Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders - Wikidata - wikimedia - TriplyDB

Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders

Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders

http://www.wikidata.org/entity/Q33416254

about

ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization Diagnosis and treatment of inherited thrombocytopenias.Progress in understanding the diagnosis and molecular genetics of macrothrombocytopenias.Immature platelet fraction measurement is influenced by platelet size and is a useful parameter for discrimination of macrothrombocytopenia.Analyses of Genetic and Clinical Parameters for Screening Patients With Inherited Thrombocytopenia with Small or Normal-Sized Platelets.Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia.Genomics of platelet disorders.Gfi1b controls integrin signaling-dependent cytoskeleton dynamics and organization in megakaryocytes.Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders.Epidural anesthesia for labor and delivery in a patient with May-Hegglin anomaly: a case report.Bleeding is not the main clinical issue in many patients with inherited thrombocytopaenias.Evaluation of the immature platelet fraction contribute to the differential diagnosis of hereditary, immune and other acquired thrombocytopenias.New roles for mean platelet volume measurement in the clinical practice?Platelet abnormalities in a family with von Willebrand disease type 2B (V1316M) and association with bleeding score.Microdialysis SPR: diffusion-gated sensing in blood.Diagnosis and treatment of MYH9-RD in an Australasian cohort with thrombocytopenia.Mutations of the integrin αIIb/β3 intracytoplasmic salt bridge cause macrothrombocytopenia and enlarged platelet α-granules.Mutations of RUNX1 in families with inherited thrombocytopenia.Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim.Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases.Mean platelet diameter measurements to classify inherited thrombocytopenias.Challenges on the diagnostic approach of inherited platelet function disorders: Is a paradigm change necessary?Prevalence of Bleeding Symptoms among Adolescents and Young Adults in the Capital City of Saudi Arabia.

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Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders

http://www.wikidata.org/entity/Q33416254

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2014 nî lūn-bûn

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2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2014 թվականի հուլիսին 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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P2860

Guidelines for the investigation and management of idiopathic thrombocytopenic purpura in adults, children and in pregnancy.

Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease.

Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia.

Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations.

Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation)

Genetics of familial forms of thrombocytopenia.

Inherited thrombocytopenias frequently diagnosed in adults.

Wiskott-Aldrich syndrome: a comprehensive review.

Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life study

MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.

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