-
1
-
-
84965236793
-
Hereditary familial congenital haemorrhagic nephritis
-
Alport A: Hereditary familial congenital haemorrhagic nephritis. Br Med J 1:504-506, 1927
-
(1927)
Br Med J
, vol.1
, pp. 504-506
-
-
Alport, A.1
-
3
-
-
0021846608
-
Renal prognosis in women with hereditary nephritis
-
Grunfeld J-P, Noel L, Hafez S, et al: Renal prognosis in women with hereditary nephritis. Clin Nephrol 23:276-271, 1985
-
(1985)
Clin Nephrol
, vol.23
, pp. 276-1271
-
-
Grunfeld, J.-P.1
Noel, L.2
Hafez, S.3
-
4
-
-
0018942488
-
Hereditary nephropathy (Alport syndrome): Correlation of clinical data with glomerular basement membrane alterations
-
Rumpelt H-J: Hereditary nephropathy (Alport syndrome): Correlation of clinical data with glomerular basement membrane alterations. Clin Nephrol 13:203-207, 1980
-
(1980)
Clin Nephrol
, vol.13
, pp. 203-207
-
-
Rumpelt, H.-J.1
-
6
-
-
0028353676
-
Deletions in the COL4A5 collagen gene in X-linked Alport syndrome: Characterization of the pathological transcripts in nonrenal cells and correlation with disease expression
-
Antignac C, Knebelmann B, Drouot L, et al: Deletions in the COL4A5 collagen gene in X-linked Alport syndrome: Characterization of the pathological transcripts in nonrenal cells and correlation with disease expression. J Clin Invest 93:1195-1207, 1994
-
(1994)
J Clin Invest
, vol.93
, pp. 1195-1207
-
-
Antignac, C.1
Knebelmann, B.2
Drouot, L.3
-
7
-
-
13144272919
-
Analysis of the COL4A5 gene in patients with Alport syndrome disclosed two deletions and one point mutation affecting a splice site
-
Netzer K, Pullig O, Renders L, et al: Analysis of the COL4A5 gene in patients with Alport syndrome disclosed two deletions and one point mutation affecting a splice site. Kidney Int 43:250, 1992
-
(1992)
Kidney Int
, vol.43
, pp. 250
-
-
Netzer, K.1
Pullig, O.2
Renders, L.3
-
8
-
-
0026792994
-
Alport syndrome and diffuse leiomyomatosis: Deletions in the 5′ end of the COL4A5 collagen gene
-
Antignac C, Zhou J, Sanak M, et al: Alport syndrome and diffuse leiomyomatosis: Deletions in the 5′ end of the COL4A5 collagen gene. Kidney Int 42:1178-1183, 1992
-
(1992)
Kidney Int
, vol.42
, pp. 1178-1183
-
-
Antignac, C.1
Zhou, J.2
Sanak, M.3
-
9
-
-
0028981590
-
Deletions of both a5(IV) and a6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumours
-
Heidet L, Dahan K, Zhou J, et al: Deletions of both a5(IV) and a6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumours. Hum Mol Genet 4:99-108, 1995
-
(1995)
Hum Mol Genet
, vol.4
, pp. 99-108
-
-
Heidet, L.1
Dahan, K.2
Zhou, J.3
-
10
-
-
0029943825
-
A mutation causing Alport syndrome with tardive hearing loss is common in the western United States
-
Barker D, Pruchno C, Jiang X, et al: A mutation causing Alport syndrome with tardive hearing loss is common in the western United States. Am J Hum Genet 58:1157-1165, 1996
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1157-1165
-
-
Barker, D.1
Pruchno, C.2
Jiang, X.3
-
11
-
-
0028168648
-
Identification of mutations in the A3(IV) and A4(IV) collagen genes in autosomal recessive Alport syndrome
-
Mochizuki T, Lemmink HH, Mariyama M, et al: Identification of mutations in the A3(IV) and A4(IV) collagen genes in autosomal recessive Alport syndrome. Nature Genet 8:77-81, 1994
-
(1994)
Nature Genet
, vol.8
, pp. 77-81
-
-
Mochizuki, T.1
Lemmink, H.H.2
Mariyama, M.3
-
12
-
-
0022444831
-
The Goodpasture antigen in Alport's syndrome: Studies with a monoclonal antibody
-
Savage COS, Pusey CD, Kershaw MJ, et al: The Goodpasture antigen in Alport's syndrome: Studies with a monoclonal antibody. Kidney Int 30:107-112, 1986
-
(1986)
Kidney Int
, vol.30
, pp. 107-112
-
-
Savage, C.O.S.1
Pusey, C.D.2
Kershaw, M.J.3
-
13
-
-
0026694770
-
Immunochemical studies of the Alport antigen
-
Kleppel MM, Fan WW, Cheong HI, et al: Immunochemical studies of the Alport antigen. Kidney Int 41:1629-1637, 1992
-
(1992)
Kidney Int
, vol.41
, pp. 1629-1637
-
-
Kleppel, M.M.1
Fan, W.W.2
Cheong, H.I.3
-
14
-
-
0027974208
-
