Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sandra Disse-Nicodeme"'
Autor:
Anne-Marie Houot, Pierre Corvol, Sandra Disse-Nicodeme, Jean-Marie Gasc, Céline Delaloy, Xavier Jeunemaitre, Jingyu Lu
Publikováno v:
Molecular and Cellular Biology. 23:9208-9221
WNK1 is a serine-threonine kinase, the expression of which is affected in pseudohypoaldosteronism type II, a Mendelian form of arterial hypertension. We characterized human WNK1 transcripts to determine the molecular mechanisms governing WNK1 express
Publikováno v:
Clinical and Experimental Pharmacology and Physiology. 28:1048-1052
1. Familial hyperkalaemic hypertension (FHH), also called pseudohypoaldosteronism type II (PHA2) or Gordon syndrome, is a rare Mendelian-form of low-renin hypertension. The first cases of FHH were reported approximately 30 years ago and they describe
Autor:
Graham Lipkin, Yvon Berland, Frederick H. Wilson, Murat Gunel, Haim Mayan, Kazuhiko Ishikawa, Morgan P. Feely, Isabelle Desitter, David V. Milford, Keith A. Choate, Zvi Farfel, David B. Simon, Bertrand Dussol, Jean-Michel Achard, Sandra Disse-Nicodeme, Robert J. Unwin, Xavier Jeunemaitre, Richard P. Lifton, Carol Nelson-Williams
Publikováno v:
Science. 293:1107-1112
Hypertension is a major public health problem of largely unknown cause. Here, we identify two genes causing pseudohypoaldosteronism type II, a Mendelian trait featuring hypertension, increased renal salt reabsorption, and impaired K + and H + excreti
Autor:
Albert Fournier, Sandra Disse-Nicodeme, Xavier Jeunemaitre, Pierre Corvol, David G. Warnock, B.éatrice Fiquet-Kempf, Jean-Michel Achard
Publikováno v:
The American journal of medicine. 114(6)
The familial hyperkalemic hypertension syndromes (1,2), also referred to as Gordon syndrome (3) or pseudohypoaldosteronism type 2 (4), are rare, autosomal dominant forms of hyperkalemia characterized by impaired renal potassium secretion, hyperchlore
Autor:
Béatrice Fiquet-Kempf, Jacky Potier, Isabelle Desitter, Michel Delahousse, Nora Stern, Jean-Louis Ader, Anne-Marie Houot, Sandra Disse-Nicodeme, Xavier Jeunemaitre
Publikováno v:
Journal of hypertension. 19(11)
Background Familial hyperkalaemic hypertension (FHH) is a Mendelian form of low-renin hypertension characterized by hyperkalaemia and hyperchloraemic acidosis despite a normal glomerular filtration rate. To date, three different loci have been identi
Publikováno v:
médecine/sciences. 17:959
Autor:
Xavier Jeunemaitre, Pierre Corvol, Anne-Marie Houot, Isabelle Desitter, Albert Fournier, Jean-Michel Achard, Sandra Disse-Nicodeme
Publikováno v:
The American Journal of Human Genetics. (2):302-310
Pseudohypoaldosteronism type II (PHA2) is a rare autosomal dominant form of volume-dependent low-renin hypertension characterized by hyperkalemia and hyperchloremic acidosis but also by a normal glomerular filtration rate. These features, together wi