-
1
-
-
0038713089
-
Hypomagnesemia and hypermagnesemia
-
Topf J.M., and Murray P.T. Hypomagnesemia and hypermagnesemia. Rev Endocr Metab Disord 4 2 (2003) 195-206
-
(2003)
Rev Endocr Metab Disord
, vol.4
, Issue.2
, pp. 195-206
-
-
Topf, J.M.1
Murray, P.T.2
-
2
-
-
16244420082
-
Magnesium deficiency in critical illness
-
Tong G.M., and Rude R.K. Magnesium deficiency in critical illness. J Intensive Care Med 20 1 (2005) 3-17
-
(2005)
J Intensive Care Med
, vol.20
, Issue.1
, pp. 3-17
-
-
Tong, G.M.1
Rude, R.K.2
-
3
-
-
0020660652
-
A high prevalence of hypomagnesemia in hospitalized patients
-
Wong E.T., Rude R.K., Singer F.R., et al. A high prevalence of hypomagnesemia in hospitalized patients. Am J Clin Pathol 79 3 (1983) 348-352
-
(1983)
Am J Clin Pathol
, vol.79
, Issue.3
, pp. 348-352
-
-
Wong, E.T.1
Rude, R.K.2
Singer, F.R.3
-
4
-
-
0023831211
-
Prevalence and clinical implications of hypocalcemia in acutely ill patients in a medical intensive care setting
-
Desai T.K., Carlson R.W., Geheb M.A., et al. Prevalence and clinical implications of hypocalcemia in acutely ill patients in a medical intensive care setting. Am J Med 84 2 (1988) 209-214
-
(1988)
Am J Med
, vol.84
, Issue.2
, pp. 209-214
-
-
Desai, T.K.1
Carlson, R.W.2
Geheb, M.A.3
-
5
-
-
0024589247
-
Hypomagnesemia in patients in postoperative intensive care
-
Chernow B., Bamberger F., Stoiko M., et al. Hypomagnesemia in patients in postoperative intensive care. Chest 95 2 (1989) 391-397
-
(1989)
Chest
, vol.95
, Issue.2
, pp. 391-397
-
-
Chernow, B.1
Bamberger, F.2
Stoiko, M.3
-
6
-
-
0023741328
-
Muscle and serum magnesium in pulmonary intensive care unit patients
-
Fiaccadori E., Del Canale S., Coffrini E., et al. Muscle and serum magnesium in pulmonary intensive care unit patients. Crit Care Med 16 8 (1988) 751-760
-
(1988)
Crit Care Med
, vol.16
, Issue.8
, pp. 751-760
-
-
Fiaccadori, E.1
Del Canale, S.2
Coffrini, E.3
-
8
-
-
0037031196
-
Tetany secondary to the use of a proton-pump inhibitor
-
Subbiah V., and Tayek J.A. Tetany secondary to the use of a proton-pump inhibitor. Ann Intern Med 137 3 (2002) 219
-
(2002)
Ann Intern Med
, vol.137
, Issue.3
, pp. 219
-
-
Subbiah, V.1
Tayek, J.A.2
-
9
-
-
33750320388
-
Proton pump inhibitors and hypomagnesemic hypoparathyroidism
-
Epstein M., McGrath S., and Law F. Proton pump inhibitors and hypomagnesemic hypoparathyroidism. N Engl J Med 355 17 (2006) 1834-1836
-
(2006)
N Engl J Med
, vol.355
, Issue.17
, pp. 1834-1836
-
-
Epstein, M.1
McGrath, S.2
Law, F.3
-
10
-
-
47549099241
-
Severe hypomagnaesemia in long-term users of proton-pump inhibitors
-
Cundy T., and Dissanayake A. Severe hypomagnaesemia in long-term users of proton-pump inhibitors. Clin Endocrinol 69 2 (2008) 338-341
-
(2008)
Clin Endocrinol
, vol.69
, Issue.2
, pp. 338-341
-
-
Cundy, T.1
Dissanayake, A.2
-
11
-
-
47849120063
-
Omeprazole and refractory hypomagnesemia
-
10.1136/bmj.39505.738981.BE
-
Shabajee N., Lamb E.J., Sturgess I., and Sumathipala R.W. Omeprazole and refractory hypomagnesemia. BMJ 337 (2008) a425 10.1136/bmj.39505.738981.BE
-
(2008)
BMJ
, vol.337
-
-
Shabajee, N.1
Lamb, E.J.2
Sturgess, I.3
Sumathipala, R.W.4
-
12
-
-
66449111985
-
Hypomagnesemia due to use of proton pump inhibitors-a review
-
Kuipers M.T., Thang H.D., and Arntzhenius A.B. Hypomagnesemia due to use of proton pump inhibitors-a review. Neth J Med 67 5 (2009) 169-172
-
(2009)
Neth J Med
, vol.67
, Issue.5
, pp. 169-172
-
-
Kuipers, M.T.1
Thang, H.D.2
Arntzhenius, A.B.3
-
13
-
-
0033574249
-
A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group
-
