Skip to search formSkip to main contentSkip to account menu

High molecular weight kininogen deficiency

Known as: Fitzgerald factor deficiency, Williams factor deficiency, HMWK Deficiency 
A rare autosomal recessive inherited disorder characterized by prolonged partial thromboplastin time and absence of bleeding diathesis.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2001
2001
Summary A 66 year old male, referred for cardiac surgery, was found to have high molecular weight kininogen deficiency (activity… 
Review
1990
Review
1990
Analyses of the kininogen (KGN) molecule and KGN gene status in five Japanese families with high-molecular-weight (HMW) KGN… 
Highly Cited
1986
Highly Cited
1986
High mol wt kininogen (HMWK), the major cofactor-substrate of the contact phase of coagulation, is contained within and secreted… 
Review
1985
Review
1985
The pollination biology of Drymonia serrulata was studied in central Panama. D. serrulata produces a small number of flowers… 
Highly Cited
1982
Highly Cited
1982
Kinins are potent vasodilator peptides that may participate in the regulation of local blood flow and blood pressure. Here we… 
1981
1981
Fujiwara trait, the first case of kininogen deficiency in Japan previously reported which did not show any clinical symptom… 
Highly Cited
1976
Highly Cited
1976
A secific, sensitive, and reproducible radioimmunoassay for human Hageman factor (HF, factory XII) has been developed with…