Frequency and clinical spectrum of rare inherited coagulopathies - A tricenter study

Journal of the Pakistan Medical Association

Volumn 58, Issue 8, 2008, Pages 441-444

  Khalid, Safoorah ^a   Bilwani, Fareena ^a   Adil, Salman Naseem ^a   Khurshid, Mohammad ^a  

^a AGA KHAN UNIVERSITY HOSPITAL   (Pakistan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BLEEDING TENDENCY; BLEEDING TIME; BLOOD CLOTTING DISORDER; BLOOD CLOTTING FACTOR 10 DEFICIENCY; BLOOD CLOTTING FACTOR 12 DEFICIENCY; BLOOD CLOTTING FACTOR 13 DEFICIENCY; BLOOD CLOTTING FACTOR 5 DEFICIENCY; BLOOD CLOTTING FACTOR 7 DEFICIENCY; CHILD; FEMALE; FIBRINOGEN DEFECT; HEMOPHILIA A; HEMOPHILIA B; HUMAN; INHERITED COAGULOPATHY; MAJOR CLINICAL STUDY; MALE; PROTHROMBIN DEFICIENCY; SCREENING; THROMBOCYTE AGGREGATION; THROMBOCYTE COUNT; ADOLESCENT; BLOOD CLOTTING TEST; HEALTH SURVEY; INFANT; MASS SCREENING; MIDDLE AGED; PAKISTAN; PRESCHOOL CHILD; QUESTIONNAIRE; RISK FACTOR;

ADOLESCENT; ADULT; BLOOD COAGULATION DISORDERS, INHERITED; BLOOD COAGULATION TESTS; CHILD; CHILD, PRESCHOOL; FEMALE; HEALTH SURVEYS; HUMANS; INFANT; MALE; MASS SCREENING; MIDDLE AGED; PAKISTAN; PLATELET COUNT; QUESTIONNAIRES; RISK FACTORS;

EID: 48249110775     PISSN: 00309982     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

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