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Annals of Neurology|September 7, 2004
Novel PINK1 mutations in early-onset parkinsonismYasuko Hatano, Yuanzhe Li, Kenichi Sato, et al.
Molecular Genetics and Metabolism|April 3, 2004
Genetic testing of glycogen storage disease type Ib in Japan: five novel G6PT1 mutations and a rapid detection method for a prevalent mutation W118RKanako Kojima, Shigeo Kure, Fumiaki Kamada, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 12, 2008
Familial Parkinsonism with digenic parkin and PINK1 mutationsManabu Funayama, Yuanzhe Li, Tak-Hong Tsoi, et al.
Eneurologicalsci|April 30, 2020
Monoamine oxidase B rs1799836 G allele polymorphism is a risk factor for early development of levodopa-induced dyskinesia in Parkinson's diseaseShoko Kakinuma, Minako Beppu, Setsu Sawai, et al.
International Breastfeeding Journal|March 6, 2022
Risk factors for discontinuation of exclusive breast feeding within 1month: a retrospective cohort study in JapanShun Yasuda, Toma Fukuda, Naoya Toba, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2006
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countriesHiroyuki Tomiyama, Yuanzhe Li, Manabu Funayama, et al.
The EMBO Journal|May 8, 2020
Homeostatic and pathogenic roles of GM3 ganglioside molecular species in TLR4 signaling in obesityHirotaka Kanoh, Takahiro Nitta, Shinji Go, et al.
Magnetic Resonance in Medical Sciences : MRMS : an Official Journal of Japan Society of Magnetic Resonance in Medicine|November 20, 2024
Image-based Re-evaluation of the JCOG0911 Study Focusing on Tumor Volume and Survival, Disease Progression Diagnosis, and Radiomic Prognostication for Newly Diagnosed GlioblastomaManabu Kinoshita, Yasutaka Fushimi, Tomohiko Masumoto, et al.
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