Natural history of patients with congenital dysfibrinogenemia. - Wikidata - awgldk - TriplyDB

Natural history of patients with congenital dysfibrinogenemia.

Natural history of patients with congenital dysfibrinogenemia.

http://www.wikidata.org/entity/Q34974082

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Thrombosis in Inherited Fibrinogen Disorders.Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His.Update on inherited disorders of haemostasis and pregnancy.A novel mutation in exon 2 of FGB caused by c.221G>T † substitution, predicting the replacement of the native Arginine at position 74 with a Leucine (p.Arg74Leu † ) in a proband from a Kurdish family with dysfibrinogenaemia and familial venous and a Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management.Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories.What Is the Biological and Clinical Relevance of Fibrin?Can the phenotype of inherited fibrinogen disorders be predicted?The amplitude of coagulation curves from thrombin time tests allows dysfibrinogenemia caused by the common mutation FGG-Arg301 to be distinguished from hypofibrinogenemia.Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation.Clinical conditions responsible for hyperviscosity and skin ulcers complications.Not fibrin(ogen), but fibrinogen or fibrin Dysfibrinogenemia with Subgaleal Hematoma: An Unusual Presentation.A Chinese family with congenital Dysfibrinogenemia carries a heterozygous missense mutation in FGA: Concerning the genetic abnormality and clinical treatment.Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization.Acute renal artery infarction secondary to dysfibrinogenemia.Management of dysfibrinogenemia in pregnancy: A case report.Dysfibrinogenemia-associated novel heterozygous mutation, Shanghai (FGA c.169_180+2 del), leads to N-terminal truncation of fibrinogen Aα chain and impairs fibrin polymerization.Therapeutic plasma exchange and pregnancy: A case report and guidelines for performing plasma exchange in a pregnant patient.Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders Identification and characterization of novel mutations implicated in congenital fibrinogen disorders

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Natural history of patients with congenital dysfibrinogenemia.

http://www.wikidata.org/entity/Q34974082

description

2014 nî lūn-bûn

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2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2014 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Natural history of patients with congenital dysfibrinogenemia.

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Natural history of patients with congenital dysfibrinogenemia.

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Natural history of patients with congenital dysfibrinogenemia.

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Natural history of patients with congenital dysfibrinogenemia.

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Natural history of patients with congenital dysfibrinogenemia.

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Natural history of patients with congenital dysfibrinogenemia.

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Natural history of patients with congenital dysfibrinogenemia.

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Natural history of patients with congenital dysfibrinogenemia.

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Natural history of patients with congenital dysfibrinogenemia.

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Natural history of patients with congenital dysfibrinogenemia

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Christine Biron

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Emmanuel de Maistre

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Jérémie Koegel

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Marc Blondon

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Marguerite Neerman-Arbez

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Philippe Gautier

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Philippe de Moerloose

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Véronique Tintillier

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P2860

Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia

The role of fibrin matrices and tissue factor in early-term trophoblast proliferation and spreading

Executive summary: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines

Mechanisms of fibrin polymerization and clinical implications

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

Comparisons of the fibrin networks during pregnancy, nonpregnancy and pregnancy during dysfibrinogenaemia using the scanning electron microscope.

Molecular basis for fibrinogen Dusart (A alpha 554 Arg-->Cys) and its association with abnormal fibrin polymerization and thrombophilia.

Conception, early pregnancy loss, and time to clinical pregnancy: a population-based prospective study.

Fibrinogen stabilizes placental-maternal attachment during embryonic development in the mouse.

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