Results 251 to 260 of about 1,017,222 (288)
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Amyloidosis with factor X deficiency

THE AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1972
B, Bernhardt   +3 more
openaire   +2 more sources

Factor II, Factor V and Factor X Deficiencies

2009
Inherited deficiencies of factors II, V and X (FII, FV, FX) are rare (estimated frequencies are: FII, 1 in 2,000,000; FV, 1 in 1,000,000; and FX, 1 in 500,000). Patients who are homozygous or compound heterozygous for defects in the FII, FV or FX genes can have moderate to severe bleeding symptoms, with patients having FX deficiency more likely to ...
openaire   +1 more source

Factor X Deficiency in Primary Amyloidosis

New England Journal of Medicine, 1980
R P, Fogdall, D P, Fischbach
openaire   +2 more sources

Human dendritic cell deficiency: the missing ID?

Nature Reviews Immunology, 2011
Mathew Collin   +2 more
exaly  

[Congenital factor X deficiency, the Prower-Stuart deficiency].

Bilten za hematologiju i transfuziju, 1983
The congenital deficit of factor-X is extremely rare and usually goes with mild bleeding tendency. The variations of the factor-X activities are described individually and depend on the tests used, that is: activating factor-X by tissue or blood thromboplastin, Russel's Viper Venom, by neutralisation of the antibodies or immunoprecipitation.
openaire   +1 more source

Vitamin B12 deficiency

Nature Reviews Disease Primers, 2017
Ralph Green   +2 more
exaly  

Congenital Factor X Deficiency

2018
Fateme Roshanzamir, Akbar Dorgalaleh
openaire   +1 more source

Severe factor X deficiency and successful pregnancy

BJOG: An International Journal of Obstetrics & Gynaecology, 1994
J C, Konje   +4 more
openaire   +2 more sources

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