5
Dillon, M.J.6
-
31
-
-
84856300896
-
KCNJ5 mutations in European families with nonglucocorticoid remediable familial hyperaldosteronism
-
Mulatero P., Tauber P., Zennaro M.C., Monticone S., Lang K., Beuschlein F., et al. KCNJ5 mutations in European families with nonglucocorticoid remediable familial hyperaldosteronism. Hypertension 2012, 59:235-240.
-
(2012)
Hypertension
, vol.59
, pp. 235-240
-
-
Mulatero, P.1
Tauber, P.2
Zennaro, M.C.3
Monticone, S.4
Lang, K.5
Beuschlein, F.6
-
32
-
-
84863696622
-
Polyuric-polydipsic syndrome in a pediatric case of non-glucocorticoid remediable familial hyperaldosteronism
-
Mussa A., VCamilla R., Monticone S., Porta F., Tessaris D., Verna F., et al. Polyuric-polydipsic syndrome in a pediatric case of non-glucocorticoid remediable familial hyperaldosteronism. Endocr J 2012, 59:497-502.
-
(2012)
Endocr J
, vol.59
, pp. 497-502
-
-
Mussa, A.1
VCamilla, R.2
Monticone, S.3
Porta, F.4
Tessaris, D.5
Verna, F.6
-
33
-
-
84864592834
-
A novel point mutation in the KCNJ5 gene causing primary hyperaldosteronism and early-onset autosomal dominant hypertension
-
Charmandari E., Sertedaki A., Kino T., Merakou C., Hoffman D.A., Hatch M.M., et al. A novel point mutation in the KCNJ5 gene causing primary hyperaldosteronism and early-onset autosomal dominant hypertension. J Clin Endocrinol Metab 2012, 97:E1532-9.
-
(2012)
J Clin Endocrinol Metab
, vol.97
-
-
Charmandari, E.1
Sertedaki, A.2
Kino, T.3
Merakou, C.4
Hoffman, D.A.5
Hatch, M.M.6
-
34
-
-
4544293557
-
Dopamine receptor expression and function in human normal adrenal gland and adrenal tumors
-
Pivonello R., Ferone D., de Herder W.W., de Krijger R.R., Waaijers M., Mooij D.M., et al. Dopamine receptor expression and function in human normal adrenal gland and adrenal tumors. J Clin Endocrinol Metab 2004, 89:4493-4502.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 4493-4502
-
-
Pivonello, R.1
Ferone, D.2
de Herder, W.W.3
de Krijger, R.R.4
Waaijers, M.5
Mooij, D.M.6
-
35
-
-
0026095840
-
The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization
-
Tannin G.M., Agarwal A.K., Monder C., New M.I., White P.C. The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization. J Biol Chem 1991, 266:16653-16658.
-
(1991)
J Biol Chem
, vol.266
, pp. 16653-16658
-
-
Tannin, G.M.1
Agarwal, A.K.2
Monder, C.3
New, M.I.4
White, P.C.5
-
36
-
-
0020698346
-
Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. A study of 25 patients
-
Zachmann M., Tassinari D., Prader A. Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. A study of 25 patients. J Clin Endocrinol Metab 1983, 56:222-229.
-
(1983)
J Clin Endocrinol Metab
, vol.56
, pp. 222-229
-
-
Zachmann, M.1
Tassinari, D.2
Prader, A.3
-
37
-
-
0020080763
-
Clinical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency
-
Rosler A., Leiberman E., Sack J., Landau H., Benderly A., Moses S.W., et al. Clinical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. Horm Res 1982, 16:133-141.
-
(1982)
Horm Res
, vol.16
, pp. 133-141
-
-
Rosler, A.1
Leiberman, E.2
Sack, J.3
Landau, H.4
Benderly, A.5
Moses, S.W.6
-
38
-
-
0034520495
-
Hormonal hypertension in children: 11beta-hydroxylase deficiency and apparent mineralocorticoid excess
-
Cerame B.I., New M.I. Hormonal hypertension in children: 11beta-hydroxylase deficiency and apparent mineralocorticoid excess. J Pediatr Endocrinol Metab 2000, 13:1537-1547.
-
(2000)
J Pediatr Endocrinol Metab
, vol.13
, pp. 1537-1547
-
-
Cerame, B.I.1
New, M.I.2
-
39
-
-
0034914294
-
Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11beta-hydroxylase) and CYP11B2(aldosterone synthase) cause steroid 11beta-hydroxylase deficiency and congenital adrenal hyperplasia
-
Portrat S., Mulatero P., Curnow K.M., Chaussain J.L., Morel Y., Pascoe L. Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11beta-hydroxylase) and CYP11B2(aldosterone synthase) cause steroid 11beta-hydroxylase deficiency and congenital adrenal hyperplasia. J Clin Endocrinol Metab 2001, 86:3197-3201.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 3197-3201
-
-
Portrat, S.1
Mulatero, P.2
Curnow, K.M.3
Chaussain, J.L.4
Morel, Y.5
Pascoe, L.6
-
41
-
-
0842291524
-
Two prevalent CYP17 mutations and genotype-phenotype correlations in 24 Brazilian patients with 17-hydroxylase deficiency
-
Costa-Santos M., Kater C.E., Auchus R.J. Two prevalent CYP17 mutations and genotype-phenotype correlations in 24 Brazilian patients with 17-hydroxylase deficiency. J Clin Endocrinol Metab 2004, 89:49-60.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 49-60
-
-
Costa-Santos, M.1
Kater, C.E.2
Auchus, R.J.3
-
42
-
-
0023943706
-
Structural characterization of normal and mutant human steroid 17 alpha-hydroxylase genes: molecular basis of one example of combined 17 alpha-hydroxylase/17,20 lyase deficiency
-
Kagimoto M., Winter J.S., Kagimoto K., Simpson E.R., Waterman M.R. Structural characterization of normal and mutant human steroid 17 alpha-hydroxylase genes: molecular basis of one example of combined 17 alpha-hydroxylase/17,20 lyase deficiency. Mol Endocrinol 1988, 2:564-570.
-
(1988)
Mol Endocrinol
, vol.2
, pp. 564-570
-
-
Kagimoto, M.1
Winter, J.S.2
Kagimoto, K.3
Simpson, E.R.4
Waterman, M.R.5
-
43
-
-
0031252385
-
The genetic and functional basis of isolated 17,20-lyase deficiency
-
Geller D.H., Auchus R.J., Mendonca B.B., Miller W.L. The genetic and functional basis of isolated 17,20-lyase deficiency. Nat Genet 1997, 17:201-205.
-
(1997)
Nat Genet
, vol.17
, pp. 201-205
-
-
Geller, D.H.1
Auchus, R.J.2
Mendonca, B.B.3
Miller, W.L.4
-
44
-
-
0017711792
-
Evidence for an unidentified steroid in a child with apparent mineralocorticoid hypertension
-
New M.I., Levine L.S., Biglieri E.G., VPareira J., Ulick S. Evidence for an unidentified steroid in a child with apparent mineralocorticoid hypertension. J Clin Endocrinol Metab 1977, 44:924-933.
-
(1977)
J Clin Endocrinol Metab
, vol.44
, pp. 924-933
-
-
New, M.I.1
Levine, L.S.2
Biglieri, E.G.3
VPareira, J.4
Ulick, S.5
-
45
-
-
0018598286
-
A syndrome of apparent mineralocorticoid excess associated with defects in the peripheral metabolism of cortisol
-
Ulick S., Levine L.S., Gunczler P., Zanconato G., Ramirez L.C., Rauh W., et al. A syndrome of apparent mineralocorticoid excess associated with defects in the peripheral metabolism of cortisol. J Clin Endocrinol Metab 1979, 49:757-764.
-
(1979)
J Clin Endocrinol Metab
, vol.49
, pp. 757-764
-
-
Ulick, S.1
Levine, L.S.2
Gunczler, P.3
Zanconato, G.4
Ramirez, L.C.5
Rauh, W.6
-
46
-
-
0023221667
-
Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor
-
Arriza J.L., Weinberger C., Cerelli G., Glaser T.M., Handelin B.L., Housman D.E., et al. Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor. Science 1987, 237:268-275.
-
(1987)
Science
, vol.237
, pp. 268-275
-
-
Arriza, J.L.1
Weinberger, C.2
Cerelli, G.3
Glaser, T.M.4
Handelin, B.L.5
Housman, D.E.6
-
47
-
-
2542624590
-
Renal mineralocorticoid receptors and hippocampal corticosterone-binding species have identical intrinsic steroid specificity
-
Krozowski Z.S., Funder J.W. Renal mineralocorticoid receptors and hippocampal corticosterone-binding species have identical intrinsic steroid specificity. Proc Natl Acad Sci USA 1983, 80:6056-6060.
-
(1983)
Proc Natl Acad Sci USA
, vol.80
, pp. 6056-6060
-
-
Krozowski, Z.S.1
Funder, J.W.2
-
48
-
-
0029160972
-
Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase
-
Mune T., Rogerson F.M., Nikkila H., Agarwal A.K., White P.C. Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase. Nat Genet 1995, 10:394-399.
-
(1995)
Nat Genet
, vol.10
, pp. 394-399
-
-
Mune, T.1
Rogerson, F.M.2
Nikkila, H.3
Agarwal, A.K.4
White, P.C.5
-
49
-
-
0033105754
-
Hypertension in mice lacking 11beta-hydroxysteroid dehydrogenase type 2
-
Kotelevtsev Y., Brown R.W., Fleming S., Kenyon C., Edwards C.R., Seckl J.R., et al. Hypertension in mice lacking 11beta-hydroxysteroid dehydrogenase type 2. J Clin Invest 1999, 103:683-689.
-
(1999)
J Clin Invest
, vol.103
, pp. 683-689
-
-
Kotelevtsev, Y.1
Brown, R.W.2
Fleming, S.3
Kenyon, C.4
Edwards, C.R.5
Seckl, J.R.6
-
50
-
-
0034745750
-
Congenital deficiency of 11beta-hydroxysteroid dehydrogenase (apparent mineralocorticoid excess syndrome): diagnostic value of urinary free cortisol and cortisone
-
Palermo M., Delitala G., Mantero F., Stewart P.M., Shackleton C.H. Congenital deficiency of 11beta-hydroxysteroid dehydrogenase (apparent mineralocorticoid excess syndrome): diagnostic value of urinary free cortisol and cortisone. J Endocrinol Invest 2001, 24:17-23.
