-
1
-
-
0031758412
-
Renal tract abnormalities detected in Australian preschool children
-
DOI 10.1046/j.1440-1754.1998.00269.x
-
Hogg RJ, Harris S, Lawrence DM, Henning PH, Wigg N, Jureidini KF: Renal tract abnormalities detected in Australian preschool children. J Paediatr Child Health 34: 420-424, 1998 (Pubitemid 28481725)
-
(1998)
Journal of Paediatrics and Child Health
, vol.34
, Issue.5
, pp. 420-424
-
-
Hogg, R.J.1
Harris, S.2
Lawrence, D.M.3
Henning, P.H.4
Wigg, N.5
Jureidini, K.F.6
-
2
-
-
0022628803
-
Importance of occult haematuria found at screening
-
Ritchie CD, Bevan EA, Collier SJ: Importance of occult haematuria found at screening. Br Med J 292: 681-683, 1986
-
Br Med J
, vol.292
, Issue.681-683
, pp. 1986
-
-
Ritchie, C.D.1
Bevan, E.A.2
Collier, S.J.3
-
3
-
-
0141674966
-
Thin basement membrane nephropathy
-
DOI 10.1046/j.1523-1755.2003.00234.x
-
Savige J, Rana K, Tonna S, Buzza M, Dagher H, Wang YY: Thin basement membrane nephropathy. Kidney Int 64: 1169-1178, 2003 (Pubitemid 37153781)
-
(2003)
Kidney International
, vol.64
, Issue.4
, pp. 1169-1178
-
-
Savige, J.1
Rana, K.2
Tonna, S.3
Buzza, M.4
Dagher, H.5
Wang, Y.Y.6
-
4
-
-
0038469583
-
Alport's syndrome, Goodpasture's syndrome, and type IV collagen
-
DOI 10.1056/NEJMra022296
-
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 (Pubitemid 36706542)
-
(2003)
New England Journal of Medicine
, vol.348
, Issue.25
, pp. 2543-2556
-
-
Hudson, B.G.1
Tryggvason, K.2
Sundaramoorthy, M.3
Neilson, E.G.4
-
5
-
-
0021013258
-
X-linked inheritance of Alport syndrome: Family P revisited
-
Hasstedt SJ, Atkin CL: X-linked inheritance of Alport syndrome: Family P revisited. Am J Hum Genet 35: 1241-1251, 1983 (Pubitemid 14201175)
-
(1983)
American Journal of Human Genetics
, vol.35
, Issue.6
, pp. 1241-1251
-
-
Hasstedt, S.J.1
Atkin, C.L.2
-
6
-
-
23144432647
-
Alport syndrome in southern Sweden
-
Persson U, Hertz JM, Wieslander J, Segelmark M: Alport syndrome in southern Sweden. Clin Nephrol 64: 85-90, 2005 (Pubitemid 41079003)
-
(2005)
Clinical Nephrology
, vol.64
, Issue.2
, pp. 85-90
-
-
Persson, U.1
Hertz, J.M.2
Wieslander, J.3
Segelmark, M.4
-
7
-
-
79960968577
-
Retinal abnormalities characteristic of inherited renal disease
-
Savige J, Ratnaike S, Colville D: Retinal abnormalities characteristic of inherited renal disease. J AmSocNephrol 22: 1403-1415, 2011
-
(2011)
J AmSocNephrol
, vol.22
, pp. 1403-1415
-
-
Savige, J.1
Ratnaike, S.2
Colville, D.3
-
8
-
-
0019449140
-
Alport's syndrome. A report of 58 cases and a review of the literature
-
DOI 10.1016/0002-9343(81)90571-4
-
Gubler M, Levy M, Broyer M, Naizot C, Gonzales G, Perrin D, Habib R: Alport's syndrome. A report of 58 cases and a review of the literature. Am J Med 70: 493-505, 1981 (Pubitemid 11153813)
-
(1981)
American Journal of Medicine
, vol.70
, Issue.3
, pp. 493-505
-
-
Gubler, M.1
Levy, M.2
Broyer, M.3
-
9
-
-
12044253337
-
Type iv collagen alpha 5 chain. Normal distribution and abnormalities in x-linked alport syndrome revealed by monoclonal antibody
-
Yoshioka K, Hino S, Takemura T, Maki S, Wieslander J, Takekoshi Y, Makino H, Kagawa M, Sado Y, Kashtan CE: Type IV collagen alpha 5 chain. Normal distribution and abnormalities in X-linked Alport syndrome revealed by monoclonal antibody. Am J Pathol 144: 986-996, 1994
-
(1994)
Am J Pathol
, vol.144
, pp. 986-996
-
-
Yoshioka, K.1
Hino, S.2
Takemura, T.3
Maki, S.4
Wieslander, J.5
Takekoshi, Y.6
Makino, H.7
Kagawa, M.8
Sado, Y.9
Kashtan, C.E.10
-
10
-
-
0025292712
-
Identification of mutations in the col4a5 collagen gene in alport syndrome
-
Barker DF, Hostikka SL, Zhou J, Chow LT, Oliphant AR, Gerken SC, Gregory MC, Skolnick MH, Atkin CL, Tryggvason K: Identification of mutations in the COL4A5 collagen gene in Alport syndrome. Science 248: 1224-1227, 1990
-
(1990)
Science
, vol.248
, pp. 1224-1227
-
-
Barker, D.F.1
Hostikka, S.L.2
Zhou, J.3
Chow, L.T.4
Oliphant, A.R.5
Gerken, S.C.6
Gregory, M.C.7
Skolnick, M.H.8
Atkin, C.L.9
Tryggvason, K.10
-
11
-
-
0028168648
-
Identification of mutations in the alpha3(IV) and alpha4(IV) collagen genes in autosomal recessive Alport syndrome
-
DOI 10.1038/ng0994-77
-
Mochizuki T, Lemmink HH, Mariyama M, Antignac C, Gubler MC, Pirson Y, Verellen-Dumoulin C, Chan B, Schröder CH, Smeets HJ, et al: Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome. Nat Genet 8: 77-81, 1994 (Pubitemid 2122272)
