-
1
-
-
0019293138
-
Glomerular basement membrane changes in hereditary glomerular diseases
-
GUBLER MC, LEVY M, NAIZOT C, HABIB R: Glomerular basement membrane changes in hereditary glomerular diseases. Renal Physiol Biochem 3:405-413, 1980
-
(1980)
Renal Physiol Biochem
, vol.3
, pp. 405-413
-
-
Gubler, M.C.1
Levy, M.2
Naizot, C.3
Habib, R.4
-
2
-
-
0024575447
-
Inherited defects of renal basement membranes
-
NOEL LH, GUBLER MC, BOBRIE G, SAVAGE COS, LOCKWOOD CM, GRUNFELD JP: Inherited defects of renal basement membranes. Adv Nephrol 18:77-94, 1989
-
(1989)
Adv Nephrol
, vol.18
, pp. 77-94
-
-
Noel, L.H.1
Gubler, M.C.2
Bobrie, G.3
Savage, C.O.S.4
Lockwood, C.M.5
Grunfeld, J.P.6
-
3
-
-
0141859455
-
Hereditary nephritis (Alport's Syndrome) and benign recurrent hematuria (thin glomerular basement membrane disease)
-
chapter 38, edited by TISHER CC, BRENNER BM, Philadelphia, JB Lippincott Co.
-
KASHTAN CE, TOCHIMARU H, SIBLEY RK, MICHAEL AF, VERNIER RL: Hereditary nephritis (Alport's Syndrome) and benign recurrent hematuria (thin glomerular basement membrane disease), chapter 38, in Renal Pathology with Clinical and Functional Correlations (vol 2), edited by TISHER CC, BRENNER BM, Philadelphia, JB Lippincott Co., 1989, p. 1164
-
(1989)
Renal Pathology with Clinical and Functional Correlations
, vol.2
, pp. 1164
-
-
Kashtan, C.E.1
Tochimaru, H.2
Sibley, R.K.3
Michael, A.F.4
Vernier, R.L.5
-
4
-
-
84913918633
-
Nail-patella syndrome (osteo-onychodysplasia), lipodystropy, Fabry's disease (angiokeratoma corporis diffusum universale), and familial lecithin-cholesterol acyltransferase deficiency
-
chapter 39, edited by TISHER CC, BRENNER BM, Philadelphia, J.B. Lippincott Co.
-
COHEN AH, ADLER SG: Nail-patella syndrome (osteo-onychodysplasia), lipodystropy, Fabry's disease (angiokeratoma corporis diffusum universale), and familial lecithin-cholesterol acyltransferase deficiency, chapter 39, in Renal Pathology with Clinical and Functional Correlations (vol 2), edited by TISHER CC, BRENNER BM, Philadelphia, J.B. Lippincott Co., 1989, p. 1191
-
(1989)
Renal Pathology with Clinical and Functional Correlations
, vol.2
, pp. 1191
-
-
Cohen, A.H.1
Adler, S.G.2
-
5
-
-
0022859333
-
Nephronophthisis: A tubular basement membrane defect
-
COHEN AH, HOYER JR: Nephronophthisis: A tubular basement membrane defect. Lab Invest 55:564-592, 1986
-
(1986)
Lab Invest
, vol.55
, pp. 564-592
-
-
Cohen, A.H.1
Hoyer, J.R.2
-
6
-
-
0014391203
-
Congenital microcephaly with hiatus hernia and nephrotic syndrome in two siblings
-
GALLOWAY WH, MOWAT AP: Congenital microcephaly with hiatus hernia and nephrotic syndrome in two siblings. J Med Genet 5:319-321, 1968
-
(1968)
J Med Genet
, vol.5
, pp. 319-321
-
-
Galloway, W.H.1
Mowat, A.P.2
-
7
-
-
0017121915
-
Congenital microcephaly, hiatus hernia and nephrotic syndrome: An autosomal recessive syndrome
-
SHAPIRO LR, DUNCAN PA, FARNSWORTH PB, LEFKOWITZ M: Congenital microcephaly, hiatus hernia and nephrotic syndrome: An autosomal recessive syndrome. Birth Defects 12:275-278, 1976
-
(1976)
Birth Defects
, vol.12
, pp. 275-278
-
-
Shapiro, L.R.1
Duncan, P.A.2
Farnsworth, P.B.3
Lefkowitz, M.4
-
8
-
-
0020320571
