Acute clinical events in 299 homozygous sickle cell patients living in france

European Journal of Haematology

Volumn 65, Issue 3, 2000, Pages 155-164

  Neonato, Maria Grazia ^a,b   Guilloud Bataille, Monique ^c   Beauvais, Pierre ^d   Bégué, Pierre ^d   Belloy, Marie ^b   Benkerrou, Malika ^b   Ducrocq, Rolande ^b   Maier Redelsperger, Micheline ^a,b   De Montalembert, Mariane ^e   Quinet, Béatrice ^d   Elion, Jacques ^b   Feingold, Josué ^c   Girot, Robert ^a,b  

^a HÔPITAL TENON   (France)

^b HÔPITAL ROBERT DEBRÉ   (France)

^c INSERM   (France)

^d ARMAND TROUSSEAU HOSPITAL   (France)

^e HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Thalassemia; Globin gene cluster haplotypes; Anaemia; Infections; Sickle cell disease

Indexed keywords

BETA GLOBIN;

ADOLESCENT; AFRICA; ALPHA THALASSEMIA; ANEMIA; ARTICLE; CARIBBEAN ISLANDS; CHILD; FEMALE; FRANCE; GENE CLUSTER; GENETIC EPISTASIS; GEOGRAPHY; GLOBIN GENE; HAPLOTYPE; HOMOZYGOSITY; HUMAN; IMMIGRANT; MAJOR CLINICAL STUDY; MALE; MENINGITIS; OSTEOMYELITIS; PAIN; PRIORITY JOURNAL; SEPTICEMIA; SICKLE CELL ANEMIA; SICKLE CELL CRISIS; STROKE;

ACUTE DISEASE; ADOLESCENT; ALPHA-THALASSEMIA; ANEMIA, SICKLE CELL; CEREBROVASCULAR ACCIDENT; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; FEMALE; FRANCE; GENOTYPE; HUMANS; MALE; MENINGITIS; OSTEOMYELITIS; PHENOTYPE; RISK FACTORS; SEPSIS;

EID: 0033857950     PISSN: 09024441     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-0609.2000.90210.x     Document Type: Article

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