Results 271 to 280 of about 1,008,107 (310)

Factor X Deficiency in Primary Amyloidosis

New England Journal of Medicine, 1979
MANY patients with acquired factor X deficiency associated with primary amyloidosis have a severe bleeding disorder.1 2 3 4 A Because administered factor X is rapidly removed from circulation, conc...
P R, Greipp, R A, Kyle, E J, Bowie
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[Factor X deficiency and pregnancy].

Annales francaises d'anesthesie et de reanimation, 2002
Factor X deficiency is one of the rarest inherited coagulation disorders. It is an autosomal recessive inherited disease. In its homozygous form factor X deficiency has an estimated prevalence of 1: 500,000. However in its heterozygous form it has an estimated frequency of 1: 500 to 1: 2000.
K, Rezig, N, Diar, D, Benabidallah, J, Audibert   +3 more
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Amyloidosis with factor X deficiency

THE AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1972
B, Bernhardt, M, Valletta, J, Brook, I, Lejnieks   +3 more
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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

Genomic predictors of response to PD-1 inhibition in children with germline DNA replication repair deficiency

Nature Medicine, 2022
Anirban Das, Daniel Morgenstern, Ailish C Coblentz   +2 more
exaly  

Factor X Deficiency

2004
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Factor X Deficiency in Primary Amyloidosis

New England Journal of Medicine, 1980
R P, Fogdall, D P, Fischbach
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Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child

Nature Medicine, 2021
Masato Ogishi, Rui Yang, Caner Aytekin
exaly  

Poly(ADP-Ribose) polymerase (PARP) inhibitors: Exploiting a synthetic lethal strategy in the clinic

Ca-A Cancer Journal for Clinicians, 2011
Timothy A Yap, Johann Sebastian de Bono
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.
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