-
(1994)
Nature Genetics
, vol.8
, Issue.1
, pp. 77-81
-
-
Mochizuki, T.1
Lemmink, H.H.2
Mariyama, M.3
Antignac, C.4
Gubler, M.C.5
Pirson, Y.6
Verellen-Dumoulin, C.7
Chan, B.8
Schroder, C.H.9
Smeets, H.J.10
Reeders, S.T.11
-
12
-
-
0021958902
-
Genetic heterogeneity of Alport syndrome
-
Feingold J, Bois E, Chompret A, Broyer M, Gubler MC, Grünfeld JP: Genetic heterogeneity of Alport syndrome. Kidney Int 27: 672-677, 1985 (Pubitemid 15092195)
-
(1985)
Kidney International
, vol.27
, Issue.4
, pp. 672-677
-
-
Feingold, J.1
Bois, E.2
Chompret, A.3
-
13
-
-
0033746069
-
Autosomal dominant alport syndrome caused by a col4a3 splice site mutation
-
van der LoopFT,Heidet L,Timmer ED, van den Bosch BJ, Leinonen A, Antignac C, Jefferson JA, Maxwell AP, Monnens LA, Schröder CH, Smeets HJ: Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation. Kidney Int 58: 1870-1875, 2000
-
(2000)
Kidney Int
, vol.58
, pp. 1870-1875
-
-
Van Der Loop, F.T.1
Heidet, L.2
Timmer, E.D.3
Van Den Bosch, B.J.4
Leinonen, A.5
Antignac, C.6
Jefferson, J.A.7
Maxwell, A.P.8
Monnens, L.A.9
Schröder, C.H.10
Smeets, H.J.11
-
14
-
-
0028070269
-
Association of thin glomerular basement membrane with other glomerulopathies
-
Cosio FG, Falkenhain ME, Sedmak DD: Association of thin glomerular basement membrane with other glomerulopathies. Kidney Int 46: 471-474, 1994 (Pubitemid 24253055)
-
(1994)
Kidney International
, vol.46
, Issue.2
, pp. 471-474
-
-
Cosioa, F.G.1
Falkenhain, M.E.2
Sedmak, D.D.3
-
15
-
-
0034073758
-
X-linked Alport syndrome: Natural history in 195 families and genotype- phenotype correlations in males
-
Jais JP, Knebelmann B, Giatras I, De Marchi M, Rizzoni G, Renieri A, Weber M, Gross O, Netzer KO, Flinter F, Pirson Y, Verellen C, Wieslander J, Persson U, Tryggvason K, Martin P, Hertz JM, Schröder C, Sanak M, Krejcova S, CarvalhoMF, Saus J, Antignac C, Smeets H, Gubler MC: X-linked Alport syndrome: Natural history in 195 families and genotype-phenotype correlations in males. J Am Soc Nephrol 11: 649-657, 2000 (Pubitemid 30171874)
-
(2000)
Journal of the American Society of Nephrology
, vol.11
, Issue.4
, pp. 649-657
-
-
Jais, J.P.1
Knebelmann, B.2
Giatras, I.3
De Marchi, M.4
Rizzoni, G.5
Renieri, A.6
Weber, M.7
Gross, O.8
Netzer, K.-O.9
Flinter, F.10
Pirson, Y.11
Verellen, C.12
Wieslander, J.13
Persson, U.14
Tryggvason, K.15
Martin, P.16
Hertz, J.M.17
Schroder, C.18
Sanak, M.19
Krejcova, S.20
Carvalho, M.F.21
Saus, J.22
Antignac, C.23
Smeets, H.24
Gubler, M.C.25
more..
-
16
-
-
84861197421
-
Clinical utility gene card for alport syndrome
-
Hertz JM, Thomassen M, Storey H, Flinter F: Clinical utility gene card for Alport syndrome Eur J Hum Genet 20: 6, 2012
-
(2012)
Eur J Hum Genet
, vol.20
, pp. 6
-
-
Hertz, J.M.1
Thomassen, M.2
Storey, H.3
Flinter, F.4
-
17
-
-
34247898894
-
Diagnosis of Alport syndrome without biopsy?
-
DOI 10.1007/s00467-006-0376-z
-
Gubler MC: Diagnosis of Alport syndrome without biopsy? Pediatr Nephrol 22: 621-625, 2007 (Pubitemid 46691515)
-
(2007)
Pediatric Nephrology
, vol.22
, Issue.5
, pp. 621-625
-
-
Gubler, M.C.1
-
18
-
-
0141566829
-
X-linked Alport syndrome: Natural history and genotype-phenotype correlations in girls and women belonging to 195 families: A "European Community Alport Syndrome Concerted Action" study
-
DOI 10.1097/01.ASN.0000090034.71205.74
-
Jais JP, Knebelmann B, Giatras I, De Marchi M, Rizzoni G, Renieri A, Weber M, Gross O, Netzer KO, Flinter F, Pirson Y, Dahan K, Wieslander J, Persson U, Tryggvason K, Martin P, Hertz JM, Schröder C, Sanak M, Carvalho MF, Saus J, Antignac C, Smeets H, Gubler MC: X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: A "European Community Alport Syndrome Concerted Action" study. J Am Soc Nephrol 14: 2603-2610, 2003 (Pubitemid 37169346)
-
(2003)
Journal of the American Society of Nephrology
, vol.14
, Issue.10
, pp. 2603-2610
-
-
Jais, J.P.1
Knebelmann, B.2
Giatras, I.3
De Marchi, M.4
Rizzoni, G.5
Renieri, A.6
Weber, M.7
Gross, O.8
Netzer, K.-O.9
Flinter, F.10
Pirson, Y.11
Dahan, K.12
Wieslander, J.13
Persson, U.14
Tryggvason, K.15
Martin, P.16
Hertz, J.M.17
Schroder, C.18
Sanak, M.19
Carvalho, M.F.20
Saus, J.21
Antignac, C.22
Smeets, H.23
Gubler, M.C.24
more..
