نتایج جستجو برای: pseudohypoaldosteronism type 1
تعداد نتایج: 3647227 فیلتر نتایج به سال:
Regulation of the SLC12 family of membrane transporters including NCCT involves a scaffold of interacting proteins including the STE 20 kinase SPAK and the WNK kinases, WNK 1 and WNK 4, which are mutated in the hypertensive syndrome of pseudohypoaldosteronism type 2 (PHAII). WNK4 regulates NCCT by affecting forward trafficking to the surface membrane. Studies in Xenopus using kinase dead WNK4 s...
introduction to define the clinical features, biochemical and histological findings and outcome of three forms of autoimmune hepatitis. materials and methods in a cross sectional study between november 2001 to january 2008 in tehran and mashhad university of medical sciences, 61 children who diagnosed as aih (40 girls and 21 boys) have been analyzed for their clinical, serological, and histol...
Ante/neonatal Bartter syndrome (BS) is a rare hereditary disorder. It is characterized by renal salt wasting, hypokalaemic metabolic alkalosis, high renin and aldosterone but normal blood pressure. We report a low birth weight newborn baby who presented with repeated apnoea shortly after birth as well as hyponatraemia, hypochloraemia, hyperkalaemia and metabolic acidosis. Her biochemical featur...
Lyndall Gordon's recent biography, Lives Like Loaded Guns: Emily Dickinson and Her Family's Feuds (2010), tells with high verve the story of generational infighting over poet Emily Dickinson's posthumous presentation to the world. Equally dramatic is Gordon's hypothesis that Dickinson suffered from epilepsy, which led Gordon to seemingly solve the ineffable mystery of Dickinson's reclusion, a c...
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