Results 171 to 180 of about 5,300 (203)
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[A family with hereditary hypofibrinogenemia].

Schweizerische medizinische Wochenschrift, 1977
A family with congenital hypofibrinogenemia (fibrinogen levels of 60-90 mg%) has been studied. Out of 19 members tested, 11 exhibit this trait, which follows a strictly autosomal-dominant pattern of inheritance. Congenital hypofibrinogenemia appears to be a separate entity which can be distinguished from heterozygous individuals of congenital ...
N, Pfluger, D, Gehrig
openaire   +1 more source

HYPOFIBRINOGENEMIA IN OBSTETRICS

Obstetrical & Gynecological Survey, 1961
R. C. MURRAY, F. J. HOFMEISTER
openaire   +1 more source

Hypofibrinogenemia

New England Journal of Medicine, 1957
openaire   +1 more source

CLINICAL CONSIDERATIONS IN HYPOFIBRINOGENEMIA

Annals of the New York Academy of Sciences, 1959
openaire   +2 more sources

Spontaneous resolution of hypofibrinogenemia associated with death of a twin in utero: A case report

American Journal of Obstetrics and Gynecology, 1988
Nancy C Chescheir, John W Seeds
exaly  

Congenital Hypofibrinogenemia

2009
Nils Peters   +199 more
openaire   +1 more source

Rapid and Correct Prediction of Thrombocytopenia and Hypofibrinogenemia With Rotational Thromboelastometry in Cardiac Surgery

Journal of Cardiothoracic and Vascular Anesthesia, 2014
Rik H G Olde Engberink   +2 more
exaly  

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