-
19
-
-
75749130327
-
Alport retinopathy results from "severe" col4a5 mutations and predicts early renal failure
-
Tan R, Colville D, Wang YY, Rigby L, Savige J: Alport retinopathy results from "severe" COL4A5 mutations and predicts early renal failure. Clin J AmSocNephrol 5: 34-38, 2010
-
(2010)
Clin J AmSocNephrol
, vol.5
, pp. 34-38
-
-
Tan, R.1
Colville, D.2
Wang, Y.Y.3
Rigby, L.4
Savige, J.5
-
20
-
-
34250426039
-
Split and extremely thin glomerular basement membranes in hereditary nephropathy (alport's syndrome)
-
Rumpelt HJ, Langer KH, Schärer K, Straub E, Thoenes W: Split and extremely thin glomerular basement membranes in hereditary nephropathy (Alport's syndrome). Virchows Arch A Pathol Anat Histol 364: 225-233, 1974
-
(1974)
Virchows Arch A Pathol Anat Histol
, vol.364
, pp. 225-233
-
-
Rumpelt, H.J.1
Langer, K.H.2
Schärer, K.3
Straub, E.4
Thoenes, W.5
-
21
-
-
0028939722
-
Autosomal recessive alport syndrome: Immunohistochemical study of type iv collagen chain distribution
-
GublerMC, Knebelmann B, Beziau A, Broyer M, Pirson Y, Haddoum F, Kleppel MM, Antignac C: 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
Broyer, M.4
Pirson, Y.5
Haddoum, F.6
Kleppel, M.M.7
Antignac, C.8
-
22
-
-
0032918906
-
Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin
-
DOI 10.1046/j.1523-1755.1999.00357.x
-
van der Loop FT, Monnens LA, Schröder CH, Lemmink HH, Breuning MH, Timmer ED, Smeets HJ: Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin. Kidney Int 55: 1217-1224, 1999 (Pubitemid 29157117)
-
(1999)
Kidney International
, vol.55
, Issue.4
, pp. 1217-1224
-
-
Van Der Loop, F.T.L.1
Monnens, L.A.H.2
Schroder, C.H.3
Lemmink, H.H.4
Breuning, M.H.5
Timmer, E.D.J.6
Smeets, H.J.M.7
-
23
-
-
33645370508
-
Is genetic testing of healthy pre-symptomatic children with possible alport syndrome ethical?
-
Copelovitch L, Kaplan BS: Is genetic testing of healthy pre-symptomatic children with possible Alport syndrome ethical? Pediatr Nephrol 21: 455-456, 2006
-
(2006)
Pediatr Nephrol
, vol.21
, pp. 455-456
-
-
Copelovitch, L.1
Kaplan, B.S.2
-
24
-
-
79251490731
-
The value of clinical criteria in identifying patients with x-linked alport syndrome
-
Hanson H, Storey H, Pagan J, Flinter F: The value of clinical criteria in identifying patients with X-linked Alport syndrome. Clin JAmSoc Nephrol 6: 198-203, 2011
-
(2011)
Clin JAmSoc Nephrol
, vol.6
, pp. 198-203
-
-
Hanson, H.1
Storey, H.2
Pagan, J.3
Flinter, F.4
-
25
-
-
0036934214
-
Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome
-
DOI 10.1007/s00439-002-0830-3
-
King K, Flinter FA, Nihalani V, Green PM: Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome. Hum Genet 111: 548-554, 2002 (Pubitemid 36075087)
-
(2002)
Human Genetics
, vol.111
, Issue.6
, pp. 548-554
-
-
King, K.1
Flinter, F.A.2
Nihalani, V.3
Green, P.M.4
-
26
-
-
56749096786
-
Mlpa and cdna analysis improves col4a5 mutation detection in x-linked alport syndrome
-
Hertz JM, Juncker I,Marcussen N:MLPA and cDNA analysis improves COL4A5 mutation detection in X-linked Alport syndrome. Clin Genet 74: 522-530, 2008
-
(2008)
Clin Genet
, vol.74
, pp. 522-530
-
-
Hertz, J.M.1
Juncker, I.2
Marcussen, N.3
-
27
-
-
16244419028
-
Detection of mutations in the COL4A5 gene by analyzing cDNA of skin fibroblasts
-
DOI 10.1111/j.1523-1755.2005.00204.x
-
Wang F, Wang Y, Ding J, Yang J: Detection of mutations in the COL4A5 gene by analyzing cDNA of skin fibroblasts. Kidney Int 67: 1268-1274, 2005 (Pubitemid 40463103)
-
(2005)
Kidney International
, vol.67
, Issue.4
, pp. 1268-1274
-
-
Wang, F.1
Wang, Y.2
Ding, J.3
Yang, J.4
-
28
-
-
34447626817
-
