✦ LIBER ✦

Two factor XI mutations in a Chinese family with factor XI deficiency

✍ Scribed by W.Y. Au; J.W. Cheung; C.C.K. Lam; Y.L. Kwong

Publisher: John Wiley and Sons
Year: 2003
Tongue: English
Weight: 132 KB
Volume: 74
Category: Article
ISSN: 0361-8609
DOI: 10.1002/ajh.10396

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Factor XI deficiency in a Bedouin family

✍ Hatskelzon, Lev; Dvilansky, A.; Holcberg, Gershon 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 119 KB 👁 2 views

To prevent heat illnesses, a high index of suspicion should be maintained during a heat wave or while using unacclimatized workers in heavy labor. Employers should measure wet bulb globe temperature index (which correlates with deep body temperature) and plan work schedules within permissible thresh

Factor XI gene mutations in factor XI de

Factor XI gene mutations in factor XI deficient patients of the Czech Republic

✍ Giancarlo Castaman; Sofia H. Giacomelli; David Habart; Rosanna Asselta; Stefano 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 345 KB 👁 2 views

Compound heterozygosity for two novel mu

Compound heterozygosity for two novel mutations in a severe factor XI deficiency

✍ Akiko Tsukahara; Takayuki Yamada; Akira Takagi; Takashi Murate; Tadashi Matsushi 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 259 KB 👁 2 views

A novel mutation that leads to a congeni

A novel mutation that leads to a congenital factor XI deficiency in a Japanese family

✍ Sato, Eriko; Kawamata, Norihiko; Kato, Atsushi; Oshimi, Kazuo 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 175 KB 👁 2 views

We have identified a novel mutation leading to a congenital deficiency of the coagulation factor XI (FXI) in a Japanese family. A propositus was a 42-year-old female patient without bleeding tendency. Coagulant activity and the antigen level of FXI in her plasma were below the detectable range. The

High incidence of factor XI deficiency i

High incidence of factor XI deficiency in Gaucher's disease

✍ A. Berrebi; S. D. H. Malnick; E. J. Vorst; D. Stein 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 118 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