-
1
-
-
0027925829
-
Autosomal dominant polycystic kidney disease
-
Gabow PA: Autosomal dominant polycystic kidney disease. N Engl J Med 329:332-342, 1993
-
(1993)
N Engl J Med
, vol.329
, pp. 332-342
-
-
Gabow, P.A.1
-
2
-
-
0031005534
-
Extrarenal manifestations of ADPKD
-
Perrone RD: Extrarenal manifestations of ADPKD. Kidney Int 51:2022-2036, 1997
-
(1997)
Kidney Int
, vol.51
, pp. 2022-2036
-
-
Perrone, R.D.1
-
3
-
-
0035960436
-
Autosomal dominant polycystic kidney disease: Modification of disease progression
-
Peters DJM, Breuning MH: Autosomal dominant polycystic kidney disease: Modification of disease progression. Lancet 358:1439-1444, 2001
-
(2001)
Lancet
, vol.358
, pp. 1439-1444
-
-
Peters, D.J.M.1
Breuning, M.H.2
-
4
-
-
0037334326
-
Polycystic kidney disease-the ciliary connection
-
Ong ACM, Wheatley DN: Polycystic kidney disease-the ciliary connection. Lancet 361:774-776, 2003
-
(2003)
Lancet
, vol.361
, pp. 774-776
-
-
Ong, A.C.M.1
Wheatley, D.N.2
-
5
-
-
0036256982
-
Molecular basis of polycystic kidney disease: PKD1, PKD2 and PKHD1
-
Harris PC: Molecular basis of polycystic kidney disease: PKD1, PKD2 and PKHD1. Curr Opin Nephrol Hypertens 11:309-314, 2002
-
(2002)
Curr Opin Nephrol Hypertens
, vol.11
, pp. 309-314
-
-
Harris, P.C.1
-
6
-
-
0030582668
-
The molecular basis of focal cyst formation in autosomal dominant polycystic kidney disease type I
-
Qian F, Watnick TJ, Onuchic LF, Germino GG: The molecular basis of focal cyst formation in autosomal dominant polycystic kidney disease type I. Cell 87:979-987, 1996
-
(1996)
Cell
, vol.87
, pp. 979-987
-
-
Qian, F.1
Watnick, T.J.2
Onuchic, L.F.3
Germino, G.G.4
-
7
-
-
0028297227
-
Why renal cysts grow
-
Gardner KD Jr, Glew RH, Evan AP, McAteer JA, Bernstein J: Why renal cysts grow. Am J Physiol 266:353-359, 1994
-
(1994)
Am J Physiol
, vol.266
, pp. 353-359
-
-
Gardner Jr., K.D.1
Glew, R.H.2
Evan, A.P.3
McAteer, J.A.4
Bernstein, J.5
-
8
-
-
0029823868
-
The etiology, pathogenesis, and treatment of autosomal dominant polycystic kidney disease: Recent advances
-
Grantham JJ: The etiology, pathogenesis, and treatment of autosomal dominant polycystic kidney disease: Recent advances. Am J Kidney Dis 28:788-803, 1996
-
(1996)
Am J Kidney Dis
, vol.28
, pp. 788-803
-
-
Grantham, J.J.1
-
9
-
-
0028351429
-
Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1
-
Ravine D, Gibson RN, Walker RG, Sheffield LJ, Kincaid-Smith P, Danks DM: Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1. Lancet 343:824-827, 1994
-
(1994)
Lancet
, vol.343
, pp. 824-827
-
-
Ravine, D.1
Gibson, R.N.2
Walker, R.G.3
Sheffield, L.J.4
Kincaid-Smith, P.5
Danks, D.M.6
-
10
-
-
0035184559
-
Rapid MR imaging detection of renal cysts: Age-based standards
-
Nascimento AB, Mitchell DG, Zhang X-M, Kamishima T, Parker L, Holland GA: Rapid MR imaging detection of renal cysts: Age-based standards. Radiology 221:628-632, 2001
-
(2001)
Radiology
, vol.221
, pp. 628-632
-
-
Nascimento, A.B.1
Mitchell, D.G.2
Zhang, X.-M.3
Kamishima, T.4
Parker, L.5
Holland, G.A.6
-
11
-
-
0035171856
-
Mutation analysis of the entire PKD1 gene: Genetic and diagnostic implications
-
Rosetti S, Strmecki L, Gamble V, et al: Mutation analysis of the entire PKD1 gene: Genetic and diagnostic implications. Am J Hum Genet 68:355-363, 2001