-
(2001)
J Endocrinol Invest
, vol.24
, pp. 17-23
-
-
Palermo, M.1
Delitala, G.2
Mantero, F.3
Stewart, P.M.4
Shackleton, C.H.5
-
51
-
-
79957909024
-
Apparent mineralocorticoid excess: time of manifestation and complications despite treatment
-
Knops N.B., Monnens L.A., Lenders J.W., Levtchenko E.N. Apparent mineralocorticoid excess: time of manifestation and complications despite treatment. Pediatrics 2011, 127:e1610-e1614.
-
(2011)
Pediatrics
, vol.127
-
-
Knops, N.B.1
Monnens, L.A.2
Lenders, J.W.3
Levtchenko, E.N.4
-
52
-
-
0023242981
-
Mineralocorticoid activity of liquorice: 11-beta-hydroxysteroid dehydrogenase deficiency comes of age
-
Stewart P.M., Wallace A.M., Valentino R., Burt D., Shackleton C.H., Edwards C.R. Mineralocorticoid activity of liquorice: 11-beta-hydroxysteroid dehydrogenase deficiency comes of age. Lancet 1987, 2:821-824.
-
(1987)
Lancet
, vol.2
, pp. 821-824
-
-
Stewart, P.M.1
Wallace, A.M.2
Valentino, R.3
Burt, D.4
Shackleton, C.H.5
Edwards, C.R.6
-
53
-
-
84882865510
-
Pseudohypoaldosteronism Type 1 and Hypertension Exacerbated in Pregnancy
-
Elsevier, London, San Diego, New York, R.P. Lifton, S. Somlo, G.H. Giebisch, D.W. Seldin (Eds.)
-
Geller D.S. Pseudohypoaldosteronism Type 1 and Hypertension Exacerbated in Pregnancy. Genetic diseases of the kidney. burlingon 2009, 301-312. Elsevier, London, San Diego, New York. R.P. Lifton, S. Somlo, G.H. Giebisch, D.W. Seldin (Eds.).
-
(2009)
Genetic diseases of the kidney. burlingon
, pp. 301-312
-
-
Geller, D.S.1
-
54
-
-
0034617130
-
Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy
-
Geller D.S., Farhi A., Pinkerton N., Fradley M., Moritz M., Spitzer A., et al. Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy. Science 2000, 289:119-123.
-
(2000)
Science
, vol.289
, pp. 119-123
-
-
Geller, D.S.1
Farhi, A.2
Pinkerton, N.3
Fradley, M.4
Moritz, M.5
Spitzer, A.6
-
55
-
-
22444438401
-
Crystal structure of a mutant mineralocorticoid receptor responsible for hypertension
-
Fagart J., Huyet J., Pinon G.M., Rochel M., Mayer C., Rafestin-Oblin M.E. Crystal structure of a mutant mineralocorticoid receptor responsible for hypertension. Nat Struct Mol Biol 2005, 12:554-555.
-
(2005)
Nat Struct Mol Biol
, vol.12
, pp. 554-555
-
-
Fagart, J.1
Huyet, J.2
Pinon, G.M.3
Rochel, M.4
Mayer, C.5
Rafestin-Oblin, M.E.6
-
56
-
-
0001182641
-
A familial renal disorder stimulating primary aldosteronism but with negligible aldosterone secretion
-
Liddle G.W., Bledsoe T., Coppage W.S. A familial renal disorder stimulating primary aldosteronism but with negligible aldosterone secretion. Trans Assoc Am Physicians 1963, 76:199-213.
-
(1963)
Trans Assoc Am Physicians
, vol.76
, pp. 199-213
-
-
Liddle, G.W.1
Bledsoe, T.2
Coppage, W.S.3
-
57
-
-
0027946089
-
Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel
-
Shimkets R.A., Warnock D.G., Bositis C.M., Nelson-Williams C., Hansson J.H., Schambelan M., et al. Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel. Cell 1994, 79:407-414.
-
(1994)
Cell
, vol.79
, pp. 407-414
-
-
Shimkets, R.A.1
Warnock, D.G.2
Bositis, C.M.3
Nelson-Williams, C.4
Hansson, J.H.5
Schambelan, M.6
-
58
-
-
0029092801
-
Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome
-
Hansson J.H., Nelson-Williams C., Suzuki H., Schild L., Shimkets R., Lu Y., et al. Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome. Nat Genet 1995, 11:76-82.
-
(1995)
Nat Genet
, vol.11
, pp. 76-82
-
-
Hansson, J.H.1
Nelson-Williams, C.2
Suzuki, H.3
Schild, L.4
Shimkets, R.5
Lu, Y.6
-
60
-
-
0028252575
-
Membrane topology of the epithelial sodium channel in intact cells
-
Canessa C.M., Merillat A.M., Rossier B.C. Membrane topology of the epithelial sodium channel in intact cells. Am J Physiol 1994, 267:C1682-C1690.
-
(1994)
Am J Physiol
, vol.267
-
-
Canessa, C.M.1
Merillat, A.M.2
Rossier, B.C.3
-
61
-
-
0029586683
-
A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation of channel activity
-
Hansson J.H., Schild L., Lu Y., Wilson T.A., Gautschi I., Shimkets R., et al. A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation of channel activity. Proc Natl Acad Sci USA 1995, 92:11495-11499.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 11495-11499
-
-
Hansson, J.H.1
Schild, L.2
Lu, Y.3
Wilson, T.A.4
Gautschi, I.5
Shimkets, R.6
-
63
-
-
0029046975
-
A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system
-
Schild L., Canessa C.M., Shimkets R.A., Gautschi I., Lifton R.P., Rossier B.C. A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system. Proc Natl Acad Sci USA 1995, 92:5699-5703.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 5699-5703
-
-
Schild, L.1
Canessa, C.M.2
Shimkets, R.A.3
Gautschi, I.4
Lifton, R.P.5
Rossier, B.C.6
-
64
-
-
0030451774
-
Cell surface expression of the epithelial Na channel and a mutant causing Liddle syndrome: a quantitative approach
-
Firsov D., Schild L., Gautschi I., Merillat A.M., Schneeberger E., Rossier B.C. Cell surface expression of the epithelial Na channel and a mutant causing Liddle syndrome: a quantitative approach. Proc Natl Acad Sci USA 1996, 93:15370-15375.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 15370-15375
-
-
Firsov, D.1
Schild, L.2
Gautschi, I.3
Merillat, A.M.4
Schneeberger, E.5
Rossier, B.C.6
-
67
-
-
0036911032
-
Liddle's syndrome associated with a point mutation in the extracellular domain of the epithelial sodium channel gamma subunit
-
Hiltunen T.P., Hannila-Handelberg T., Petajaniemi N., Kantola I., Tikkanen I., Virtamo J., et al. Liddle's syndrome associated with a point mutation in the extracellular domain of the epithelial sodium channel gamma subunit. J Hypertens 2002, 20:2383-2390.
-
(2002)
J Hypertens
, vol.20
, pp. 2383-2390
-
-
Hiltunen, T.P.1
Hannila-Handelberg, T.2
Petajaniemi, N.3
Kantola, I.4
Tikkanen, I.5
Virtamo, J.6
-
68
-
-
0028154726
-
Brief report: liddle's syndrome revisited - a disorder of sodium reabsorption in the distal tubule
-
Botero-Velez M., Curtis J.J., Warnock D.G. Brief report: liddle's syndrome revisited - a disorder of sodium reabsorption in the distal tubule. N Engl J Med 1994, 330:178-181.
-
(1994)
N Engl J Med
, vol.330
, pp. 178-181
-
-
Botero-Velez, M.1
Curtis, J.J.2
Warnock, D.G.3
-
69
-
-
0032749231
-
A mouse model for Liddle's syndrome
-
Pradervand S., Wang Q., Burnier M., Beermann F., Horisberger J.D., Hummler E., et al. A mouse model for Liddle's syndrome. J Am Soc Nephrol 1999, 10:2527-2533.
-
(1999)
J Am Soc Nephrol
, vol.10
, pp. 2527-2533
-
-
Pradervand, S.1
Wang, Q.2
Burnier, M.3
Beermann, F.4
Horisberger, J.D.5
Hummler, E.6
-
70
-
-
75949143620
-
Hypertension and hyperpotassaemia without Renal disease in a young male
-
Paver W.K., Pauline G.J. Hypertension and hyperpotassaemia without Renal disease in a young male. Med J Aust 1964, 2:305-306.
-
(1964)
Med J Aust
, vol.2
, pp. 305-306
-
-
Paver, W.K.1
Pauline, G.J.2
-
71
-
-
84949312562
-
Familial hyperpotassemia and hypertension accompanied by normal plasma aldosterone levels: possible hereditary cell membrane defect
-
Farfel Z., Iaina A., Rosenthal T., Waks U., Shibolet S., Gafni J. Familial hyperpotassemia and hypertension accompanied by normal plasma aldosterone levels: possible hereditary cell membrane defect. Arch Intern Med 1978, 138:1828-1832.
-
(1978)
Arch Intern Med
, vol.138
, pp. 1828-1832
-
-
Farfel, Z.1
Iaina, A.2
Rosenthal, T.3
Waks, U.4
Shibolet, S.5
Gafni, J.6
-
72
-
-
0017121382
-
Familial hyperkalemia and hypertension
-
Farfel Z., Rosenthal T., Shibolet S., Iaina A., Gafni J. Familial hyperkalemia and hypertension. Harefuah 1976, 90:468-470.
-
(1976)
Harefuah
, vol.90
, pp. 468-470
-
-
Farfel, Z.1
Rosenthal, T.2
Shibolet, S.3
Iaina, A.4
Gafni, J.5
-
73
-
-
0018900933
-
Familial hyperkalaemia responsive to benzothiadiazine diuretic
-
Lee M.R., Morgan D.B. Familial hyperkalaemia responsive to benzothiadiazine diuretic. Lancet 1980, 1:879.
