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Article

Transient hemiparesis in a 14-year-old boy with MYH9 disorders.

International journal of hematology - 1 Sept 2012

Kitamura Katsumasa, Kunishima Shinji, Tahara Mayu, Ogiwara Shigetoshi, Dobata Nana, Dobata Tomoyuki, Sugihara Akemi, Nakashima Taiji, Sasaki Yasushi, Nagumo Kiyoshi, Kubota Mitsuru, Kinugawa Yoshikazu, Ieko Masahiro, Kumaki Satoru

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 22821427
DOI: 10.1007/s12185-012-1149-z

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

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Transient hemiparesis in a 14-year-old boy with MYH9 disorders.PMID 22821427Read ↗

Early diagnosis improves the quality of life in MYH9 disorder.Semantic proximity Read ↗

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

A case of MYH9 disorders caused by a novel mutation (p.K74E).Semantic proximity Read ↗

Description of a novel mutation leading to MYH9-related disease.Semantic proximity Read ↗

Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review.Semantic proximity Read ↗

Familial hemiplegic migraine in Indian children-a tertiary center experience.Semantic proximity Read ↗

Cerebral arteriopathy and ischemic stroke in a pediatric MYH11 patientSemantic proximity Read ↗

A Longitudinal Exploration of<i>CACNA1A</i>-related Hemiplegic Migraine in ChildrenSemantic proximity Read ↗

Alternating Hemiplegia of Childhood in Korea: a Case Report.Semantic proximity Read ↗

A D1424N mutation in the MYH9 gene results in macrothrombocytopenia and granulocytic inclusion bodies in a Chinese inherited macrothrombocytopenia pedigree.Semantic proximity Read ↗

Diagnostic and therapeutic aspects of hemiplegic migraine.Semantic proximity Read ↗

Alternating Hemiplegia of Childhood with Novel Features.Semantic proximity Read ↗

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