-
(2001)
Am J Hum Genet
, vol.68
, pp. 355-363
-
-
Rosetti, S.1
Strmecki, L.2
Gamble, V.3
-
12
-
-
0028725184
-
Overt proteinuria and microalbuminuria in autosomal dominant polycystic kidney disease
-
Chapman AB, Johnson AM, Gabow PA, Schrier RW: Overt proteinuria and microalbuminuria in autosomal dominant polycystic kidney disease. J Am Soc Nephrol 5:1349-1354, 1994
-
(1994)
J Am Soc Nephrol
, vol.5
, pp. 1349-1354
-
-
Chapman, A.B.1
Johnson, A.M.2
Gabow, P.A.3
Schrier, R.W.4
-
13
-
-
0038460302
-
The seventh report of the joint national committee on prevention, detection, evaluation, and treatment of high blood pressure: The JNC 7 report
-
Chobanian AV, Bakris GL, Black HR, 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 289:2560-2572, 2003
-
(2003)
JAMA
, vol.289
, pp. 2560-2572
-
-
Chobanian, A.V.1
Bakris, G.L.2
Black, H.R.3
-
14
-
-
0034998124
-
Diuretics versus angiotensin converting enzyme inhibitors in autosomal dominant polycystic kidney disease
-
Ecder T, Edelstein CL, Fick-Brosnahan GM, et al: Diuretics versus angiotensin converting enzyme inhibitors in autosomal dominant polycystic kidney disease. Am J Nephrol 21:98-103, 2001
-
(2001)
Am J Nephrol
, vol.21
, pp. 98-103
-
-
Ecder, T.1
Edelstein, C.L.2
Fick-Brosnahan, G.M.3
-
15
-
-
0030732925
-
Left ventricular hypertrophy in autosomal dominant polycystic kidney disease
-
Chapman AB, Johnson AM, Rainguet S, Hossak K, Gabow PA, Schrier RW: Left ventricular hypertrophy in autosomal dominant polycystic kidney disease. J Am Soc Nephrol 8:1292-1297, 1997
-
(1997)
J Am Soc Nephrol
, vol.8
, pp. 1292-1297
-
-
Chapman, A.B.1
Johnson, A.M.2
Rainguet, S.3
Hossak, K.4
Gabow, P.A.5
Schrier, R.W.6
-
16
-
-
0032943188
-
Reversal of left ventricular hypertrophy with angiotensin converting enzyme inhibition in hypertensive patients with autosomal dominant polycystic kidney disease
-
Ecder T, Edelstein CL, Chapman AB, et al: Reversal of left ventricular hypertrophy with angiotensin converting enzyme inhibition in hypertensive patients with autosomal dominant polycystic kidney disease. Nephrol Dial Transplant 14:1113-1116, 1999
-
(1999)
Nephrol Dial Transplant
, vol.14
, pp. 1113-1116
-
-
Ecder, T.1
Edelstein, C.L.2
Chapman, A.B.3
-
17
-
-
0035161149
-
Hypertension in autosomal-dominant polycystic kidney disease: Early occurrence and unique aspects
-
Ecder T, Schrier RW: Hypertension in autosomal-dominant polycystic kidney disease: Early occurrence and unique aspects. J Am Soc Nephrol 12:194-200, 2001
-
(2001)
J Am Soc Nephrol
, vol.12
, pp. 194-200
-
-
Ecder, T.1
Schrier, R.W.2
-
18
-
-
0001839544
-
Clinical management of autosomal dominant polycystic kidney disease
-
Bennett WM, Elzinga LW: Clinical management of autosomal dominant polycystic kidney disease. Kidney Int suppl 42:S74-S79, 1993
-
(1993)
Kidney Int Suppl
, vol.42
-
-
Bennett, W.M.1
Elzinga, L.W.2
-
19
-
-
0025887509
-
Renal manifestations: Complication management and long-term outcome of autosomal dominant polycystic kidney disease
-
Gabow PA, Bennett WM: Renal manifestations: Complication management and long-term outcome of autosomal dominant polycystic kidney disease. Semin Nephrol 11:643-652, 1991
-
(1991)
Semin Nephrol
, vol.11
, pp. 643-652
-
-
Gabow, P.A.1
