Pancytopenia and Bone Marrow Hypoplasia in a Case of Paroxysmal Nocturnal Hemoglobinuria
Author:
Publisher
Wiley
Subject
Internal Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.0954-6820.1963.tb16505.x/fullpdf
Reference31 articles.
1. Paroxysmal nocturnal hemoglobinuria. H. Erythrocyte acetylcholinesterase defect;Auditore;Amer. J. Med.,1959
2. Survival of blood platelets labelled with chromium;Aas;J. Clin. Invest.,1958
3. Spektralphotometrische Eisenbestimmung mit o-Phenantrolin und αα'-Dipyridyl;Borei;Biochem. Z.,1943
4. Paroxysmal nocturnal hemoglobinuria: Case complicated by aregenerative (aplastic) crisis;Crosby;Ann. intern. Med.,1953
5. Refractory anaemia (Fanconi type): Its incidence in three members of one family, with in one case a relationship to chronic haemolytic anaemia with nocturnal haemoglobinuria (Marchiafava-Micheli disease or “nocturnal haemoglobinuria”);Dacie;Arch. Dis. Childh.,1944
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1. THE SUCROSE HAEMOLYSIS TEST IN PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA;Acta Medica Scandinavica;2009-04-24
2. Paroxysmal Nocturnal Haemoglobinuria in Aplastic Anaemia;Clinics in Haematology;1978-10
3. Paroxysmal Nocturnal Haemoglobinuria and Refractory Marrow Failure Treated by Marrow Transplantation;British Journal of Haematology;1973-06
4. BIBLIOGRAPHY;Blood Platelets in Man and Animals;1969
5. THE VARIED PATTERN OF APLASTIC ANAEMIA IN CHILDHOOD;Journal of Paediatrics and Child Health;1966-12
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