Yuta Ichinose
Yamanashi, Japan
Last Updated: 09/26/2026
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Found 31 publications
Age-related changes in blood pressure and heart rates of patients with Parkinson's disease.
Journal: Journal of clinical hypertension (Greenwich, Conn.)
Published: August 12, 2020
A patient with ossification of the yellow ligament and ventriculomegaly with 22q11.2 deletion syndrome undiagnosed until adulthood.
Journal: Heliyon
Published: July 15, 2020
Conjugal multiple system atrophy: Be cautious when calculating numbers of probability.
Journal: Parkinsonism & related disorders
Published: June 29, 2020
A Japanese SPG4 Patient with a Confirmed De Novo Mutation of the SPAST Gene.
Journal: Internal medicine (Tokyo, Japan)
Published: June 12, 2020
RFC1 repeat expansion in Japanese patients with late-onset cerebellar ataxia.
Journal: Journal of human genetics
Published: April 24, 2020
The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1.
Journal: Neurobiology of aging
Published: March 05, 2020
Conjugal multiple system atrophy: Computing chance or investigating real patients?
Journal: Parkinsonism & related disorders
Published: March 03, 2020
Variants in saposin D domain of prosaposin gene linked to Parkinson's disease.
Journal: Brain : a journal of neurology
Published: October 11, 2019
Conjugal cerebellar type of multiple system atrophy: Person-to-person transmission?
Journal: Parkinsonism & related disorders
Published: October 08, 2019
Sympathetic outflow to skin predicts central autonomic dysfunction in multiple system atrophy.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: September 19, 2019
VPS13D-related disorders presenting as a pure and complicated form of hereditary spastic paraplegia.
VPS13D-related disorders presenting as a pure and complicated form of hereditary spastic paraplegia.
Journal: Molecular genetics & genomic medicine
Published: July 25, 2019
UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes.
Journal: Journal of human genetics
Published: June 16, 2019
Last Updated: 09/26/2026