Immunohistochemical study of α1-5 chains of type IV collagen in hereditary nephritis
-
Nakanishi K, Yoshikawa N, Iijima K, et al: Immunohistochemical study of α1-5 chains of type IV collagen in hereditary nephritis. Kidney Int 46:1413-1421, 1994
-
(1994)
Kidney Int
, vol.46
, pp. 1413-1421
-
-
Nakanishi, K.1
Yoshikawa, N.2
Iijima, K.3
-
15
-
-
0024442303
-
Distribution of familial nephritis antigen in normal tissue and renal basement membranes of patients with homozygous and heterozygous Alport familial nephritis
-
Kleppel MM, Kashtan C, Santi PA, et al: Distribution of familial nephritis antigen in normal tissue and renal basement membranes of patients with homozygous and heterozygous Alport familial nephritis. Lab Invest 61:278, 1989
-
(1989)
Lab Invest
, vol.61
, pp. 278
-
-
Kleppel, M.M.1
Kashtan, C.2
Santi, P.A.3
-
16
-
-
0025350089
-
Abnormally thin glomerular basement membrane and the Goodpasture epitope
-
Pettersson E, Tornroth T, Wieslander J: Abnormally thin glomerular basement membrane and the Goodpasture epitope. Clin Nephrol 33:105-109, 1990
-
(1990)
Clin Nephrol
, vol.33
, pp. 105-109
-
-
Pettersson, E.1
Tornroth, T.2
Wieslander, J.3
-
17
-
-
0022629020
-
Immunohistochemical localization of glomerular basement membrane antigens in various renal diseases
-
Hara M, Mase D, Inaba S, et al: Immunohistochemical localization of glomerular basement membrane antigens in various renal diseases. Virchows Arch 408:403-419, 1986
-
(1986)
Virchows Arch
, vol.408
, pp. 403-419
-
-
Hara, M.1
Mase, D.2
Inaba, S.3
-
18
-
-
0023032361
-
Nephritogenic antigen determinants in epidermal and renal basement membranes of kindreds with Alport-type familial nephritis
-
Kashtan C, Fish A, Kleppel M, et al: Nephritogenic antigen determinants in epidermal and renal basement membranes of kindreds with Alport-type familial nephritis. J Clin Invest 78:1035-1044, 1986
-
(1986)
J Clin Invest
, vol.78
, pp. 1035-1044
-
-
Kashtan, C.1
Fish, A.2
Kleppel, M.3
-
19
-
-
0028330824
-
A monoclonal antibody marker for Alport syndrome identifies the Alport antigen as the α5 chain of type TV collagen
-
Ding J, Kashtan CE, Fan WW, et al: A monoclonal antibody marker for Alport syndrome identifies the Alport antigen as the α5 chain of type TV collagen. Kidney Int 45:1504-1506, 1994
-
(1994)
Kidney Int
, vol.45
, pp. 1504-1506
-
-
Ding, J.1
Kashtan, C.E.2
Fan, W.W.3
-
21
-
-
0020580195
-
Quantitative glomerular morphology of the normal human kidney
-
Steffes M, Barbosa J, Basgen J, et al: Quantitative glomerular morphology of the normal human kidney. Lab Invest 49:82-86, 1983
-
(1983)
Lab Invest
, vol.49
, pp. 82-86
-
-
Steffes, M.1
Barbosa, J.2
Basgen, J.3
-
22
-
-
0023543664
-
Glomerular basement membrane and lamina densa in infants and children: An ultrastructural evaluation
-
Vogler C, McAdams A, Homan S: Glomerular basement membrane and lamina densa in infants and children: An ultrastructural evaluation. Pediatr Pathol 7:527-534, 1987
-
(1987)
Pediatr Pathol
, vol.7
, pp. 527-534
-
-
Vogler, C.1
McAdams, A.2
Homan, S.3
-
23
-
-
0019792531
-
The glomerular basal lamina in hereditary nephritis
-
Yoshikawa N, Cameron AH, White RHR: The glomerular basal lamina in hereditary nephritis. J Pathol 135:199-209, 1981
-
(1981)
J Pathol
, vol.135
, pp. 199-209
-
-
Yoshikawa, N.1
Cameron, A.H.2
White, R.H.R.3
-
24
-
-
0030369741
-
Expression of type IV collagen a3 and α4 chain mRNA in X-linked Alport syndrome
-
Nakanishi K, Yoskikawa N, Iijima K, et al: Expression of type IV collagen a3 and α4 chain mRNA in X-linked Alport syndrome. J Am Soc Nephrol 7:938-945, 1996
-
(1996)
J Am Soc Nephrol
, vol.7
, pp. 938-945
-
-
Nakanishi, K.1
Yoskikawa, N.2
Iijima, K.3
-
25
-
-
0028939722
-
Autosomal recessive Alport syndrome: Immunohistochemical study of type IV collagen chain distribution
-
Gubler MC, Knebelmann B, Beziau A, et al: Autosomal recessive Alport syndrome: Immunohistochemical study of type IV collagen chain distribution. Kidney Int 47:1142-1147, 1995
-
(1995)
Kidney Int
, vol.47
, pp. 1142-1147
-
-
Gubler, M.C.1
Knebelmann, B.2
Beziau, A.3
|