Literature DB >> 16221700

Alpha-galactosidase activity should be examined in patients with proteinuria: what have we learned from a family affected with Fabry disease?

Ni-Chung Lee, Dau-Ming Niu, Ching-Yuang Lin, Kwang-Jen Hsiao, An-Hang Yang, Yee-Yung Ng.   

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Year:  2005        PMID： 16221700     DOI： 10.1093/ndt/gfi191

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN： 0931-0509            Impact factor:   5.992


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  2 in total

1.  A renal variant of Fabry disease: A case with a novel Gal A hemizygote mutation.

Authors:  Jorge H Mukdsi; Silvina Gutiérrez; Belén Barrón; Pablo Novoa; Segundo Fernández; Ana B de Diller; Alicia I Torres; Richard N Formica; Marcelo Orías
Journal:  J Nephropathol       Date:  2012-10-01

2.  A Renal Variant of Fabry Disease Diagnosed by the Presence of Urinary Mulberry Cells.

Authors:  Homare Shimohata; Yujiro Ogawa; Hiroshi Maruyama; Kouichi Hirayama; Masaki Kobayashi
Journal:  Intern Med       Date:  2016-12-01       Impact factor: 1.271
  2 in total

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