-
(1980)
Lancet
, vol.1
, pp. 879
-
-
Lee, M.R.1
Morgan, D.B.2
-
74
-
-
0019480065
-
Mineralocorticoid-resistant renal hyperkalemia without salt wasting (type II pseudohypoaldosteronism): role of increased renal chloride reabsorption
-
Schambelan M., Sebastian A., Rector F.C. Mineralocorticoid-resistant renal hyperkalemia without salt wasting (type II pseudohypoaldosteronism): role of increased renal chloride reabsorption. Kidney Int 1981, 19:716-727.
-
(1981)
Kidney Int
, vol.19
, pp. 716-727
-
-
Schambelan, M.1
Sebastian, A.2
Rector, F.C.3
-
75
-
-
17944373014
-
Human hypertension caused by mutations in WNK kinases
-
Wilson F.H., Disse-Nicodeme S., Choate K.A., Ishikawa K., Nelson-Williams C., Desitter I., et al. Human hypertension caused by mutations in WNK kinases. Science 2001, 293:1107-1112.
-
(2001)
Science
, vol.293
, pp. 1107-1112
-
-
Wilson, F.H.1
Disse-Nicodeme, S.2
Choate, K.A.3
Ishikawa, K.4
Nelson-Williams, C.5
Desitter, I.6
-
76
-
-
0037382807
-
WNK kinases regulate thiazide-sensitive Na-Cl co-transport
-
Yang C.L., Angell J., Mitchell R., Ellison D.H. WNK kinases regulate thiazide-sensitive Na-Cl co-transport. J Clin Invest 2003, 111:1039-1045.
-
(2003)
J Clin Invest
, vol.111
, pp. 1039-1045
-
-
Yang, C.L.1
Angell, J.2
Mitchell, R.3
Ellison, D.H.4
-
79
-
-
11144354175
-
Disease-causing mutant WNK4 increases paracellular chloride permeability and phosphorylates claudins
-
Yamauchi K., Rai T., Kobayashi K., Sohara E., Suzuki T., Itoh T., et al. Disease-causing mutant WNK4 increases paracellular chloride permeability and phosphorylates claudins. Proc Natl Acad Sci USA 2004, 101:4690-4694.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 4690-4694
-
-
Yamauchi, K.1
Rai, T.2
Kobayashi, K.3
Sohara, E.4
Suzuki, T.5
Itoh, T.6
-
80
-
-
33749118898
-
Wnk4 controls blood pressure and potassium homeostasis via regulation of mass and activity of the distal convoluted tubule
-
Lalioti M.D., Zhang J., Volkman H.M., Kahle K.T., Hoffmann K.E., Toka H.R., et al. Wnk4 controls blood pressure and potassium homeostasis via regulation of mass and activity of the distal convoluted tubule. Nat Genet 2006, 38:1124-1132.
-
(2006)
Nat Genet
, vol.38
, pp. 1124-1132
-
-
Lalioti, M.D.1
Zhang, J.2
Volkman, H.M.3
Kahle, K.T.4
Hoffmann, K.E.5
Toka, H.R.6
-
82
-
-
79953304695
-
The WNK kinase network regulating sodium, potassium, and blood pressure
-
Hoorn E.J., Nelson J.H., McCormick J.A., Ellison D.H. The WNK kinase network regulating sodium, potassium, and blood pressure. J Am Soc Nephrol 2011, 22:605-614.
-
(2011)
J Am Soc Nephrol
, vol.22
, pp. 605-614
-
-
Hoorn, E.J.1
Nelson, J.H.2
McCormick, J.A.3
Ellison, D.H.4
-
83
-
-
84882556519
-
The Syndrome of Hypertension and Hyperkalemia (Pseudohypoaldosteronism Type II): WNK Kinases regulate the balance between renal salt reabsorption and potassium secretion
-
Elsevier, Burlington, London, San Diego, New York, R.P. Lifton, S. Somlo, G. Giebisch, D.W. Seldin (Eds.)
-
Kahle K.T., Wilson F.H., Lifton R.P. The Syndrome of Hypertension and Hyperkalemia (Pseudohypoaldosteronism Type II): WNK Kinases regulate the balance between renal salt reabsorption and potassium secretion. Genetic diseases of the kidney 2009, 313-329. Elsevier, Burlington, London, San Diego, New York. R.P. Lifton, S. Somlo, G. Giebisch, D.W. Seldin (Eds.).
-
(2009)
Genetic diseases of the kidney
, pp. 313-329
-
-
Kahle, K.T.1
Wilson, F.H.2
Lifton, R.P.3
-
84
-
-
0037457965
-
Molecular pathogenesis of inherited hypertension with hyperkalemia: the Na-Cl co-transporter is inhibited by wild-type but not mutant WNK4
-
Wilson F.H., Kahle K.T., Sabath E., Lalioti M.D., Rapson A.K., Hoover R.S., et al. Molecular pathogenesis of inherited hypertension with hyperkalemia: the Na-Cl co-transporter is inhibited by wild-type but not mutant WNK4. Proc Natl Acad Sci USA 2003, 100:680-684.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 680-684
-
-
Wilson, F.H.1
Kahle, K.T.2
Sabath, E.3
Lalioti, M.D.4
Rapson, A.K.5
Hoover, R.S.6
-
85
-
-
67650533826
-
WNK4 diverts the thiazide-sensitive NaCl co-transporter to the lysosome and stimulates AP-3 interaction
-
Subramanya A.R., Liu J., Ellison D.H., Wade J.B., Welling P.A. WNK4 diverts the thiazide-sensitive NaCl co-transporter to the lysosome and stimulates AP-3 interaction. J Biol Chem 2009, 284:18471-18480.
-
(2009)
J Biol Chem
, vol.284
, pp. 18471-18480
-
-
Subramanya, A.R.1
Liu, J.2
Ellison, D.H.3
Wade, J.B.4
Welling, P.A.5
-
86
-
-
34147121186
-
-
He G, Wang HR, Huang SK, Huang CL. Intersectin links WNK kinases to endocytosis of ROMK1. J Clin Invest 2007;117:1078-87.
-
He G, Wang HR, Huang SK, Huang CL. Intersectin links WNK kinases to endocytosis of ROMK1. J Clin Invest 2007;117:1078-87.
-
-
-
-
89
-
-
31944441600
-
Antagonistic regulation of ROMK by long and kidney-specific WNK1 isoforms
-
Lazrak A., Liu Z., Huang C.L. Antagonistic regulation of ROMK by long and kidney-specific WNK1 isoforms. Proc Natl Acad Sci USA 2006, 103:1615-1620.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 1615-1620
-
-
Lazrak, A.1
Liu, Z.2
Huang, C.L.3
-
90
-
-
22544472397
-
WNK1 activates SGK1 to regulate the epithelial sodium channel
-
Xu B.E., Stippec S., Chu P.Y., Lazrak A., Li X.J., Lee B.H., et al. WNK1 activates SGK1 to regulate the epithelial sodium channel. Proc Natl Acad Sci USA 2005, 102:10315-10320.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 10315-10320
-
-
Xu, B.E.1
Stippec, S.2
Chu, P.Y.3
Lazrak, A.4
Li, X.J.5
Lee, B.H.6
-
91
-
-
33748430618
-
Overexpression of human WNK1 increases paracellular chloride permeability and phosphorylation of claudin-4 in MDCKII cells
-
Ohta A., Yang S.S., Rai T., Chiga M., Sasaki S., Uchida S. Overexpression of human WNK1 increases paracellular chloride permeability and phosphorylation of claudin-4 in MDCKII cells. Biochem Biophys Res Commun 2006, 349:804-808.
-
(2006)
Biochem Biophys Res Commun
, vol.349
, pp. 804-808
-
-
Ohta, A.1
Yang, S.S.2
Rai, T.3
Chiga, M.4
Sasaki, S.5
Uchida, S.6
-
92
-
-
63149133727
-
Angiotensin II signaling increases activity of the renal Na-Cl co-transporter through a WNK4-SPAK-dependent pathway
-
San-Cristobal P., Pacheco-Alvarez D., Richardson C., Ring A.M., Vazquez N., Rafiqi F.H., et al. Angiotensin II signaling increases activity of the renal Na-Cl co-transporter through a WNK4-SPAK-dependent pathway. Proc Natl Acad Sci USA 2009, 106:4384-4389.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 4384-4389
-
-
San-Cristobal, P.1
Pacheco-Alvarez, D.2
Richardson, C.3
Ring, A.M.4
Vazquez, N.5
Rafiqi, F.H.6
-
93
-
-
78751654853
-
The WNKs: atypical protein kinases with pleiotropic actions
-
McCormick J.A., Ellison D.H. The WNKs: atypical protein kinases with pleiotropic actions. Physiol Rev 2011, 91:177-219.
-
(2011)
Physiol Rev
, vol.91
, pp. 177-219
-
-
McCormick, J.A.1
Ellison, D.H.2
-
95
-
-
57449120881
-
Deletion of WNK1 first intron results in misregulation of both isoforms in renal and extrarenal tissues
-
Delaloy C., Elvira-Matelot E., Clemessy M., Zhou X.O., Imbert-Teboul M., Houot A.M., et al. Deletion of WNK1 first intron results in misregulation of both isoforms in renal and extrarenal tissues. Hypertension 2008, 52:1149-1154.
-
(2008)
Hypertension
, vol.52
, pp. 1149-1154
-
-
Delaloy, C.1
Elvira-Matelot, E.2
Clemessy, M.3
Zhou, X.O.4
Imbert-Teboul, M.5
Houot, A.M.6
-
96
-
-
84856431125
-
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
-
Boyden L.M., Choi M., Choate K.A., Nelson-Williams C.J., Farhi A., Toka H.R., et al. Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities. Nature 2012, 482:98-102.
-
(2012)
Nature
, vol.482
, pp. 98-102
-
-
Boyden, L.M.1
Choi, M.2
Choate, K.A.3
Nelson-Williams, C.J.4
Farhi, A.5
Toka, H.R.6
-
97
-
-
84859425383
-
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron
-
Louis-Dit-Picard H., Barc J., Trujillano D., Miserey-Lenkei S., Bouatia-Naji N., Pylypenko O., et al. KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron. Nat Genet 2012, 44:456-460.
