-
1
-
-
78649655193
-
Diabetes insipidus
-
Geary DF, Schaefer F (eds) Philadelphia, Mosby Elsevier
-
Bockenhauer D: Diabetes insipidus; in Geary DF, Schaefer F (eds): Comprehensive Pediatric Nephrology. Philadelphia, Mosby Elsevier, 2008, pp 489-498.
-
(2008)
Comprehensive Pediatric Nephrology
, pp. 489-498
-
-
Bockenhauer, D.1
-
2
-
-
57049184564
-
Antenatal Bart-ter's syndrome: Why is this not a lethal condition?
-
Bockenhauer D, Cruwys M, Kleta R, Halperin LF, Wildgoose P, Souma T, Nukiwa N, Cheema-Dhadli S, Chong CK, Kamel KS, Davids MR, Halperin ML: Antenatal Bart-ter's syndrome: why is this not a lethal condition? QJM 2008; 101:927-942.
-
(2008)
QJM
, vol.101
, pp. 927-942
-
-
Bockenhauer, D.1
Cruwys, M.2
Kleta, R.3
Halperin, L.F.4
Wildgoose, P.5
Souma, T.6
Nukiwa, N.7
Cheema-Dhadli, S.8
Chong, C.K.9
Kamel, K.S.10
Davids, M.R.11
Halperin, M.L.12
-
3
-
-
70349846324
-
Vasopressin type 2 receptor V88M mutation: Molecular basis of partial and complete nephrogenic diabetes insipidus
-
Bockenhauer D, Carpentier E, Rochdi D, Van't Hoff W, Breton B, Bernier V, Bouvier M, Bichet DG: Vasopressin type 2 receptor V88M mutation: molecular basis of partial and complete nephrogenic diabetes insipidus. Nephron Physiol 2010; 114: p1-p10.
-
(2010)
Nephron Physiol
, vol.114
-
-
Bockenhauer, D.1
Carpentier, E.2
Rochdi, D.3
Van'T Hoff, W.4
Breton, B.5
Bernier, V.6
Bouvier, M.7
Bichet, D.G.8
-
5
-
-
0023231429
-
Prevalence, pathogenesis, and treatment of renal dysfunction associated with chronic lithium therapy
-
Boton R, Gaviria M, Batlle DC: Prevalence, pathogenesis, and treatment of renal dysfunction associated with chronic lithium therapy. Am J Kidney Dis 1987; 10:329-345.
-
(1987)
Am J Kidney Dis
, vol.10
, pp. 329-345
-
-
Boton, R.1
Gaviria, M.2
Batlle, D.C.3
-
6
-
-
0036083443
-
Aquaporins in the kidney: From molecules to medicine
-
Nielsen S, Frokiaer J, Marples D, Kwon TH, Agre P, Knepper MA: Aquaporins in the kidney: from molecules to medicine. Physiol Rev 2002; 82: 205-244.
-
(2002)
Physiol Rev
, vol.82
, pp. 205-244
-
-
Nielsen, S.1
Frokiaer, J.2
Marples, D.3
Kwon, T.H.4
Agre, P.5
Knepper, M.A.6
-
7
-
-
0023856917
-
Hemody-namic and coagulation responses to 1-desa-mino [8-D-arginine] vasopressin in patients w it h congen ita l neph rogenic diabete s i nsipi-dus
-
Bichet DG, Razi M, Lonergan M, Arthus MF, Papukna V, Kortas C, Barjon JN: Hemody-namic and coagulation responses to 1-desa-mino [8-D-arginine] vasopressin in patients w it h congen ita l neph rogenic diabete s i nsipi-dus. N Engl J Med 1988; 318:881-887.
-
(1988)
N Engl J Med
, vol.318
, pp. 881-887
-
-
Bichet, D.G.1
Razi, M.2
Lonergan, M.3
Arthus, M.F.4
Papukna, V.5
Kortas, C.6
Barjon, J.N.7
-
8
-
-
0021356905
-
The various renal manifestations of the nephropathic form of cysti-nosis
-
Lemire J, Kaplan BS: The various renal manifestations of the nephropathic form of cysti-nosis. A m J Nephrol 1984; 4: 81-85.
-
(1984)
A M J Nephrol
, vol.4
, pp. 81-85
-
-
Lemire, J.1
Kaplan, B.S.2
-
9
-
-
0028248722
-
Nephropathic cystinosis: Report of 2 cases and review of the literature (in Portuguese)
-
Knoepfelmacher M, Rocha R, Salgado LR, Semer M, Voss D, Wajchenberg BL, Liber-man B: Nephropathic cystinosis: report of 2 cases and review of the literature (in Portuguese). Rev Assoc Med Bras 1994; 40:43-46.
-
(1994)
Rev Assoc Med Bras
, vol.40
, pp. 43-46
-
-
Knoepfelmacher, M.1
Rocha, R.2
Salgado, L.R.3
Semer, M.4
Voss, D.5
Wajchenberg, B.L.6
Liber-Man, B.7
-
10
-
-
0023947484
-
Nephrogenic diabetes insipidus, cystinosis, and vitamin D
-
Katzir Z, Shvil Y, Landau H, Kidrony G, Popovtzer MM: Nephrogenic diabetes insipidus, cystinosis, and vitamin D. Arch Dis Child 1988; 63: 548-550.