-
Kongenitale mikrozephalie mit maskelhypotonie und nephrotoschem syndrom
-
METZKE H, BROMME W: Kongenitale mikrozephalie mit maskelhypotonie und nephrotoschem syndrom [Congenital microcephaly with muscle hypotonia and the nephrotic syndrome]. Padiatire und Grenzgebiete 21:39-41, 1982
-
(1982)
Padiatire und Grenzgebiete
, vol.21
, pp. 39-41
-
-
Metzke, H.1
Bromme, W.2
-
9
-
-
0020554785
-
Pachygyria and congenital nephrosis disorder of migration and neuronal orientation
-
Berl
-
ROBAIN O, DEONNA T: Pachygyria and congenital nephrosis disorder of migration and neuronal orientation. Acta Neuropathol (Berl) 60:137-141, 1983
-
(1983)
Acta Neuropathol
, vol.60
, pp. 137-141
-
-
Robain, O.1
Deonna, T.2
-
10
-
-
0021441625
-
Association d'un syndrome néphrotique à début précocc et d'une microcéphalie: A propos de 4 observations dans deux familes
-
GAUDELUS J, LEVERGER G, RAULT G, NATHANSON M, GIORNO JL, BOCCON-GIBOD L, LEVY M, BROYER M: Association d'un syndrome néphrotique à début précocc et d'une microcéphalie: A propos de 4 observations dans deux familes. Arch Fr Pediatr 41:409-415, 1984
-
(1984)
Arch Fr Pediatr
, vol.41
, pp. 409-415
-
-
Gaudelus, J.1
Leverger, G.2
Rault, G.3
Nathanson, M.4
Giorno, J.L.5
Boccon-Gibod, L.6
Levy, M.7
Broyer, M.8
-
11
-
-
0023594948
-
Congenital microcephaly, infantile spasms, psychomotor retardation, and nephrotic syndrome in two siblings
-
ROOS RAC, MAASWINKEL-MOOY PD, V.D. LOO EM, KANHAI HHH: Congenital microcephaly, infantile spasms, psychomotor retardation, and nephrotic syndrome in two siblings. Eur J Pediatr 146:532-536, 1987
-
(1987)
Eur J Pediatr
, vol.146
, pp. 532-536
-
-
Roos, R.A.C.1
Maaswinkel-Mooy, P.D.2
V.D. Loo, E.M.3
Kanhai, H.H.H.4
-
12
-
-
0025050872
-
Familial infantile nephrotic syndrome with ocular abnormalities
-
GLASTRE C, COCHAT P, BOUVIER R, COLON S, COTTIN X, GIFFEN D, WRIGHT C, DIJOUD F, DAVID L: Familial infantile nephrotic syndrome with ocular abnormalities. Pediatr Nephrol 4:340-342 1990
-
(1990)
Pediatr Nephrol
, vol.4
, pp. 340-342
-
-
Glastre, C.1
Cochat, P.2
Bouvier, R.3
Colon, S.4
Cottin, X.5
Giffen, D.6
Wright, C.7
Dijoud, F.8
David, L.9
-
13
-
-
0021322629
-
Interstitial Tamm-Horsfall protein in rejecting renal allografts: Identification and morphologic pattern of injury
-
COHEN AH, BORDER WA, RAJFER J, DUMKE A, GLASSOCK RJ: Interstitial Tamm-Horsfall protein in rejecting renal allografts: Identification and morphologic pattern of injury. Lab Invest 50:519-525, 1984
-
(1984)
Lab Invest
, vol.50
, pp. 519-525
-
-
Cohen, A.H.1
Border, W.A.2
Rajfer, J.3
Dumke, A.4
Glassock, R.J.5
-
14
-
-
0019958324
-
Production and characterization of a monoclonal antibody to human type IV collagen
-
SAKAI LY, ENGVALL E, HOLLISTER DW, BURGESON RE: Production and characterization of a monoclonal antibody to human type IV collagen. Am J Pathol 108:310-318, 1982
-
(1982)
Am J Pathol
, vol.108
, pp. 310-318
-
-
Sakai, L.Y.1
Engvall, E.2
Hollister, D.W.3
Burgeson, R.E.4
-
15
-
-
0021874923
-
Structural studies of human basement membrane collagen with the use of a monoclonal antibody
-
