-
1
-
-
0028270861
-
Alport syndrome: Clinical, molecular and genetic aspects
-
Sessa A, Renieri A, Battaglia C. Alport syndrome: clinical, molecular and genetic aspects. J Nephrol 1994; 7: 102-116
-
(1994)
J Nephrol
, vol.7
, pp. 102-116
-
-
Sessa, A.1
Renieri, A.2
Battaglia, C.3
-
2
-
-
0015736575
-
Alport's syndrome: A consideration of pathogenesis
-
Spear GS. Alport's syndrome: a consideration of pathogenesis. Clin Nephrol 1973; 1: 336-337
-
(1973)
Clin Nephrol
, vol.1
, pp. 336-337
-
-
Spear, G.S.1
-
3
-
-
0016291994
-
Hereditary nephropathy with nerve deafness (Alport's syndrome): Electron microscopic studies on the renal glomerulus
-
Sessa A, Cioffi A, Conte F, D'Amico G. Hereditary nephropathy with nerve deafness (Alport's syndrome): electron microscopic studies on the renal glomerulus. Nephron 1974; 13: 404-415
-
(1974)
Nephron
, vol.13
, pp. 404-415
-
-
Sessa, A.1
Cioffi, A.2
Conte, F.3
D'Amico, G.4
-
4
-
-
0025174012
-
Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome
-
Hostikka SL, Eddy RL, Byers MG, Hoyhtya M, Shows TB, Tryggvason K. Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome. Proc Natl Acad Sci USA 1990; 87: 1606-1610
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 1606-1610
-
-
Hostikka, S.L.1
Eddy, R.L.2
Byers, M.G.3
Hoyhtya, M.4
Shows, T.B.5
Tryggvason, K.6
-
5
-
-
0028069132
-
Mutations in the type IV collagen alfa-3 (COL4A3) gene in autosomal recessive Alport syndrome
-
Lemmink HH, Mochizuki T, Van den Heuvel LP et al. Mutations in the type IV collagen alfa-3 (COL4A3) gene in autosomal recessive Alport syndrome. Hum Mol Genet 1994; 3: 1269-1273
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1269-1273
-
-
Lemmink, H.H.1
Mochizuki, T.2
Van Den Heuvel, L.P.3
-
6
-
-
1842430334
-
Autosomal dominant Alport syndrome linked to markers on 29 flanking the COL4A3:COL4A4 genes
-
27th Annual Meeting ASN, Orlando 1994.
-
Jefferson JA, Hughes AE, Hill C, Maxwell AP, Doherty CC, Nevin NC. Autosomal dominant Alport syndrome linked to markers on 29 flanking the COL4A3:COL4A4 genes. 27th Annual Meeting ASN, Orlando 1994. JASN 1994; 5: 647, 43
-
(1994)
JASN
, vol.5
, pp. 647
-
-
Jefferson, J.A.1
Hughes, A.E.2
Hill, C.3
Maxwell, A.P.4
Doherty, C.C.5
Nevin, N.C.6
-
7
-
-
0016200996
-
The nonspecificity of the ultrastructure lesion in hereditary nephritis: With additional observations on benign familial hematuria
-
Hill GS, Jenis EH, Goodloe S Jr. The nonspecificity of the ultrastructure lesion in hereditary nephritis: with additional observations on benign familial hematuria. Lab Invest 1974; 31: 516-532
-
(1974)
Lab Invest
, vol.31
, pp. 516-532
-
-
Hill, G.S.1
Jenis, E.H.2
Goodloe Jr., S.3
-
8
-
-
0015428067
-
Alport's syndrome emphasizing electron microscopic studies of the glomerulus
-
