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Blood Coagulation Disorders, Inherited
Known as:
Hereditary Blood Coagulation Disorders
, Coagulation Disorders, Inherited
, Hereditary Coagulation Disorders
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Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.
National Institutes of Health
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Related topics
Related topics
12 relations
Narrower (6)
Athrombia, Essential
Hereditary factor II deficiency disease
Pechet Factor Deficiency
Platelet Disorder, Familial, with Associated Myeloid Malignancy
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In Blood
Microbiological
chemically induced
nursing therapy
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2011
Highly Cited
2011
Interactions Between Ankyrin-G, Plakophilin-2, and Connexin43 at the Cardiac Intercalated Disc
Priscila Y. Sato
,
W. Coombs
,
+5 authors
M. Delmar
Circulation Research
2011
Corpus ID: 11340823
Rationale: The early description of the intercalated disc defined 3 structures, all of them involved in cell-cell communication…
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Review
2007
Review
2007
Maternal Acceptance of the Fetus: True Human Tolerance
I. Guleria
,
M. Sayegh
Journal of Immunology
2007
Corpus ID: 24549801
Induction and maintenance of immunologic tolerance in humans remains a desirable but elusive goal. Therefore, understanding the…
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Review
2007
Review
2007
Inherited Arrhythmias: A National Heart, Lung, and Blood Institute and Office of Rare Diseases Workshop Consensus Report About the Diagnosis, Phenotyping, Molecular Mechanisms, and Therapeutic…
S. Lehnart
,
Michael J Ackerman
,
+18 authors
Andrew R. Marks
Circulation
2007
Corpus ID: 16774666
The National Heart, Lung, and Blood Institute and Office of Rare Diseases at the National Institutes of Health organized a…
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Review
2006
Review
2006
The obstetric and gynaecological management of women with inherited bleeding disorders – review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors’ Organization
C. Lee
,
C. Chi
,
+4 authors
R. Kadir
Haemophilia
2006
Corpus ID: 28422177
Summary. The gynaecological and obstetric management of women with inherited coagulation disorders requires close collaboration…
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Highly Cited
2002
Highly Cited
2002
Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasia.
E. Shore
,
Jaimo Ahn
,
+8 authors
F. Kaplan
New England Journal of Medicine
2002
Corpus ID: 39943361
BACKGROUND Progressive osseous heteroplasia (POH), an autosomal dominant disorder, is characterized by extensive dermal…
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Highly Cited
2002
Highly Cited
2002
Immune reconstitution without graft-versus-host disease after haemopoietic stem-cell transplantation: a phase 1/2 study
I. André-Schmutz
,
F. Deist
,
+6 authors
M. Cavazzana‐Calvo
The Lancet
2002
Corpus ID: 45860071
Review
2002
Review
2002
Genetics of colorectal cancer: hereditary aspects and overview of colorectal tumorigenesis.
N. Fearnhead
,
J. Wilding
,
W. Bodmer
British Medical Bulletin
2002
Corpus ID: 24069063
Familial adenomatous polyposis and hereditary non-polyposis colorectal cancer are dominantly inherited conditions with 100% and…
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Highly Cited
2001
Highly Cited
2001
Clinical characteristics, aetiological factors and long-term prognosis of myocardial infarction with an absolutely normal coronary angiogram; a 3-year follow-up study of 91 patients.
A. D. Costa
,
K. Isaaz
,
E. Faure
,
S. Mourot
,
A. Cerisier
,
M. Lamaud
European Heart Journal
2001
Corpus ID: 13556187
OBJECTIVES The purpose of this study was to evaluate the clinical outcome of a large cohort of patients who suffered an acute…
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Review
1998
Review
1998
Eating disorders: progress and problems.
B. Walsh
,
M. Devlin
Science
1998
Corpus ID: 21919824
Recent research on Anorexia Nervosa and Bulimia Nervosa has yielded an increasingly detailed understanding of the range of…
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Highly Cited
1990
Highly Cited
1990
The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase.
I. Fearnley
,
J. Walker
,
+4 authors
D. Palmer
Biochemical Journal
1990
Corpus ID: 19324441
The ceroid lipofuscinoses are a group of neurodegenerative lysosomal storage diseases of children and animals that are…
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