-
(1988)
Arch Dis Child
, vol.63
, pp. 548-550
-
-
Katzir, Z.1
Shvil, Y.2
Landau, H.3
Kidrony, G.4
Popovtzer, M.M.5
-
11
-
-
0014065055
-
Pitressin-resistant hyposthe-nuria in chronic renal disease
-
Holliday MA, Egan TJ, Morris CR, Jarrah AS, Harrah JL: Pitressin-resistant hyposthe-nuria in chronic renal disease. Am J Med 1967; 42: 378-387.
-
(1967)
Am J Med
, vol.42
, pp. 378-387
-
-
Holliday, M.A.1
Egan, T.J.2
Morris, C.R.3
Jarrah, A.S.4
Harrah, J.L.5
-
12
-
-
78649666330
-
Fanconi syndrome
-
Geary DF, Schaefer F (eds) Philadelphia, Mosby Elsevier
-
Bockenhauer D, Van't Hoff W: Fanconi syndrome; in Geary DF, Schaefer F (eds): Comprehensive Pediatric Nephrology. Philadelphia, Mosby Elsevier, 2008, pp 433-450.
-
(2008)
Comprehensive Pediatric Nephrology
, pp. 433-450
-
-
Bockenhauer, D.1
Van'T Hoff, W.2
-
13
-
-
0025154745
-
Familial juvenile nephronophthisis. Pathohistology of a rare genetic disease in three siblings (in German)
-
August C, Demuth S: Familial juvenile nephronophthisis. Pathohistology of a rare genetic disease in three siblings (in German). Zentralbl Allg Pathol 1990; 136: 367-375.
-
(1990)
Zentralbl Allg Pathol
, vol.136
, pp. 367-375
-
-
August, C.1
Demuth, S.2
-
14
-
-
0017744263
-
Nephronophthisis. Renal function and histologic studies in a family
-
Brouhard BH, Srivastava RN, Travis LB, Kay MI, Beathard GA, Dodge WF, Lorentz WB Jr: Nephronophthisis. Renal function and histologic studies in a family. Nephron 1977; 19: 99-112.
-
(1977)
Nephron
, vol.19
, pp. 99-112
-
-
Brouhard, B.H.1
Srivastava, R.N.2
Travis, L.B.3
Kay, M.I.4
Beathard, G.A.5
Dodge, W.F.6
Lorentz Jr., W.B.7
-
15
-
-
0020579896
-
Nephronophthisis with massive proteinuria
-
Eiser AR, Grishman E, Neff MS, Allerhand J, Slifkin RF: Nephronophthisis with massive proteinuria. Am J Kidney Dis 1983; 2: 640-644.
-
(1983)
Am J Kidney Dis
, vol.2
, pp. 640-644
-
-
Eiser, A.R.1
Grishman, E.2
Neff, M.S.3
Allerhand, J.4
Slifkin, R.F.5
-
16
-
-
0035140597
-
New insights: Nephronophthisis-medullary cystic kidney disease
-
DOI 10.1007/s004670000518
-
Hildebrandt F, Omram H: New insights: nephronophthisis-medullary cystic kidney disease. Pediatr Nephrol 2001; 16: 168-176. (Pubitemid 32125169)
-
(2001)
Pediatric Nephrology
, vol.16
, Issue.2
, pp. 168-176
-
-
Hildebrandt, F.1
Omram, H.2
-
17
-
-
33749025551
-
Bartter syndromes and other salt-losing tubulopathies
-
Kleta R, Bockenhauer D: Bartter syndromes and other salt-losing tubulopathies. Neph-ron Physiol 2006; 104: p73-p80.
-
(2006)
Neph-ron Physiol
, vol.104
-
-
Kleta, R.1
Bockenhauer, D.2
-
18
-
-
0037082531
-
Clinical presentation of genetically defined patients with hypokalemic saltlosing tubulopathies
-
Peters M, Jeck N, Reinalter S, Leonhardt A, Tonshoff B, Klaus GG, Konrad M, Seyberth HW: Clinical presentation of genetically defined patients with hypokalemic saltlosing 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
Konrad, M.7
Seyberth, H.W.8
-
19
-
-
0029996150
-
Hypokalemia-induced down-regulation of aquaporin-2 water channel expression in rat kidney medulla and cortex
-
Marples D, Frokiaer J, Dorup J, Knepper MA, Nielsen S: Hypokalemia-induced down-regulation of aquaporin-2 water channel expression in rat kidney medulla and cortex. J Clin Invest 1996; 97: 1960-1968.
-
(1996)
J Clin Invest
, vol.97
, pp. 1960-1968
-
-
Marples, D.1
Frokiaer, J.2
Dorup, J.3
Knepper, M.A.4
Nielsen, S.5
-
20
-
-
65249093634
-
Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome
-
Brochard K, Boyer O, Bla nchard A, Loirat C, Niaudet P, Macher MA, Deschenes G, Bensman A, Decramer S, Cochat P, Morin D, Broux F, Caillez M, Guyot C, Novo R, Jeunemaitre X, Vargas-Poussou R: Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome. Nephrol Dial Transplant 2009; 24:1455-1464.
