Aritoshi Iida

Kodaira, Japan

Last Updated: 09/26/2026

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Found 74 publications

THE1 repeats: Ancient endogenous retroviruses rampaging behind sarcoid myopathy.

THE1 repeats: Ancient endogenous retroviruses rampaging behind sarcoid myopathy.

Journal: Journal of human genetics

Published: April 23, 2026

Ectopic co-expression of canonical and LINE1 and THE1A-exonizing IL23R transcripts in sarcoid myopathy.

Ectopic co-expression of canonical and LINE1 and THE1A-exonizing IL23R transcripts in sarcoid myopathy.

Journal: Journal of human genetics

Published: June 19, 2025

Two Brothers With ADSS1 Myopathy: A Report of Clinical, Radiological, and Autopsy Findings.

Two Brothers With ADSS1 Myopathy: A Report of Clinical, Radiological, and Autopsy Findings.

Journal: Neuropathology : official journal of the Japanese Society of Neuropathology

Published: November 11, 2024

Sequential development of parkinsonism in two patients with oculopharyngodistal type myopathy in GIPC1-related repeat expansion disorder.

Sequential development of parkinsonism in two patients with oculopharyngodistal type myopathy in GIPC1-related repeat expansion disorder.

Journal: Neuromuscular disorders : NMD

Published: June 30, 2024

Retrotrans-genomics identifies aberrant THE1B endogenous retrovirus fusion transcripts in the pathogenesis of sarcoidosis.

Retrotrans-genomics identifies aberrant THE1B endogenous retrovirus fusion transcripts in the pathogenesis of sarcoidosis.

Journal: Nature communications

Published: February 29, 2024

Novel CLOCK and NR1D2 variants in 64 sighted Japanese individuals with non-24-hour sleep-wake rhythm disorder.

Novel CLOCK and NR1D2 variants in 64 sighted Japanese individuals with non-24-hour sleep-wake rhythm disorder.

Journal: Sleep

Published: March 10, 2023

Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysis.

Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysis.

Journal: PLoS genetics

Published: January 21, 2023

RILPL1-related OPDM is absent in a Japanese cohort.

RILPL1-related OPDM is absent in a Japanese cohort.

Journal: American journal of human genetics

Published: November 04, 2022

Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy.

Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy.

Journal: Acta neuropathologica communications

Published: October 01, 2022

Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4.

Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4.

Journal: Acta neuropathologica

Published: September 15, 2022

Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathy.

Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathy.

Journal: Scientific reports

Published: September 08, 2022

Malignant hyperthermia and cylindrical spirals in a 4-year-old boy.

Malignant hyperthermia and cylindrical spirals in a 4-year-old boy.

Journal: Neuromuscular disorders : NMD

Published: April 27, 2022

Showing 1-12 of 74

Last Updated: 09/26/2026