Bennett, W.M.2
-
20
-
-
0033652904
-
Identification of a locus for autosomal dominant polycystic liver disease on chromosome 19 p 13.2-13.1
-
Reynolds DM, Falk CT, Li A, et al: Identification of a locus for autosomal dominant polycystic liver disease on chromosome 19 p 13.2-13.1. Am J Hum Genet 67:1598-1604, 2000
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1598-1604
-
-
Reynolds, D.M.1
Falk, C.T.2
Li, A.3
-
21
-
-
0026743940
-
Intracranial aneurysms in autosomal dominant polycystic kidney disease
-
Chapman AB, Rubinstein D, Hughes R, et al: Intracranial aneurysms in autosomal dominant polycystic kidney disease. N Engl J Med 327:916-920, 1992
-
(1992)
N Engl J Med
, vol.327
, pp. 916-920
-
-
Chapman, A.B.1
Rubinstein, D.2
Hughes, R.3
-
22
-
-
0032712803
-
Evaluation of colonic diverticular disease in autosomal dominant polycystic kidney disease without end-stage renal disease
-
Sharp CK, Zeligman BE, Johnson AM, Duley IT, Gabow PA: Evaluation of colonic diverticular disease in autosomal dominant polycystic kidney disease without end-stage renal disease. Am J Kidney Dis 34:863-868, 1999
-
(1999)
Am J Kidney Dis
, vol.34
, pp. 863-868
-
-
Sharp, C.K.1
Zeligman, B.E.2
Johnson, A.M.3
Duley, I.T.4
Gabow, P.A.5
-
23
-
-
0030929882
-
Abdominal wall hernia in autosomal dominant polycystic kidney disease
-
Morris-Stiff G, Coles G, Moore R, Jurewicz A, Lord R: Abdominal wall hernia in autosomal dominant polycystic kidney disease. Br J Surg 84:615-617, 1997
-
(1997)
Br J Surg
, vol.84
, pp. 615-617
-
-
Morris-Stiff, G.1
Coles, G.2
Moore, R.3
Jurewicz, A.4
Lord, R.5
-
24
-
-
0033840291
-
Advances in the understanding of tuberous sclerosis
-
O'Callaghan FJ, Osborne JP: Advances in the understanding of tuberous sclerosis. Arch Dis Child 83:140-142, 2000
-
(2000)
Arch Dis Child
, vol.83
, pp. 140-142
-
-
O'Callaghan, F.J.1
Osborne, J.P.2
-
25
-
-
0027619701
-
Characteristics of very early onset autosomal dominant polycystic kidney disease
-
Fick GM, Johnson AM, Strain JD, et al: Characteristics of very early onset autosomal dominant polycystic kidney disease. J Am Soc Nephrol 3:1863-1870, 1993
-
(1993)
J Am Soc Nephrol
, vol.3
, pp. 1863-1870
-
-
Fick, G.M.1
Johnson, A.M.2
Strain, J.D.3
-
26
-
-
0028541574
-
Pregnancy outcome and its relationship to progression of renal failure in autosomal dominant polycystic kidney disease
-
Chapman AB, Johnson AM, Gabow PA: Pregnancy outcome and its relationship to progression of renal failure in autosomal dominant polycystic kidney disease. J Am Soc Nephrol 5:1178-1185, 1994
-
(1994)
J Am Soc Nephrol
, vol.5
, pp. 1178-1185
-
-
Chapman, A.B.1
Johnson, A.M.2
Gabow, P.A.3
-
27
-
-
0034865003
-
Autosomal recessive polycystic kidney disease in adulthood
-
Fonck C, Chauveau D, Gagnadoux M-F, Pirson Y, Grunfeld J-P: Autosomal recessive polycystic kidney disease in adulthood. Nephrol Dial Transplant 16:1648-1652, 2001
-
(2001)
Nephrol Dial Transplant
, vol.16
, pp. 1648-1652
-
-
Fonck, C.1
Chauveau, D.2
Gagnadoux, M.-F.3
Pirson, Y.4
Grunfeld, J.-P.5
-
28
-
-
0036509712
-
The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein
-
Ward CJ, Hogan MC, Rosetti S, et al: The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein. Nat Genet 30:259-269, 2002
-
(2002)
Nat Genet
, vol.30
, pp. 259-269
