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Deficiency of coagulation factors
Known as:
clotting factor deficiency
, Coagulation Factor Deficiency Syndrome
, Coagulation Factor Deficiency
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Congenital or acquired deficiency of one of the coagulation factors. It results in bleeding.
National Institutes of Health
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Related topics
Related topics
13 relations
Acquired Coagulation Factor Deficiency
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj
F7 gene
F7 wt Allele
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Broader (1)
Blood Coagulation Disorders
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
ABSTRACTS of the 61 st Annual Meeting of the Society of Thrombosis and Hemostasis Research 15-18 February 2017 Basel , Switzerland Multianalyte determination of NOAC using LC-MS / MS and comparison…
T. Bakchoul
,
H. Schulze
,
E. Simeoni
,
W. Ouwehand
2017
Corpus ID: 35342751
S of the 61 Annual Meeting of the Society of Thrombosis and Hemostasis Research 15-18 February 2017 Basel, Switzerland The…
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2016
2016
Case Report: Keloid Scar in A Rare Congenital (Inherited) Coagulation Factor Deficiency
Abeer Alessa
,
Fai A. AlQahtani
,
M. Alotaibi
,
Hadeel AlOmran
,
Osama Alsultan
2016
Corpus ID: 212473917
Factor XIII deficiency is one of the rare bleeding diathesis, the presentation of which varies from multiple ecchymosis…
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2013
2013
Congenital clotting factor deficiency and cardiovascular disease: protected by nature?
A. Tuinenburg
2013
Corpus ID: 67883757
Since the introduction of clotting factor concentrates, life expectancy of patients with hemophilia (PWH) has increased and now…
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2006
2006
Compound heterozygosity of novel missense mutations in the γ-carboxylase gene causes hereditary combined vitamin K-dependent coagulation factor deficiency
D. Darghouth
,
K. Hallgren
,
+5 authors
K. Berkner
2006
Corpus ID: 8006915
word count: 200 Manuscript word count: 4201 Scientific heading: HEMOSTASIS, THROMBOSIS, AND VASCULAR BIOLOGY Blood First Edition…
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2004
2004
Homozygosity Mapping of a Second Gene Locus for Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors (FMFD) to Chromosome 16
A. Fregin
,
S. Rost
,
W. Wolz
,
A. Krebsova
,
C. Müller
,
J. Oldenburg
2004
Corpus ID: 83387042
Familial multiple coagulation factor deficiency (FMFD) of factors II, VII, IX, X, protein C and protein S is a very rare bleeding…
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2001
2001
[Ring chromosome 13 and congenital coagulation factor deficiency].
M. RuizDelPrado
,
J. AlfonsoLanda
,
C. CristóbalNavas
,
J. BlázquezRegidor
,
Pérez Marrodán Ja
,
A. MartínNuño
Anales espanoles de pediatria
2001
Corpus ID: 77690835
2001
2001
Assessment of the resonance thromboelastograph CS-3 for differentiation of coagulation disorders: a pilot in vitro investigation of simulated post-cardiopulmonary bypass coagulopathies.
A. Koster
,
R. Hansen
,
Jürgen Schulz
,
M. Kukucka
,
T. Fischer
,
H. Kuppe
The journal of extra-corporeal technology
2001
Corpus ID: 22496590
Resonance thromboelastography (RTG), a further development of the thromboelastogram (TEG), has been designed for improved…
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2001
2001
Because purpura results from extravasation of blood into the skin , the lesions do not blanch with pressure . Evaluating the Child with Purpura
A. Leung
2001
Corpus ID: 38390926
www.aafp.org/afp AMERICAN FAMILY PHYSICIAN 419 vessel wall and, in response to the exposed subendothelial collagen, release…
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1998
1998
#696 Complex coagulation factor deficiency in noonans syndrome
J. Ramdas
,
R. Warrier
,
Y. Lacassie
,
L. Yu
1998
Corpus ID: 71511947
1992
1992
Extracorporeal Hemoperfusion Over the Human and Baboon Liver
T. Lie
1992
Corpus ID: 68026884
The liver supports life by three characteristic functions: excretion, synthesis, and detoxification. In acute hepatic damage, the…
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