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

A nationwide survey of MYH9-related disease in Japan.

Clinical and experimental nephrology - 1 Jan 2024

Shirai Yoko, Miura Kenichiro, Hamada Riku, Ishikura Kenji, Kunishima Shinji, Hattori Motoshi

Abstract excerpt

BACKGROUND: MYH9-related disease (MYH9-RD) is characterized by congenital macrothrombocytopenia, Döhle body-like granulocyte inclusions, and nephropathy, which may progress to end-stage kidney disease (ESKD). However, information on the effects of renin-angiotensin system (RAS) inhibitors on kidney survival is currently lacking and the outcomes of kidney replacement therapy (KRT) in MYH9-RD are largely unknown....

Read the complete abstract on PubMed

Topics

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

Share to Antihypertensive Agents
Share to Cross-Sectional Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hearing Loss, Sensorineural

Share to Kidney Failure, Chronic

Share to Mutation

Share to Myosin Heavy Chains

Share to Thrombocytopenia

Source

Identifiers

PMID: 37733142
DOI: 10.1007/s10157-023-02404-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A nationwide survey of MYH9-related disease in Japan.PMID 37733142Read ↗

Renal manifestations of patients with MYH9-related disorders.Semantic proximity Read ↗

Management of patients with severe Epstein syndrome: Review of four patients who received living-donor renal transplantation.Semantic proximity Read ↗

Clinical and genetic characteristics of 40 patients with nonmuscle myosin heavy chain 9-related disease (MYH9-RD) misdiagnosed as immune thrombocytopenia: a retrospective analysis in China.Semantic proximity Read ↗

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

CKD in MYH9-related disorders.Semantic proximity Read ↗

[Gene analysis and clinical features of MYH9-related disease].Semantic proximity Read ↗

MYH9-related inherited thrombocytopenia: the genetic spectrum, underlying mechanisms, clinical phenotypes, diagnosis, and management approachesSemantic proximity Read ↗

The Potential Impact of MYH9 (rs3752462) and ELMO1 (rs741301) Genetic Variants on the Risk of Nephrotic Syndrome Incidence.Semantic proximity Read ↗

Research Advances in the Physiological and Pathological Function of MYH9 and NMIIA.Semantic proximity Read ↗

Advances in the understanding of MYH9 disorders.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 ↗

Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with the progression of IgA nephropathy in Chinese.Semantic proximity Read ↗

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