-
-
Ward, C.J.1
Hogan, M.C.2
Rosetti, S.3
-
29
-
-
12244300887
-
Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1)
-
Bergmann C, Senderek J, Sedlacek B, et al: Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1). J Am Soc Nephrol 14:76-89, 2003
-
(2003)
J Am Soc Nephrol
, vol.14
, pp. 76-89
-
-
Bergmann, C.1
Senderek, J.2
Sedlacek, B.3
-
30
-
-
0036707893
-
Genetics and pathogenesis of polycystic kidney disease
-
Igarashi P, Somlo S: Genetics and pathogenesis of polycystic kidney disease. J Am Soc Nephrol 13:2384-2398, 2002
-
(2002)
J Am Soc Nephrol
, vol.13
, pp. 2384-2398
-
-
Igarashi, P.1
Somlo, S.2
-
31
-
-
0027621009
-
Autosomal recessive polycystic kidney disease: Issues regarding the variability of clinical presentation
-
Shaikewitz ST, Chapman AB: Autosomal recessive polycystic kidney disease: Issues regarding the variability of clinical presentation. J Am Soc Nephrol 3:1858-1862, 1993
-
(1993)
J Am Soc Nephrol
, vol.3
, pp. 1858-1862
-
-
Shaikewitz, S.T.1
Chapman, A.B.2
-
32
-
-
0024314037
-
Polycystic kidney diseases in childhood
-
Kaplan BS, Kaplan P, Rosenberg HK, Lamothe E, Rosenblatt DS: Polycystic kidney diseases in childhood. J Pediatr 115:867-880, 1989
-
(1989)
J Pediatr
, vol.115
, pp. 867-880
-
-
Kaplan, B.S.1
Kaplan, P.2
Rosenberg, H.K.3
Lamothe, E.4
Rosenblatt, D.S.5
-
33
-
-
0032815492
-
Making the diagnosis of Alport's syndrome
-
Pirson Y: Making the diagnosis of Alport's syndrome. Kidney Int 56:760-775, 1999
-
(1999)
Kidney Int
, vol.56
, pp. 760-775
-
-
Pirson, Y.1
-
34
-
-
0038469583
-
Alport's syndrome, Goodpasture's syndrome, and type IV collagen
-
Hudson BG, Tryggvason K, Sundaramoorthy M, Neilson EG: Alport's syndrome, Goodpasture's syndrome, and type IV collagen. N Engl J Med 348:2543-2556, 2003
-
(2003)
N Engl J Med
, vol.348
, pp. 2543-2556
-
-
Hudson, B.G.1
Tryggvason, K.2
Sundaramoorthy, M.3
Neilson, E.G.4
-
35
-
-
0031720662
-
Alport syndrome and thin glomerular basement membrane disease
-
Kashtan CE: Alport syndrome and thin glomerular basement membrane disease. J Am Soc Nephrol 9:1736-1750, 1998
-
(1998)
J Am Soc Nephrol
, vol.9
, pp. 1736-1750
-
-
Kashtan, C.E.1
-
36
-
-
0036020918
-
Meta-analysis of genotype-phenotype correlation in X-linked Alport syndrome: Impact on clinical counselling
-
Gross O, Netzer KO, Lambrecht R, Seibold S, Weber M: Meta-analysis of genotype-phenotype correlation in X-linked Alport syndrome: Impact on clinical counselling. Nephrol Dial Transplant 17:1218-1227, 2002
-
(2002)
Nephrol Dial Transplant
, vol.17
, pp. 1218-1227
-
-
Gross, O.1
Netzer, K.O.2
Lambrecht, R.3
Seibold, S.4
Weber, M.5
-
37
-
-
0035537907
-
Familial Henaturic syndromes - Alport syndrome, thin glomerular basement membrane disease and Fechtner/Epstein syndromes
-
Kashtan CE: Familial Henaturic syndromes-Alport syndrome, thin glomerular basement membrane disease and Fechtner/Epstein syndromes. Contrib Nephrol 136:79-99, 2001
-
(2001)
Contrib Nephrol
, vol.136
, pp. 79-99
-
-
Kashtan, C.E.1
-
38
-
-
0030065754
-
In hereditary nephritis angiotensin-converting enzyme inhibition decreases proteinuria and may slow the rate of progression
-
Cohen EP, Lemann J Jr: In hereditary nephritis angiotensin-converting enzyme inhibition decreases proteinuria and may slow the rate of progression. Am J Kidney Dis 27:199-203, 1996
