autosomal dominant tubulointerstitial kidney disease, focal segmental glomerulosclerosis, Alport syndrome, and atypical ...
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AI-based method shows promise for pathological diagnosis of hereditary kidney diseasesAlport syndrome is a genetic disorder associated with kidney dysfunction, sensorineural hearing loss, and ocular abnormalities. In the kidneys, hematuria occurs in the early stages of the disease ...
Data from Eloxx’s proof-of-concept trial in patients with nonsense mutation Alport Syndrome (NMAS) presented in late-breaking presentation at American Society of Nephrology (ASN) Kidney Week New ...
The National Kidney Foundation (NKF) is proud to announce that its KidneyCARE (Community Access to Research Equity)™ Study – ...
She remained extremely active by traveling with friends internationally, hiking with the “Mountain Mamas,” biking, skiing, dragon boating, paddling, gardening and singing with Mountain Song.
EAST STROUDSBURG, Pa. - 20-year-old Kyrsten Lerch is like so many young women: Her story is only just beginning, and she has so much to be excited for.
C3 Glomerulopathy (C3G), Focal Segmental Glomerulosclerosis (FSGS), Polycystic Kidney Disease (PKD), Alport Syndrome, Fabry Disease, and more. By capturing diverse patient experiences, the study ...
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