Levey A.S., Bosch J.P., Lewis J.B., Greene T., Rogers N., and Roth D. A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group. Ann Intern Med 130 6 (1999) 461-470
-
(1999)
Ann Intern Med
, vol.130
, Issue.6
, pp. 461-470
-
-
Levey, A.S.1
Bosch, J.P.2
Lewis, J.B.3
Greene, T.4
Rogers, N.5
Roth, D.6
-
14
-
-
0019128309
-
Renal tubular maximum for magnesium in normal, hyperparathyroid, and hypoparathyroid man
-
Rude R.K., Bethune J.E., and Singer F.R. Renal tubular maximum for magnesium in normal, hyperparathyroid, and hypoparathyroid man. J Clin Endocrinol Metab 51 6 (1980) 1425-1431
-
(1980)
J Clin Endocrinol Metab
, vol.51
, Issue.6
, pp. 1425-1431
-
-
Rude, R.K.1
Bethune, J.E.2
Singer, F.R.3
-
15
-
-
0036284259
-
Magnesium in critical illness: metabolism, assessment and treatment
-
Noronha J.L., and Matuschak G.M. Magnesium in critical illness: metabolism, assessment and treatment. Intensive Care Med 28 6 (2002) 667-679
-
(2002)
Intensive Care Med
, vol.28
, Issue.6
, pp. 667-679
-
-
Noronha, J.L.1
Matuschak, G.M.2
-
16
-
-
0033029532
-
Hypomagnesemia
-
Agus Z.S. Hypomagnesemia. J Am Soc Nephrol 10 7 (1999) 1616-1622
-
(1999)
J Am Soc Nephrol
, vol.10
, Issue.7
, pp. 1616-1622
-
-
Agus, Z.S.1
-
17
-
-
49649114443
-
Molecular mechanisms of magnesium homeostasis: insights from human disease
-
Alexander R.T., Hoenderop J.G.J., and Bindels R.J.M. Molecular mechanisms of magnesium homeostasis: insights from human disease. J Am Soc Nephrol 19 8 (2008) 1451-1458
-
(2008)
J Am Soc Nephrol
, vol.19
, Issue.8
, pp. 1451-1458
-
-
Alexander, R.T.1
Hoenderop, J.G.J.2
Bindels, R.J.M.3
-
18
-
-
40049101450
-
Recent developments in intestinal magnesium absorption
-
Quamme G.A. Recent developments in intestinal magnesium absorption. Curr Opin Gastroenterol 24 2 (2008) 230-235
-
(2008)
Curr Opin Gastroenterol
, vol.24
, Issue.2
, pp. 230-235
-
-
Quamme, G.A.1
-
19
-
-
64149132666
-
Function and regulation of claudins in the thick ascending limb of Henle
-
Gunzel D., and Yu A.S.L. Function and regulation of claudins in the thick ascending limb of Henle. Eur J Physiol 458 1 (2009) 77-88
-
(2009)
Eur J Physiol
, vol.458
, Issue.1
, pp. 77-88
-
-
Gunzel, D.1
Yu, A.S.L.2
-
20
-
-
0035139184
-
Magnesium transport in the distal convoluted tubule
-
Dai L.J., Ritchie G., Kerstan D., Kang H.S., Cole D.E.C., and Quamme G.A. Magnesium transport in the distal convoluted tubule. Physiol Rev 81 1 (2001) 51-84
-
(2001)
Physiol Rev
, vol.81
, Issue.1
, pp. 51-84
-
-
Dai, L.J.1
Ritchie, G.2
Kerstan, D.3
Kang, H.S.4
Cole, D.E.C.5
Quamme, G.A.6
-
21
-
-
55249086295
-
Insights into the molecular regulation of the epithelial magnesium channel TRPM6
-
Cao G., Hoenderop J.G.J., and Bindels R.J.M. Insights into the molecular regulation of the epithelial magnesium channel TRPM6. Curr Opin Nephrol Hypertens 17 4 (2008) 373-378
-
(2008)
Curr Opin Nephrol Hypertens
, vol.17
, Issue.4
, pp. 373-378
-
-
Cao, G.1
Hoenderop, J.G.J.2
Bindels, R.J.M.3
-
23
-
-
34548835794
-
Hypomagnesemia in patients with type 2 diabetes
-
Pham P.C., Pham P.M., Pham S.V., Miller J.M., and Pham P.T. Hypomagnesemia in patients with type 2 diabetes. Clin J Am Soc Nephrol 2 2 (2007) 366-373
-
(2007)
Clin J Am Soc Nephrol
, vol.2
, Issue.2
, pp. 366-373
-
-
Pham, P.C.1
Pham, P.M.2
Pham, S.V.3
Miller, J.M.4
Pham, P.T.5
-
24
-
-
18244431922
-
Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene
-
Weber S., Hoffmann K., Jeck N., et al. Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene. Eur J Hum Genet 8 6 (2000) 414-422
-
(2000)
Eur J Hum Genet
, vol.8
, Issue.6
, pp. 414-422
-
-
Weber, S.1
Hoffmann, K.2
Jeck, N.3
-
25
-
-
33751097262
-
Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement
