✦ LIBER ✦

Combined deficiencies of factor vlll (ahf) and factor xi (pta)

✍ Scribed by Eric Chun-Yet Lian; Daniel Deykin; Donald R. Harkness

Publisher: John Wiley and Sons
Year: 1976
Tongue: English
Weight: 383 KB
Volume: 1
Category: Article
ISSN: 0361-8609
DOI: 10.1002/ajh.2830010306

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Factor XI deficiency: Genetic and clinic

Factor XI deficiency: Genetic and clinical studies of a single kindred

✍ Craig E. Litz; William R. Swaim; Agustin P. Dalmasso 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 435 KB 👁 1 views

A four-generation 25-member kindred with Factor XI:C deficiency is reported. Factor XI:C levels in heterorygotes varied from 15 to 58940, suggesting that Factor XI:C values for homozygote determination should be less than 15%. The frequency of bleeding was not correlated with Factor XI:C levels in t

Congenital combined deficiency of factor

Congenital combined deficiency of factor V and factor VIII with acquired ichthyosis, epidermodysplasia verruciformis, and immunological abnormalities

✍ Hisashi Tsurumi; Takeshi Takahashi; Hisataka Moriwaki; Yasutoshi Muto 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 195 KB 👁 2 views

Inherited combined deficiency of factor

Inherited combined deficiency of factor V and factor VIII: Report of a case with normal factor VIII antigen and ristocetin-induced platelet aggregation

✍ Dr. P. L. Cimo; J. L. Moake; M. F. Gonzalez; E. A. Natelson; K. R. Fox 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 English ⚖ 381 KB 👁 2 views

Combined factor V/VIII deficiency: A cas

Combined factor V/VIII deficiency: A case report including levels of factor V and factor VIII coagulant and antigen as well as protein C inhibitor

✍ Janet M. Brown; Nancy R. Selik; Mary Jo Voelpel; Dr. Eberhard F. Mammen 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 English ⚖ 398 KB 👁 2 views

Combined hereditary factor XI (plasma th

Combined hereditary factor XI (plasma thromboplastin antecedent) deficiency, von Willebrand's disease, and xeroderma pigmentosum in a Japanese family

✍ Masayuki Sano; Hidehiko Saito; Yoshinori Shimamoto; Isamu Sugiura; Haruhiko Ohts 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 369 KB 👁 2 views

## H.S., I.S.) Japan We report a 28-year-old-Japanese male who had a skin tumor derived from variant type xeroderma pigmentosum (XP), combined with factor XI (FXI) deficiency and type llB von Willebrand's disease (vWd). The patient had abnormal bleeding history on tooth extraction. FXI clotting ac

A novel missense mutation causing abnorm

A novel missense mutation causing abnormal LMAN1 in a Japanese patient with combined deficiency of factor V and factor VIII

✍ Takayuki Yamada; Yuta Fujimori; Atsuo Suzuki; Yuhri Miyawaki; Akira Takagi; Taka 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 350 KB 👁 2 views