Literature DB >> 19615561

Hereditary renal tubular disorders.

Vimal Chadha1, Uri S Alon.   

Abstract

The multiple and complex functions of the renal tubule in regulating water, electrolyte, and mineral homeostasis make it prone to numerous genetic abnormalities resulting in malfunction. The phenotypic expression depends on the mode of interference with the normal physiology of the segment affected, and whether the abnormality is caused by loss of function or, less commonly, gain of function. In this review we address the current knowledge about the association between the genetics and clinical manifestations and treatment of representative disorders affecting the length of the nephron.

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Year:  2009        PMID: 19615561     DOI: 10.1016/j.semnephrol.2009.03.013

Source DB:  PubMed          Journal:  Semin Nephrol        ISSN: 0270-9295            Impact factor:   5.299


  11 in total

Review 1.  Tumor-induced osteomalacia.

Authors:  William H Chong; Alfredo A Molinolo; Clara C Chen; Michael T Collins
Journal:  Endocr Relat Cancer       Date:  2011-06-08       Impact factor: 5.678

Review 2.  Pathophysiology and clinical presentations of salt-losing tubulopathies.

Authors:  Hannsjörg W Seyberth
Journal:  Pediatr Nephrol       Date:  2015-07-16       Impact factor: 3.714

Review 3.  Distal convoluted tubule.

Authors:  James A McCormick; David H Ellison
Journal:  Compr Physiol       Date:  2015-01       Impact factor: 9.090

Review 4.  [Electrolyte disorders].

Authors:  M Girndt
Journal:  Internist (Berl)       Date:  2011-08       Impact factor: 0.743

Review 5.  The population genetics of chronic kidney disease: insights from the MYH9-APOL1 locus.

Authors:  Saharon Rosset; Shay Tzur; Doron M Behar; Walter G Wasser; Karl Skorecki
Journal:  Nat Rev Nephrol       Date:  2011-05-03       Impact factor: 28.314

6.  RenalTube: a network tool for clinical and genetic diagnosis of primary tubulopathies.

Authors:  Natalia Mejía; Fernando Santos; Félix Claverie-Martín; Víctor García-Nieto; Gema Ariceta; Luis Castaño
Journal:  Eur J Pediatr       Date:  2013-02-07       Impact factor: 3.183

7.  [Chronic pain and artificial diseases].

Authors:  C Roch; C Knöchlein; J Albrecht
Journal:  Schmerz       Date:  2014-10       Impact factor: 1.107

Review 8.  Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects.

Authors:  Hannsjörg W Seyberth; Karl P Schlingmann
Journal:  Pediatr Nephrol       Date:  2011-04-19       Impact factor: 3.714

9.  An infant with poor weight gain and hypochloremic metabolic alkalosis: a case report.

Authors:  Ahmed H Alhammadi; Mohamed Khalifa; Lolwa Alnaimi
Journal:  Int J Gen Med       Date:  2014-07-25

10.  Nonmuscle myosin 2 proteins encoded by Myh9, Myh10, and Myh14 are uniquely distributed in the tubular segments of murine kidney.

Authors:  Karla L Otterpohl; Ryan G Hart; Claire Evans; Kameswaran Surendran; Indra Chandrasekar
Journal:  Physiol Rep       Date:  2017-12
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