scholarly journals Surgery in patients with congenital factor VII deficiency: A single center experience

2012 ◽  
Vol 47 (4) ◽  
pp. 281 ◽  
Author(s):  
Shin-Hee Kim ◽  
Young Shil Park ◽  
Kee-Hwan Kwon ◽  
Jae Hoon Lee ◽  
Kwang Chul Kim ◽  
...  
1961 ◽  
Vol 05 (01) ◽  
pp. 087-092 ◽  
Author(s):  
F. J Cleton ◽  
E. A Loeliger

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.


2006 ◽  
Vol 17 (6) ◽  
pp. 695-705 ◽  
Author(s):  
Hideji HANABUSA ◽  
Kazushige OYAMA ◽  
Satoshi WATANABE ◽  
Yuzuru SAKAKIBARA ◽  
Yuji HIRAMATSU ◽  
...  

Haemophilia ◽  
2016 ◽  
Vol 22 (5) ◽  
pp. 752-759 ◽  
Author(s):  
M. Napolitano ◽  
M. N. D. Di Minno ◽  
A. Batorova ◽  
A. Dolce ◽  
M. Giansily-Blaizot ◽  
...  

2018 ◽  
pp. 239-259
Author(s):  
Mahmood Shams ◽  
Akbar Dorgalaleh

Medicine ◽  
2019 ◽  
Vol 98 (40) ◽  
pp. e17360
Author(s):  
Juan He ◽  
Wei Zhou ◽  
Hui Lv ◽  
Li Tao ◽  
XiaoWen Chen ◽  
...  

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