-
(2012)
Nat Genet
, vol.44
, pp. 456-460
-
-
Louis-Dit-Picard, H.1
Barc, J.2
Trujillano, D.3
Miserey-Lenkei, S.4
Bouatia-Naji, N.5
Pylypenko, O.6
-
98
-
-
0031279143
-
Hereditary defect in biosynthesis of aldosterone: aldosterone synthase deficiency 1964-1997
-
Peter M., Fawaz L., Drop S.L., Visser H.K., Sippell W.G. Hereditary defect in biosynthesis of aldosterone: aldosterone synthase deficiency 1964-1997. J Clin Endocrinol Metab 1997, 82:3525-3528.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3525-3528
-
-
Peter, M.1
Fawaz, L.2
Drop, S.L.3
Visser, H.K.4
Sippell, W.G.5
-
99
-
-
0344823584
-
An aldosterone biosynthetic defect in a salt-losing disorder
-
Ulick S., Gautier E., Vetter K.K., Markello J.R., Yaffe S., Lowe C.U. An aldosterone biosynthetic defect in a salt-losing disorder. J Clin Endocrinol Metab 1964, 24:669-672.
-
(1964)
J Clin Endocrinol Metab
, vol.24
, pp. 669-672
-
-
Ulick, S.1
Gautier, E.2
Vetter, K.K.3
Markello, J.R.4
Yaffe, S.5
Lowe, C.U.6
-
100
-
-
0026771282
-
Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency
-
Pascoe L., Curnow K.M., Slutsker L., Rosler A., White P.C. Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency. Proc Natl Acad Sci USA 1992, 89:4996-5000.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 4996-5000
-
-
Pascoe, L.1
Curnow, K.M.2
Slutsker, L.3
Rosler, A.4
White, P.C.5
-
101
-
-
0027218610
-
Congenitally defective aldosterone biosynthesis in humans: inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients
-
Mitsuuchi Y., Kawamoto T., Miyahara K., Ulick S., Morton D.H., Naiki Y., et al. Congenitally defective aldosterone biosynthesis in humans: inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients. Biochem Biophys Res Commun 1993, 190:864-869.
-
(1993)
Biochem Biophys Res Commun
, vol.190
, pp. 864-869
-
-
Mitsuuchi, Y.1
Kawamoto, T.2
Miyahara, K.3
Ulick, S.4
Morton, D.H.5
Naiki, Y.6
-
102
-
-
0035185578
-
Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene
-
Kayes-Wandover K.M., Tannin G.M., Shulman D., Peled D., Jones K.L., Karaviti L., et al. Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene. J Clin Endocrinol Metab 2001, 86:5379-5382.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 5379-5382
-
-
Kayes-Wandover, K.M.1
Tannin, G.M.2
Shulman, D.3
Peled, D.4
Jones, K.L.5
Karaviti, L.6
-
103
-
-
3142610292
-
HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation
-
White P.C., New M.I., Dupont B. HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation. Proc Natl Acad Sci USA 1984, 81:7505-7509.
-
(1984)
Proc Natl Acad Sci USA
, vol.81
, pp. 7505-7509
-
-
White, P.C.1
New, M.I.2
Dupont, B.3
-
104
-
-
0001502287
-
The adrenogenital syndrome
-
contd
-
Bongiovanni A.M., Root A.W. The adrenogenital syndrome. N Engl J Med 1963, 268:1283-1289. contd.
-
(1963)
N Engl J Med
, vol.268
, pp. 1283-1289
-
-
Bongiovanni, A.M.1
Root, A.W.2
-
105
-
-
0042901202
-
Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene
-
Higashi Y., Yoshioka H., Yamane M., Gotoh O., Fujii-Kuriyama Y. Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene. Proc Natl Acad Sci USA 1986, 83:2841-2845.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 2841-2845
-
-
Higashi, Y.1
Yoshioka, H.2
Yamane, M.3
Gotoh, O.4
Fujii-Kuriyama, Y.5
-
106
-
-
77956588420
-
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline
-
Speiser P.W., Azziz R., Baskin L.S., Ghizzoni L., Hensle T.W., Merke D.P., et al. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab 2010, 95:4133-4160.
-
(2010)
J Clin Endocrinol Metab
, vol.95
, pp. 4133-4160
-
-
Speiser, P.W.1
Azziz, R.2
Baskin, L.S.3
Ghizzoni, L.4
Hensle, T.W.5
Merke, D.P.6
-
107
-
-
0026893712
-
Congenital adrenal hyperplasia due to point mutations in the type II 3 beta-hydroxysteroid dehydrogenase gene
-
Rheaume E., Simard J., Morel Y., Mebarki F., Zachmann M., Forest M.G., et al. Congenital adrenal hyperplasia due to point mutations in the type II 3 beta-hydroxysteroid dehydrogenase gene. Nat Genet 1992, 1:239-245.
-
(1992)
Nat Genet
, vol.1
, pp. 239-245
-
-
Rheaume, E.1
Simard, J.2
Morel, Y.3
Mebarki, F.4
Zachmann, M.5
Forest, M.G.6
-
108
-
-
0028944669
-
-
3rd, Clark BJ, Stocco DM, Saenger P, et al. Role of steroidogenic acute regulatory protein in adrenal and gonadal steroidogenesis.
-
Lin D, Sugawara T, Strauss JF 3rd, Clark BJ, Stocco DM, Saenger P, et al. Role of steroidogenic acute regulatory protein in adrenal and gonadal steroidogenesis. Science 1995; 267:1828-31.
-
(1995)
Science
, vol.267
, pp. 1828-31
-
-
Lin, D.1
Sugawara, T.2
Strauss, J.F.3
-
109
-
-
0001601125
-
A salt wasting syndrome in infancy
-
Cheek D.B., Perry J.W. A salt wasting syndrome in infancy. Arch Dis Child 1958, 33:252-256.
-
(1958)
Arch Dis Child
, vol.33
, pp. 252-256
-
-
Cheek, D.B.1
Perry, J.W.2
-
110
-
-
0028143993
-
Pseudohypoaldosteronism with increased sweat and saliva electrolyte values and frequent lower respiratory tract infections mimicking cystic fibrosis
-
Hanukoglu A., Bistritzer T., Rakover Y., Mandelberg A. Pseudohypoaldosteronism with increased sweat and saliva electrolyte values and frequent lower respiratory tract infections mimicking cystic fibrosis. J Pediatr 1994, 125:752-755.
-
(1994)
J Pediatr
, vol.125
, pp. 752-755
-
-
Hanukoglu, A.1
Bistritzer, T.2
Rakover, Y.3
Mandelberg, A.4
-
111
-
-
0033565228
-
Pulmonary epithelial sodium-channel dysfunction and excess airway liquid in pseudohypoaldosteronism
-
Kerem E., Bistritzer T., Hanukoglu A., Hofmann T., Zhou Z., Bennett W., et al. Pulmonary epithelial sodium-channel dysfunction and excess airway liquid in pseudohypoaldosteronism. N Engl J Med 1999, 341:156-162.
-
(1999)
N Engl J Med
, vol.341
, pp. 156-162
-
-
Kerem, E.1
Bistritzer, T.2
Hanukoglu, A.3
Hofmann, T.4
Zhou, Z.5
Bennett, W.6
-
112
-
-
13344295074
-
Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1
-
Chang S.S., Grunder S., Hanukoglu A., Rosler A., Mathew P.M., Hanukoglu I., et al. Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1. Nat Genet 1996, 12:248-253.
-
(1996)
Nat Genet
, vol.12
, pp. 248-253
-
-
Chang, S.S.1
Grunder, S.2
Hanukoglu, A.3
Rosler, A.4
Mathew, P.M.5
Hanukoglu, I.6
-
113
-
-
0030068042
-
A novel splice-site mutation in the gamma subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families
-
Strautnieks S.S., Thompson R.J., Gardiner R.M., Chung E. A novel splice-site mutation in the gamma subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families. Nat Genet 1996, 13:248-250.
-
(1996)
Nat Genet
, vol.13
, pp. 248-250
-
-
Strautnieks, S.S.1
Thompson, R.J.2
Gardiner, R.M.3
Chung, E.4
-
115
-
-
0032531425
-
Role of gammaENaC subunit in lung liquid clearance and electrolyte balance in newborn mice. Insights into perinatal adaptation and pseudohypoaldosteronism
-
Barker P.M., Nguyen M.S., Gatzy J.T., Grubb B., Norman H., Hummler E., et al. Role of gammaENaC subunit in lung liquid clearance and electrolyte balance in newborn mice. Insights into perinatal adaptation and pseudohypoaldosteronism. J Clin Invest 1998, 102:1634-1640.
-
(1998)
J Clin Invest
, vol.102
, pp. 1634-1640
-
-
Barker, P.M.1
Nguyen, M.S.2
Gatzy, J.T.3
Grubb, B.4
Norman, H.5
Hummler, E.6
-
116
-
-
12644300654
-
A mouse model for the renal salt-wasting syndrome pseudohypoaldosteronism
-
Hummler E., Barker P., Talbot C., Wang Q., Verdumo C., Grubb B., et al. A mouse model for the renal salt-wasting syndrome pseudohypoaldosteronism. Proc Natl Acad Sci USA 1997, 94:11710-11715.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 11710-11715
-
-
Hummler, E.1
Barker, P.2
Talbot, C.3
Wang, Q.4
Verdumo, C.5
Grubb, B.6
-
117
-
-
0029935712
-
Early death due to defective neonatal lung liquid clearance in alpha-ENaC-deficient mice
-
Hummler E., Barker P., Gatzy J., Beermann F., Verdumo C., Schmidt A., et al. Early death due to defective neonatal lung liquid clearance in alpha-ENaC-deficient mice. Nat Genet 1996, 12:325-328.
-
(1996)
Nat Genet
, vol.12
, pp. 325-328
-
-
Hummler, E.1
Barker, P.2
Gatzy, J.3
Beermann, F.4
Verdumo, C.5
Schmidt, A.6
-
118
-
-
82455206354
-
Unimpaired postnatal respiratory adaptation in a preterm human infant with a homozygous ENaC-alpha unit loss-of-function mutation
-
Huppmann S., Lankes E., Schnabel D., Buhrer C. Unimpaired postnatal respiratory adaptation in a preterm human infant with a homozygous ENaC-alpha unit loss-of-function mutation. J Perinatol 2011, 31:802-803.
