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Protein S Deficiency
Known as:
Protein S Deficiency [Disease/Finding]
, Protein S Deficiencies
, s protein deficiency
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An autosomal dominant disorder showing decreased levels of plasma protein S antigen or activity, associated with venous thrombosis and pulmonary…
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National Institutes of Health
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Related topics
Related topics
11 relations
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie
Congenital Bleeding Disorder
Hematopoietic and Lymphoid Cell
Hematopoietic and Lymphoid Tissue
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2002
Highly Cited
2002
Calciphylaxis in a Patient with Rheumatoid Arthritis without Renal Failure and Hyperparathyroidism: The Possible Role of Long-Term Steroid Use and Protein S Deficiency
C. Korkmaz
,
E. Du¨ndar
,
I. Zubaroğlu
Clinical Rheumatology
2002
Corpus ID: 12049758
Abstract Calciphylaxis is a rare and life-threatening condition of progressive cutaneous necrosis secondary to small and medium…
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1998
1998
Recurrent Warfarin-Induced Skin Necrosis in Kindreds with Protein S Deficiency
S. Sallah
,
J. Abdallah
,
G. Gagnon
Pathophysiology of Haemostasis and Thrombosis
1998
Corpus ID: 46762929
Warfarin-induced skin necrosis is a rare complication of anticoagulant treatment. The incidence of this complication is…
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1997
1997
Two Distinct Novel Splice Site Mutations in a Compound Heterozygous Patient with Protein S Deficiency
T. Yamazaki
,
A. Katsumi
,
+7 authors
Hidehiko Saito
Thrombosis and Haemostasis
1997
Corpus ID: 20156649
Summary Genetic analysis revealed two distinct novel splice site mutations in a compound heterozygous patient with protein S…
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1996
1996
Molecular basis of protein S deficiency in three families also showing independent inheritance of factor V leiden.
N. Beauchamp
,
M. Daly
,
P. Cooper
,
M. Makris
,
F. Preston
,
I. Peake
Blood
1996
Corpus ID: 1051146
The molecular basis of type I or III Protein S deficiency has been investigated in three kindred also showing independent…
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Highly Cited
1995
Highly Cited
1995
Homozygous APC-resistance Combined with Inherited Type I Protein S Deficiency in a Young Boy with Severe Thrombotic Disease
Bengt Zöller
,
X. He
,
B. Dahlbäck
Thrombosis and Haemostasis
1995
Corpus ID: 35849925
Summary Inherited resistance to activated protein C (APC) is a frequent cause of familial thrombosis. It is associated with a…
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Review
1995
Review
1995
A Review of Mutations Causing Deficiencies of Antithrombin, Protein C and Protein S
M. Aiach
,
S. Gandrille
,
J. Emmerich
Thrombosis and Haemostasis
1995
Corpus ID: 13126923
The mutations observed in patients with antithrombin and protein C deficiencies are mostly substitutions of one nucleotide, or…
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1994
1994
Coumarin-induced skin necrosis associated with acquired protein S deficiency and antiphospholipid antibody syndrome.
Marie‐José Wattiaux
,
Robert Hervé
,
A. Robert
,
Jean Cabane
,
Bruno Housset
,
Jean-claude Imbert
Arthritis & Rheumatism
1994
Corpus ID: 38990985
We report a case of skin necrosis occurring during coumarin treatment in a patient with acquired protein S deficiency and the…
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1991
1991
Skin necrosis following prolonged administration of coumarin in a patient with inherited protein S deficiency
S. Goldberg
,
C. Kessler
,
B. L. Yalisove
,
M. Elgart
,
C. Orthner
American journal of hematology/oncology
1991
Corpus ID: 6152238
Depression of the vitamin K‐dependent modulators of coagulation during the initial phase of oral anticoagulant therapy may lead…
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1990
1990
Type I protein S deficiency and skin necrosis.
A. Craig
,
D. Taberner
,
A. Fisher
,
D. Foster
,
J. Mitra
Postgraduate medical journal
1990
Corpus ID: 26621644
A kindred with Type I protein S deficiency is described in which the index case developed skin necrosis during induction of oral…
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1989
1989
A Mutation in the Protein S Pseudogene Is Linked to Protein S Deficiency in a Thrombophilic Family
H. K. Ploos van Amstel
,
P. Reitsma
,
K. Hamulyák
,
Christine Die-Smulders
,
P. Mannucci
,
R. Bertina
Thrombosis and Haemostasis
1989
Corpus ID: 21919352
Summary Probands from 15 unrelated families with hereditary protein S deficiency type I, that is having a plasma total protein S…
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