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Article

Giant platelet syndromes and the MYH9 mutations.

Laboratory hematology : official publication of the International Society for Laboratory Hematology - 1 Jan 2004

Balduini Carlo L

Abstract excerpt

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Topics

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Share to Bernard-Soulier Syndrome
Share to Blood Platelets
Share to Megakaryocytes
Share to Molecular Motor Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Myosin Heavy Chains

Share to Platelet Activation

Share to Signal Transduction

Share to Thrombocytopenia

Source

Identifiers

PMID: 15529446

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Giant platelet syndromes and the MYH9 mutations.PMID 15529446Read ↗

MYH-9 Related Platelet Disorders: Strategies for Management and DiagnosisSemantic proximity Read ↗

MYH9-Related Platelet DisordersSemantic proximity Read ↗

A case report of a family with MYH9 gene mutation-related disease in an ethnic minority group and literature review.Semantic proximity Read ↗

Historical hematology: May–Hegglin anomalySemantic proximity Read ↗

Hereditary thrombocytopenias: a growing list of disordersSemantic proximity Read ↗

MYH9 gene mutations associated with bleeding.Semantic proximity Read ↗

[MYH9-related macrothrombocytopenia].Semantic proximity Read ↗

A family with an MYH9-related disorder with different phenotypes masquerading as immune thrombocytopaenia: an underreported disorder in Taiwan.Semantic proximity Read ↗

[Analysis of clinical phenotype and gene mutation characteristics of MYH9-related disorder].Semantic proximity Read ↗

Inherited Platelet Disorders: Diagnosis and Management.Semantic proximity Read ↗

A rare case of MYH9 disorders presenting with macrothrombocytopenia and deafness caused by MYH9-R702C mutation.Semantic proximity Read ↗

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.Semantic proximity Read ↗

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