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Hiroyo Yoshino

Showing results (1-10 of 78) with videos related to

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Clinical Parkinsonism & Related Disorders|May 1, 2026
Deep brain stimulation in <i>VPS13C</i>-associated Parkinson's disease: a longitudinal case studyHiroyuki Sumikura, Naoki Tani, Hiroyo Yoshino, et al.
Stem Cell Research|February 3, 2024
Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson's disease with PARK2 mutationKei-Ichi Ishikawa, Ayami Okuzumi, Hiroyo Yoshino, et al.
Journal of the Neurological Sciences|July 19, 2017
Parkin mutation may be associated with serious akinesia in a patient with Parkinson's diseaseYuto Uchihara, Hiroshi Kataoka, Hiroyo Yoshino, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 7, 2012
Pseudo-heterozygous rearrangement mutation of parkinManabu Funayama, Hiroyo Yoshino, Yuanzhe Li, et al.
Parkinson'S Disease|February 15, 2011
Nonmotor Symptoms in Patients with PARK2 MutationsAsako Yoritaka, Yumi Shimo, Yasushi Shimo, et al.
Frontiers in Neurology|June 20, 2022
Clinical Manifestations and Molecular Backgrounds of Parkinson's Disease Regarding Genes Identified From Familial and Population StudiesKenya Nishioka, Yuzuru Imai, Hiroyo Yoshino, et al.
Stem Cell Research|May 12, 2026
Generation of hiPSCs (JUCGRMi008-A) from a β-propeller protein-associated neurodegeneration patient with WDR45 mutationRino Kamikura, Xing Liu, Kei-Ichi Ishikawa, et al.
Stem Cell Research|December 28, 2023
Generation of three clones (JUCGRMi002-A, B, C) of induced pluripotent stem cells from a Parkinson's disease patient with SNCA duplicationKei-Ichi Ishikawa, Takahiro Shiga, Hiroyo Yoshino, et al.
Parkinsonism & Related Disorders|January 7, 2018
Genetic analysis of TMEM230 in Japanese patients with familial Parkinson's diseaseSilvio A Conedera, Yuanzhe Li, Manabu Funayama, et al.
Eneurologicalsci|January 17, 2022
A complex form of hereditary spastic paraplegia harboring a novel variant, p.W1515*, in the <i>SPG11</i> geneKensuke Daida, Yosuke Nishioka, Yuanzhe Li, et al.
Pageof 8

Showing results (1-10 of 78) with videos related to

Sort By:
Pageof 8
Clinical Parkinsonism & Related Disorders|May 1, 2026
Deep brain stimulation in <i>VPS13C</i>-associated Parkinson's disease: a longitudinal case studyHiroyuki Sumikura, Naoki Tani, Hiroyo Yoshino, et al.
Stem Cell Research|February 3, 2024
Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson's disease with PARK2 mutationKei-Ichi Ishikawa, Ayami Okuzumi, Hiroyo Yoshino, et al.
Journal of the Neurological Sciences|July 19, 2017
Parkin mutation may be associated with serious akinesia in a patient with Parkinson's diseaseYuto Uchihara, Hiroshi Kataoka, Hiroyo Yoshino, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 7, 2012
Pseudo-heterozygous rearrangement mutation of parkinManabu Funayama, Hiroyo Yoshino, Yuanzhe Li, et al.
Parkinson'S Disease|February 15, 2011
Nonmotor Symptoms in Patients with PARK2 MutationsAsako Yoritaka, Yumi Shimo, Yasushi Shimo, et al.
Frontiers in Neurology|June 20, 2022
Clinical Manifestations and Molecular Backgrounds of Parkinson's Disease Regarding Genes Identified From Familial and Population StudiesKenya Nishioka, Yuzuru Imai, Hiroyo Yoshino, et al.
Stem Cell Research|May 12, 2026
Generation of hiPSCs (JUCGRMi008-A) from a β-propeller protein-associated neurodegeneration patient with WDR45 mutationRino Kamikura, Xing Liu, Kei-Ichi Ishikawa, et al.
Stem Cell Research|December 28, 2023
Generation of three clones (JUCGRMi002-A, B, C) of induced pluripotent stem cells from a Parkinson's disease patient with SNCA duplicationKei-Ichi Ishikawa, Takahiro Shiga, Hiroyo Yoshino, et al.
Parkinsonism & Related Disorders|January 7, 2018
Genetic analysis of TMEM230 in Japanese patients with familial Parkinson's diseaseSilvio A Conedera, Yuanzhe Li, Manabu Funayama, et al.
Eneurologicalsci|January 17, 2022
A complex form of hereditary spastic paraplegia harboring a novel variant, p.W1515*, in the <i>SPG11</i> geneKensuke Daida, Yosuke Nishioka, Yuanzhe Li, et al.
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