Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Case of an hemodialysis patient with MYH9 disorders].

Nihon Jinzo Gakkai shi - 1 Jan 2011

Ishida Ryo, Kusaba Tetsuro, Kirita Yuhei, Matsuoka Eiko, Nakayama Mayuka, Uchiyama Hitoji, Kajita Yoshihiro

Abstract excerpt

A 70-year-old woman was admitted to our hospital for repair of vascular access for maintenance hemodialysis. She had been undergoing the maintenance hemodialysis for 20 years, however, her underlying renal disease had not been identified. The laboratory data on admission revealed marked thrombocytopenia with giant platelets and a Dohle body-like cytoplasmic inclusion body in granulocytes. The same hematological...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Diagnosis, Differential
Share to Hearing Loss, Sensorineural

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Kidney Failure, Chronic

Share to Molecular Motor Proteins

Share to Myosin Heavy Chains

Share to Renal Dialysis

Share to Thrombocytopenia

Source

Identifiers

PMID: 21516706

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Case of an hemodialysis patient with MYH9 disorders].PMID 21516706Read ↗

[Clinical features and gene analyses of six patients with MYH9-related disease].Semantic proximity Read ↗

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

Advances in the understanding of MYH9 disorders.Semantic proximity Read ↗

[A non-familial May-Hegglin anomaly accompanying with MYH9 gene R1933X mutation and I1626V polymorphism].Semantic proximity Read ↗

Successful living-related kidney transplantation in MYH9-related disorder with macrothrombocytopenia: lessons for the clinical nephrologist.Semantic proximity Read ↗

[Clinical manifestations and gene mutations of a Chinese family with MYH9-related syndrome].Semantic proximity Read ↗

[Nonmuscle myosin heavy chain 9 gene mutations related disease: a family report].Semantic proximity Read ↗

MYH9 disorder: Identification and a novel mutation in patients with macrothrombocytopenia.Semantic proximity Read ↗

[Identification of nonmuscle mysin heavy chain 9 gene mutation in a May-Hegglin anomaly family].Semantic proximity Read ↗

[MYH9-related macrothrombocytopenia].Semantic proximity Read ↗

[May-Hegglin anomaly: past and present--novel diagnostic test and new concept of the disease].Semantic proximity Read ↗

Association of a novel in-frame deletion mutation of the MYH9 gene with end-stage renal failure: case report and review of the literature.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.