Literature DB >> 19902262

Focal segmental glomerulosclerosis in a boy with Dent-2 disease.

Kazunari Kaneko, Masafumi Hasui, Atsuko Hata, Daisuke Hata, Kandai Nozu.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2009        PMID： 19902262     DOI： 10.1007/s00467-009-1362-z

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.714


× No keyword cloud information.
  5 in total

1.  OCRL1 mutations in patients with Dent disease phenotype in Japan.

Authors:  Takashi Sekine; Kandai Nozu; Rashmi Iyengar; Xue Jun Fu; Masafumi Matsuo; Ryojiro Tanaka; Kazumoto Iijima; Emiko Matsui; Yutaka Harita; Jun Inatomi; Takashi Igarashi
Journal:  Pediatr Nephrol       Date:  2007-03-24       Impact factor: 3.714

2.  Association of Gitelman's syndrome and focal glomerulosclerosis.

Authors:  F Bulucu; A Vural; M Yenicesu; K Caglar
Journal:  Nephron       Date:  1998       Impact factor: 2.847

3.  Hypothesis: Dent disease is an underrecognized cause of focal glomerulosclerosis.

Authors:  Lawrence Copelovitch; Martin A Nash; Bernard S Kaplan
Journal:  Clin J Am Soc Nephrol       Date:  2007-08-08       Impact factor: 8.237

4.  Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis.

Authors:  Hajime Yamazaki; Kandai Nozu; Ichiei Narita; Michio Nagata; Yoshimi Nozu; Xue Jun Fu; Masafumi Matsuo; Kazumoto Iijima; Fumitake Gejyo
Journal:  Pediatr Nephrol       Date:  2008-10-02       Impact factor: 3.714

5.  Advanced renal insufficiency in a 34-year-old man with Lowe syndrome.

Authors:  Lothar Schramm; Andreas Gal; Josef Zimmermann; Kai-Olaf Netzer; Ekkehart Heidbreder; Kai Lopau; Hermann Gröne; Christoph Wanner
Journal:  Am J Kidney Dis       Date:  2004-03       Impact factor: 8.860
  5 in total
  11 in total

1.  A patient with Dent disease and features of Bartter syndrome caused by a novel mutation of CLCN5.

Authors:  Takayuki Okamoto; Toshihiro Tajima; Tomoya Hirayama; Satoshi Sasaki
Journal:  Eur J Pediatr       Date:  2011-09-20       Impact factor: 3.183

2.  Diagnosis and treatment of Dent disease in 10 Chinese boys.

Authors:  Guohua He; Hongwen Zhang; Fang Wang; Xiaoyu Liu; Huijie Xiao; Yong Yao
Journal:  Intractable Rare Dis Res       Date:  2017-02

3.  Clinical and laboratory features of Macedonian children with OCRL mutations.

Authors:  Velibor Tasic; Vladimir J Lozanovski; Petar Korneti; Nadica Ristoska-Bojkovska; Vesna Sabolic-Avramovska; Zoran Gucev; Michael Ludwig
Journal:  Pediatr Nephrol       Date:  2011-01-20       Impact factor: 3.714

4.  Nonfunction of the ECT2 gene may cause renal tubulointerstitial injury leading to focal segmental glomerulosclerosis.

Authors:  Akane Izu; Keisuke Sugimoto; Shinsuke Fujita; Hitomi Nishi; Yutaka Takemura; Mitsuru Okada; Tsukasa Takemura
Journal:  Clin Exp Nephrol       Date:  2012-05-03       Impact factor: 2.801

5.  The Lowe syndrome protein OCRL1 is required for endocytosis in the zebrafish pronephric tubule.

Authors:  Francesca Oltrabella; Grzegorz Pietka; Irene Barinaga-Rementeria Ramirez; Aleksandr Mironov; Toby Starborg; Iain A Drummond; Katherine A Hinchliffe; Martin Lowe
Journal:  PLoS Genet       Date:  2015-04-02       Impact factor: 5.917

Review 6.  The oculocerebrorenal syndrome of Lowe: an update.

Authors:  Arend Bökenkamp; Michael Ludwig
Journal:  Pediatr Nephrol       Date:  2016-03-24       Impact factor: 3.714

7.  Splicing Analysis of Exonic OCRL Mutations Causing Lowe Syndrome or Dent-2 Disease.

Authors:  Lorena Suarez-Artiles; Ana Perdomo-Ramirez; Elena Ramos-Trujillo; Felix Claverie-Martin
Journal:  Genes (Basel)       Date:  2018-01-04       Impact factor: 4.096

Review 8.  Genetic testing in steroid-resistant nephrotic syndrome: why, who, when and how?

Authors:  Rebecca Preston; Helen M Stuart; Rachel Lennon
Journal:  Pediatr Nephrol       Date:  2017-11-27       Impact factor: 3.714

9.  A role for OCRL in glomerular function and disease.

Authors:  Rebecca Preston; Richard W Naylor; Graham Stewart; Agnieszka Bierzynska; Moin A Saleem; Martin Lowe; Rachel Lennon
Journal:  Pediatr Nephrol       Date:  2019-12-06       Impact factor: 3.714

Review 10.  Proteinuria in Dent disease: a review of the literature.

Authors:  Youri van Berkel; Michael Ludwig; Joanna A E van Wijk; Arend Bökenkamp
Journal:  Pediatr Nephrol       Date:  2016-10-18       Impact factor: 3.714
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.