Defining the phenotypes of sickle cell disease

Hemoglobin

Volumn 35, Issue 5-6, 2011, Pages 511-519

  Ballas, Samir K ^a  

^a THOMAS JEFFERSON UNIVERSITY   (United States)

Author keywords

Complications; Definition; Genotype; Phenotype; Sickle cell anemia; Sickle cell disease

Indexed keywords

BETA GLOBIN; HEMOGLOBIN; HEMOGLOBIN C;

ACUTE CHEST SYNDROME; ACUTE KIDNEY FAILURE; APLASTIC CRISIS; ASPLENIA; AVASCULAR NECROSIS; BONE DISEASE; CEREBROVASCULAR ACCIDENT; CHRONIC KIDNEY FAILURE; COGNITIVE DEFECT; DEMETHYLATION; DISEASE PREDISPOSITION; DISEASE SEVERITY; DNA METHYLATION; EPIGENETICS; ERYTHROPOIESIS; EYE DISEASE; GASTROINTESTINAL DISEASE; GENE ACTIVATION; GENE INACTIVATION; GENE MUTATION; GENETIC EPISTASIS; HAND FOOT SYNDROME; HEMATURIA; HEMOGLOBIN BLOOD LEVEL; HEMOLYSIS; HEMOLYTIC ANEMIA; HEMOSIDEROSIS; HEPATOBILIARY DISEASE; HEREDITY; HUMAN; HYPERHEMOLYSIS; HYPERVISCOSITY SYNDROME; INTRAHEPATIC CHOLESTASIS; KIDNEY DISEASE; LEG ULCER; LUNG DISEASE; MULTIPLE ORGAN FAILURE; MUSCLE DISEASE; NEUROIMAGING; NEUROLOGIC DISEASE; NEUROPATHIC PAIN; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PLEIOTROPY; PRIAPISM; PROTEIN BLOOD LEVEL; PROTEINURIA; RETINA DETACHMENT; REVIEW; SCINTISCANNING; SICKLE CELL ANEMIA; SKIN DISEASE; SKIN ULCER; TRANSFUSIONAL HEMOSIDEROSIS; TRANSIENT ISCHEMIC ATTACK; UROGENITAL TRACT DISEASE; VITREOUS HEMORRHAGE;

ANEMIA, SICKLE CELL; EPIGENESIS, GENETIC; HUMANS; PHENOTYPE; RISK FACTORS;

EID: 81055133480     PISSN: 03630269     EISSN: 1532432X     Source Type: Journal    
DOI: 10.3109/03630269.2011.610477     Document Type: Review

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