-
(1996)
Am J Kidney Dis
, vol.27
, pp. 199-203
-
-
Cohen, E.P.1
Lemann Jr., J.2
-
39
-
-
0032986645
-
Long-term effects of cyclosporine A in Alport's syndrome
-
Callis L, Vila A, Carrera M, Nieto J: Long-term effects of cyclosporine A in Alport's syndrome. Kidney Int 55:1051-1056, 1999
-
(1999)
Kidney Int
, vol.55
, pp. 1051-1056
-
-
Callis, L.1
Vila, A.2
Carrera, M.3
Nieto, J.4
-
40
-
-
0033621858
-
Identification of alpha3, alpha4, and alpha5 chains of type IV collagen as alloantigens for Alport posttransplant anti-glomerular basement membrane antibodies
-
Kalluri R, Torre A, Shield CF III, et al: Identification of alpha3, alpha4, and alpha5 chains of type IV collagen as alloantigens for Alport posttransplant anti-glomerular basement membrane antibodies. Transplantation 69:679-684, 2000
-
(2000)
Transplantation
, vol.69
, pp. 679-684
-
-
Kalluri, R.1
Torre, A.2
Shield III, C.F.3
-
41
-
-
19044382459
-
Quantitative analysis of glomerular type IV collagen alpha3-5 chain expression in children with thin basement membrane disease
-
Ueda T, Nakajima M, Akazawa H, et al: Quantitative analysis of glomerular type IV collagen alpha3-5 chain expression in children with thin basement membrane disease. Nephron 92:271-278, 2002
-
(2002)
Nephron
, vol.92
, pp. 271-278
-
-
Ueda, T.1
Nakajima, M.2
Akazawa, H.3
-
42
-
-
0037225967
-
Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)
-
Ghiggeri GM, Caridi G, Magrini U, et al: Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome). Am J Kidney Dis 41:95-104, 2003
-
(2003)
Am J Kidney Dis
, vol.41
, pp. 95-104
-
-
Ghiggeri, G.M.1
Caridi, G.2
Magrini, U.3
-
43
-
-
0034023746
-
National Institute of Health consensus conference: Tuberous sclerosis complex
-
Hyman MH, Whittemore VH: National Institute of Health consensus conference: Tuberous sclerosis complex. Arch Neurol 57:662-665, 2000
-
(2000)
Arch Neurol
, vol.57
, pp. 662-665
-
-
Hyman, M.H.1
Whittemore, V.H.2
-
45
-
-
0036266203
-
Biochemical and molecular genetic basis of Fabry disease
-
Pastores GM, Lien YHH: Biochemical and molecular genetic basis of Fabry disease. J Am Soc Nephrol 13:S130-S133, 2002 (suppl 2)
-
(2002)
J Am Soc Nephrol
, vol.13
, Issue.SUPPL. 2
-
-
Pastores, G.M.1
Lien, Y.H.H.2
-
46
-
-
0036266877
-
Natural history and treatment of renal involvement in Fabry disease
-
Branton M, Schiffmann R, Kopp JB: Natural history and treatment of renal involvement in Fabry disease. J Am Soc Nephrol 13:S139-S143, 2002 (suppl 2)
-
(2002)
J Am Soc Nephrol
, vol.13
, Issue.SUPPL. 2
-
-
Branton, M.1
Schiffmann, R.2
Kopp, J.B.3
-
48
-
-
0035811624
-
Safety and efficacy of recombinant human (alpha)-galactosidase A replacement therapy in Fabry's disease
-
Eng CM, Guffon N, Wilcox WR, et al: Safety and efficacy of recombinant human (alpha)-galactosidase A replacement therapy in Fabry's disease. N Engl J Med 345:9-16, 2001
-
(2001)
N Engl J Med
, vol.345
, pp. 9-16
-
-
Eng, C.M.1
Guffon, N.2
Wilcox, W.R.3
-
49
-
-
0036263496
-
End-stage renal disease in patients with Fabry disease
-
Obrador GT, Ojo A, Thadhani R: End-stage renal disease in patients with Fabry disease. J Am Soc Nephrol 13:S144-S146, 2002 (suppl 2)
-
(2002)
J Am Soc Nephrol
, vol.13
, Issue.SUPPL. 2
-
-
