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Literature DB >> 7566631

Lack of H-ATPase in distal nephron causing hypokalaemic distal RTA in a patient with Sjögren's syndrome.

B Bastani, L Haragsim, S Gluck, K C Siamopoulos.

Abstract

Entities: Disease Gene Species

Mesh：

Substances：

Year: 1995 PMID： 7566631

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

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8 in total

1. Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene.

Authors: L J Bruce; D L Cope; G K Jones; A E Schofield; M Burley; S Povey; R J Unwin; O Wrong; M J Tanner
Journal: J Clin Invest Date: 1997-10-01 Impact factor: 14.808

2. Acquired gitelman syndrome.

Authors: Yong Kyun Kim; Ho Cheol Song; Yong-Soo Kim; Euy Jin Choi
Journal: Electrolyte Blood Press Date: 2009-06-30

Review 3. Regulated acid-base transport in the collecting duct.

Authors: Carsten A Wagner; Olivier Devuyst; Soline Bourgeois; Nilufar Mohebbi
Journal: Pflugers Arch Date: 2009-03-07 Impact factor: 3.657

Review 4. [Interstitial nephritis].

Authors: J Halbritter; C Mayer; F M Rasche; K Amann; T H Lindner
Journal: Internist (Berl) Date: 2009-09 Impact factor: 0.743

Lack of H-ATPase in distal nephron causing hypokalaemic distal RTA in a patient with Sjögren's syndrome.

1. Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene.

2. Acquired gitelman syndrome.

Review 3. Regulated acid-base transport in the collecting duct.

Review 4. [Interstitial nephritis].

5. Secondary Sjogren's syndrome presenting with hypokalemic periodic paralysis.

6. Primary Sjogren's syndrome presenting as hypokalemic paralysis: A case series.

7. Hypokalemic Paralysis due to Primary Sjögren Syndrome: Case Report and Review of the Literature.

Review 8. Differential diagnosis of perinatal Bartter, Bartter and Gitelman syndromes.