Transfusion in patients with hemoglobinopathies;Transfusion des patients atteints d'hémoglobinopathies

Transfusion Clinique et Biologique

Volumn 7, Issue 6, 2000, Pages 553-558

  Montalembert, M De ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Hemolysis; Sickle cell disease; Splenic sequestration; Thalassemia

Indexed keywords

ALPHA GLOBIN; BETA GLOBIN;

ALPHA THALASSEMIA; ANEMIA; BETA THALASSEMIA; BLOOD TRANSFUSION; DAILY LIFE ACTIVITY; ERYTHROCYTE CONCENTRATE; ERYTHROCYTE TRANSFUSION; FOLIC ACID DEFICIENCY; FRANCE; HEMOGLOBIN DETERMINATION; HEMOGLOBINOPATHY; HEMOLYSIS; HOMOZYGOTE; HUMAN; INCIDENCE; IRON DEFICIENCY; MEDICAL DECISION MAKING; PARVOVIRUS; PRENATAL DIAGNOSIS; REVIEW; SCREENING; SICKLE CELL ANEMIA; TREATMENT INDICATION; TREATMENT OUTCOME;

EID: 0034520055     PISSN: 12467820     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1246-7820(01)80006-9     Document Type: Article

References (10)

1. Les modalités de la transfusion sanguine dans la drépanocytose et dans la thalassémie
2. Comparison of a transfusion preparation of newly formed red cells standard washed red cells transfusions in patients with homozygous beta-thalassemia
3. Indications for transfusion in sickle cell disease
4. Transfusion management of sickle cell disease
5. A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease
6. Controversies in transfusion in sickle cell disease
7. Alloimmunization in sickle cell anemia and transfusion of racially unmatched blood
8. Incidence de l'allo-immunisation antiérythrocytaire chez les patients porteurs d'un syndrome drépanocytaire majeur transfusé
9. La transfusion dans la drépanocytose
10. Structural and functional consequences of antigenic modulation of red blood cells with methoxypoly (Ethylene Glycol)