Spear GS, Slusser RJ. Alport's syndrome emphasizing electron microscopic studies of the glomerulus. Am J Pathol 1972; 69: 213-224
-
(1972)
Am J Pathol
, vol.69
, pp. 213-224
-
-
Spear, G.S.1
Slusser, R.J.2
-
9
-
-
0015421264
-
Characteristic ultrastructural lesions of the glomerular basement membrane in progressive nephritis (Alport's syndrome)
-
Hinglais M, Grünfeld JP, Bois E. Characteristic ultrastructural lesions of the glomerular basement membrane in progressive nephritis (Alport's syndrome). Lab Invest 1972; 27: 473-487
-
(1972)
Lab Invest
, vol.27
, pp. 473-487
-
-
Hinglais, M.1
Grünfeld, J.P.2
Bois, E.3
-
10
-
-
0015955413
-
Hereditary nephritis with a characteristic renal lesion
-
Sherman RL, Churg J, Yudis M. Hereditary nephritis with a characteristic renal lesion. Am J Med 1974; 56: 44-51
-
(1974)
Am J Med
, vol.56
, pp. 44-51
-
-
Sherman, R.L.1
Churg, J.2
Yudis, M.3
-
11
-
-
0025002684
-
Correlation of glomerular basement membrane alterations with clinical data in progressive hereditary nephritis (Alport's syndrome)
-
Basta-Jovanovic G, Venkataseshan VS. Churg J. Correlation of glomerular basement membrane alterations with clinical data in progressive hereditary nephritis (Alport's syndrome). Am J Kidney Dis 1990; 16: 51-56
-
(1990)
Am J Kidney Dis
, vol.16
, pp. 51-56
-
-
Basta-Jovanovic, G.1
Venkataseshan, V.S.2
Churg, J.3
-
13
-
-
0024445449
-
Thin membrane nephropathy: A clinico-pathological study
-
Aarons I, Smith PS, Davies RA, Woodroffe AJ, Clarkson AR. Thin membrane nephropathy: a clinico-pathological study. Clin Nephrol 1989; 32: 151-158
-
(1989)
Clin Nephrol
, vol.32
, pp. 151-158
-
-
Aarons, I.1
Smith, P.S.2
Davies, R.A.3
Woodroffe, A.J.4
Clarkson, A.R.5
-
14
-
-
0025295803
-
Incidence of thin membrane nephropathy: Morphometric investigation of a population sample
-
Dische FE, Anderson VER, Keane SJ, Taube D, Bewick M, Parsons V. Incidence of thin membrane nephropathy: morphometric investigation of a population sample. J Clin Pathol 1990; 43: 457-460
-
(1990)
J Clin Pathol
, vol.43
, pp. 457-460
-
-
Dische, F.E.1
Anderson, V.E.R.2
Keane, S.J.3
Taube, D.4
Bewick, M.5
Parsons, V.6
-
15
-
-
0028070269
-
Association of thin glomerular basement membrane with other glomerulopathies
-
Cosio FG, Falkenhan ME, Sedmak DD. Association of thin glomerular basement membrane with other glomerulopathies. Kidney Int 1994; 46: 471-474
-
(1994)
Kidney Int
, vol.46
, pp. 471-474
-
-
Cosio, F.G.1
Falkenhan, M.E.2
Sedmak, D.D.3
-
16
-
-
0026271678
-
Glomerular basement membrane thinning is acquired in minimal change disease
-
Coleman M, Stirling JW. Glomerular basement membrane thinning is acquired in minimal change disease. Am J Nephrol 1991; 11: 437-438
-
(1991)
Am J Nephrol
, vol.11
, pp. 437-438
-
-
Coleman, M.1
Stirling, J.W.2
-
17
-
-
0025167916
-
Thin membrane nephropathy: How thin is thin?