-
(2011)
J Perinatol
, vol.31
, pp. 802-803
-
-
Huppmann, S.1
Lankes, E.2
Schnabel, D.3
Buhrer, C.4
-
119
-
-
0031861245
-
Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I
-
Geller D.S., Rodriguez-Soriano J., Vallo Boado A., Schifter S., Bayer M., Chang S.S., et al. Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I. Nat Genet 1998, 19:279-281.
-
(1998)
Nat Genet
, vol.19
, pp. 279-281
-
-
Geller, D.S.1
Rodriguez-Soriano, J.2
Vallo Boado, A.3
Schifter, S.4
Bayer, M.5
Chang, S.S.6
-
120
-
-
33646357245
-
Autosomal dominant pseudohypoaldosteronism type 1: mechanisms, evidence for neonatal lethality, and phenotypic expression in adults
-
Geller D.S., Zhang J., Zennaro M.C., Vallo-Boado A., Rodriguez-Soriano J., Furu L., et al. Autosomal dominant pseudohypoaldosteronism type 1: mechanisms, evidence for neonatal lethality, and phenotypic expression in adults. J Am Soc Nephrol 2006, 17:1429-1436.
-
(2006)
J Am Soc Nephrol
, vol.17
, pp. 1429-1436
-
-
Geller, D.S.1
Zhang, J.2
Zennaro, M.C.3
Vallo-Boado, A.4
Rodriguez-Soriano, J.5
Furu, L.6
-
121
-
-
80555134763
-
Mineralocorticoid receptor mutations and a severe recessive pseudohypoaldosteronism type 1
-
Hubert E.L., Teissier R., Fernandes-Rosa F.L., Fay M., Rafestin-Oblin M.E., Jeunemaitre X., et al. Mineralocorticoid receptor mutations and a severe recessive pseudohypoaldosteronism type 1. J Am Soc Nephrol 2011, 22:1997-2003.
-
(2011)
J Am Soc Nephrol
, vol.22
, pp. 1997-2003
-
-
Hubert, E.L.1
Teissier, R.2
Fernandes-Rosa, F.L.3
Fay, M.4
Rafestin-Oblin, M.E.5
Jeunemaitre, X.6
-
123
-
-
0032814854
-
Rescue of the mineralocorticoid receptor knock-out mouse
-
Bleich M., Warth R., Schmidt-Hieber M., Schulz-Baldes A., Hasselblatt P., Fisch D., et al. Rescue of the mineralocorticoid receptor knock-out mouse. Pflugers Arch 1999, 438:245-254.
-
(1999)
Pflugers Arch
, vol.438
, pp. 245-254
-
-
Bleich, M.1
Warth, R.2
Schmidt-Hieber, M.3
Schulz-Baldes, A.4
Hasselblatt, P.5
Fisch, D.6
-
124
-
-
50849151835
-
Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome
-
Bartter F.C., Pronove P., Gill J.R., Maccardle R.C. Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome. Am J Med 1962, 33:811-828.
-
(1962)
Am J Med
, vol.33
, pp. 811-828
-
-
Bartter, F.C.1
Pronove, P.2
Gill, J.R.3
Maccardle, R.C.4
-
126
-
-
0018772568
-
Growth characteristics in patients with Bartter's syndrome
-
Simopoulos A.P. Growth characteristics in patients with Bartter's syndrome. Nephron 1979, 23:130-135.
-
(1979)
Nephron
, vol.23
, pp. 130-135
-
-
Simopoulos, A.P.1
-
127
-
-
0024411986
-
Hypercalciuric Bartter syndrome: resolution of nephrocalcinosis with indomethacin
-
Matsumoto J., Han B.K., Restrepo de Rovetto C., Welch T.R. Hypercalciuric Bartter syndrome: resolution of nephrocalcinosis with indomethacin. AJR Am J Roentgenol 1989, 152:1251-1253.
-
(1989)
AJR Am J Roentgenol
, vol.152
, pp. 1251-1253
-
-
Matsumoto, J.1
Han, B.K.2
Restrepo de Rovetto, C.3
Welch, T.R.4
-
128
-
-
0028787681
-
Infantile variant of Bartter syndrome and sensorineural deafness: a new autosomal recessive disorder
-
Landau D., Shalev H., Ohaly M., Carmi R. Infantile variant of Bartter syndrome and sensorineural deafness: a new autosomal recessive disorder. Am J Med Genet 1995, 59:454-459.
-
(1995)
Am J Med Genet
, vol.59
, pp. 454-459
-
-
Landau, D.1
Shalev, H.2
Ohaly, M.3
Carmi, R.4
-
129
-
-
0015576864
-
Studies on the site of renal salt loss in a patient with Bartter's syndrome
-
Chaimovitz C., Levi J., Better O.S., Oslander L., Benderli A. Studies on the site of renal salt loss in a patient with Bartter's syndrome. Pediatr Res 1973, 7:89-94.
-
(1973)
Pediatr Res
, vol.7
, pp. 89-94
-
-
Chaimovitz, C.1
Levi, J.2
Better, O.S.3
Oslander, L.4
Benderli, A.5
-
130
-
-
0017319455
-
Role of prostaglandins in the pathogenesis of Bartter's syndrome
-
Fichman M.P., Telfer N., Zia P., Speckart P., Golub M., Rude R. Role of prostaglandins in the pathogenesis of Bartter's syndrome. Am J Med 1976, 60:785-797.
-
(1976)
Am J Med
, vol.60
, pp. 785-797
-
-
Fichman, M.P.1
Telfer, N.2
Zia, P.3
Speckart, P.4
Golub, M.5
Rude, R.6
-
131
-
-
0017286809
-
Bartter's syndrome with hyperplasia of renomedullary cells: successful treatment with indomethacin
-
Verberckmoes R., van Damme B.B., Clement J., Amery A., Michielsen P. Bartter's syndrome with hyperplasia of renomedullary cells: successful treatment with indomethacin. Kidney Int 1976, 9:302-307.
-
(1976)
Kidney Int
, vol.9
, pp. 302-307
-
-
Verberckmoes, R.1
van Damme, B.B.2
Clement, J.3
Amery, A.4
Michielsen, P.5
-
132
-
-
0017134973
-
Bartter's syndrome: a disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis
-
Gill J.R., Frolich J.C., Bowden R.E., Taylor A.A., Keiser H.R., Seyberth H.W., et al. Bartter's syndrome: a disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis. Am J Med 1976, 61:43-51.
-
(1976)
Am J Med
, vol.61
, pp. 43-51
-
-
Gill, J.R.1
Frolich, J.C.2
Bowden, R.E.3
Taylor, A.A.4
Keiser, H.R.5
Seyberth, H.W.6
-
133
-
-
0030032699
-
Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl co-transporter NKCC2
-
Simon D.B., Karet F.E., Hamdan J.M., DiPietro A., Sanjad S.A., Lifton R.P. Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl co-transporter NKCC2. Nat Genet 1996, 13:183-188.
-
(1996)
Nat Genet
, vol.13
, pp. 183-188
-
-
Simon, D.B.1
Karet, F.E.2
Hamdan, J.M.3
DiPietro, A.4
Sanjad, S.A.5
Lifton, R.P.6
-
134
-
-
0034625084
-
Uncompensated polyuria in a mouse model of Bartter's syndrome
-
Takahashi N., Chernavvsky D.R., Gomez R.A., Igarashi P., Gitelman H.J., Smithies O. Uncompensated polyuria in a mouse model of Bartter's syndrome. Proc Natl Acad Sci USA 2000, 97:5434-5439.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 5434-5439
-
-
Takahashi, N.1
Chernavvsky, D.R.2
Gomez, R.A.3
Igarashi, P.4
Gitelman, H.J.5
Smithies, O.6
-
135
-
-
0029794875
-
+ channel, ROMK
-
+ channel, ROMK. Nat Genet 1996, 14:152-156.
-
(1996)
Nat Genet
, vol.14
, pp. 152-156
-
-
Simon, D.B.1
Karet, F.E.2
Rodriguez-Soriano, J.3
Hamdan, J.H.4
DiPietro, A.5
Trachtman, H.6
-
136
-
-
0029095609
-
An ATP-regulated, inwardly rectifying potassium channel from rat kidney (ROMK)
-
Hebert S.C. An ATP-regulated, inwardly rectifying potassium channel from rat kidney (ROMK). Kidney Int 1995, 48:1010-1016.
-
(1995)
Kidney Int
, vol.48
, pp. 1010-1016
-
-
Hebert, S.C.1
-
137
-
-
0029133210
-
Renal potassium channels: an overview
-
Giebisch G. Renal potassium channels: an overview. Kidney Int 1995, 48:1004-1009.
-
(1995)
Kidney Int
, vol.48
, pp. 1004-1009
-
-
Giebisch, G.1
-
138
-
-
0037082531
-
Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies
-
Peters M., Jeck N., Reinalter S., Leonhardt A., Tonshoff B., Klaus G.G., et al. Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies. Am J Med 2002, 112:183-190.
-
(2002)
Am J Med
, vol.112
, pp. 183-190
-
-
Peters, M.1
Jeck, N.2
Reinalter, S.3
Leonhardt, A.4
Tonshoff, B.5
Klaus, G.G.6
-
139
-
-
0037339228
-
Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome
-
Finer G., Shalev H., Birk O.S., Galron D., Jeck N., Sinai-Treiman L., et al. Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome. J Pediatr 2003, 142:318-323.
-
(2003)
J Pediatr
, vol.142
, pp. 318-323
-
-
Finer, G.1
Shalev, H.2
Birk, O.S.3
Galron, D.4
Jeck, N.5
Sinai-Treiman, L.6
-
140
-
-
0028012361
-
Postnatal maturation of potassium transport in rabbit cortical collecting duct
-
Satlin L.M. Postnatal maturation of potassium transport in rabbit cortical collecting duct. Am J Physiol 1994, 266:F57-F65.
-
(1994)
Am J Physiol
, vol.266
-
-
Satlin, L.M.1
-
141
-
-
0030779090
-
+ conductance in maturing rabbit principal cell
-
+ conductance in maturing rabbit principal cell. Am J Physiol 1997, 272:F397-F404.
