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Hereditary Nephritis and Thin Glomerular Basement Membrane Lesion
Author / Creator:Lusco, Mark A. ; Fogo, Agnes B.
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Glomerular diseases, 2021-08, Vol.1 (3), p.135-144
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Clinicopathological Features of Hereditary Nephritis in the Iranian Population: Analysis of a 14-Year Survey in Kidney Biopsies From a Large Referral Center
Author / Creator:Emami, Amir ; Nili, Fatemeh ; Sotoudeh Anvari, Maryam ; Salarvand, Samaneh ; Seirafi, Golnar
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2024-01, Vol.27 (1), p.8-14
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Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type I...
Author / Creator:Zheng, K ; Thorner, P S ; Marrano, P ; Baumal, R ; McInnes, R R
Publisher:United States: National Acad Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 1994-04, Vol.91 (9), p.3989-3993
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Canine X Chromosome-Linked Hereditary Nephritis: A Genetic Model for Human X-Linked Hereditary Nephritis Resulting from a Single Base Mutation in the Gene Encoding the α5 Chain of Collagen Type IV
Author / Creator:Zheng, Keqin ; Thorner, Paul S. ; Marrano, Paula ; Baumal, Reuben ; McInnes, Roderick R.
Publisher:Washington, DC: National Academy of Sciences of the United States of America
Journal title:Proceedings of the National Academy of Sciences - PNAS, 1994-04, Vol.91 (9), p.3989-3993
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Alport syndromes: phenotypic heterogeneity of progressive hereditary nephritis
Author / Creator:Kashtan, C. E.
Publisher:Germany: Springer Nature B.V
Journal title:Pediatric nephrology (Berlin, West), 2000-06, Vol.14 (6), p.502-512
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Podocyte Depletion in Thin GBM and Alport Syndrome
Author / Creator:Wickman, Larysa ; Hodgin, Jeffrey B. ; Wang, Su Q. ; Afshinnia, Farsad ; Kershaw, David ; Wiggins, Roger C.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2016-05, Vol.11 (5), p.e0155255-e0155255
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Long-term outcome among females with Alport syndrome from a single pediatric center
Author / Creator:Goka, Selasie ; Copelovitch, Lawrence ; Levy Erez, Daniella
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2021-04, Vol.36 (4), p.945-951
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Alport syndrome: ACE2 administration slows kidney damage
Author / Creator:Lieben, Liesbet
Publisher:England: Nature Publishing Group
Journal title:Nature reviews. Nephrology, 2017-05, Vol.13 (5), p.261
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Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome
Author / Creator:Liu, Jian-Hong ; Wei, Xiu-Xiu ; Li, Ang ; Cui, Ying-Xia ; Xia, Xin-Yi ; Qin, Wei-Song ; Zhang, Ming-Chao ; Gao, Er-Zhi ; Sun, Jun ; Gao, Chun-Lin ; Liu, Feng-Xia ; Wu, Qiu-Yue ; Li, Wei-Wei ; Asan ; Liu, Zhi-Hong ; Li, Xiao-Jun
Publisher:United States: Public Library of Science
Journal title:PloS one, 2017-05, Vol.12 (5), p.e0177685
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Renal, auricular, and ocular outcomes of Alport syndrome and their current management
Author / Creator:Zhang, Yanqin ; Ding, Jie
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2018-08, Vol.33 (8), p.1309-1316
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Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis
Author / Creator:Chiereghin, Chiara ; Robusto, Michela ; Mastrangelo, Antonio ; Castorina, Pierangela ; Montini, Giovanni ; Giani, Marisa ; Duga, Stefano ; Asselta, Rosanna ; Soldà, Giulia
Publisher:United States: Public Library of Science
Journal title:PloS one, 2017-06, Vol.12 (6), p.e0178630
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Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy
Author / Creator:Weber, Stefanie ; Strasser, Katja ; Rath, Sabine ; Kittke, Achim ; Beicht, Sonja ; Alberer, Martin ; Lange-Sperandio, Bärbel ; Hoyer, Peter F. ; Benz, Marcus R. ; Ponsel, Sabine ; Weber, Lutz T. ; Klein, Hanns-Georg ; Hoefele, Julia
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2016-06, Vol.31 (6), p.941-955
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X-linked Alport syndrome: pathogenic variant features and further auditory genotype-phenotype correlations in males
Author / Creator:Zhang, Xiao ; Zhang, Yanqin ; Zhang, Yanmei ; Gu, Hongbo ; Chen, Zhe ; Ren, Lei ; Lu, Xingxing ; Chen, Li ; Wang, Fang ; Liu, Yuhe ; Ding, Jie
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2018-12, Vol.13 (1), p.229-11, Article 229
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RNA-seq analysis of gene expression profiles in isolated stria vascularis from wild-type and Alport mice reveals key pathways underling Alport strial pathogenesis
Author / Creator:Dufek, Brianna ; Meehan, Daniel T. ; Delimont, Duane ; Wilhelm, Kevin ; Samuelson, Gina ; Coenen, Ross ; Madison, Jacob ; Doyle, Edward ; Smyth, Brendan ; Phillips, Grady ; Gratton, Michael Anne ; Cosgrove, Dominic
Publisher:United States: Public Library of Science
Journal title:PloS one, 2020-08, Vol.15 (8), p.e0237907
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Bilateral spontaneous lens capsule rupture in Alport's syndrome
Author / Creator:Lohchab, Monica ; Arora, Ritu
Publisher:India: Wolters Kluwer India Pvt. Ltd
Journal title:Indian journal of ophthalmology, 2019-03, Vol.67 (3), p.406-406
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An overlap of Alport syndrome and rheumatoid arthritis in a patient and literature review
Author / Creator:Tang, Xiaofei ; Ding, Qiuling ; Xu, Dong ; Yang, Songtao ; Xiao, Yuefei ; Liu, Jian
Publisher:England: BioMed Central Ltd
Journal title:BMC nephrology, 2019-07, Vol.20 (1), p.277-5, Article 277
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Prospective study on the potential of RAAS blockade to halt renal disease in Alport syndrome patients with heterozygous mutations
Author / Creator:Stock, Johanna ; Kuenanz, Johannes ; Glonke, Niklas ; Sonntag, Joseph ; Frese, Jenny ; Tönshoff, Burkhard ; Höcker, Britta ; Hoppe, Bernd ; Feldkötter, Markus ; Pape, Lars ; Lerch, Christian ; Wygoda, Simone ; Weber, Manfred ; Müller, Gerhard-Anton ; Gross, Oliver
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2017-01, Vol.32 (1), p.131-137
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X-Linked Alport Dogs Demonstrate Mesangial Filopodial Invasion of the Capillary Tuft as an Early Event in Glomerular Damage
Author / Creator:Clark, Sabrina D. ; Nabity, Mary B. ; Cianciolo, Rachel E. ; Dufek, Brianna ; Cosgrove, Dominic
Publisher:United States: Public Library of Science
Journal title:PloS one, 2016-12, Vol.11 (12), p.e0168343
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An overview of the multi-pronged approach in the diagnosis of Alport syndrome for 22 children in Northeast China
Author / Creator:Zhang, Li ; Sun, Bai-chao ; Zhao, Bing-gang ; Ma, Qing-shan
Publisher:England: BioMed Central Ltd
Journal title:BMC nephrology, 2020-07, Vol.21 (1), p.294-13, Article 294
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Anterior lenticonus associated with Alport syndrome
Author / Creator:Jinagal, Jitender ; Gupta, Gaurav ; Thattaruthody, Faisal ; Nada, Ritambhra ; Ram, Jagat
Publisher:India: Wolters Kluwer India Pvt. Ltd
Journal title:Indian journal of ophthalmology, 2018-09, Vol.66 (9), p.1330-1331
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Showing 1 to 20 of 170 results

