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Toshitaka Kawarai

University of Tokushima
University of Toronto

171

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4920

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Ataxia with vitamin E deficiency in the Philippines : A case report of two siblings.

2021 The Journal of Medical Investigation
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Rapid-Onset Dystonia-Parkinsonism Phenotype Consistency for a Novel Variant of ATP1A3 in Patients Across 3 Global Populations

2021 Neurology Genetics
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Clinico‐genetic study of two Japanese pedigrees with hereditary spastic paraparesis and Alzheimer's disease: Genetics/molecular genetics

2020 Alzheimers & Dementia
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A case of cervical dystonia with GNAL mutation and a subsequent shift in laterality of torticollis after temporary remission

2020 Neurology and Clinical Neuroscience
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Recurrent de novo missense variant E210K in UBTF causes juvenile dystonia-parkinsonism.

2020 Neurological Sciences
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Withdrawal: Cytosolic proteins regulate α-synuclein dissociation from presynaptic membranes.

2020 Journal of Biological Chemistry
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A novel AIFM1 missense mutation in a Japanese patient with ataxic sensory neuronopathy and hearing impairment

2020 Journal of the Neurological Sciences
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Clinicopathological co-morbidity of progressive supranuclear palsy and amyotrophic lateral sclerosis

2019 Journal of the Neurological Sciences
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Lesser motor disability in adulthood: A ten-year follow-up of a dyskinetic patient with ADCY5 mutation

2019 Journal of the Neurological Sciences
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MiR-33a is a therapeutic target in SPG4-related hereditary spastic paraplegia human neurons

2019 Clinical Science
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