Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene

Haemophilia ◽  
2009 ◽  
Vol 15 (1) ◽  
pp. 267-280 ◽  
Author(s):  
F. H. HERRMANN ◽  
K. WULFF ◽  
G. AUERSWALD ◽  
S. SCHULMAN ◽  
J. ASTERMARK ◽  
...  
Keyword(s):  
Latin America ◽  
Clinical Manifestation ◽  
Factor Vii ◽  
Factor Vii Deficiency

scholarly journals Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V

Haematologica ◽  
2008 ◽  
Vol 93 (8) ◽  
pp. 1273-1275 ◽  
Author(s):  
F. H. Herrmann ◽  
K. Wulff ◽  
R. Strey ◽  
A. Siegemund ◽  
J. Astermark ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Clinical Manifestation ◽  
Factor Vii ◽  
Factor Vii Deficiency

Molecular Biology and Clinical Manifestation of Hereditary Factor VII Deficiency

2000 ◽  
Vol Volume 26 (Number 4) ◽  
pp. 0393-0400 ◽  
Author(s):  
Falko H. Herrmann ◽  
Karin Wulff ◽  
Karin Auberger ◽  
Volker Aumann ◽  
Frauke Bergmann ◽  
...  
Keyword(s):  
Molecular Biology ◽  
Clinical Manifestation ◽  
Factor Vii ◽  
Hereditary Factor ◽  
Factor Vii Deficiency

Inherited Factor VII Deficiency: Genetics and Molecular Pathology

1995 ◽  
Vol 74 (01) ◽  
pp. 313-321 ◽  
Author(s):  
Edward G D Tuddenham ◽  
Susan Pemberton ◽  
David N Cooper
Keyword(s):  
Molecular Pathology ◽  
Factor Vii ◽  
Factor Vii Deficiency

Two Typical Hereditary Charts of Congenital Factor VII Deficiency

1961 ◽  
Vol 05 (01) ◽  
pp. 087-092 ◽  
Author(s):  
F. J Cleton ◽  
E. A Loeliger
Keyword(s):  
Factor Vii ◽  
Autosomal Gene ◽  
Homozygous State ◽  
Recessive Character ◽  
Factor Vii Deficiency ◽  
Complete Penetrance ◽  
Coagulation Defect ◽  
Haemorrhagic Diathesis ◽  
Intermediate Expression ◽  
Congenital Factor

SummaryThe inheritance of congenital factor VII deficiency was investigated in 2 unrelated families. Out of 68 individuals, 4 (3 proven and 1 highly probable) were found to have severe factor VII deficiency (<C 0.1% factor VII), and 29 appeared to be heterozygotes (30—60% factor VII). The coagulation defect is due to an autosomal gene of intermediate expression and complete penetrance. The recessive character of the haemorrhagic diathesis due to the homozygous state for the abnormal gene is clearly demonstrated.

Paracetamol poisoning unmasking factor VII deficiency

2002 ◽  
Vol 14 (4) ◽  
pp. 441-443 ◽  
Author(s):  
Andrew P. Chilton ◽  
Tariq Hussain ◽  
Elwyn Elias
Keyword(s):  
Factor Vii ◽  
Paracetamol Poisoning ◽  
Factor Vii Deficiency

scholarly journals Efficacy and safety of recombinant factor VIIa preparation (NovoSeven) for patients with congenital factor VII deficiency

2006 ◽  
Vol 17 (6) ◽  
pp. 695-705 ◽  
Author(s):  
Hideji HANABUSA ◽  
Kazushige OYAMA ◽  
Satoshi WATANABE ◽  
Yuzuru SAKAKIBARA ◽  
Yuji HIRAMATSU ◽  
...  
Keyword(s):  
Recombinant Factor Viia ◽  
Factor Viia ◽  
Factor Vii ◽  
Efficacy And Safety ◽  
Factor Vii Deficiency ◽  
Congenital Factor
Sign in / Sign up

Export Citation Format

Share Document