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pro vyhledávání: '"Kristina Roche"'
Autor:
Penelope Poyah, Joel Bergman, Laurette Geldenhuys, Glenda Wright, Noreen M. Walsh, Peter Hull, Kristina Roche, Michael L. West
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 8 (2021)
Rationale: Primary hyperoxaluria (PH) is a rare autosomal recessive disorder more commonly diagnosed in children or adolescents. Owing to its rarity and heterogeneous phenotype, it is often underrecognized, resulting in delayed diagnosis, including d
Externí odkaz:
https://doaj.org/article/e151fc151c6a43de9c36dd4a7880aaff
Autor:
Kristina Roche, Glenda R Wright, Penelope Poyah, Laurette Geldenhuys, Michael West, Joel C. Bergman, Noreen M. Walsh, Peter R. Hull
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 8 (2021)
Canadian Journal of Kidney Health and Disease
Canadian Journal of Kidney Health and Disease
Rationale: Primary hyperoxaluria (PH) is a rare autosomal recessive disorder more commonly diagnosed in children or adolescents. Owing to its rarity and heterogeneous phenotype, it is often underrecognized, resulting in delayed diagnosis, including d
Publikováno v:
Blood. 134:2447-2447
Background: A recognized complication of exposure to heparin is the development of heparin-induced thrombocytopenia (HIT) and heparin-induced thrombocytopenia with thrombosis (HITT). The frequency of HIT in patients exposed to unfractionated heparin