Literature DB >> 9399056

X-linked Alport syndrome with normal distribution of collagen IV alpha chains in epidermal basement membrane.

I Naito1, S Nomura, S Inoue, M Kagawa, T Matsubara, T Araki, M Taki, H Ohmori, K Manabe, S Kawai, G Osawa, Y Sado.   

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Year:  1997        PMID： 9399056     DOI： 10.1159/000059891

Source DB:  PubMed          Journal:  Contrib Nephrol        ISSN： 0302-5144            Impact factor:   1.580


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  4 in total

1.  Siblings with Alport's syndrome showing unique staining patterns for alpha5(IV) and alpha6(IV) chains of collagen type IV.

Authors:  Takayuki Tsuji; Yoshihide Fujigaki; Masanori Sakakima; Yoshikazu Sado; Akira Hishida
Journal:  Clin Exp Nephrol       Date:  2010-03-09       Impact factor: 2.801

2.  COL4A3/COL4A4 mutations and features in individuals with autosomal recessive Alport syndrome.

Authors:  Helen Storey; Judy Savige; Vanessa Sivakumar; Stephen Abbs; Frances A Flinter
Journal:  J Am Soc Nephrol       Date:  2013-09-19       Impact factor: 10.121

3.  The value of clinical criteria in identifying patients with X-linked Alport syndrome.

Authors:  Helen Hanson; Helen Storey; Judith Pagan; Frances Flinter
Journal:  Clin J Am Soc Nephrol       Date:  2010-09-30       Impact factor: 8.237

4.  COL4A6 is dispensable for autosomal recessive Alport syndrome.

Authors:  Tomohiro Murata; Kan Katayama; Toshitaka Oohashi; Timo Jahnukainen; Tomoko Yonezawa; Yoshikazu Sado; Eiji Ishikawa; Shinsuke Nomura; Karl Tryggvason; Masaaki Ito
Journal:  Sci Rep       Date:  2016-07-05       Impact factor: 4.379
  4 in total

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