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Article

Early diagnosis improves the quality of life in MYH9 disorder.

Pediatric blood & cancer - 1 Feb 2012

Shiota Mitsutaka, Kunishima Shinji, Hamabata Takayuki, Nakata Masatoshi, Hata Daisuke

Abstract excerpt

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21796764
DOI: 10.1002/pbc.23268

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Early diagnosis improves the quality of life in MYH9 disorder.PMID 21796764Read ↗

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

Somatic mosaicism in MYH9 disorders: the need to carefully evaluate apparently healthy parents.Semantic proximity Read ↗

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

Transient hemiparesis in a 14-year-old boy with MYH9 disorders.Semantic proximity Read ↗

Identification of a novel MYH9-related disease-associated mutation with multiple faintly staining Döhle-like bodies.Semantic proximity Read ↗

Gene symbol: MYH7.Semantic proximity Read ↗

Gene symbol: MYH7.Semantic proximity Read ↗

The Cardiovascular Manifestations and Management Recommendations for Ogden SyndromeSemantic proximity Read ↗

The Cardiovascular Manifestations and Management Recommendations for Ogden Syndrome.Semantic proximity Read ↗

Diagnosis and Therapy in MCT8 Deficiency: Ongoing ChallengesSemantic proximity Read ↗

Novel variant of MYH9 associated with mild evaluation of MYH9 related disorder in a Chinese family.Semantic proximity Read ↗

Two females with distinct de novo missense pathogenic variants in MED12 and vastly differing phenotypes.Semantic proximity Read ↗

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