HR GRALNICK, BS COLLER, NR SHULMAN, … - Annals of Internal Medicine, 1977 - annals.org.p.angrylapdog.com Hemophilia and von Willebrand disease are two congenital hemorrhagic disorders
associated with a deficiency of factor VIII activity. Newly developed assays for
the factor VIII/von Willebrand factor antigen and for the ristocetin ... Cited by 23 - Related articles - All 2 versions
H Takahashi, K Koike, T Nakamura, M Itoh, I … - Nippon Ketsueki Gakkai zasshi: journal of Japan …, 1979 - ncbi.nlm.nih.gov 1: Nippon Ketsueki Gakkai Zasshi. 1979 Feb;42(1):44-52. An atypical case
of von Willebrand's disease with an isolated deficiency ... Cited by 5 - Related articles
高橋芳右， 小池和夫， 伊藤正一， 服部晃， 小林 … - 臨床血液, 1980 - J-STAGE The clinicalfeatures of47 patients with von Willebrand's disease were studied．
Nose bleedingwas the most common symptom and ecchymoses，bleeding after tooth
extraction，glnglValbleeding and prolonged bleedings from trivial wounds ... Cited by 1 - Related articles
K Hasler, D Böttcher, R Engelhardt - Annals of Hematology, 1979 - Springer Zusammenfassung. Berichtet wird fiber eine Familie mit einer Variante des yon
Willebrand-Jfirgens-Syndroms. Bei den Mitgliedern dieser Familie war ein
qualitativer Defekt des Faktor VIII/von Willebrand Faktor Proteins nachzu- ... Cited by 2 - Related articles
[CITATION] 正常人における DDAVP (1-deamino-8-D-arginine vasopressin) 投与後の第 VIII 因子の性状
D Böttcher, K Hasler, AH Sutor, D Mair - Annals of Hematology, 1976 - Springer Zusammenfassung Die bei 5 yon 8 Kindern einer Familie beobachtete angeborene
hiimorrhagische Diathese war gerinnungsanalytisch charakterisiert durch
verl~ingerte Blumngszeiten, verminderte Adh~tsivit~iten und verminderte ... Cited by 3 - Related articles
LW Hoyer - Progress in hemostasis and thrombosis, 1976 - ncbi.nlm.nih.gov 1: Prog Hemost Thromb. 1976;3:231-87. Von Willebrand's disease. Hoyer LW.
Publication Types: Historical Article; Research Support ... Cited by 67 - Related articles - All 2 versions
