HEREDITARY HEMORRHAGIC TELANGIECTASIA AND DISSEMINATED INTRAVASCULAR COAGULATION: A NEW CLINICAL SYNDROME

Annals of the New York Academy of Sciences

Volumn 370, Issue 1, 1981, Pages 851-854

  Bick, Rodger L ^a,b,c  

^a San Joaquin Hematology Oncology Medical Group ^*  (United States)

^b WAYNE STATE UNIVERSITY   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HEPARIN;

ACUTE DISEASE; ARTICLE; BLOOD CLOTTING FACTOR 11 DEFICIENCY; CHRONIC DISEASE; DISSEMINATED INTRAVASCULAR CLOTTING; HEMOSTASIS; HUMAN; RENDU OSLER WEBER DISEASE; SYNDROME; THROMBOCYTE; VON WILLEBRAND DISEASE; BLEEDING; BLOOD AND HEMOPOIETIC SYSTEM; HUMAN CELL; MAJOR CLINICAL STUDY; TELANGIECTASIA; THROMBOSIS;

ACUTE DISEASE; BLOOD PLATELETS; CHRONIC DISEASE; DISSEMINATED INTRAVASCULAR COAGULATION; FACTOR XI DEFICIENCY; HEMOSTASIS; HEPARIN; HUMAN; SYNDROME; TELANGIECTASIA, HEREDITARY HEMORRHAGIC; VON WILLEBRAND DISEASE;

EID: 0019729477     PISSN: 00778923     EISSN: 17496632     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1981.tb29791.x     Document Type: Article

References (10)

1. Familial haemorrhagic telangiectasis
2. On a family form of recurrent epistaxis associated with telangiectasia of the skin and mucous membranes
3. On multiple hereditary telangiectasia with recurrent hemorrhages
4. Pulmonary artenovenous fistulae and hereditary hemorrhagic telangiectasis
5. Splenomegaly and hepatic enlargement in hereditary hemorrhagic telangiectasis
6. Vascular disorders associated with thrombohemorrhagic phenomena
7. Telangiectasia
8. Disseminated intravascular coagulation and related syndromes: Etiology, pathophysiology, diagnosis and management
9. Chronic defibrination syndrome due to a giant hemangioma associated with microangiopathic hemolytic anemia