-
(1997)
Am J Physiol
, vol.272
-
-
Satlin, L.M.1
Palmer, L.G.2
-
142
-
-
0037020096
-
Impaired renal NaCl absorption in mice lacking the ROMK potassium channel, a model for type II Bartter's syndrome
-
Lorenz J.N., Baird N.R., Judd L.M., Noonan W.T., Andringa A., Doetschman T., et al. Impaired renal NaCl absorption in mice lacking the ROMK potassium channel, a model for type II Bartter's syndrome. J Biol Chem 2002, 277:37871-37880.
-
(2002)
J Biol Chem
, vol.277
, pp. 37871-37880
-
-
Lorenz, J.N.1
Baird, N.R.2
Judd, L.M.3
Noonan, W.T.4
Andringa, A.5
Doetschman, T.6
-
143
-
-
16944366243
-
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
-
Simon D.B., Bindra R.S., Mansfield T.A., Nelson-Williams C., Mendonca E., Stone R., et al. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III. Nat Genet 1997, 17:171-178.
-
(1997)
Nat Genet
, vol.17
, pp. 171-178
-
-
Simon, D.B.1
Bindra, R.S.2
Mansfield, T.A.3
Nelson-Williams, C.4
Mendonca, E.5
Stone, R.6
-
144
-
-
0030851745
-
Localization and induction by dehydration of ClC-K chloride channels in the rat kidney
-
Vandewalle A., Cluzeaud F., Bens M., Kieferle S., Steinmeyer K., Jentsch T.J. Localization and induction by dehydration of ClC-K chloride channels in the rat kidney. Am J Physiol 1997, 272:F678-F688.
-
(1997)
Am J Physiol
, vol.272
-
-
Vandewalle, A.1
Cluzeaud, F.2
Bens, M.3
Kieferle, S.4
Steinmeyer, K.5
Jentsch, T.J.6
-
145
-
-
0028292022
-
Two isoforms of a chloride channel predominantly expressed in thick ascending limb of Henle's loop and collecting ducts of rat kidney
-
Adachi S., Uchida S., Ito H., Hata M., Hiroe M., Marumo F., et al. Two isoforms of a chloride channel predominantly expressed in thick ascending limb of Henle's loop and collecting ducts of rat kidney. J Biol Chem 1994, 269:17677-17683.
-
(1994)
J Biol Chem
, vol.269
, pp. 17677-17683
-
-
Adachi, S.1
Uchida, S.2
Ito, H.3
Hata, M.4
Hiroe, M.5
Marumo, F.6
-
146
-
-
0028360729
-
Two highly homologous members of the ClC chloride channel family in both rat and human kidney
-
Kieferle S., Fong P., Bens M., Vandewalle A., Jentsch T.J. Two highly homologous members of the ClC chloride channel family in both rat and human kidney. Proc Natl Acad Sci USA 1994, 91:6943-6947.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 6943-6947
-
-
Kieferle, S.1
Fong, P.2
Bens, M.3
Vandewalle, A.4
Jentsch, T.J.5
-
147
-
-
0033667558
-
Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype
-
Jeck N., Konrad M., Peters M., Weber S., Bonzel K.E., Seyberth H.W. Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype. Pediatr Res 2000, 48:754-758.
-
(2000)
Pediatr Res
, vol.48
, pp. 754-758
-
-
Jeck, N.1
Konrad, M.2
Peters, M.3
Weber, S.4
Bonzel, K.E.5
Seyberth, H.W.6
-
148
-
-
0031937693
-
Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome
-
Brennan T.M., Landau D., Shalev H., Lamb F., Schutte B.C., Walder R.Y., et al. Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome. Am J Hum Genet 1998, 62:355-361.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 355-361
-
-
Brennan, T.M.1
Landau, D.2
Shalev, H.3
Lamb, F.4
Schutte, B.C.5
Walder, R.Y.6
-
149
-
-
0035189356
-
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
-
Birkenhager R., Otto E., Schurmann M.J., Vollmer M., Ruf E.M., Maier-Lutz I., et al. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. Nat Genet 2001, 29:310-314.
-
(2001)
Nat Genet
, vol.29
, pp. 310-314
-
-
Birkenhager, R.1
Otto, E.2
Schurmann, M.J.3
Vollmer, M.4
Ruf, E.M.5
Maier-Lutz, I.6
-
151
-
-
1642366722
-
Salt wasting and deafness resulting from mutations in two chloride channels
-
Schlingmann K.P., Konrad M., Jeck N., Waldegger P., Reinalter S.C., Holder M., et al. Salt wasting and deafness resulting from mutations in two chloride channels. N Engl J Med 2004, 350:1314-1319.
-
(2004)
N Engl J Med
, vol.350
, pp. 1314-1319
-
-
Schlingmann, K.P.1
Konrad, M.2
Jeck, N.3
Waldegger, P.4
Reinalter, S.C.5
Holder, M.6
-
152
-
-
40649112131
-
Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness
-
Nozu K., Inagaki T., Fu X.J., Nozu Y., Kaito H., Kanda K., et al. Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness. J Med Genet 2008, 45:182-186.
-
(2008)
J Med Genet
, vol.45
, pp. 182-186
-
-
Nozu, K.1
Inagaki, T.2
Fu, X.J.3
Nozu, Y.4
Kaito, H.5
Kanda, K.6
-
153
-
-
0032947011
-
Overt nephrogenic diabetes insipidus in mice lacking the CLC-K1 chloride channel
-
Matsumura Y., Uchida S., Kondo Y., Miyazaki H., Ko S.B., Hayama A., et al. Overt nephrogenic diabetes insipidus in mice lacking the CLC-K1 chloride channel. Nat Genet 1999, 21:95-98.
-
(1999)
Nat Genet
, vol.21
, pp. 95-98
-
-
Matsumura, Y.1
Uchida, S.2
Kondo, Y.3
Miyazaki, H.4
Ko, S.B.5
Hayama, A.6
-
155
-
-
10144256536
-
A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor
-
Pearce S.H., Williamson C., Kifor O., Bai M., Coulthard M.G., Davies M., et al. A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor. N Engl J Med 1996, 335:1115-1122.
-
(1996)
N Engl J Med
, vol.335
, pp. 1115-1122
-
-
Pearce, S.H.1
Williamson, C.2
Kifor, O.3
Bai, M.4
Coulthard, M.G.5
Davies, M.6
-
156
-
-
0036707879
-
Functional characterization of a calcium-sensing receptor mutation in severe autosomal dominant hypocalcemia with a Bartter-like syndrome
-
Vargas-Poussou R., Huang C., Hulin P., Houillier P., Jeunemaitre X., Paillard M., et al. Functional characterization of a calcium-sensing receptor mutation in severe autosomal dominant hypocalcemia with a Bartter-like syndrome. J Am Soc Nephrol 2002, 13:2259-2266.
-
(2002)
J Am Soc Nephrol
, vol.13
, pp. 2259-2266
-
-
Vargas-Poussou, R.1
Huang, C.2
Hulin, P.3
Houillier, P.4
Jeunemaitre, X.5
Paillard, M.6
-
157
-
-
0037206034
-
Association between activating mutations of calcium-sensing receptor and Bartter's syndrome
-
Watanabe S., Fukumoto S., Chang H., Takeuchi Y., Hasegawa Y., Okazaki R., et al. Association between activating mutations of calcium-sensing receptor and Bartter's syndrome. Lancet 2002, 360:692-694.
-
(2002)
Lancet
, vol.360
, pp. 692-694
-
-
Watanabe, S.1
Fukumoto, S.2
Chang, H.3
Takeuchi, Y.4
Hasegawa, Y.5
Okazaki, R.6
-
159
-
-
0023588270
-
Role of prostaglandins in hyperprostaglandin E syndrome and in selected renal tubular disorders
-
Seyberth H.W., Koniger S.J., Rascher W., Kuhl P.G., Schweer H. Role of prostaglandins in hyperprostaglandin E syndrome and in selected renal tubular disorders. Pediatr Nephrol 1987, 1:491-497.
-
(1987)
Pediatr Nephrol
, vol.1
, pp. 491-497
-
-
Seyberth, H.W.1
Koniger, S.J.2
Rascher, W.3
Kuhl, P.G.4
Schweer, H.5
-
160
-
-
21344446137
-
A founder mutation in the CLCNKB gene causes bartter syndrome type III in Spain
-
Rodriguez-Soriano J., Vallo A., Perez de Nanclares G., Bilbao J.R., Castano L. A founder mutation in the CLCNKB gene causes bartter syndrome type III in Spain. Pediatr Nephrol 2005, 20:891-896.
-
(2005)
Pediatr Nephrol
, vol.20
, pp. 891-896
-
-
Rodriguez-Soriano, J.1
Vallo, A.2
Perez de Nanclares, G.3
Bilbao, J.R.4
Castano, L.5
-
161
-
-
0036318596
-
Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome
-
Reinalter S.C., Jeck N., Brochhausen C., Watzer B., Nusing R.M., Seyberth H.W., et al. Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome. Kidney Int 2002, 62:253-260.
-
(2002)
Kidney Int
, vol.62
, pp. 253-260
-
-
Reinalter, S.C.1
Jeck, N.2
Brochhausen, C.3
Watzer, B.4
Nusing, R.M.5
Seyberth, H.W.6
-
162
-
-
33645108887
-
Option of pre-emptive nephrectomy and renal transplantation for Bartter's syndrome
-
Chaudhuri A., Salvatierra O., Alexander S.R., Sarwal M.M. Option of pre-emptive nephrectomy and renal transplantation for Bartter's syndrome. Pediatr Transplant 2006, 10:266-270.
-
(2006)
Pediatr Transplant
, vol.10
, pp. 266-270
-
-
Chaudhuri, A.1
Salvatierra, O.2
Alexander, S.R.3
Sarwal, M.M.4
-
164
-
-
0026512508
-
Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: bartter and Gitelman syndromes
-
Bettinelli A., Bianchetti M.G., Girardin E., Caringella A., Cecconi M., Appiani A.C., et al. Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: bartter and Gitelman syndromes. J Pediatr 1992, 120:38-43.
