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Publication : blood coagulation fibrinolysis an international journal in haemostasis and thrombosis
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Academic Journal

Lupus anticoagulant hypoprothrombinemia syndrome with multiple and high-titer antiphospholipid antibodies strongly interfered with coagulation assays.

  • Authors : Sugasaki M; Department of Medical Technology, Tokushima University Hospital, Tokushima.; Nakamura S

Subjects: Hypoprothrombinemias*/Hypoprothrombinemias*/Hypoprothrombinemias*/complications ; Antiphospholipid Syndrome* ; Blood Coagulation Disorders, Inherited*Dysprothrombinemia

  • Source: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis [Blood Coagul Fibrinolysis] 2024 Apr 01; Vol. 35 (3), pp. 149-153. Date of Electronic Publisher: Lippincott Williams And Wilkins Country of Publication: England NLM ID: 9102551 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Lupus anticoagulant - hypoprothrombinemia syndrome: a rare cause of intracranial bleeding.

  • Authors : Sreedharanunni S; aDepartment of Hematology bDepartment of Internal Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.; Ahluwalia J

Subjects: Antiphospholipid Syndrome/Antiphospholipid Syndrome/Antiphospholipid Syndrome/*complications ; Hematoma, Subdural/Hematoma, Subdural/Hematoma, Subdural/*complications ; Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*complications

  • Source: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis [Blood Coagul Fibrinolysis] 2017 Jul; Vol. 28 (5), pp. 416-418.Publisher: Lippincott Williams And Wilkins Country of Publication: England NLM ID: 9102551 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Lupus anticoagulant-hypoprothrombinemia syndrome and catastrophic antiphospholipid syndrome in a patient with antidomain I antibodies.

  • Authors : Galland J; aNancy University Hospital, Vascular Medicine Division and Regional Competence, Center for Rare Vascular And Systemic Autoimmune DiseasesbDijon University Hospital, Haematology laboratory, Nancy, FrancecBiochemistry, Cardiovascular Research Institute Maastricht (CARIM), Maastricht, University, Maastricht, the NetherlandsdNancy University Hospital, Nuclear Medecine & Nancyclotep Experimental Imaging, PlatformeUniversité de LorrainefInserm, UMR_S 1116gNancy University Hospital, Department of Critical Care Medicine, Nancy, France.; Mohamed S

Subjects: Antiphospholipid Syndrome/Antiphospholipid Syndrome/Antiphospholipid Syndrome/*diagnosis ; Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*diagnosis ; Lupus Coagulation Inhibitor/Lupus Coagulation Inhibitor/Lupus Coagulation Inhibitor/*blood

  • Source: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis [Blood Coagul Fibrinolysis] 2016 Jul; Vol. 27 (5), pp. 580-2.Publisher: Lippincott Williams And Wilkins Country of Publication: England NLM ID: 9102551 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Low plasma concentrations of coagulation factors II, VII and XI indicate increased risk among elderly with symptoms of heart failure.

  • Authors : Alehagen U; Department of Cardiology, Heart Center, University Hospital of Linköping, Linköping, Sweden. ; Dahlström U

Subjects: Cardiovascular Diseases/Cardiovascular Diseases/Cardiovascular Diseases/*mortality ; Factor VII Deficiency/Factor VII Deficiency/Factor VII Deficiency/*epidemiology ; Factor XI Deficiency/Factor XI Deficiency/Factor XI Deficiency/*epidemiology

  • Source: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis [Blood Coagul Fibrinolysis] 2010 Jan; Vol. 21 (1), pp. 62-9.Publisher: Lippincott Williams And Wilkins Country of Publication: England NLM ID: 9102551 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Fatal pulmonary embolism and pulmonary hemorrhage in lupus anticoagulant hypoprothrombinemia syndrome: a case report and review of literature.

  • Authors : Chen X; Department of Pathology and Laboratory Medicine, University of Kansas Health System, Kansas City, Kansas.; Nedved D

Subjects: Hemorrhage/Hemorrhage/Hemorrhage/*etiology ; Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*complications ; Lupus Coagulation Inhibitor/Lupus Coagulation Inhibitor/Lupus Coagulation Inhibitor/*blood

  • Source: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis [Blood Coagul Fibrinolysis] 2018 Dec; Vol. 29 (8), pp. 708-713.Publisher: Lippincott Williams And Wilkins Country of Publication: England NLM ID: 9102551 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Inherited factor II deficiency with paradoxical hypercoagulability: a case report.

Subjects: Blood Coagulation Tests/Blood Coagulation Tests/Blood Coagulation Tests/*methods ; Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*genetics ; Thrombophilia/Thrombophilia/Thrombophilia/*etiology

  • Source: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis [Blood Coagul Fibrinolysis] 2018 Mar; Vol. 29 (2), pp. 223-226.Publisher: Lippincott Williams And Wilkins Country of Publication: England NLM ID: 9102551 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up study.

  • Authors : Girolami A; aDepartment of Medicine, University of Padua Medical SchoolbDivision of Medicine, Padua City Hospital, Padua, Italy.; Santarossa C

Subjects: Heterozygote*; Hemorrhage/Hemorrhage/Hemorrhage/*genetics ; Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*genetics

  • Source: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis [Blood Coagul Fibrinolysis] 2017 Dec; Vol. 28 (8), pp. 623-626.Publisher: Lippincott Williams And Wilkins Country of Publication: England NLM ID: 9102551 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

A case of congenital prothrombin deficiency and idiopathic thrombocytopenic purpura in a pregnant female.

  • Authors : Harel R; Hematology/Oncology Faculty, NSLIJ/Lenox Hill Hospital, New York, USA.; Shani D

Subjects: Hemorrhagic Disorders/Hemorrhagic Disorders/Hemorrhagic Disorders/*complications ; Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*complications ; Purpura, Thrombocytopenic, Idiopathic/Purpura, Thrombocytopenic, Idiopathic/Purpura, Thrombocytopenic, Idiopathic/*complications

  • Source: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis [Blood Coagul Fibrinolysis] 2017 Jan; Vol. 28 (1), pp. 100-101.Publisher: Lippincott Williams And Wilkins Country of Publication: England NLM ID: 9102551 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Congenital deficiencies and abnormalities of prothrombin.

  • Authors : Girolami A; University of Padua Medical School, Institute of Medical Semeiotics, Italy.; Scarano L

Subjects: Chromosomes, Human, Pair 11* ; Point Mutation*; Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*congenital

  • Source: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis [Blood Coagul Fibrinolysis] 1998 Oct; Vol. 9 (7), pp. 557-69.Publisher: Lippincott Williams And Wilkins Country of Publication: England NLM ID: 9102551 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Two novel mutations in the prothrombin gene cause severe bleeding in a compound heterozygous patient.

  • Authors : Poort SR; Hemostasis and Thrombosis Research Center, Department of Hematology, Leiden University Medical School, The Netherlands.; Njo KT

Subjects: Heterozygote* ; Point Mutation*; Hemorrhage/Hemorrhage/Hemorrhage/*genetics

  • Source: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis [Blood Coagul Fibrinolysis] 1998 Nov; Vol. 9 (8), pp. 761-4.Publisher: Lippincott Williams And Wilkins Country of Publication: England NLM ID: 9102551 Publication Model: Print Cited Medium: Print ISSN:

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  • 1-10 of  13 results for ""Hypoprothrombinemias""