[PDF] from cnrs.frF Gundel, S Eber… - Annals of hematology, 2011 - Springer ...hereditaryspherocytosis in the neonatal period ... Dear Editor, Although hereditaryspherocytosis (HS) is a common disorder of the red cell membrane, it is diagnosed in only one third of affected infants during the first year of life [1] and rarely in the newborn period. ... Related articles - All 5 versions
CL Snyder - AAP Grand Rounds, 2011 - Am Acad Pediatrics ... SURGERY Partial Splenectomy for HereditarySpherocytosis. Source: Buesing KL, Tracy ET, Kiernan C, et al. ... PICO Question: Among children with hereditaryspherocytosis, is partial splenectomy a viable treatment option? Question type: Intervention. Study design: Case series. ... Related articles
[HTML] from nih.govS Iijima, T Ohzeki… - Yonsei Medical Journal, 2011 - ncbi.nlm.nih.gov ... Copyright : Yonsei University College of Medicine 2011. HereditarySpherocytosis Coexisting with UDP-Glucuronosyltransferase Deficiency Highly Suggestive of Crigler-Najjar Syndrome Type II. ... Guidelines for the diagnosis and management of hereditaryspherocytosis. ... Related articles - All 9 versions
KL Buesing, ET Tracy, C Kiernan, AC Pastor… - Journal of Pediatric …, 2011 - Elsevier ... APSA Papers. Partial splenectomy for hereditaryspherocytosis: a multi-institutional review. ... Partial splenectomy has emerged as a surgical option for selected children with hereditaryspherocytosis, with the goal of reducing anemia while preserving splenic function. ... Related articles - All 3 versions
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