Literature DB >> 23364648

A long-term follow-up of an Imerslund-Grasbeck syndrome patient with proteinuria.

Zafer Ercan, Mehmet E Demir, Turgay Ulas, Muharrem Ingec, Mehmet Horoz.   

Abstract

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Year:  2013        PMID: 23364648     DOI: 10.3265/Nefrologia.pre2012.Aug.11661

Source DB:  PubMed          Journal:  Nefrologia        ISSN: 0211-6995            Impact factor:   2.033


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  3 in total

1.  Clinical and genetic characterization of children with cubilin variants.

Authors:  Neslihan Cicek; Harika Alpay; Sercin Guven; Ceren Alavanda; Özde Nisa Türkkan; Serim Pul; Ece Demirci; Nurdan Yıldız; Pınar Ata; Ibrahim Gokce
Journal:  Pediatr Nephrol       Date:  2022-09-16       Impact factor: 3.651

2.  Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.

Authors:  Mathilda Bedin; Olivia Boyer; Aude Servais; Yong Li; Laure Villoing-Gaudé; Marie-Josephe Tête; Alexandra Cambier; Julien Hogan; Veronique Baudouin; Saoussen Krid; Albert Bensman; Florie Lammens; Ferielle Louillet; Bruno Ranchin; Cecile Vigneau; Iseline Bouteau; Corinne Isnard-Bagnis; Christoph J Mache; Tobias Schäfer; Lars Pape; Markus Gödel; Tobias B Huber; Marcus Benz; Günter Klaus; Matthias Hansen; Kay Latta; Olivier Gribouval; Vincent Morinière; Carole Tournant; Maik Grohmann; Elisa Kuhn; Timo Wagner; Christine Bole-Feysot; Fabienne Jabot-Hanin; Patrick Nitschké; Tarunveer S Ahluwalia; Anna Köttgen; Christian Brix Folsted Andersen; Carsten Bergmann; Corinne Antignac; Matias Simons
Journal:  J Clin Invest       Date:  2020-01-02       Impact factor: 14.808

3.  CUBN gene mutations may cause focal segmental glomerulosclerosis (FSGS) in children.

Authors:  Jing Yang; Yongli Xu; Linxia Deng; Luowen Zhou; Liru Qiu; Yu Zhang; Jianhua Zhou
Journal:  BMC Nephrol       Date:  2022-01-03       Impact factor: 2.388

  3 in total

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