نتایج جستجو برای: sickle cell anaemia

تعداد نتایج: 1695368  

Journal: :Archives of disease in childhood 1988
C Vermylen G Cornu M Philippe J Ninane A Borja D Latinne A Ferrant J L Michaux G Sokal

Sickle cell anaemia is still responsible for severe crippling and death in young patients living in developing countries. Apart from prophylaxis and treatment of infections, no active treatment can be safely proposed in such areas of the world. Therefore a bone marrow transplantation was performed in 12 patients staying in Belgium and planning to return to Africa. Twelve patients, aged between ...

Journal: :International endodontic journal 2004
A Demirbaş Kaya B O Aktener C Unsal

AIM To investigate radiographic manifestations of sickle cell anaemia (SCA) and whether or not a pulpal necrosis may develop without a pathological history. METHODOLOGY Thirty-six patients with homozygous SCA were evaluated, and a further 36 individuals without SCA were included in the study as a control group. All 72 patients participating in the study ranged between the ages of 16 and 40 ye...

Ghodsi Daneshbod,

Sickle cell-thalassemia associated with glucose- 6-phosphate dehydrogenese deficiency is re­ported in an Iranian family. The father had sickle trait and G.6.P.D. deficiency, the mother minor thalassemia, one of the sons siclc:le ceH-thailasemiia., the oth-er sickle cell trait; the daughter had sickle cell-thalassemia and was carrier of G.6.P.D. deficiellcy. 

Fatemeh Kianpour Ghahfarokhi, Khoda Morad Zandian, Mohammad Pedram,

Background: Studies have demonstrated that sickle cell trait can be found in an asymptomatic healthy carrier with normal complete blood count (CBC) and red blood cell (RBC) indices. According to Iranian Ministry of Health bulletin instructions, prenuptial Thalassemia Screening Program (TSP) primarily depends on RBC indices which are measured through a routine CBC. Only when these levels are bel...

Journal: :Journal of clinical pathology 1952
P PIZZOLATO L RAIDER

In the course of a study of bone marrow in blood dyscrasias and other pathological states an increase of megakaryocytes was found to be rather frequent in idiopathic thrombocytopenic purpura, sickle cell anaemia, Hodgkin's disease, microcytic hypochromic anaemia, polycythaemia vera, and pregnancy. Simultaneously with this study, two patients with unexplained mild anaemia and no definite clinica...

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