Homozygous Factor V Leiden mutation in sickle cell anaemia [1]

British Journal of Haematology

Volumn 116, Issue 1, 2002, Pages 236-

  Kordes, U ^a   Janka Schaub, G ^a   Kulozik, A ^a   Schneppenheim, R ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

Author keywords

Factor V Leiden mutation; Sickle cell anaemia

Indexed keywords

ALPHA GLOBIN; BLOOD CLOTTING FACTOR 5 LEIDEN; HEMOGLOBIN F; HYDROXYUREA;

ARTERY THROMBOSIS; BLOOD LEVEL; BLOOD TRANSFUSION; CELL ADHESION; CELL COUNT; CHOLECYSTITIS; CLINICAL TRIAL; DISEASE COURSE; DISEASE SEVERITY; FEMUR HEAD NECROSIS; GENE DELETION; HOMOZYGOSITY; HUMAN; INFARCTION; IRAQ; LABORATORY TEST; LETTER; MEDICAL RECORD; MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; OCCLUSION; OSTEOMYELITIS; PATHOPHYSIOLOGY; PATIENT COMPLIANCE; PREVALENCE; PRIORITY JOURNAL; RECURRENT DISEASE; RISK ASSESSMENT; RISK FACTOR; SALMONELLA; SAUDI ARABIA; SICKLE CELL ANEMIA; SICKLE CELL TRAIT; SOUTHERN BLOTTING; STROKE; THROMBOGENESIS;

ADOLESCENT; ADULT; ANEMIA, SICKLE CELL; FACTOR V; FEMALE; HOMOZYGOTE; HUMANS; RISK FACTORS; VENOUS THROMBOSIS;

EID: 0036164905     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2002.3242_1.x     Document Type: Letter

References (3)

1. Inherited thrombophilia: Resistance to activated protein C as a pathogenic factor of venous thromboembolism
2. Two different forms of homozygous sickle cell disease occur in Saudi Arabia
3. Antiphospholipid antibodies, proteins C and S, and coagulation changes in sickle cell disease