Genetic testing for x-linked alport syndrome by direct sequencing of col4a5 cdna from hair root rna samples
-
Tazon-Vega, B, Ars, E, Burset, M, Santin, S, Ruiz, P, Fernandez-Llama, P,Ballarin, J&Torra, R: Genetic testing for X-linked Alport syndrome by direct sequencing of COL4A5 cDNA from hair root RNA samples. Am J Kidney Dis 50: 257 e1-14, 2007
-
(2007)
Am J Kidney Dis
, vol.50
-
-
Tazon-Vega, B.1
Ars, E.2
Burset, M.3
Santin, S.4
Ruiz, P.5
Fernandez-Llama, P.6
Ballarin, J.7
Torra, R.8
-
29
-
-
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 genotypephenotype correlation in X-linked Alport syndrome: Impact on clinical counselling.Nephrol Dial Transplant 17: 1218-1227, 2002 (Pubitemid 34812066)
-
(2002)
Nephrology Dialysis Transplantation
, vol.17
, Issue.7
, pp. 1218-1227
-
-
Gross, O.1
Netzer, K.-O.2
Lambrecht, R.3
Seibold, S.4
Weber, M.5
-
30
-
-
34447573030
-
Alport syndrome and the X chromosome: Implications of a diagnosis of Alport syndrome in females
-
DOI 10.1093/ndt/gfm024
-
Kashtan CE: Alport syndrome and the X chromosome: Implications of a diagnosis of Alport syndrome in females. Nephrol Dial Transplant 22: 1499-1505, 2007 (Pubitemid 47073745)
-
(2007)
Nephrology Dialysis Transplantation
, vol.22
, Issue.6
, pp. 1499-1505
-
-
Kashtan, C.E.1
-
31
-
-
33746922312
-
Renal transplantation in patients with Alport syndrome
-
DOI 10.1111/j.1399-3046.2006.00528.x
-
Kashtan CE: Renal transplantation in patients with Alport syndrome. Pediatr Transplant 10: 651-657, 2006 (Pubitemid 44186284)
-
(2006)
Pediatric Transplantation
, vol.10
, Issue.6
, pp. 651-657
-
-
Kashtan, C.E.1
-
32
-
-
68549085536
-
Opinion:ocular features aid the diagnosis of alport syndrome
-
Savige J, ColvilleD:Opinion:Ocular features aid the diagnosis of Alport syndrome. Nat Rev Nephrol 5: 356-360, 2009
-
(2009)
Nat Rev Nephrol
, vol.5
, pp. 356-360
-
-
Savige, J.1
Colville, D.2
-
33
-
-
1542330045
-
Enalapril in children with Alport syndrome
-
DOI 10.1007/s00467-003-1366-z
-
Proesmans W, Van Dyck M: Enalapril in children with Alport syndrome. Pediatr Nephrol 19: 271-275, 2004 (Pubitemid 38313009)
-
(2004)
Pediatric Nephrology
, vol.19
, Issue.3
, pp. 271-275
-
-
Proesmans, W.1
Van Dyck, M.2
-
34
-
-
33750993170
-
The effect of aldosterone blockade in patients with Alport syndrome
-
DOI 10.1007/s00467-006-0270-8
-
Kaito H, Nozu K, Iijima K, Nakanishi K, Yoshiya K, Kanda K, Przybyslaw Krol R, Yoshikawa N, Matsuo M: The effect of aldosterone blockade in patients with Alport syndrome. Pediatr Nephrol 21: 1824-1829, 2006 (Pubitemid 44741159)
-
(2006)
Pediatric Nephrology
, vol.21
, Issue.12
, pp. 1824-1829
-
-
Kaito, H.1
Nozu, K.2
Iijima, K.3
Nakanishi, K.4
Yoshiya, K.5
Kanda, K.6
Przybyslaw Krol, R.7
Yoshikawa, N.8
Matsuo, M.9
-
35
-
-
84857109752
-
Early angiotensinconverting enzyme inhibition in alport syndrome delays renal failure and improves life expectancy
-
Gross O, Licht C, Anders HJ, Hoppe B, Beck B, Tonshoff B, Hocker B, Wygoda S, Ehrich JH, Pape L, Konrad M, Rascher W, Dotsch J, Muller-Wiefel DE, Hoyer P, Knebelmann B, Pirson Y, Grunfeld JP, Niaudet P, Cochat P, Heidet L, Lebbah S, Torra R, Friede T, Lange K, Muller GA, Weber M: Early angiotensinconverting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy. Kidney Int 81:494-501, 2012
-
(2012)
Kidney Int
, vol.81
, pp. 494-501
-
-
Gross, O.1
Licht, C.2
Anders, H.J.3
Hoppe, B.4
Beck, B.5
Tonshoff, B.6
Hocker, B.7
Wygoda, S.8
Ehrich, J.H.9
Pape, L.10
Konrad, M.11
Rascher, W.12
Dotsch, J.13
Muller-Wiefel, D.E.14
Hoyer, P.15
Knebelmann, B.16
Pirson, Y.17
Grunfeld, J.P.18
Niaudet, P.19
Cochat, P.20
Heidet, L.21
Lebbah, S.22
Torra, R.23
Friede, T.24
Lange, K.25
Muller, G.A.26
Weber, M.27
more..
