Literature DB >> 9832636

The molecular basis of hypokalaemic alkalosis: Bartter's and Gitelman's syndromes.

S Bhandari, J H Turney.   

Abstract

Entities:  

Mesh：

Year:  1998        PMID： 9832636     DOI： 10.1159/000045209

Source DB:  PubMed          Journal:  Nephron        ISSN： 1660-8151            Impact factor:   2.847


× No keyword cloud information.
  4 in total

1.  Two novel genotypes of the thiazide-sensitive Na-Cl cotransporter (SLC12A3) gene in patients with Gitelman's syndrome.

Authors:  Noriko Aoi; Tomohiro Nakayama; Yoshiko Tahira; Akira Haketa; Minako Yabuki; Tadataka Sekiyama; Chie Nakane; Hiroaki Mano; Hideomi Kawachi; Naoyuki Sato; Masayoshi Soma; Kouichi Matsumoto
Journal:  Endocrine       Date:  2007-04       Impact factor: 3.633

2.  Long-term Clinical Course after Living Kidney Donation by a Patient with Gitelman Syndrome Harboring a Compound Heterozygous Mutation of the SLC12A3 Gene.

Authors:  Sahoko Kamejima; Izumi Yamamoto; Akiko Tajiri; Yudo Tanno; Ichiro Ohkido; Takashi Yokoo
Journal:  Intern Med       Date:  2020-12-15       Impact factor: 1.271

Review 3.  Calcium Transport in the Kidney and Disease Processes.

Authors:  Ramy M Hanna; Rebecca S Ahdoot; Kamyar Kalantar-Zadeh; Lena Ghobry; Ira Kurtz
Journal:  Front Endocrinol (Lausanne)       Date:  2022-03-01       Impact factor: 5.555

4.  KCC3a, a Strong Candidate Pathway for K+ Loss in Alkalemia.

Authors:  Mohammed Zubaerul Ferdaus; Andrew Scott Terker; Rainelli Koumangoye; Eric Delpire
Journal:  Front Cell Dev Biol       Date:  2022-07-07
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.