6 papers found
Mitochondrial DNA mutations in renal disease: an overview
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure
Acidosis and Deafness in Patients with Recessive Mutations in FOXI1
Clinical and diagnostic features of Bartter and Gitelman syndromes
Hyponatremia and cyst growth in neonatal polycystic kidney disease: a case for aquaretics?
EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10.
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