-
Konrad M., Schaller A., Seelow D., et al. Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement. Am J Hum Genet 79 5 (2006) 949-957
-
(2006)
Am J Hum Genet
, vol.79
, Issue.5
, pp. 949-957
-
-
Konrad, M.1
Schaller, A.2
Seelow, D.3
-
26
-
-
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., et al. Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family. Nat Genet 31 2 (2002) 166-170
-
(2002)
Nat Genet
, vol.31
, Issue.2
, pp. 166-170
-
-
Schlingmann, K.P.1
Weber, S.2
Peters, M.3
-
27
-
-
0033763089
-
Dominant isolated renal magnesium loss is caused by misrouting of the Na+,K(+)-ATPase gamma-subunit
-
Meij I.C., Koenderink J.B., van Bokhoven H., et al. Dominant isolated renal magnesium loss is caused by misrouting of the Na+,K(+)-ATPase gamma-subunit. Nat Genet 26 3 (2000) 265-266
-
(2000)
Nat Genet
, vol.26
, Issue.3
, pp. 265-266
-
-
Meij, I.C.1
Koenderink, J.B.2
van Bokhoven, H.3
-
28
-
-
34547700632
-
Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia
-
Groenestege W.M., Thebault S., van der Wijst J., et al. Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia. J Clin Invest 117 8 (2007) 2260-2267
-
(2007)
J Clin Invest
, vol.117
, Issue.8
, pp. 2260-2267
-
-
Groenestege, W.M.1
Thebault, S.2
van der Wijst, J.3
-
29
-
-
0030032699
-
Bartter's syndrome, hypokalemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2
-
Simon D.B., Karet F.E., Hamdan J.M., Di Pietro A., Sanjad S.A., and Lifton R.P. Bartter's syndrome, hypokalemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2. Nat Genet 13 2 (1996) 183-188
-
(1996)
Nat Genet
, vol.13
, Issue.2
, pp. 183-188
-
-
Simon, D.B.1
Karet, F.E.2
Hamdan, J.M.3
Di Pietro, A.4
Sanjad, S.A.5
Lifton, R.P.6
-
30
-
-
0037082531
-
Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies
-
Peters M., Jeck N., Reinalter S., et al. Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies. Am J Med 112 3 (2002) 183-190
-
(2002)
Am J Med
, vol.112
, Issue.3
, pp. 183-190
-
-
Peters, M.1
Jeck, N.2
Reinalter, S.3
-
31
-
-
16944366243
-
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
-
Simon D.B., Bindra R.S., Mansfield T.A., et al. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III. Nat Genet 17 2 (1997) 171-178
-
(1997)
Nat Genet
, vol.17
, Issue.2
, pp. 171-178
-
-
Simon, D.B.1
Bindra, R.S.2
Mansfield, T.A.3
-
32
-
-
0035189356
-
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
-
Birkenhager R., Otto E., Schurmann M.J., et al. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. Nat Genet 29 3 (2001) 310-314
-
(2001)
Nat Genet
, vol.29
, Issue.3
, pp. 310-314
-
-
Birkenhager, R.1
Otto, E.2
Schurmann, M.J.3
-
33
-
-
1642366722
-
Salt wasting and deafness resulting from mutations in two chloride channels
-
Schlingmann K.P., Konrad M., Jeck N., et al. Salt wasting and deafness resulting from mutations in two chloride channels. N Engl J Med 350 13 (2004) 1314-1319
-
(2004)
N Engl J Med
, vol.350
, Issue.13
, pp. 1314-1319
-
-
Schlingmann, K.P.1
Konrad, M.2
Jeck, N.3
-
34
-
-
9044235777
-
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter
-
Simon D.B., Nelson-Williams C., Bia M.J., et al. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter. Nat Genet 12 1 (1996) 24-30
-
(1996)
Nat Genet
, vol.12
, Issue.1
, pp. 24-30
-
-
Simon, D.B.1
Nelson-Williams, C.2
Bia, M.J.3
-
35
-
-
0037206034
-
Association between activating mutations of calcium-sensing receptor and Bartter's syndrome
-
Watanabe S., Fukumoto S., Chang H., et al. Association between activating mutations of calcium-sensing receptor and Bartter's syndrome. Lancet 360 9334 (2002) 692-694
-
(2002)
Lancet
, vol.360
, Issue.9334