-
36
-
-
85190672931
-
Safety and efficacy of the ace-inhibitor ramipril in alport syndrome: The double-blind, randomized, placebo-controlled, multicenter phase iii early pro-tect alport trial in pediatric patients [published online july 1, 2012]
-
doi:10.5402/2012/436046
-
Gross O, Friede T, Hilgers R, Görlitz A, Gavénis K, Ahmed R, Dürr U: Safety and efficacy of the ACE-inhibitor ramipril in Alport syndrome: The double-blind, randomized, placebo-controlled, multicenter phase III EARLY PRO-TECT Alport trial in pediatric patients [published online July 1, 2012]. ISRN Pediatr doi:10.5402/2012/436046
-
ISRN Pediatr
-
-
Gross, O.1
Friede, T.2
Hilgers, R.3
Görlitz, A.4
Gavénis, K.5
Ahmed, R.6
Dürr, U.7
-
37
-
-
84870405692
-
Clinical practice recommendations for the treatment of alport syndrome: A statement of the alport syndrome research collaborative
-
Kashtan CE, Ding J, Gregory M, Gross O, Heidet L, Knebelmann B, Rheault M, Licht C: Clinical practice recommendations for the treatment of Alport syndrome: A statement of the Alport Syndrome Research Collaborative. Pediatr Nephrol 28:5-11, 2013
-
(2013)
Pediatr Nephrol
, vol.28
, pp. 5-11
-
-
Kashtan, C.E.1
Ding, J.2
Gregory, M.3
Gross, O.4
Heidet, L.5
Knebelmann, B.6
Rheault, M.7
Licht, C.8
-
38
-
-
34047115353
-
Nephroprotective effect of the HMG-CoA-reductase inhibitor cerivastatin in a mouse model of progressive renal fibrosis in Alport syndrome
-
DOI 10.1093/ndt/gfl810
-
Koepke ML, Weber M, Schulze-Lohoff E, Beirowski B, Segerer S, Gross O: Nephroprotective effect of the HMG-CoA-reductase inhibitor cerivastatin in a mouse model of progressive renal fibrosis in Alport syndrome. Nephrol Dial Transplant 22: 1062-1069, 2007 (Pubitemid 46523419)
-
(2007)
Nephrology Dialysis Transplantation
, vol.22
, Issue.4
, pp. 1062-1069
-
-
Koepke, M.-L.1
Weber, M.2
Schulze-Lohoff, E.3
Beirowski, B.4
Segerer, S.5
Gross, O.6
-
39
-
-
33646266237
-
Stage-specific action of matrix metalloproteinases influences progressive hereditary kidney disease
-
Zeisberg M, Khurana M, Rao VH, Cosgrove D, Rougier JP, Werner MC, Shield CF, Werb Z, Kalluri R: Stage-specific action of matrix metalloproteinases influences progressive hereditary kidney disease. PLoS Med 3: e100, 2006
-
(2006)
PLoS Med
, vol.3
-
-
Zeisberg, M.1
Khurana, M.2
Rao, V.H.3
Cosgrove, D.4
Rougier, J.P.5
Werner, M.C.6
Shield, C.F.7
Werb, Z.8
Kalluri, R.9
-
40
-
-
23844552355
-
Delayed chemokine receptor 1 blockade prolongs survival in collagen 4A3-deficient mice with alport disease
-
DOI 10.1681/ASN.2004100871
-
Ninichuk V, GrossO, Reichel C, Khandoga A, Pawar RD, Ciubar R, Segerer S, Belemezova E, Radomska E, Luckow B, Perez de Lema G, Murphy PM, Gao JL, Henger A, Kretzler M, Horuk R,Weber M, Krombach F, Schlöndorff D, Anders HJ: Delayed chemokine receptor 1 blockade prolongs survival in collagen 4A3-deficient mice with Alport disease.J Am Soc Nephrol 16: 977-985, 2005 (Pubitemid 41710308)
-
(2005)
Journal of the American Society of Nephrology
, vol.16
, Issue.4
, pp. 977-985
-
-
Ninichuk, V.1
Gross, O.2
Reichel, C.3
Khandoga, A.4
Pawar, R.D.5
Ciubar, R.6
Segerer, S.7
Belemezova, E.8
Radomska, E.9
Luckow, B.10
Perez De Lema, G.11
Murphy, P.M.12
Gao, J.-L.13
Henger, A.14
Kretzler, M.15
Horuk, R.16
Weber, M.17
Krombach, F.18
Anders, H.-J.19
-
41
-
-
26944490766
-
Nephroprotection by antifibrotic and anti-inflammatory effects of the vasopeptidase inhibitor AVE7688
-
DOI 10.1111/j.1523-1755.2005.00423.x, PII 4494615
-
Gross O, Koepke ML, Beirowski B, Schulze-Lohoff E, Segerer S, Weber M: Nephroprotection by antifibrotic and anti-inflammatory effects of the vasopeptidase inhibitor AVE7688. Kidney Int 68: 456-463, 2005 (Pubitemid 43323100)
-
(2005)
Kidney International
, vol.68
, Issue.2
, pp. 456-463
-
-
Gross, O.1
Koepke, M.-L.2
Beirowski, B.3
Schulze-Lohoff, E.4
Segerer, S.5
Weber, M.6
-
42
-
-
33646561825
-
Bone-marrow-derived stem cells repair basement membrane collagen defects and reverse genetic kidney disease
-
DOI 10.1073/pnas.0601436103
-
Sugimoto H, Mundel TM, Sund M, Xie L, Cosgrove D, Kalluri R: Bone-marrow-derived stem cells repair basement membrane collagen defects and reverse genetic kidney disease. Proc Natl Acad Sci U S A 103: 7321-7326, 2006 (Pubitemid 43727831)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.19
, pp. 7321-7326
-
-
Sugimoto, H.1
Mundel, T.M.2
Sund, M.3
Xie, L.4
Cosgrove, D.5
Kalluri, R.6
-
43
-
-
33750547298
-
Bone marrow-derived cells contribute to podocyte regeneration and amelioration of renal disease in a mouse model of Alport syndrome
-
DOI 10.1634/stemcells.2006-0201
-
Prodromidi EI, Poulsom R, Jeffery R, RoufosseCA, Pollard PJ, PuseyCD,CookHT: Bone marrow-derived cells contribute to podocyte regeneration and amelioration of renal disease in a mouse model of Alport syndrome. Stem Cells 24: 2448-2455, 2006 (Pubitemid 44674305)
-
(2006)
Stem Cells
, vol.24
, Issue.11
, pp. 2448-2455
-
-
Prodromidi, E.I.1
Poulsom, R.2
Jeffery, R.3
Roufosse, C.A.4
Pollard, P.J.5
Pusey, C.D.6
Cook, H.T.7
-
44
-
-
0029557146
-
Renal allograft survival according to primary diagnosis: A report of the North American Pediatric Renal Transplant Cooperative Study
-
DOI 10.1007/BF00868709
-
Kashtan CE, McEnery PT, Tejani A, Stablein DM: Renal allograft survival according to primary diagnosis: a report of the North American Pediatric Renal Transplant Cooperative Study. PediatrNephrol 9: 679-684, 1995 (Pubitemid 26003665)
-
(1995)
Pediatric Nephrology
, vol.9
, Issue.6
, pp. 679-684
-
-
Kashtan, C.E.1
McEnery, P.T.2
Tejani, A.3
Stablein, D.M.4
-
45
-
-
84874603461
-
Grosso:outcomes ofmale patientswithalport syndrome undergoing renal replacement therapy
-
Temme J, Kramer A, Jager KJ, Lange K, Peters F, Muller GA, Kramar R, Heaf JG, Finne P, Palsson R, Reisæter AV, Hoitsma AJ, MetcalfeW, Postorino M, Zurriaga O, Santos JP, Ravani P, Jarraya F, Verrina E, Dekker FW, GrossO:Outcomes ofmale patientswithAlport syndrome undergoing renal replacement therapy. Clin J AmSoc Nephrol 7: 1969-1976, 2012
-
(2012)
Clin J AmSoc Nephrol
, vol.7
, pp. 1969-1976
-
-
Temme, J.1
Kramer, A.2
Jager, K.J.3
Lange, K.4
Peters, F.5
Muller, G.A.6
Kramar, R.7
Heaf, J.G.8
Finne, P.9
Palsson, R.10
Reisæter, A.V.11
Hoitsma, A.J.12
Metcalfe, W.13
Postorino, M.14
Zurriaga, O.15
Santos, J.P.16
Ravani, P.17
Jarraya, F.18
Verrina, E.19
Dekker, F.W.20
more..