DIERINGER H, HOLLISTER DW, GLANVILLE RW, SAKAI LY, KUHN K: Structural studies of human basement membrane collagen with the use of a monoclonal antibody. Biochem J 227:217-222, 1985
-
(1985)
Biochem J
, vol.227
, pp. 217-222
-
-
Dieringer, H.1
Hollister, D.W.2
Glanville, R.W.3
Sakai, L.Y.4
Kuhn, K.5
-
16
-
-
0017975964
-
Changes in glomerular basement membrane antigen(s) with age
-
ANAND SK, LANDING BH, HEUSER ET, OLSON DT, GRUSHKIN CM, LIEBERMAN E: Changes in glomerular basement membrane antigen(s) with age. J Pediatr 92:952-953, 1978
-
(1978)
J Pediatr
, vol.92
, pp. 952-953
-
-
Anand, S.K.1
Landing, B.H.2
Heuser, E.T.3
Olson, D.T.4
Grushkin, C.M.5
Lieberman, E.6
-
17
-
-
0020058318
-
Diffuse mesangial sclerosis and ocular abnormalities in two siblings
-
BARAKAT AY, KHOURY LA, ALLAM CK, NAJJAR SS: Diffuse mesangial sclerosis and ocular abnormalities in two siblings. Int J Pediatr Nephrol 3:33-35, 1982
-
(1982)
Int J Pediatr Nephrol
, vol.3
, pp. 33-35
-
-
Barakat, A.Y.1
Khoury, L.A.2
Allam, C.K.3
Najjar, S.S.4
-
18
-
-
0018834240
-
Infantile nephrotic syndrome with diffuse mesangial sclerosis: A disturbance of glomerular basement membrane development
-
RUMPELT HJ, BACHMANN HJ: Infantile nephrotic syndrome with diffuse mesangial sclerosis: A disturbance of glomerular basement membrane development. Clin Nephrol 13:146-150, 1980
-
(1980)
Clin Nephrol
, vol.13
, pp. 146-150
-
-
Rumpelt, H.J.1
Bachmann, H.J.2
-
19
-
-
0002668646
-
Nephrotic syndrome in the first year of life
-
(chapt 40), edited by TISHER CC, BRENNER BM, Philadelphia, JB Lippincott Co
-
SIBLEY RK, STRIEGEL J, MELVIN T: Nephrotic syndrome in the first year of life (chapt 40), in Renal Pathology with Clinical and Functional Correlations, edited by TISHER CC, BRENNER BM, Philadelphia, JB Lippincott Co, 1989, p. 1214
-
(1989)
Renal Pathology with Clinical and Functional Correlations
, pp. 1214
-
-
Sibley, R.K.1
Striegel, J.2
Melvin, T.3
-
20
-
-
0025778181
-
Focal and segmental glomerulosclerosis associated with infantile spasms in five mentally retarded children: A morphological analysis on mesangiolysis
-
JOH K, USUI N, AIZAWAS, YAMAGUCHI Y, CHIBA S, TAKAHASHI T, MURAMATSU Y, SAKAI S: Focal and segmental glomerulosclerosis associated with infantile spasms in five mentally retarded children: A morphological analysis on mesangiolysis. Am J Kidney Dis 17:569-577, 1991
-
(1991)
Am J Kidney Dis
, vol.17
, pp. 569-577
-
-
Joh, K.1
Usui, N.2
Aizawas3
Yamaguchi, Y.4
Chiba, S.5
Takahashi, T.6
Muramatsu, Y.7
Sakai, S.8
-
21
-
-
12644284558
-
Basement membranes-organization and function
-
chapter 1, edited by PRICE RG, HUDSON BG, London, Academic Press
-
PRICE RG, RAND-WEAVER M: Basement membranes-organization and function, chapter 1, in Renal Basement Membranes in Health and Disease, edited by PRICE RG, HUDSON BG, London, Academic Press, 1987, p. 3
-
(1987)
Renal Basement Membranes in Health and Disease
, pp. 3
-
-
Price, R.G.1
Rand-Weaver, M.2
-
22
-
-
0018578024
-
Glomerular microfibrils in renal disease: A comparative electron microscopic study
-
HSU H-C, CHURG J: Glomerular microfibrils in renal disease: A comparative electron microscopic study. Kidney Int 16:497-504, 1979
-
(1979)
Kidney Int
, vol.16
, pp. 497-504
-
-
Hsu, H.-C.1
Churg, J.2
|