Literature DB >> 20650908

Expanding the clinical spectrum of congenital nephrotic syndrome caused by NPHS1 mutations.

Nathalie Godefroid1, Karin Dahan.   

Abstract

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Year:  2010        PMID： 20650908     DOI： 10.1093/ndt/gfq434

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


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  3 in total

1.  GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome.

Authors:  Tobias Hermle; Ronen Schneider; David Schapiro; Daniela A Braun; Amelie T van der Ven; Jillian K Warejko; Ankana Daga; Eugen Widmeier; Makiko Nakayama; Tilman Jobst-Schwan; Amar J Majmundar; Shazia Ashraf; Jia Rao; Laura S Finn; Velibor Tasic; Joel D Hernandez; Arvind Bagga; Sawsan M Jalalah; Sherif El Desoky; Jameela A Kari; Kristen M Laricchia; Monkol Lek; Heidi L Rehm; Daniel G MacArthur; Shrikant Mane; Richard P Lifton; Shirlee Shril; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2018-06-29       Impact factor: 10.121

2.  Congenital nephrotic syndrome with prolonged renal survival without renal replacement therapy.

Authors:  William Wong; Maxwell Clarke Morris; Tonya Kara
Journal:  Pediatr Nephrol       Date:  2013-08-15       Impact factor: 3.714

Review 3.  Congenital nephrotic syndrome: is early aggressive treatment needed? Yes.

Authors:  Tuula Hölttä; Hannu Jalanko
Journal:  Pediatr Nephrol       Date:  2020-05-06       Impact factor: 3.714
  3 in total

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