-
46
-
-
0024211467
-
Anti-glomerular basement membrane antibody-mediated nephritis complicating transplantation in a patient with Alport's syndrome
-
Fleming SJ, Savage CO, McWilliam LJ, Pickering SJ, Ralston AJ, Johnson RW, Ackrill P: Anti-glomerular basement membrane antibody-mediated nephritis complicating transplantation in a patient with Alport's syndrome. Transplantation 46: 857-859, 1988 (Pubitemid 19013231)
-
(1988)
Transplantation
, vol.46
, Issue.6
, pp. 857-859
-
-
Fleming, S.J.1
Savage, C.O.S.2
McWilliam, L.J.3
Pickering, S.J.4
Ralston, A.J.5
Greenwood Johnson, R.W.6
Ackrill, P.7
-
47
-
-
0025582010
-
Renal transplantation in alport's syndrome. Personal experience in twelve patients
-
Berardinelli L, Pozzoli E, Raiteri M, Canal R, Tonello G, Tarantino A, Vegeto A: Renal transplantation in Alport's syndrome. Personal experience in twelve patients. Contrib Nephrol 80: 131-134, 1990
-
(1990)
Contrib Nephrol
, vol.80
, pp. 131-134
-
-
Berardinelli, L.1
Pozzoli, E.2
Raiteri, M.3
Canal, R.4
Tonello, G.5
Tarantino, A.6
Vegeto, A.7
-
48
-
-
0030913337
-
The clinical spectrum of type IV collagen mutations
-
DOI 10.1002/(SICI)1098-1004(1997)9:6<477::AID-HUMU1>3.0.CO;2-#
-
Lemmink HH, Schröder CH, Monnens LA, Smeets HJ: The clinical spectrum of type IV collagen mutations.HumMutat 9: 477-499, 1997 (Pubitemid 27250812)
-
(1997)
Human Mutation
, vol.9
, Issue.6
, pp. 477-499
-
-
Lemmink, H.H.1
Schroder, C.H.2
Monnens, L.A.H.3
Smeets, H.J.M.4
-
49
-
-
1642520777
-
Retransplantation in Alport post-transplant anti-GBM disease
-
DOI 10.1111/j.1523-1755.2004.00428.x
-
BrowneG, Brown PA, TomsonCR, Fleming S, Allen A, Herriot R, Pusey CD, Rees AJ, Turner AN: Retransplantation in Alport post-transplant anti-GBM disease. Kidney Int 65: 675-681, 2004 (Pubitemid 38130665)
-
(2004)
Kidney International
, vol.65
, Issue.2
, pp. 675-681
-
-
Browne, G.1
Brown, P.A.J.2
Tomson, C.R.V.3
Fleming, S.4
Allen, A.5
Herriot, R.6
Pusey, C.D.7
Rees, A.J.8
Turner, A.N.9
-
50
-
-
0035721629
-
A comparison of the clinical, histopathologic, and ultrastructural phenotypes in carriers of X-linked and autosomal recessive Alport's syndrome
-
Dagher H, Buzza M, Colville D, Jones C, Powell H, Fassett R,WilsonD, Agar J, Savige J: A comparison of the clinical, histopathologic, and ultrastructural phenotypes in carriers of X-linked and autosomal recessive Alport's syndrome. Am J Kidney Dis 38: 1217-1228, 2001 (Pubitemid 34193106)
-
(2001)
American Journal of Kidney Diseases
, vol.38
, Issue.6
, pp. 1217-1228
-
-
Dagher, H.1
Buzza, M.2
Colville, D.3
Jones, C.4
Powell, H.5
Fassett, R.6
Wilson, D.7
Agar, J.8
Savige, J.9
-
51
-
-
0018942488
-
Hereditary nephropathy (alport syndrome): Correlation of clinical data with glomerular basement membrane alterations
-
Rumpelt HJ: 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
-
52
-
-
84859330714
-
Incidence of renal failure and nephroprotection by raas inhibition in heterozygous carriers of x-chromosomal and autosomal recessive alport mutations
-
Temme J, Peters F, Lange K, Pirson Y, Heidet L, Torra R, Grunfeld JP, Weber M, Licht C, MüllerGA, GrossO: Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations. Kidney Int 81: 779-783, 2012
-
(2012)
Kidney Int
, vol.81
, pp. 779-783
-
-
Temme, J.1
Peters, F.2
Lange, K.3
Pirson, Y.4
Heidet, L.5
Torra, R.6
Grunfeld, J.P.7
Weber, M.8
Licht, C.9
Müller, G.A.10
Gross, O.11
-
53
-
-
0021846608
-
Renal prognosis in women with hereditary nephritis
-
Grünfeld JP, Noël LH, Hafez S, Droz D: Renal prognosis in women with hereditary nephritis. Clin Nephrol 23: 267-271, 1985 (Pubitemid 15059835)
-
(1985)
Clinical Nephrology
, vol.23
, Issue.6
, pp. 267-271
-
-
Grunfeld, J.-P.1
Noel, L.-H.2
Hafez, S.3
Droz, D.4
-
54
-
-
65249087306
-
Living donor kidney transplantation from relatives with mild urinary abnormalities in alport syndrome: Long-term risk, benefit and outcome
-