Obrador, G.T.1
Ojo, A.2
Thadhani, R.3
-
50
-
-
0036266230
-
Cardiac involvement in Anderson-Fabry disease
-
Kampmann C, Baehner F, Ries M, Beck M: Cardiac involvement in Anderson-Fabry disease. J Am Soc Nephrol 13:S147-S149, 2002 (suppl 2)
-
(2002)
J Am Soc Nephrol
, vol.13
, Issue.SUPPL. 2
-
-
Kampmann, C.1
Baehner, F.2
Ries, M.3
Beck, M.4
-
51
-
-
0036266968
-
Anderson-Fabry disease: Extrarenal, neurologic manifestations
-
Kolodny EH, Pastores GM: Anderson-Fabry disease: Extrarenal, neurologic manifestations. J Am Soc Nephrol 13:S150-S153, 2002 (suppl 2)
-
(2002)
J Am Soc Nephrol
, vol.13
, Issue.SUPPL. 2
-
-
Kolodny, E.H.1
Pastores, G.M.2
-
52
-
-
0035537906
-
Medullary cystic kidney disease: Past and present
-
Scolari F, Viola BF, Prati E, et al: Medullary cystic kidney disease: Past and present. Contrib Nephrol 136:68-78, 2001
-
(2001)
Contrib Nephrol
, vol.136
, pp. 68-78
-
-
Scolari, F.1
Viola, B.F.2
Prati, E.3
-
53
-
-
7344237404
-
Autosomal dominant medullary cystic kidney disease: Evidence of gene locus heterogeneity
-
Fuchshuber A, Deltas CC, Berthold S, et al: Autosomal dominant medullary cystic kidney disease: Evidence of gene locus heterogeneity. Nephrol Dial Transplant 13:1955-1957, 1998
-
(1998)
Nephrol Dial Transplant
, vol.13
, pp. 1955-1957
-
-
Fuchshuber, A.1
Deltas, C.C.2
Berthold, S.3
-
54
-
-
0033358592
-
Identification of a new locus for medullary cystic disease on chromosome 16p12
-
Scolari F, Puzzer D, Amoroso A, et al: Identification of a new locus for medullary cystic disease on chromosome 16p12. Am J Hum Genet 64:1655-1660, 1999
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1655-1660
-
-
Scolari, F.1
Puzzer, D.2
Amoroso, A.3
-
55
-
-
0033848676
-
Molecular genetics of nephronophthisis and medullary cystic kidney disease
-
Hildebrandt F, Otto E: Molecular genetics of nephronophthisis and medullary cystic kidney disease. J Am Soc Nephrol 11:1753-1761, 2000
-
(2000)
J Am Soc Nephrol
, vol.11
, pp. 1753-1761
-
-
Hildebrandt, F.1
Otto, E.2
-
56
-
-
0030994938
-
Late occurrence of cysts in autosomal dominant medullary cystic kidney disease
-
Neumann HP, Zauner I, Strahm B, et al: Late occurrence of cysts in autosomal dominant medullary cystic kidney disease. Nephrol Dial Transplant 12:1242-1246, 1997
-
(1997)
Nephrol Dial Transplant
, vol.12
, pp. 1242-1246
-
-
Neumann, H.P.1
Zauner, I.2
Strahm, B.3
-
57
-
-
7344268573
-
Autosomal dominant medullary cystic disease: A disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus
-
Scolari F, Ghiggeri GM, Casari G, et al: Autosomal dominant medullary cystic disease: A disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus. Nephrol Dial Transplant 13:2536-2546, 1998
-
(1998)
Nephrol Dial Transplant
, vol.13
, pp. 2536-2546
-
-
Scolari, F.1
Ghiggeri, G.M.2
Casari, G.3
-
58
-
-
0034763887
-
Familial juvenile hyperuricemic nephropathy and autosomal dominant medullary cystic kidney disease type 2: Two facets of the same disease?
-
Dahan K, Fuchshuber A, Adamis S, et al: Familial juvenile hyperuricemic nephropathy and autosomal dominant medullary cystic kidney disease type 2: Two facets of the same disease? J Am Soc Nephrol 12:2348-2357, 2001
-
(2001)
J Am Soc Nephrol
, vol.12
, pp. 2348-2357
-
-
Dahan, K.1
Fuchshuber, A.2
Adamis, S.3
|