, pp. 692-694
-
-
Watanabe, S.1
Fukumoto, S.2
Chang, H.3
-
36
-
-
65249156553
-
Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10
-
Scholl U.I., Choi M., Liu T., et al. Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10. Proc Natl Acad Sci U S A 106 14 (2009) 5842-5847
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, Issue.14
, pp. 5842-5847
-
-
Scholl, U.I.1
Choi, M.2
Liu, T.3
-
37
-
-
65649112786
-
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations
-
Bockenhauer D., Feather S., Stanescu H.C., et al. Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations. N Engl J Med 360 19 (2009) 1960-1970
-
(2009)
N Engl J Med
, vol.360
, Issue.19
, pp. 1960-1970
-
-
Bockenhauer, D.1
Feather, S.2
Stanescu, H.C.3
-
38
-
-
65249096581
-
A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia
-
Glaudemans B., van derWijst J., Scola R.H., et al. A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia. J Clin Invest 119 4 (2009) 936-942
-
(2009)
J Clin Invest
, vol.119
, Issue.4
, pp. 936-942
-
-
Glaudemans, B.1
van derWijst, J.2
Scola, R.H.3
-
39
-
-
8444228909
-
A cluster of metabolic defects caused by mutation in a mitochondrial tRNA
-
Wilson F.H., Hariri A., Farhi A., et al. A cluster of metabolic defects caused by mutation in a mitochondrial tRNA. Science 306 5699 (2004) 1190-1194
-
(2004)
Science
, vol.306
, Issue.5699
, pp. 1190-1194
-
-
Wilson, F.H.1
Hariri, A.2
Farhi, A.3
-
40
-
-
0017183721
-
Functional hypoparathyroidism and parathyroid hormone and organ resistance in human magnesium deficiency
-
Rude R.K., Oldham S.B., and Singer F.R. Functional hypoparathyroidism and parathyroid hormone and organ resistance in human magnesium deficiency. Clin Endocrinol (Oxf) 5 3 (1976) 209-224
-
(1976)
Clin Endocrinol (Oxf)
, vol.5
, Issue.3
, pp. 209-224
-
-
Rude, R.K.1
Oldham, S.B.2
Singer, F.R.3
-
41
-
-
0014526029
-
Hypocalcemia due to hypomagnesemia and reversible parathyroid hormone unresponsiveness
-
Estep H., Shaw W.A., Watlington C., Hobe R., Holland W., and Tucker S.G. Hypocalcemia due to hypomagnesemia and reversible parathyroid hormone unresponsiveness. J Clin Endocrinol Metab 29 6 (1969) 842-848
-
(1969)
J Clin Endocrinol Metab
, vol.29
, Issue.6
, pp. 842-848
-
-
Estep, H.1
Shaw, W.A.2
Watlington, C.3
Hobe, R.4
Holland, W.5
Tucker, S.G.6
-
42
-
-
0031769533
-
Effect of intravenous ranitidine and omeprazole on intestinal absorption of water, sodium and macronutrients in patients with intestinal resection
-
Jeppesen P.B., Staun M., Tjellesen L., and Mortensen P.B. Effect of intravenous ranitidine and omeprazole on intestinal absorption of water, sodium and macronutrients in patients with intestinal resection. Gut 43 6 (1998) 763-769
-
(1998)
Gut
, vol.43
, Issue.6
, pp. 763-769
-
-
Jeppesen, P.B.1
Staun, M.2
Tjellesen, L.3
Mortensen, P.B.4
-
43
-
-
0029156271
-
Hypochlorhydria from short-term omeprazole treatment does not inhibit intestinal absorption of calcium, phosphorus, magnesium or zinc from food in humans
-
Serfaty-Lacrosniere C., Wood R.J., Voytko D., et al. Hypochlorhydria from short-term omeprazole treatment does not inhibit intestinal absorption of calcium, phosphorus, magnesium or zinc from food in humans. J Am Coll Nutr 14 4 (1995) 364-368
-
(1995)
J Am Coll Nutr
, vol.14
, Issue.4
, pp. 364-368
-
-
Serfaty-Lacrosniere, C.1
Wood, R.J.2
Voytko, D.3
-
44
-
-
0021123904
-
Intracellular magnesium loss after diuretic administration
-
Dyckner T., and Wester P.O. Intracellular magnesium loss after diuretic administration. Drugs 28 suppl 1 (1984) 161-166
-
(1984)
Drugs
, vol.28
, Issue.SUPPL. 1
, pp. 161-166
-
-
Dyckner, T.1
Wester, P.O.2
|