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by Ren, H and Li, L and Yu, JY and Wu, S and Zhou, SS and Zheng, Y and Sun, WX
MEDICINE, ISSN 0025-7974, 07/2019, Volume 98, Issue 28, pp. e16256 - e16256
Rationale: Fabry's disease is an X-linked inherited syndrome. Herein, we presented an unusual case of Fabry disease coexisting with immunoglobulin A... 
Fabry disease | MEDICINE, GENERAL & INTERNAL | IGA NEPHROPATHY | immunoglobulin A nephropathy | Alport syndrome | Medical research | Medicine, Experimental | Alport's syndrome | Research | Immunoglobulin A | Fabry's disease | Risk factors | Index Medicus | Abridged Index Medicus
Journal Article
Nephrology Dialysis Transplantation, ISSN 0931-0509, 2017, Volume 32, Issue 6, pp. 916 - 924
Journal Article
1996, Contributions to nephrology, ISBN 3805561938, Volume 117., 204
Book
Journal of the American Society of Nephrology, ISSN 1046-6673, 03/2018, Volume 29, Issue 3, pp. 949 - 960
Pierson syndrome is a congenital nephrotic syndrome with eye and neurologic defects caused by mutations in laminin β2 (LAMB2), a major component of the... 
laminin | glomerular basement membrane | nephrotic syndrome | Alport syndrome | Basic Research
Journal Article
KIDNEY INTERNATIONAL, ISSN 0085-2538, 05/2018, Volume 93, Issue 5, pp. 1045 - 1051
Mutations in the genes COL4A3, COL4A4, and COL4A5 affect the synthesis, assembly, deposition, or function of the collagen IV alpha 345 molecule, the major... 
chronic kidney disease | GLOMERULAR-BASEMENT-MEMBRANE | GENOTYPE-PHENOTYPE CORRELATIONS | proteinuria | COL4A3/COL4A4 MUTATIONS | NATURAL-HISTORY | WOMEN | INHIBITION | 195 FAMILIES | Alport syndrome | DISEASE | RENAL-FAILURE | UROLOGY & NEPHROLOGY | AUTOSOMAL-DOMINANT
Journal Article
Kidney International, ISSN 0085-2538, 10/2014, Volume 86, Issue 4, pp. 679 - 684
Alport syndrome, historically referred to as hereditary glomerulonephritis with sensorineural deafness and anterior lenticonus, is a genetic disease of... 
ACE inhibitors | proteinuria | glomerulus | Alport syndrome | FIBROSIS | GLOMERULAR-BASEMENT-MEMBRANE | COLLAGEN-IV | GENOTYPE-PHENOTYPE CORRELATIONS | NATURAL-HISTORY | THERAPY | 195 FAMILIES | MOUSE MODEL | UROLOGY & NEPHROLOGY | MUTATIONS | PROGRESSION | Meeting Report
Journal Article
Journal Article
Laryngoscope Investigative Otolaryngology, ISSN 2378-8038, 08/2018, Volume 3, Issue 4, pp. 311 - 314
To describe the histopathologic findings within the human cochlea in X-linked Alport syndrome. Histopathologic analysis of cellular elements within the human... 
otopathology | Alport's syndrome | temporal bone histopathology | temporal bone histology
Journal Article
Kidney International, ISSN 0085-2538, 03/2012, Volume 81, Issue 5, pp. 494 - 501
Journal Article