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[PDF] from cnrs.frF Gundel, S Eber… - Annals of hematology, 2011 - Springer
... hereditary spherocytosis in the neonatal period ... Dear Editor, Although hereditary spherocytosis
(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. ...
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CL Snyder - AAP Grand Rounds, 2011 - Am Acad Pediatrics
... SURGERY Partial Splenectomy for Hereditary Spherocytosis. Source: Buesing KL, Tracy ET,
Kiernan C, et al. ... PICO Question: Among children with hereditary spherocytosis, is partial
splenectomy a viable treatment option? Question type: Intervention. Study design: Case series. ...
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[HTML] from nih.govS Iijima, T Ohzeki… - Yonsei Medical Journal, 2011 - ncbi.nlm.nih.gov
... Copyright : Yonsei University College of Medicine 2011. Hereditary Spherocytosis Coexisting
with UDP-Glucuronosyltransferase Deficiency Highly Suggestive of Crigler-Najjar Syndrome
Type II. ... Guidelines for the diagnosis and management of hereditary spherocytosis. ...
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A Wree, A Canbay, H Müller-Beißenhirtz… - Z …, 2011 - thieme-connect.com
© Georg Thieme Verlag KG Stuttgart · New York. Excessive Bilirubin Elevation in a Patient with
Hereditary Spherocytosis and Intrahepatic Cholestasis. ... Seitenanfang. Abstract. Hereditary
spherocytosis is a common hemolytic anemia with an estimated incidence of 1 / 2500 births. ...
KL Buesing, ET Tracy, C Kiernan, AC Pastor… - Journal of Pediatric …, 2011 - Elsevier
... APSA Papers. Partial splenectomy for hereditary spherocytosis: a multi-institutional review. ... Partial
splenectomy has emerged as a surgical option for selected children with hereditary spherocytosis,
with the goal of reducing anemia while preserving splenic function. ...
Related articles - All 3 versions

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