Literature DB >> 11692471

Familial hyperkalemic hypertension (Gordon syndrome): evidence for phenotypic variability in a study of 7 families.

S Disse-Nicodème, J M Achard, J Potier, M Delahousse, B Fiquet-Kempf, N Stern, A Blanchard, J C Guilbaud, P Niaudet, D Chauveau, B Dussol, Y Berland, P Dequiedt, J L Ader, M Paillard, J P Grünfeld, A Fournier, P Corvol, X Jeunemaitre.   

Abstract

Entities:  

Mesh：

Year:  2001        PMID： 11692471

Source DB:  PubMed          Journal:  Adv Nephrol Necker Hosp        ISSN： 0084-5957


× No keyword cloud information.
  2 in total

1.  Multiple promoters in the WNK1 gene: one controls expression of a kidney-specific kinase-defective isoform.

Authors:  Celine Delaloy; Jingyu Lu; Anne-Marie Houot; Sandra Disse-Nicodeme; Jean-Marie Gasc; Pierre Corvol; Xavier Jeunemaitre
Journal:  Mol Cell Biol       Date:  2003-12       Impact factor: 4.272

2.  Rare cause of severe hypertension in an adolescent boy presenting with short stature: Answers.

Authors:  Zehra Yavas Abali; Gozde Yesil; Tarık Kirkgoz; Neslihan Cicek; Harika Alpay; Serap Turan; Abdullah Bereket; Tulay Guran
Journal:  Pediatr Nephrol       Date:  2019-09-16       Impact factor: 3.714
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.