Gross O, Weber M, Fries JW, Müller GA: Living donor kidney transplantation from relatives with mild urinary abnormalities in Alport syndrome: Long-term risk, benefit and outcome. Nephrol Dial Transplant 24: 1626-1630, 2009
-
(2009)
Nephrol Dial Transplant
, vol.24
, pp. 1626-1630
-
-
Gross, O.1
Weber, M.2
Fries, J.W.3
Müller, G.A.4
-
55
-
-
0031596221
-
Comparison of α5(IV) collagen chain expression in skin with disease severity in women with X-linked alport syndrome
-
Nakanishi K, Iijima K, Kuroda N, Inoue Y, Sado Y, Nakamura H, Yoshikawa N: Comparison of alpha5(IV) collagen chain expression in skin with disease severity in women with X-linked Alport syndrome. J Am Soc Nephrol 9: 1433-1440, 1998 (Pubitemid 28354553)
-
(1998)
Journal of the American Society of Nephrology
, vol.9
, Issue.8
, pp. 1433-1440
-
-
Nakanishi, K.1
Iijima, K.2
Kuroda, N.3
Inoue, Y.4
Sado, Y.5
Nakamura, H.6
Yoshikawa, N.7
-
56
-
-
0031778196
-
X-linked Alport syndrome in females
-
DOI 10.1016/S0046-8177(98)90123-X
-
Meleg-Smith S,Magliato S, Cheles M, Garola RE, Kashtan CE: X-linked Alport syndrome in females. Hum Pathol 29: 404-408, 1998 (Pubitemid 28231907)
-
(1998)
Human Pathology
, vol.29
, Issue.4
, pp. 404-408
-
-
Meleg-Smith, S.1
Magliato, S.2
Cheles, M.3
Garola, R.E.4
Kashtan, C.E.5
-
57
-
-
0030730733
-
Assessment of long-term risks for living related kidney donors by 24-h blood pressure monitoring and testing for microalbuminuria
-
Eberhard OK, Kliem V, Offner G, Oldhafer K, Fangmann J, Pichlmay R,KochKM, Brunkhorst R: Assessment of long-term risks for living related kidney donors by 24-h blood pressure monitoring and testing for microalbuminuria. Clin Transplant 11: 415-419, 1997 (Pubitemid 27460437)
-
(1997)
Clinical Transplantation
, vol.11
, Issue.5
, pp. 415-419
-
-
Eberhard, O.K.1
Kliem, V.2
Offner, G.3
Oldhafer, K.4
Fangmann, J.5
Pichlmay, R.6
Koch, K.M.7
Brunkhorst, R.8
-
58
-
-
65249091927
-
Women with alport syndrome: Risks and rewards of kidney donation
-
Kashtan CE: Women with Alport syndrome: risks and rewards of kidney donation. Nephrol Dial Transplant 24: 1369-1370, 2009
-
(2009)
Nephrol Dial Transplant
, vol.24
, pp. 1369-1370
-
-
Kashtan, C.E.1
-
59
-
-
19944402848
-
Case records of the massachusetts general hospital. Weekly clinicopathological exercises. Case 40-2004 -A 42-year-old woman with long-standing hematuria
-
Steele DJ, Michaels PJ: Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 40-2004 -A 42-year-old woman with long-standing hematuria. N Engl JMed 351: 2851-2859, 2004
-
(2004)
N Engl JMed
, vol.351
, pp. 2851-2859
-
-
Steele, D.J.1
Michaels, P.J.2
-
60
-
-
71149115618
-
Pregnancy complicated with alport syndrome: A good obstetric outcome and failure to diagnose an infant born to a mother with alport syndrome by umbilical cord immunofluorescence staining
-
Matsubara S, Ueda Y, Takahashi H, Nagai T, Kuwata T, Muto S, Yamaguchi T, Takizawa T, Suzuki M: Pregnancy complicated with Alport syndrome: a good obstetric outcome and failure to diagnose an infant born to a mother with Alport syndrome by umbilical cord immunofluorescence staining. J Obstet Gynaecol Res 35: 1109-1114, 2009
-
(2009)
J Obstet Gynaecol Res
, vol.35
, pp. 1109-1114
-
-
Matsubara, S.1
Ueda, Y.2
Takahashi, H.3
Nagai, T.4
Kuwata, T.5
Muto, S.6
Yamaguchi, T.7
Takizawa, T.8
Suzuki, M.9
-
61
-
-
0028919872
-
Bull terrier hereditary nephritis: A model for autosomal dominant alport syndrome
-
Hood JC, Savige J, Hendtlass A, Kleppel MM, Huxtable CR, Robinson WF: Bull terrier hereditary nephritis: a model for autosomal dominant Alport syndrome. Kidney Int 47: 758-765, 1995
-
(1995)
Kidney Int
, vol.47
, pp. 758-765
-
-
Hood, J.C.1
Savige, J.2
Hendtlass, A.3
Kleppel, M.M.4
Huxtable, C.R.5
Robinson, W.F.6
-
62
-
-
18844406535
-
Thin basement membrane nephropathy and renal transplantation
-
DOI 10.1016/j.semnephrol.2005.01.012, PII S0270929505000161
-
Ierino FL, Kanellis J: Thin basement membrane nephropathy and renal transplantation. Semin Nephrol 25: 184-187, 2005 (Pubitemid 40692803)
