Familial infantile thrombotic thrombocytopenic purpura

Journal of Pediatric Hematology/Oncology

Volumn 18, Issue 2, 1996, Pages 171-174

  Daghistani, Doured ^a   Jimenez, Joaquin J ^b   Moake, Joel L ^c   Ledford, Marlies R ^b   Yunis, Adel A ^b  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MIAMI   (United States)

^c HOUSTON METHODIST HOSPITAL   (United States)

Author keywords

thrombotic thrombocytopenic purpura

Indexed keywords

FRESH FROZEN PLASMA; VON WILLEBRAND FACTOR;

ARTICLE; BLOOD TRANSFUSION; CLINICAL ARTICLE; CONSANGUINITY; FAMILIAL DISEASE; FEMALE; HUMAN; PRESCHOOL CHILD; PRIORITY JOURNAL; THROMBOTIC THROMBOCYTOPENIC PURPURA;

FEMALE; HUMANS; INFANT; PURPURA, THROMBOTIC THROMBOCYTOPENIC; RISTOCETIN; VON WILLEBRAND FACTOR;

EID: 0029897061     PISSN: 10774114     EISSN: None     Source Type: Journal    
DOI: 10.1097/00043426-199605000-00015     Document Type: Article

References (10)

1. Ruggenenti P, Remuzzi G. Thrombotic thrombocytopenic purpura and related disorders. Hematol Oncol Clin North Am 1990;4:219-41.
2. Fuchs WE, George JN, Dotin LN, et al. Thrombotic thrombocytopenic purpura: occurrence two years apart during late pregnancy in two sisters. JAMA 1976;235:2126-7.
3. Wallace DC, Lovric A, Clubb JS, et al. Thrombotic thrombocytopenic purpura in four siblings. Am J Med 1974;58:724-34.
4. Elias M, Horowitz J, Tal I, et al. Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome in three siblings. Arch Dis Child 1988;63:644-6.
5. Moake JL, Rudy CK, Troll JH, et al. Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura. N Engl J Med 1982;307:1432-5.
6. Ledford MR, Kent JW, Civantos F. A comparative study of three methods for the visualization of vWF multimers. Thromb Haemost 1990;64:569-75.
7. Frangos JA, Moake JL, Nolasco LH, et al. Cryosupematant regulates accumulation of unusually large vWF from endothelial cells. Am J Physiol 1989;256:1635-44.
8. Phillips MD, Moake JL, Nolasco L, et al. Plasma von Willibrand factor processing activity functions like a disulfide bond reductase: reversible decrease of multimer size. Thromb Haemostas 1993;69:2342.
9. Moake JL, Turner NA, Stathopoulos NA, et al. Involvement of large plasma vWF multimers and unusually large vWF forms derived from endothelial cells in shear stress induced platelet aggregation. J Clin Invest 1986;78:1456.
10. Katz JA, Moake JL, McPherson PD, et al. The relationship between human development and disappearance of unusually large von Willibrand factor multimers from plasma. Blood 1989;73:1851-8.