Literature DB >> 20625829

Focal segmental glomerulosclerosis in association with Gitelman syndrome.

Mevlut Ceri1, Selman Unverdi, Mustafa Altay, Hatice Unverdi, Ilhan Kurultak, Rahmi Yılmaz, Arzu Ensari, Murat Duranay.   

Abstract

Gitelman syndrome (GS) is an autosomal recessive disorder characterized by hypokalemia, metabolic alkalosis, hypomagnesemia and hypocalciuria. Glomerulonephritis associated with GS is rarely documented in the literature. We present an adult patient with GS whose renal biopsy revealed focal segmental glomerulosclerosis.

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Year:  2010        PMID： 20625829     DOI： 10.1007/s11255-010-9802-z

Source DB:  PubMed          Journal:  Int Urol Nephrol        ISSN： 0301-1623            Impact factor:   2.370


  14 in total

Review 1.  Hypokalaemic salt-losing tubulopathies: an evolving story.

Authors:  Israel Zelikovic
Journal:  Nephrol Dial Transplant       Date:  2003-09       Impact factor: 5.992

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

Review 3.  The renin-angiotensin system and progression of renal disease: from hemodynamics to cell biology.

Authors:  Gunter Wolf; Ulrike Butzmann; Ulrich O Wenzel
Journal:  Nephron Physiol       Date:  2003-01

Review 4.  Gitelman's syndrome: towards genotype-phenotype correlations?

Authors:  Eva Riveira-Munoz; Qing Chang; René J Bindels; Olivier Devuyst
Journal:  Pediatr Nephrol       Date:  2006-10-24       Impact factor: 3.714

5.  C1q nephropathy in association with Gitelman syndrome: a case report.

Authors:  Coral Hanevold; Ayesa Mian; Rory Dalton
Journal:  Pediatr Nephrol       Date:  2006-09-06       Impact factor: 3.714

Review 6.  Angiotensin II and gene expression in the kidney.

Authors:  S Klahr; J Morrissey
Journal:  Am J Kidney Dis       Date:  1998-01       Impact factor: 8.860

7.  Kidney transplant in Gitelman's syndrome. Report of the first case.

Authors:  Lorenzo A Calò; Francesco Marchini; Paul A Davis; Paolo Rigotti; Elisa Pagnin; Andrea Semplicini
Journal:  J Nephrol       Date:  2003 Jan-Feb       Impact factor: 3.902

8.  Expression of transforming growth factor-beta isoforms in human glomerular diseases.

Authors:  T Yamamoto; N A Noble; A H Cohen; C C Nast; A Hishida; L I Gold; W A Border
Journal:  Kidney Int       Date:  1996-02       Impact factor: 10.612

9.  Expression of types I, II, and III TGF-beta receptors in human glomerulonephritis.

Authors:  T Yamamoto; T Watanabe; N Ikegaya; Y Fujigaki; K Matsui; H Masaoka; M Nagase; A Hishida
Journal:  J Am Soc Nephrol       Date:  1998-12       Impact factor: 10.121

10.  Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.

Authors:  D B Simon; C Nelson-Williams; M J Bia; D Ellison; F E Karet; A M Molina; I Vaara; F Iwata; H M Cushner; M Koolen; F J Gainza; H J Gitleman; R P Lifton
Journal:  Nat Genet       Date:  1996-01       Impact factor: 38.330
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  3 in total

1.  Fanconi syndrome and severe polyuria: an uncommon clinicobiological presentation of a Gitelman syndrome.

Authors:  Karim Bouchireb; Olivia Boyer; Lamisse Mansour-Hendili; Arnaud Garnier; Laurence Heidet; Patrick Niaudet; Remi Salomon; Rosa Vargas Poussou
Journal:  BMC Pediatr       Date:  2014-08-11       Impact factor: 2.125

2.  A case of Gitelman syndrome with membranous nephropathy.

Authors:  Xiafei Guo; Shanshen Yu; Jia Sun; Lijun Mou
Journal:  BMC Nephrol       Date:  2022-07-26       Impact factor: 2.585

3.  A case of hypokalemia and proteinuria with a new mutation in the SLC12A3 Gene.

Authors:  Qin Chen; Yaqin Wu; Jingya Zhao; Ying Jia; Wei Wang
Journal:  BMC Nephrol       Date:  2018-10-19       Impact factor: 2.388
  3 in total

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