-
(2005)
Seminars in Nephrology
, vol.25
, Issue.3
, pp. 184-187
-
-
Ierino, F.L.1
Kanellis, J.2
-
63
-
-
60149106148
-
Alport syndrome and thin glomerular basement membrane nephropathy: A practical approach to diagnosis
-
Haas M: Alport syndrome and thin glomerular basement membrane nephropathy: A practical approach to diagnosis. Arch Pathol Lab Med 133: 224-232, 2009
-
(2009)
Arch Pathol Lab Med
, vol.133
, pp. 224-232
-
-
Haas, M.1
-
64
-
-
0025350089
-
Abnormally thin glomerular basement membrane and the Goodpasture epitope
-
Pettersson E, Törnroth T, Wieslander J: Abnormally thin glomerular basement membrane and the Goodpasture epitope. Clin Nephrol 33: 105-109, 1990 (Pubitemid 20103997)
-
(1990)
Clinical Nephrology
, vol.33
, Issue.3
, pp. 105-109
-
-
Pettersson, E.1
Tornroth, T.2
Wieslander, J.3
-
65
-
-
0030789006
-
Autosomal dominant Alport syndrome linked to the type IV collage α3 and α4 genes (COL4A3 and COL4A4)
-
DOI 10.1093/ndt/12.8.1595
-
Jefferson JA, Lemmink HH, Hughes AE, Hill CM, Smeets HJ, Doherty CC, Maxwell AP: Autosomal dominant Alport syndrome linked to the type IV collage alpha 3 and alpha 4 genes (COL4A3 and COL4A4). Nephrol Dial Transplant 12: 1595-1599, 1997 (Pubitemid 27346283)
-
(1997)
Nephrology Dialysis Transplantation
, vol.12
, Issue.8
, pp. 1595-1599
-
-
Jefferson, J.A.1
Lemmink, H.H.2
Hughes, A.E.3
Hill, C.M.4
Smeets, H.J.M.5
Doherty, C.C.6
Maxwell, A.P.7
-
66
-
-
0030604561
-
Randomised placebo-controlled trial of effect of ramipril on decline in glomerular filtration rate and risk of terminal renal failure in proteinuric,non-diabetic nephropathy
-
The GISEN Group (Gruppo Italiano di Studi Epidemiologici in Nefrologia)
-
The GISEN Group (Gruppo Italiano di Studi Epidemiologici in Nefrologia): Randomised placebo-controlled trial of effect of ramipril on decline in glomerular filtration rate and risk of terminal renal failure in proteinuric,non-diabetic nephropathy. Lancet 349: 1857-1863, 1997
-
(1997)
Lancet
, vol.349
, pp. 1857-1863
-
-
-
67
-
-
0035203597
-
ACE inhibitors to prevent end-stage renal disease: When to start and why possibly never to stop: A post hoc analysis of the REIN trial results
-
Ruggenenti P, Perna A, Remuzzi G; Gruppo Italiano di Studi Epidemiologici in Nefrologia: ACE inhibitors to prevent end-stage renal disease:When to start andwhy possibly never to stop: a post hoc analysis of the REIN trial results. Ramipril Efficacy in Nephropathy. J Am SocNephrol 12: 2832-2837, 2001 (Pubitemid 33115432)
-
(2001)
Journal of the American Society of Nephrology
, vol.12
, Issue.12
, pp. 2832-2837
-
-
Ruggenenti, P.1
Perna, A.2
Remuzzi, G.3
-
68
-
-
0037248954
-
Preemptive ramipril therapy delays renal failure and reduces renal fibrosis in COL4A3-knockout mice with Alport syndrome
-
DOI 10.1046/j.1523-1755.2003.00779.x
-
Gross O, Beirowski B, Koepke ML, Kuck J, Reiner M, Addicks K, Smyth N, Schulze-Lohoff E, Weber M: Preemptive ramipril therapy delays renal failure and reduces renal fibrosis in COL4A3-knockout mice with Alport syndrome. Kidney Int 63: 438-446, 2003 (Pubitemid 36126790)
-
(2003)
Kidney International
, vol.63
, Issue.2
, pp. 438-446
-
-
Gross, O.1
Beirowski, B.2
Koepke, M.-L.3
Kuck, J.4
Reiner, M.5
Addicks, K.6
Smyth, N.7
Schulze-Lohoff, E.8
Weber, M.9
-
69
-
-
0043123466
-
Living related kidney transplantation in a patient with autosomal-recessive Alport syndrome
-
DOI 10.1034/j.1399-0012.17.s10.5.x
-
Sakai K, Muramatsu M, Ogiwara H, Kawamura T, Arai K, Aikawa A, Ohara T, Mizuiri S, Joh K, Naito I, Hasegawa A: Living related kidney transplantation in a patient with autosomal-recessive Alport syndrome. Clin Transplant 17[Suppl 10]: 4-8, 2003 (Pubitemid 36958170)
-
(2003)
Clinical Transplantation
, vol.17
, Issue.SUPPL. 10
, pp. 4-8
-
-
Sakai, K.1
Muramatsu, M.2
Ogiwara, H.3
Kawamura, T.4
Arai, K.5
Aikawa, A.6
Ohara, T.7
Mizuiri, S.8
Joh, K.9
Naito, I.10
Hasegawa, A.11
|