-
(2009)
Nephrol Dial Transplant
, vol.24
, pp. 1455-1464
-
-
Brochard, K.1
Boyer, O.2
Blanchard, A.3
Loirat, C.4
Niaudet, P.5
MacHer, M.A.6
Deschenes, G.7
Bensman, A.8
Decramer, S.9
Cochat, P.10
Morin, D.11
Broux, F.12
Caillez, M.13
Guyot, C.14
Novo, R.15
Jeunemaitre, X.16
Vargas-Poussou, R.17
-
21
-
-
0030910045
-
Role of the Ca(2+)-sensing receptor in divalent mineralion homeostasis
-
Hebert SC, Brown EM, Harris HW: Role of the Ca(2+)-sensing receptor in divalent mineralion homeostasis. J Exp Biol 1997; 200: 295-302.
-
(1997)
J Exp Biol
, vol.200
, pp. 295-302
-
-
Hebert, S.C.1
Brown, E.M.2
Harris, H.W.3
-
22
-
-
0034060129
-
Does a high concentration of calcium in the urine cause an important renal concentrating defect in human subjects?
-
Lam GS, Asplin JR, Halperin ML: Does a high concentration of calcium in the urine cause an important renal concentrating defect in human subjects? Clin Sci (Lond) 2000; 98:313-319.
-
(2000)
Clin Sci (Lond)
, vol.98
, pp. 313-319
-
-
Lam, G.S.1
Asplin, J.R.2
Halperin, M.L.3
-
23
-
-
0028339017
-
Nephrogenic diabetes insipidus
-
Bichet DG: Nephrogenic diabetes insipidus. Semin Nephrol 1994; 14:349-356.
-
(1994)
Semin Nephrol
, vol.14
, pp. 349-356
-
-
Bichet, D.G.1
-
25
-
-
0019982232
-
Natural history of primary distal renal tubular acidosis treated since infancy
-
Rodriguez-Soriano J, Vallo A, Castillo G, Oliveros R: Natural history of primary distal renal tubular acidosis treated since infancy. J Pediatr 1982; 101:669-676.
-
(1982)
J Pediatr
, vol.101
, pp. 669-676
-
-
Rodriguez-Soriano, J.1
Vallo, A.2
Castillo, G.3
Oliveros, R.4
-
26
-
-
0022993254
-
Renal tubular acidosis in children. Diagnosis, treatment and prognosis
-
Santos F, Chan JC: Renal tubular acidosis in children. Diagnosis, treatment and prognosis. Am J Nephrol 1986; 6:289-295.
-
(1986)
Am J Nephrol
, vol.6
, pp. 289-295
-
-
Santos, F.1
Chan, J.C.2
-
28
-
-
33847258227
-
Combined renal tubular acidosis and diabetes insipidus in hemato-logical disease
-
Hoorn EJ, Zietse R: Combined renal tubular acidosis and diabetes insipidus in hemato-logical disease. Nat Clin Pract Nephrol 2007; 3:171-175.
-
(2007)
Nat Clin Pract Nephrol
, vol.3
, pp. 171-175
-
-
Hoorn, E.J.1
Zietse, R.2
-
29
-
-
0030058775
-
Cognitive and psychosocial functioning of patients wit h congenita l nephrogenic d iabetes insipidus
-
Hoekstra JA, van Lieburg AF, Monnens LA, Hulstijn-Dirkmaat GM, Knoers VV: Cognitive and psychosocial functioning of patients wit h congenita l nephrogenic d iabetes insipidus. Am J Med Genet 1996; 61: 81-88.
-
(1996)
Am J Med Genet
, vol.61
, pp. 81-88
-
-
Hoekstra, J.A.1
Van Lieburg, A.F.2
Monnens, L.A.3
Hulstijn-Dirkmaat, G.M.4
Knoers, V.V.5
-
30
-
-
0033868928
-
Phenotypic variability in Bartter syndrome type i
-
Bettinelli A, Ciarmatori S, Cesareo L, Tede-schi S, Ruffa G, Appiani AC, Rosini A, Grumieri G, Mercuri B, Sacco M, Leozappa G, Binda S, Cecconi M, Navone C, Curcio C, Syren ML, Casari G: Phenotypic variability in Bartter syndrome type I. Pediatr Nephrol 2000; 14:940-945.
-
(2000)
Pediatr Nephrol
, vol.14
, pp. 940-945
-
-
Bettinelli, A.1
Ciarmatori, S.2
Cesareo, L.3
Tede-Schi, S.4
Ruffa, G.5
Appiani, A.C.6
Rosini, A.7
Grumieri, G.8
Mercuri, B.9
Sacco, M.10
Leozappa, G.11
Binda, S.12
Cecconi, M.13
Navone, C.14
Curcio, C.15
Syren, M.L.16
Casari, G.17
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