Literature DB >> 16283887

Mild cystic fibrosis revealed by persistent hyponatremia during the French 2003 heat wave, associated with the S1455X C-terminus CFTR mutation.

R Epaud, E Girodon, H Corvol, F Niel, V Guigonis, A Clement, D Feldmann, A Bensman, T Ulinski.   

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Year:  2005        PMID： 16283887     DOI： 10.1111/j.1399-0004.2005.00525.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  3 in total

1.  Autosomal recessive hyponatremia due to isolated salt wasting in sweat associated with a mutation in the active site of Carbonic Anhydrase 12.

Authors:  Emad Muhammad; Neta Leventhal; Galit Parvari; Aaron Hanukoglu; Israel Hanukoglu; Vered Chalifa-Caspi; Yael Feinstein; Jenny Weinbrand; Harel Jacoby; Esther Manor; Tal Nagar; John C Beck; Val C Sheffield; Eli Hershkovitz; Ruti Parvari
Journal:  Hum Genet       Date:  2010-12-24       Impact factor: 4.132

Review 2.  Electrolyte abnormalities in cystic fibrosis: systematic review of the literature.

Authors:  Elisabetta Scurati-Manzoni; Emilio F Fossali; Carlo Agostoni; Enrica Riva; Giacomo D Simonetti; Maura Zanolari-Calderari; Mario G Bianchetti; Sebastiano A G Lava
Journal:  Pediatr Nephrol       Date:  2013-12-11       Impact factor: 3.714

Review 3.  Physiology of sweat gland function: The roles of sweating and sweat composition in human health.

Authors:  Lindsay B Baker
Journal:  Temperature (Austin)       Date:  2019-07-17
  3 in total

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