-
(1992)
J Pediatr
, vol.120
, pp. 38-43
-
-
Bettinelli, A.1
Bianchetti, M.G.2
Girardin, E.3
Caringella, A.4
Cecconi, M.5
Appiani, A.C.6
-
165
-
-
0026482217
-
Bartter's syndrome: evidence suggesting a distal tubular defect in a hypocalciuric variant of the syndrome
-
Sutton R.A., Mavichak V., Halabe A., Wilkins G.E. Bartter's syndrome: evidence suggesting a distal tubular defect in a hypocalciuric variant of the syndrome. Miner Electrolyte Metab 1992, 18:43-51.
-
(1992)
Miner Electrolyte Metab
, vol.18
, pp. 43-51
-
-
Sutton, R.A.1
Mavichak, V.2
Halabe, A.3
Wilkins, G.E.4
-
166
-
-
0028201013
-
Molecular cloning, primary structure, and characterization of two members of the mammalian electroneutral sodium-(potassium)-chloride co-transporter family expressed in kidney
-
Gamba G., Miyanoshita A., Lombardi M., Lytton J., Lee W.S., Hediger M.A., et al. Molecular cloning, primary structure, and characterization of two members of the mammalian electroneutral sodium-(potassium)-chloride co-transporter family expressed in kidney. J Biol Chem 1994, 269:17713-17722.
-
(1994)
J Biol Chem
, vol.269
, pp. 17713-17722
-
-
Gamba, G.1
Miyanoshita, A.2
Lombardi, M.3
Lytton, J.4
Lee, W.S.5
Hediger, M.A.6
-
167
-
-
0027405688
-
Primary structure and functional expression of a cDNA encoding the thiazide-sensitive, electroneutral sodium-chloride co-transporter
-
Gamba G., Saltzberg S.N., Lombardi M., Miyanoshita A., Lytton J., Hediger M.A., et al. Primary structure and functional expression of a cDNA encoding the thiazide-sensitive, electroneutral sodium-chloride co-transporter. Proc Natl Acad Sci USA 1993, 90:2749-2753.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 2749-2753
-
-
Gamba, G.1
Saltzberg, S.N.2
Lombardi, M.3
Miyanoshita, A.4
Lytton, J.5
Hediger, M.A.6
-
168
-
-
9044235777
-
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl co-transporter
-
Simon D.B., Nelson-Williams C., Bia M.J., Ellison D., Karet F.E., Molina A.M., et al. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl co-transporter. Nat Genet 1996, 12:24-30.
-
(1996)
Nat Genet
, vol.12
, pp. 24-30
-
-
Simon, D.B.1
Nelson-Williams, C.2
Bia, M.J.3
Ellison, D.4
Karet, F.E.5
Molina, A.M.6
-
169
-
-
42649084334
-
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
-
Ji W., Foo J.N., O'Roak B.J., Zhao H., Larson M.G., Simon D.B., et al. Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nat Genet 2008, 40:592-599.
-
(2008)
Nat Genet
, vol.40
, pp. 592-599
-
-
Ji, W.1
Foo, J.N.2
O'Roak, B.J.3
Zhao, H.4
Larson, M.G.5
Simon, D.B.6
-
170
-
-
0035136314
-
Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life
-
Cruz D.N., Shaer A.J., Bia M.J., Lifton R.P., Simon D.B. Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life. Kidney Int 2001, 59:710-717.
-
(2001)
Kidney Int
, vol.59
, pp. 710-717
-
-
Cruz, D.N.1
Shaer, A.J.2
Bia, M.J.3
Lifton, R.P.4
Simon, D.B.5
-
172
-
-
18544369466
-
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family
-
Schlingmann K.P., Weber S., Peters M., Niemann Nejsum L., Vitzthum H., Klingel K., et al. Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family. Nat Genet 2002, 31:166-170.
-
(2002)
Nat Genet
, vol.31
, pp. 166-170
-
-
Schlingmann, K.P.1
Weber, S.2
Peters, M.3
Niemann Nejsum, L.4
Vitzthum, H.5
Klingel, K.6
-
174
-
-
0029827662
-
Thiazide treatment of rats provokes apoptosis in distal tubule cells
-
Loffing J., Loffing-Cueni D., Hegyi I., Kaplan M.R., Hebert S.C., Le Hir M., et al. Thiazide treatment of rats provokes apoptosis in distal tubule cells. Kidney Int 1996, 50:1180-1190.
-
(1996)
Kidney Int
, vol.50
, pp. 1180-1190
-
-
Loffing, J.1
Loffing-Cueni, D.2
Hegyi, I.3
Kaplan, M.R.4
Hebert, S.C.5
Le Hir, M.6
-
176
-
-
65249156553
-
Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10
-
Scholl U.I., Choi M., Liu T., Ramaekers V.T., Hausler M.G., Grimmer J., et al. Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10. Proc Natl Acad Sci USA 2009, 106:5842-5847.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 5842-5847
-
-
Scholl, U.I.1
Choi, M.2
Liu, T.3
Ramaekers, V.T.4
Hausler, M.G.5
Grimmer, J.6
-
177
-
-
65649112786
-
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations
-
Bockenhauer D., Feather S., Stanescu H.C., Bandulik S., Zdebik A.A., Reichold M., et al. Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations. N Engl J Med 2009, 360:1960-1970.
-
(2009)
N Engl J Med
, vol.360
, pp. 1960-1970
-
-
Bockenhauer, D.1
Feather, S.2
Stanescu, H.C.3
Bandulik, S.4
Zdebik, A.A.5
Reichold, M.6
-
178
-
-
35448989687
-
Conditional knock-out of Kir4.1 leads to glial membrane depolarization, inhibition of potassium and glutamate uptake, and enhanced short-term synaptic potentiation
-
Djukic B., Casper K.B., Philpot B.D., Chin L.S., McCarthy K.D. Conditional knock-out of Kir4.1 leads to glial membrane depolarization, inhibition of potassium and glutamate uptake, and enhanced short-term synaptic potentiation. J Neurosci 2007, 27:11354-11365.
-
(2007)
J Neurosci
, vol.27
, pp. 11354-11365
-
-
Djukic, B.1
Casper, K.B.2
Philpot, B.D.3
Chin, L.S.4
McCarthy, K.D.5
-
179
-
-
0034255132
-
Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina
-
Kofuji P., Ceelen P., Zahs K.R., Surbeck L.W., Lester H.A., Newman E.A. Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina. J Neurosci 2000, 20:5733-5740.
-
(2000)
J Neurosci
, vol.20
, pp. 5733-5740
-
-
Kofuji, P.1
Ceelen, P.2
Zahs, K.R.3
Surbeck, L.W.4
Lester, H.A.5
Newman, E.A.6
-
180
-
-
0035425966
-
Kir4.1 potassium channel subunit is crucial for oligodendrocyte development and in vivo myelination
-
Neusch C., Rozengurt N., Jacobs R.E., Lester H.A., Kofuji P. Kir4.1 potassium channel subunit is crucial for oligodendrocyte development and in vivo myelination. J Neurosci 2001, 21:5429-5438.
-
(2001)
J Neurosci
, vol.21
, pp. 5429-5438
-
-
Neusch, C.1
Rozengurt, N.2
Jacobs, R.E.3
Lester, H.A.4
Kofuji, P.5
-
182
-
-
78649418068
-
Implication of Kir4.1 channel in excess potassium clearance: an in vivo study on anesthetized glial-conditional Kir4.1 knock-out mice
-
Chever O., Djukic B., McCarthy K.D., Amzica F. Implication of Kir4.1 channel in excess potassium clearance: an in vivo study on anesthetized glial-conditional Kir4.1 knock-out mice. J Neurosci 2010, 30:15769-15777.
-
(2010)
J Neurosci
, vol.30
, pp. 15769-15777
-
-
Chever, O.1
Djukic, B.2
McCarthy, K.D.3
Amzica, F.4
-
183
-
-
0037333861
-
Time course of inner ear degeneration and deafness in mice lacking the Kir4.1 potassium channel subunit
-
Rozengurt N., Lopez I., Chiu C.S., Kofuji P., Lester H.A., Neusch C. Time course of inner ear degeneration and deafness in mice lacking the Kir4.1 potassium channel subunit. Hear Res 2003, 177:71-80.
-
(2003)
Hear Res
, vol.177
, pp. 71-80
-
-
Rozengurt, N.1
Lopez, I.2
Chiu, C.S.3
Kofuji, P.4
Lester, H.A.5
Neusch, C.6
-
185
-
-
77956290593
-
KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function
-
Reichold M., Zdebik A.A., Lieberer E., Rapedius M., Schmidt K., Bandulik S., et al. KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function. Proc Natl Acad Sci USA 2010, 107:14490-14495.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 14490-14495
-
-
Reichold, M.1
Zdebik, A.A.2
Lieberer, E.3
Rapedius, M.4
Schmidt, K.5
Bandulik, S.6
-
186
-
-
80051654634
-
KCNJ10 mutations disrupt function in patients with EAST syndrome
-
Freudenthal B., Kulaveerasingam D., Lingappa L., Shah M.A., Brueton L., Wassmer E., et al. KCNJ10 mutations disrupt function in patients with EAST syndrome. Nephron Physiol 2011, 119:40-48.
-
(2011)
Nephron Physiol
, vol.119
, pp. 40-48
-
-
Freudenthal, B.1
Kulaveerasingam, D.2
Lingappa, L.3
Shah, M.A.4
Brueton, L.5
Wassmer, E.6
-
187
-
-
79953143745
-
Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome
-
Thompson D.A., Feather S., Stanescu H.C., Freudenthal B., Zdebik A.A., Warth R., et al. Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome. J Physiol 2011, 589:1681-1689.
-
(2011)
J Physiol
, vol.589
, pp. 1681-1689
-
-
Thompson, D.A.1
Feather, S.2
Stanescu, H.C.3
Freudenthal, B.4
Zdebik, A.A.5
Warth, R.6
-
188
-
-
12344282783
-
Global burden of hypertension: analysis of worldwide data
-
Kearney P.M., Whelton M., Reynolds K., Muntner P., Whelton P.K., He J. Global burden of hypertension: analysis of worldwide data. Lancet 2005, 365:217-223.
