Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 237,921,122 papers from all fields of science
Search
Sign In
Create Free Account
Factor XI Deficiency
Known as:
Rosenthal Syndromes
, Plasma Thromboplastin Antecedent Deficiency
, F11 DEFICIENCY
Expand
A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
18 relations
Congenital disorder of glycosylation type 1A
Congenital disorder of glycosylation type 1B
Congenital disorder of glycosylation type 1C
F11 gene
Expand
Broader (1)
Hemophilia A
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Clinical application of the chromogenic assay of factor VIII in haemophilia A, and different variants of von Willebrand's disease.
Stefan Lethagen
,
Hans Østergaard
,
Inga Marie Nilsson
Scandinavian Journal of Haematology
2009
Corpus ID: 39651352
A chromogenic substrate kit for determination of factor VIII activity (COATEST Factor VIII) was compared to a one-stage clotting…
Expand
2009
2009
Homozygous expression of haemophilia B in a heterozygote.
Lars Holmberg
,
I. Nilsson
,
Per Henriksson
,
Karen Helene Ørstavik
Acta Medica Scandinavica
2009
Corpus ID: 42835192
A case of clinically severe haemophilia B in a woman is described. In 1977 she was delivered of a healthy male child, showing…
Expand
2008
2008
High frequency of HLA-DR5 in Greek patients with haemophilia A and haemophilia B.
C. Papasteriades
,
M. Varla
,
+6 authors
G. Papaevangelou
Tissue Antigens
2008
Corpus ID: 31299543
Sixty unrelated Greek patients with haemophilia (46 with haemophilia A and 14 with haemophilia B) were typed for HLA-A, B and DR…
Expand
2005
2005
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency.
G. Soldà
,
R. Asselta
,
R. Ghiotto
,
M. Tenchini
,
G. Castaman
,
S. Duga
Haematologica
2005
Corpus ID: 6244908
The Glu117stop mutation in the factor XI (FXI) gene is the most common cause of FXI deficiency and might cause the disease either…
Expand
2001
2001
THE IMPACTS OF ANTECEDENT ENSO EVENT ON AIR TEMPERATURE OVER NORTHEAST CHINA IN SUMMER
Liu Shi
2001
Corpus ID: 123829592
Based on SST data of the Pacific,height field data at 500 hPa,and air temperature data of Changchun in summer,the relationship…
Expand
1985
1985
Gene deletion in an Italian haemophilia B subject.
F. Bernardi
,
L. del Senno
,
+7 authors
S. Pitruzzello
Journal of Medical Genetics
1985
Corpus ID: 2529758
DNA from 20 Italian haemophilia B patients was analysed by the Southern blotting technique and hybridisation to a factor IX cDNA…
Expand
1980
1980
Combined severe factor XI deficiency and von Willebrand's disease.
J. Chediak
,
Eugene Lambert
,
Esther I. Johnson
,
M. Telfer
American Journal of Clinical Pathology
1980
Corpus ID: 8449923
A family whose members demonstrated deficiency of factor XI and also showed mild von Willebrand’s disease is discussed. Two…
Expand
1978
1978
Effects of acute and chronic splenectomy on experimental acute renal tubular lesions.
A. Mandal
,
C. Haygood
,
+5 authors
R. Lindeman
Journal of Laboratory and Clinical Medicine
1978
Corpus ID: 24317878
The first half of this study describes the effects of acute splenectomy on epinephrine-induced ATL in the dog. Renal morphology…
Expand
1971
1971
Factor 8 inhibitors and the use of blood products in patients with haemophilia A.
E. Ikkala
,
O. Simonen
Scandinavian Journal of Haematology
1971
Corpus ID: 20915130
1967
1967
Treatment of haemophilia A with purified factor 8 obtained from human plasma by cryoprecipitation.
K. Meyer
,
J. G. Eernisse
,
J. Veltkamp
,
H. Hemker
,
E. Loeliger
Folia medica Neerlandica
1967
Corpus ID: 35279892
A few years ago it was discovered by coincidence that so-called cryoprecipitate a protein fraction which precipitates from human…
Expand