Literature DB >> 17290294

A familial childhood-onset relapsing nephrotic syndrome.

A Kitamura1, H Tsukaguchi, R Hiramoto, A Shono, T Doi, S Kagami, K Iijima.   

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Year:  2007        PMID: 17290294     DOI: 10.1038/sj.ki.5002110

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


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  13 in total

Review 1.  Translating genetic findings in hereditary nephrotic syndrome: the missing loops.

Authors:  Gentzon Hall; Rasheed A Gbadegesin
Journal:  Am J Physiol Renal Physiol       Date:  2015-03-25

Review 2.  Genetics of childhood steroid-sensitive nephrotic syndrome.

Authors:  Alana M Karp; Rasheed A Gbadegesin
Journal:  Pediatr Nephrol       Date:  2016-07-29       Impact factor: 3.714

Review 3.  Genetic testing in nephrotic syndrome--challenges and opportunities.

Authors:  Rasheed A Gbadegesin; Michelle P Winn; William E Smoyer
Journal:  Nat Rev Nephrol       Date:  2013-01-15       Impact factor: 28.314

Review 4.  Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations.

Authors:  Geneviève Benoit; Eduardo Machuca; Corinne Antignac
Journal:  Pediatr Nephrol       Date:  2010-03-24       Impact factor: 3.714

5.  Phosphorylation of nephrin triggers its internalization by raft-mediated endocytosis.

Authors:  Xiao-Song Qin; Hiroyasu Tsukaguchi; Akemi Shono; Akitsugu Yamamoto; Hidetake Kurihara; Toshio Doi
Journal:  J Am Soc Nephrol       Date:  2009-10-22       Impact factor: 10.121

6.  Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.

Authors:  Saskia F Heeringa; Christopher N Vlangos; Gil Chernin; Bernward Hinkes; Rasheed Gbadegesin; Jinhong Liu; Bethan E Hoskins; Fatih Ozaltin; Friedhelm Hildebrandt
Journal:  Nephrol Dial Transplant       Date:  2008-05-23       Impact factor: 5.992

7.  Mutation analysis of NPHS1 in a worldwide cohort of congenital nephrotic syndrome patients.

Authors:  Bugsu Ovunc; Shazia Ashraf; Virginia Vega-Warner; Detlef Bockenhauer; Neveen A Soliman Elshakhs; Mark Joseph; Friedhelm Hildebrandt
Journal:  Nephron Clin Pract       Date:  2012-05-11

Review 8.  Monogenic Causes of Proteinuria in Children.

Authors:  Onur Cil; Farzana Perwad
Journal:  Front Med (Lausanne)       Date:  2018-03-12

9.  Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).

Authors:  Dominik S Schoeb; Gil Chernin; Saskia F Heeringa; Verena Matejas; Susanne Held; Virginia Vega-Warner; Detlef Bockenhauer; Christopher N Vlangos; Khemchand N Moorani; Thomas J Neuhaus; Jameela A Kari; James MacDonald; Pawaree Saisawat; Shazia Ashraf; Bugsu Ovunc; Martin Zenker; Friedhelm Hildebrandt
Journal:  Nephrol Dial Transplant       Date:  2010-02-18       Impact factor: 5.992

Review 10.  Novel insights in the genetics of steroid-sensitive nephrotic syndrome in childhood.

Authors:  Stephanie Dufek-Kamperis; Robert Kleta; Detlef Bockenhauer; Daniel Gale; Mallory L Downie
Journal:  Pediatr Nephrol       Date:  2020-10-21       Impact factor: 3.714

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