-
(2005)
Lancet
, vol.365
, pp. 217-223
-
-
Kearney, P.M.1
Whelton, M.2
Reynolds, K.3
Muntner, P.4
Whelton, P.K.5
He, J.6
-
190
-
-
0038460302
-
The seventh report of the joint national committee on prevention, detection, evaluation, and treatment of high blood pressure: the jnc 7 report
-
Chobanian A.V., Bakris G.L., Black H.R., Cushman W.C., Green L.A., Izzo J.L., et al. The seventh report of the joint national committee on prevention, detection, evaluation, and treatment of high blood pressure: the jnc 7 report. Jama 2003, 289:2560-2572.
-
(2003)
Jama
, vol.289
, pp. 2560-2572
-
-
Chobanian, A.V.1
Bakris, G.L.2
Black, H.R.3
Cushman, W.C.4
Green, L.A.5
Izzo, J.L.6
-
191
-
-
0017761036
-
The NHLBI twin study of cardiovascular disease risk factors: methodology and summary of results
-
Feinleib M., Garrison R.J., Fabsitz R., Christian J.C., Hrubec Z., Borhani N.O., et al. The NHLBI twin study of cardiovascular disease risk factors: methodology and summary of results. Am J Epidemiol 1977, 106:284-285.
-
(1977)
Am J Epidemiol
, vol.106
, pp. 284-285
-
-
Feinleib, M.1
Garrison, R.J.2
Fabsitz, R.3
Christian, J.C.4
Hrubec, Z.5
Borhani, N.O.6
-
192
-
-
0021258966
-
Environmental and genetic sources of familial aggregation of blood pressure in Tecumseh, Michigan
-
Longini I.M., Higgins M.W., Hinton P.C., Moll P.P., Keller J.B. Environmental and genetic sources of familial aggregation of blood pressure in Tecumseh, Michigan. Am J Epidemiol 1984, 120:131-144.
-
(1984)
Am J Epidemiol
, vol.120
, pp. 131-144
-
-
Longini, I.M.1
Higgins, M.W.2
Hinton, P.C.3
Moll, P.P.4
Keller, J.B.5
-
193
-
-
11244321599
-
Heritability of daytime ambulatory blood pressure in an extended twin design
-
Kupper N., Willemsen G., Riese H., Posthuma D., Boomsma D.I., de Geus E.J. Heritability of daytime ambulatory blood pressure in an extended twin design. Hypertension 2005, 45:80-85.
-
(2005)
Hypertension
, vol.45
, pp. 80-85
-
-
Kupper, N.1
Willemsen, G.2
Riese, H.3
Posthuma, D.4
Boomsma, D.I.5
de Geus, E.J.6
-
194
-
-
67349085063
-
Genome-wide association study identifies eight loci associated with blood pressure
-
Newton-Cheh C., Johnson T., Gateva V., Tobin M.D., Bochud M., Coin L., et al. Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet 2009, 41:666-676.
-
(2009)
Nat Genet
, vol.41
, pp. 666-676
-
-
Newton-Cheh, C.1
Johnson, T.2
Gateva, V.3
Tobin, M.D.4
Bochud, M.5
Coin, L.6
-
195
-
-
67349208839
-
Genome-wide association study of blood pressure and hypertension
-
Levy D., Ehret G.B., Rice K., Verwoert G.C., Launer L.J., Dehghan A., et al. Genome-wide association study of blood pressure and hypertension. Nat Genet 2009, 41:677-687.
-
(2009)
Nat Genet
, vol.41
, pp. 677-687
-
-
Levy, D.1
Ehret, G.B.2
Rice, K.3
Verwoert, G.C.4
Launer, L.J.5
Dehghan, A.6
-
196
-
-
84863556835
-
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
-
Tennessen J.A., Bigham A.W., O'Connor T.D., Fu W., Kenny E.E., Gravel S., et al. Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science 2012, 337:64-69.
-
(2012)
Science
, vol.337
, pp. 64-69
-
-
Tennessen, J.A.1
Bigham, A.W.2
O'Connor, T.D.3
Fu, W.4
Kenny, E.E.5
Gravel, S.6
-
197
-
-
0035804277
-
Effects on blood pressure of reduced dietary sodium and the dietary approaches to stop hypertension (dash) diet. Dash-sodium collaborative research group
-
Sacks F.M., Svetkey L.P., Vollmer W.M., Appel L.J., Bray G.A., Harsha D., et al. Effects on blood pressure of reduced dietary sodium and the dietary approaches to stop hypertension (dash) diet. Dash-sodium collaborative research group. N Engl J Med 2001, 344:3-10.
-
(2001)
N Engl J Med
, vol.344
, pp. 3-10
-
-
Sacks, F.M.1
Svetkey, L.P.2
Vollmer, W.M.3
Appel, L.J.4
Bray, G.A.5
Harsha, D.6
-
198
-
-
0025771982
-
Does potassium supplementation lower blood pressure? A meta-analysis of published trials
-
Cappuccio F.P., MacGregor G.A. Does potassium supplementation lower blood pressure? A meta-analysis of published trials. J Hypertens 1991, 9:465-473.
-
(1991)
J Hypertens
, vol.9
, pp. 465-473
-
-
Cappuccio, F.P.1
MacGregor, G.A.2
-
199
-
-
0030956083
-
Effects of oral potassium on blood pressure. Meta-analysis of randomized controlled clinical trials
-
Whelton P.K., He J., Cutler J.A., Brancati F.L., Appel L.J., Follmann D., et al. Effects of oral potassium on blood pressure. Meta-analysis of randomized controlled clinical trials. Jama 1997, 277:1624-1632.
-
(1997)
Jama
, vol.277
, pp. 1624-1632
-
-
Whelton, P.K.1
He, J.2
Cutler, J.A.3
Brancati, F.L.4
Appel, L.J.5
Follmann, D.6
-
200
-
-
0041368790
-
Blood pressure response to changes in sodium and potassium intake: a metaregression analysis of randomised trials
-
Geleijnse J.M., Kok F.J., Grobbee D.E. Blood pressure response to changes in sodium and potassium intake: a metaregression analysis of randomised trials. J Hum Hypertens 2003, 17:471-480.
-
(2003)
J Hum Hypertens
, vol.17
, pp. 471-480
-
-
Geleijnse, J.M.1
Kok, F.J.2
Grobbee, D.E.3
-
201
-
-
70349238909
-
Effect of modest salt reduction on blood pressure, urinary albumin, and pulse wave velocity in white, black, and Asian mild hypertensives
-
He F.J., Marciniak M., Visagie E., Markandu N.D., Anand V., Dalton R.N., et al. Effect of modest salt reduction on blood pressure, urinary albumin, and pulse wave velocity in white, black, and Asian mild hypertensives. Hypertension 2009, 54:482-488.
-
(2009)
Hypertension
, vol.54
, pp. 482-488
-
-
He, F.J.1
Marciniak, M.2
Visagie, E.3
Markandu, N.D.4
Anand, V.5
Dalton, R.N.6
-
202
-
-
77149154383
-
Projected effect of dietary salt reductions on future cardiovascular disease
-
Bibbins-Domingo K., Chertow G.M., Coxson P.G., Moran A., Lightwood J.M., Pletcher M.J., et al. Projected effect of dietary salt reductions on future cardiovascular disease. N Engl J Med 2010, 362:590-599.
-
(2010)
N Engl J Med
, vol.362
, pp. 590-599
-
-
Bibbins-Domingo, K.1
Chertow, G.M.2
Coxson, P.G.3
Moran, A.4
Lightwood, J.M.5
Pletcher, M.J.6
-
203
-
-
84861391455
-
Institute of Medicine. Strategies to reduce sodium intake in the United States
-
The National Academies Press, Washington, DC, 49-50
-
McGuire S Institute of Medicine. Strategies to reduce sodium intake in the United States. Adv Nutr 2010, 1. The National Academies Press, Washington, DC, 49-50.
-
(2010)
Adv Nutr
, vol.1
-
-
McGuire, S.1
-
204
-
-
60749115069
-
The benefit of salt restriction in the treatment of end-stage renal disease by haemodialysis
-
Kayikcioglu M., Tumuklu M., Ozkahya M., Ozdogan O., Asci G., Duman S., et al. The benefit of salt restriction in the treatment of end-stage renal disease by haemodialysis. Nephrol Dial Transplant 2009, 24:956-962.
-
(2009)
Nephrol Dial Transplant
, vol.24
, pp. 956-962
-
-
Kayikcioglu, M.1
Tumuklu, M.2
Ozkahya, M.3
Ozdogan, O.4
Asci, G.5
Duman, S.6
-
205
-
-
0029039206
-
Interdialysis blood pressure control by long haemodialysis sessions
-
Chazot C., Charra B., Laurent G., Didier C., Vo Van C., Terrat J.C., et al. Interdialysis blood pressure control by long haemodialysis sessions. Nephrol Dial Transplant 1995, 10:831-837.
-
(1995)
Nephrol Dial Transplant
, vol.10
, pp. 831-837
-
-
Chazot, C.1
Charra, B.2
Laurent, G.3
Didier, C.4
Vo Van, C.5
Terrat, J.C.6
-
206
-
-
34548772315
-
Effect of frequent nocturnal hemodialysis vs conventional hemodialysis on left ventricular mass and quality of life: a randomized controlled trial
-
Culleton B.F., Walsh M., Klarenbach S.W., Mortis G., Scott-Douglas N., Quinn R.R., et al. Effect of frequent nocturnal hemodialysis vs conventional hemodialysis on left ventricular mass and quality of life: a randomized controlled trial. Jama 2007, 298:1291-1299.
-
(2007)
Jama
, vol.298
, pp. 1291-1299
-
-
Culleton, B.F.1
Walsh, M.2
Klarenbach, S.W.3
Mortis, G.4
Scott-Douglas, N.5
Quinn, R.R.6
-
207
-
-
0035571328
-
Mutations in the Na-Cl co-transporter reduce blood pressure in humans
-
Cruz D.N., Simon D.B., Nelson-Williams C., Farhi A., Finberg K., Burleson L., et al. Mutations in the Na-Cl co-transporter reduce blood pressure in humans. Hypertension 2001, 37:1458-1464.
-
(2001)
Hypertension
, vol.37
, pp. 1458-1464
-
-
Cruz, D.N.1
Simon, D.B.2
Nelson-Williams, C.3
Farhi, A.4
Finberg, K.5
Burleson, L.6
|