✦ LIBER ✦

Factor XII Shizuoka, a novel mutation (Ala392Thr) identified and characterized in a patient with congenital coagulation factor XII deficiency

✍ Scribed by Shuji Oguchi; Keiko Ishii; Takanori Moriki; Eiko Takeshita; Mitsuru Murata; Yasuo Ikeda; Kiyoaki Watanabe

Book ID: 116913085
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 433 KB
Volume: 115
Category: Article
ISSN: 0049-3848
DOI: 10.1016/j.thromres.2004.08.027

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Combined severe factor XII deficiency an

Combined severe factor XII deficiency and homozygous factor V Leiden mutation in a patient with venous thrombosis

✍ P Miljic; M Colovic; Lj Rakicevic; V Djordjevic; D Boskovic 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 60 KB

Surgical management in the patient with

Surgical management in the patient with congenital factor XII deficiency: Report of a case

✍ Joji Sekine; Kazuto Tsuruda; Sei-ichiro Matsunaga; Shimeru Kamihira; Kei Ueno; T 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 341 KB

Thrombus formation on transcatheter ASD

Thrombus formation on transcatheter ASD occluder device in a patient with coagulation factor XII deficiency

✍ Gastmann, Oliver ;Werner, Gerald S. ;Babic, Uros U. ;Figulla, Hans R. 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 78 KB 👁 2 views

Transcatheter occlusion of cardiac defects has become an effective and less invasive alternative to open heart surgery. Thromboembolic complications are rare events, after both surgical and transcatheter closure of atrial septal defects [Galal et al.: Eur Heart J 15:1381-1384, 1994]. We report on a

Captopril-induced changes on active and

Captopril-induced changes on active and inactive renin in a patient with factor XII congenital deficiency

✍ G. M. Patrassi; F. Mantero; F. Fallo; A. Girolami; F. H. M. Derkx 📂 Article 📅 1985 🏛 Springer 🌐 English ⚖ 303 KB

Functional characterization of a novel m

Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency

✍ E. M. PARABOSCHI; S. M. KAYIRAN; N. ÖZBEK; B. GÜRAKAN; F. PEYVANDI; I. GUELLA; S 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 178 KB

A case of atypical hemolytic uremic synd

A case of atypical hemolytic uremic syndrome due to anti-factor H antibody in a patient presenting with a factor XII deficiency identified two novel mutations

✍ Eiji Matsukuma; Yoshimitsu Gotoh; Yoshiyuki Kuroyanagi; Takuji Yamada; Mitsuji I 📂 Article 📅 2011 🏛 Springer 🌐 English ⚖ 286 KB