-
Editorial. Thin membrane nephropathy: how thin is thin? Lancet 1990; 336: 469-470
-
(1990)
Lancet
, vol.336
, pp. 469-470
-
-
-
18
-
-
0026559228
-
Glomerular basement thinning in adults: Clinicopathological correlations of a new diagnostic approach
-
McLay ALC, Jackson R, Meyboom F, Boulton Jones JM. Glomerular basement thinning in adults: clinicopathological correlations of a new diagnostic approach. Nephrol Dial Transplant 1992; 7: 191-199
-
(1992)
Nephrol Dial Transplant
, vol.7
, pp. 191-199
-
-
McLay, A.L.C.1
Jackson, R.2
Meyboom, F.3
Boulton Jones, J.M.4
-
19
-
-
9544221712
-
Overlap of Alport and thin membrane nephropathy
-
Erlangen, October
-
White RHR, Raafat F, McKay S, Fardon PA. Overlap of Alport and thin membrane nephropathy. 3rd Int Workshop on Alport Syndrome, Erlangen, October 1994
-
(1994)
3rd Int Workshop on Alport Syndrome
-
-
White, R.H.R.1
Raafat, F.2
McKay, S.3
Fardon, P.A.4
-
20
-
-
0021012526
-
Basement membrane nephropathy
-
Yum M, Bergstein JM. Basement membrane nephropathy. Hum Pathol 1983; 14: 996-1003
-
(1983)
Hum Pathol
, vol.14
, pp. 996-1003
-
-
Yum, M.1
Bergstein, J.M.2
-
21
-
-
0019449140
-
Alport's syndrome: A report of 58 cases and a review of the literature
-
Gübler MC, Levy M, Broyer M et al. Alport's syndrome: a report of 58 cases and a review of the literature. Am J Med 1981; 70: 493-505
-
(1981)
Am J Med
, vol.70
, pp. 493-505
-
-
Gübler, M.C.1
Levy, M.2
Broyer, M.3
-
22
-
-
0025653587
-
Ultrastructural lesions of tubular basement membranes and peritubular capillaries in hereditary nephritis
-
Battini G, Meroni M, Torri Tarelli L, Sessa A. Ultrastructural lesions of tubular basement membranes and peritubular capillaries in hereditary nephritis. Contrib Nephrol 1990; 80: 47-55
-
(1990)
Contrib Nephrol
, vol.80
, pp. 47-55
-
-
Battini, G.1
Meroni, M.2
Torri Tarelli, L.3
Sessa, A.4
-
23
-
-
0023933690
-
Glomerular basement membrane thickness in children. A morphometric study
-
Morita M, White RHR, Raafat F, Barnes JM, Standring D. Glomerular basement membrane thickness in children. A morphometric study. Pediatr Nephrol 1988; 2: 190-195
-
(1988)
Pediatr Nephrol
, vol.2
, pp. 190-195
-
-
Morita, M.1
White, R.H.R.2
Raafat, F.3
Barnes, J.M.4
Standring, D.5
-
24
-
-
0029191248
-
Paraffin-processed material is unsuitable for diagnosis of thin membrane disease
-
Collar J, Cattel V. Paraffin-processed material is unsuitable for diagnosis of thin membrane disease. Nephron 1995; 69: 187-188
-
(1995)
Nephron
, vol.69
, pp. 187-188
-
-
Collar, J.1
Cattel, V.2
-
25
-
-
0019463068
-
The normal human renal glomerulus
-
Haynes WDG. The normal human renal glomerulus. Virchows Arch B 1981; 35: 133-158
-
(1981)
Virchows Arch B
, vol.35
, pp. 133-158
-
-
Haynes, W.D.G.1
-
26
-
-
0021279199
-
Animal model of human diseases. Hereditary nephritis in Samoycd dogs
-
Jansen B, Thoner PS, Singh A et al. Animal model of human diseases. Hereditary nephritis in Samoycd dogs. Am J Pathol 1984; 116: 175-178
-
(1984)
Am J Pathol
, vol.116
, pp. 175-178
-
-
Jansen, B.1
Thoner, P.S.2
Singh, A.3
-
27
-
-
0015792370
-
Progressive and non-progressive hereditary chronic nephritis
-
Grünfeld JP, Bois EP, Hinglais M. Progressive and non-progressive hereditary chronic nephritis. Kidney Int 1973; 4: 216-228
-
(1973)
Kidney Int
, vol.4
, pp. 216-228
-
-
Grünfeld, J.P.1
Bois, E.P.2
Hinglais, M.3
-
28
-
-
0015922463
-
Hereditary nephritis with immunofluorescent mesangial deposits
-
Sessa A, Cioffi A, Allaria P, Conte F, D'Amico G. Hereditary nephritis with immunofluorescent mesangial deposits. Lancet 1973; 2: 853
-
(1973)
Lancet
, vol.2
, pp. 853
-
-
Sessa, A.1
Cioffi, A.2
Allaria, P.3
Conte, F.4
D'Amico, G.5
-
29
-
-
0027379064
-
Alport syndrome with type I membranoproliferative glomerulonephritis
-
Meroni M, Sessa A, Battini G et al. Alport syndrome with type I membranoproliferative glomerulonephritis. Nephron 1993; 65: 479-480
-
(1993)
Nephron
, vol.65
, pp. 479-480
-
-
Meroni, M.1
Sessa, A.2
Battini, G.3
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