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Hereditary Nephritis and Thin Glomerular Basement Membrane Lesion

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Clinicopathological Features of Hereditary Nephritis in the Iranian Population: Analysis of a 14-Year Survey in Kidney Biopsies From a Large Referral Center

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Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type I...

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Canine X Chromosome-Linked Hereditary Nephritis: A Genetic Model for Human X-Linked Hereditary Nephritis Resulting from a Single Base Mutation in the Gene Encoding the α5 Chain of Collagen Type IV

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Alport syndromes: phenotypic heterogeneity of progressive hereditary nephritis

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Podocyte Depletion in Thin GBM and Alport Syndrome

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Long-term outcome among females with Alport syndrome from a single pediatric center

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Alport syndrome: ACE2 administration slows kidney damage

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Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome

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Renal, auricular, and ocular outcomes of Alport syndrome and their current management

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Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis

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Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy

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X-linked Alport syndrome: pathogenic variant features and further auditory genotype-phenotype correlations in males

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RNA-seq analysis of gene expression profiles in isolated stria vascularis from wild-type and Alport mice reveals key pathways underling Alport strial pathogenesis

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Bilateral spontaneous lens capsule rupture in Alport's syndrome

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An overlap of Alport syndrome and rheumatoid arthritis in a patient and literature review

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Prospective study on the potential of RAAS blockade to halt renal disease in Alport syndrome patients with heterozygous mutations

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X-Linked Alport Dogs Demonstrate Mesangial Filopodial Invasion of the Capillary Tuft as an Early Event in Glomerular Damage

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An overview of the multi-pronged approach in the diagnosis of Alport syndrome for 22 children in Northeast China

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Anterior lenticonus associated with Alport syndrome

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