Literature DB >> 12937211

Hypokalaemic salt-losing tubulopathies: an evolving story.

Israel Zelikovic1.   

Abstract

Entities:  

Mesh：

Year:  2003        PMID： 12937211     DOI： 10.1093/ndt/gfg249

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


× No keyword cloud information.
  13 in total

1.  Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome.

Authors:  Natsuki Matsunoshita; Kandai Nozu; Masahide Yoshikane; Azusa Kawaguchi; Naoya Fujita; Naoya Morisada; Shingo Ishimori; Tomohiko Yamamura; Shogo Minamikawa; Tomoko Horinouchi; Keita Nakanishi; Junya Fujimura; Takeshi Ninchoji; Ichiro Morioka; Hiroaki Nagase; Mariko Taniguchi-Ikeda; Hiroshi Kaito; Kazumoto Iijima
Journal:  J Hum Genet       Date:  2018-05-30       Impact factor: 3.172

2.  Focal segmental glomerulosclerosis in association with Gitelman syndrome.

Authors:  Mevlut Ceri; Selman Unverdi; Mustafa Altay; Hatice Unverdi; Ilhan Kurultak; Rahmi Yılmaz; Arzu Ensari; Murat Duranay
Journal:  Int Urol Nephrol       Date:  2010-07-14       Impact factor: 2.370

3.  Cardiac arrhythmias and rhabdomyolysis in Bartter-Gitelman patients.

Authors:  Cinzia Cortesi; Sebastiano A G Lava; Alberto Bettinelli; Fabiana Tammaro; Olivier Giannini; Maria Caiata-Zufferey; Mario G Bianchetti
Journal:  Pediatr Nephrol       Date:  2010-06-13       Impact factor: 3.714

4.  Mutation G47R in the BSND gene causes Bartter syndrome with deafness in two Spanish families.

Authors:  Víctor García-Nieto; Carlos Flores; Maria I Luis-Yanes; Eduardo Gallego; Jesús Villar; Félix Claverie-Martín
Journal:  Pediatr Nephrol       Date:  2006-03-29       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

6.  Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafness.

Authors:  Pierre Robitaille; Aicha Merouani; Ning He; York Pei
Journal:  Eur J Pediatr       Date:  2011-04-09       Impact factor: 3.183

7.  Renal aspects of metabolic acid-base disorders in neonates.

Authors:  Silvia Iacobelli; Jean-Pierre Guignard
Journal:  Pediatr Nephrol       Date:  2018-11-19       Impact factor: 3.714

8.  Bartter syndrome: benefits and side effects of long-term treatment.

Authors:  Maria Helena Vaisbich; Maria Danisi Fujimura; Vera H Koch
Journal:  Pediatr Nephrol       Date:  2004-06-16       Impact factor: 3.714

9.  Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics.

Authors:  Natsuki Matsunoshita; Kandai Nozu; Akemi Shono; Yoshimi Nozu; Xue Jun Fu; Naoya Morisada; Naohiro Kamiyoshi; Hiromi Ohtsubo; Takeshi Ninchoji; Shogo Minamikawa; Tomohiko Yamamura; Koichi Nakanishi; Norishige Yoshikawa; Yuko Shima; Hiroshi Kaito; Kazumoto Iijima
Journal:  Genet Med       Date:  2015-04-16       Impact factor: 8.822

Review 10.  Rare Renal Diseases Can Be Used as Tools to Investigate Common Kidney Disorders.

Authors:  Mariadelina Simeoni; Sara Damiano; Giovanna Capolongo; Francesco Trepiccione; Miriam Zacchia; Giorgio Fuiano; Giovambattista Capasso
Journal:  Kidney Dis (Basel)       Date:  2017-05-25
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.