Inherited platelet disorders: a clinical approach to diagnosis and management. - Wikidata - thesis-toulmin - TriplyDB

Inherited platelet disorders: a clinical approach to diagnosis and management.

Inherited platelet disorders: a clinical approach to diagnosis and management.

http://www.wikidata.org/entity/Q33396427

about

Genotyping and phenotyping of platelet function disorders The VPS33B-binding protein VPS16B is required in megakaryocyte and platelet α-granule biogenesis.Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assay What we have learned from inherited platelet disorders.Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH.Detection of mild inherited disorders of blood coagulation: current options and personal recommendations.Current status and future prospects for platelet function testing in the diagnosis of inherited bleeding disorders.Combined variants in factor VIII and prostaglandin synthase-1 amplify hemorrhage severity across three generations of descendants.Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey.

P2860

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P2860

Inherited platelet disorders: a clinical approach to diagnosis and management.

http://www.wikidata.org/entity/Q33396427

description

2011 nî lūn-bûn

@nan

2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի օգոստոսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

@zh-hk

2011年論文

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2011年論文

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2011年论文

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name

Inherited platelet disorders: a clinical approach to diagnosis and management.

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Inherited platelet disorders: a clinical approach to diagnosis and management.

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Inherited platelet disorders: a clinical approach to diagnosis and management.

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Inherited platelet disorders: a clinical approach to diagnosis and management.

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Inherited platelet disorders: a clinical approach to diagnosis and management.

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Expert Review of Hematology

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Inherited platelet disorders: a clinical approach to diagnosis and management.

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P2093

Kelly Cox

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Victoria Price

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Walter H A Kahr

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P2860

Bernard-Soulier syndrome (hemorrhagiparous thrombocytic dystrophy)

Glanzmann thrombasthenia

Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1

Identification of the platelet ADP receptor targeted by antithrombotic drugs

Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation

X-linked thrombocytopenia caused by a novel mutation of GATA-1

Selective impairment of platelet activation to collagen in the absence of GATA1

Molecular bases of defective signal transduction in the platelet P2Y12 receptor of a patient with congenital bleeding

Calcium-dependent phospholipid scrambling by TMEM16F

Requirement of VPS33B, a member of the Sec1/Munc18 protein family, in megakaryocyte and platelet alpha-granule biogenesis

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455-472

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scholarly article

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10.1586/EHM.11.41

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4

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4

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21801136

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