遗传性球形红细胞增多症；新指南。 - Suppr

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Hereditary spherocytosis; new guidelines.

作者信息

Bolton-Maggs P H B

机构信息

Department of Clinical Haematology, Manchester Royal Infirmary, Oxford Road, Manchester M13 9WL, UK.

出版信息

Arch Dis Child. 2004 Sep;89(9):809-12. doi: 10.1136/adc.2003.034587.

DOI:10.1136/adc.2003.034587

PMID:15321852

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1763196/

Abstract

摘要

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Safety and immunogenicity of a recombinant parvovirus B19 vaccine formulated with MF59C.1.

J Infect Dis. 2003 Feb 15;187(4):675-8. doi: 10.1086/368382. Epub 2003 Feb 7.

Clinical and hematologic benefits of partial splenectomy for congenital hemolytic anemias in children.

Ann Surg. 2003 Feb;237(2):281-8. doi: 10.1097/01.SLA.0000048453.61168.8F.

Bacille Calmette-Guérin lymphadenitis.

Postgrad Med J. 2002 Jun;78(920):327-9. doi: 10.1136/pmj.78.920.327.

Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis.

Hematol J. 2000;1(3):146-52. doi: 10.1038/sj.thj.6200022.

Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis.

Blood. 2001 Jan 15;97(2):399-403. doi: 10.1182/blood.v97.2.399.

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Natural history of hereditary spherocytosis during the first year of life.

Blood. 2000 Jan 15;95(2):393-7.

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