S. Hayashi

发表

Neuronal nuclear alterations in dentatorubral-pallidoluysian atrophy: ultrastructural and morphometric studies of the cerebellar granule cells

Hitoshi Takahashi, Shintaro Hayashi, Kiyomitsu Oyanagi, 2001, Brain Research.

α-Synuclein pathology affecting Bergmann glia of the cerebellum in patients with α-synucleinopathies

A. Kakita, Hitoshi Takahashi, Y. Piao, 2003, Acta Neuropathologica.

α‐Synuclein Accumulates in Purkinje Cells in Lewy Body Disease but not in Multiple System Atrophy

T. Iwatsubo, M. Hasegawa, Hitoshi Takahashi, 2003 .

Sporadic hereditary diffuse leukoencephalopathy with axonal spheroids showing numerous lesions with restricted diffusivity caused by a novel splice site mutation in the CSF1R gene

Satoshi O. Suzuki, T. Iwaki, J. Kira, 2013 .

Impaired Cytoplasmic–Nuclear Transport of Hypoxia‐Inducible Factor‐1α in Amyotrophic Lateral Sclerosis

T. Iwaki, J. Kira, S. Hayashi, 2013, Brain pathology.

Interaction between neuronal intranuclear inclusions and promyelocytic leukemia protein nuclear and coiled bodies in CAG repeat diseases.

S. Tsuji, S. Hayashi, M. Yamada, 2001, The American journal of pathology.

Co-localization of α-synuclein and phosphorylated tau in neuronal and glial cytoplasmic inclusions in a patient with multiple system atrophy of long duration

T. Iwatsubo, M. Hasegawa, Hitoshi Takahashi, 2001, Acta Neuropathologica.

Pathological study of the diffuse myelin pallor in the anterolateral columns of the spinal cord in amyotrophic lateral sclerosis

K. Okamoto, M. Amari, S. Hayashi, 2001, Journal of the Neurological Sciences.

Late‐onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation

T. Iwatsubo, M. Hasegawa, Hitoshi Takahashi, 2002, Annals of neurology.

Juvenile Parkinson's disease with widespread Lewy bodies in the brain

S. Hayashi, I. Yoshimura, N. Yoshimura, 2004, Acta Neuropathologica.

Distribution of intracytoplasmic acidophilic granule-containing neurons in the human brain

S. Hayashi, S. Oyanagi, S. Sekiya, 2004, Acta Neuropathologica.

Pick's disease: α- and β-synuclein-immunoreactive Pick bodies in the dentate gyrus

Hitoshi Takahashi, S. Yagihashi, S. Hayashi, 2002, Acta Neuropathologica.

Neuropathology of sporadic amyotrophic lateral sclerosis of long duration

S. Tsuji, Hitoshi Takahashi, S. Hayashi, 1997, Journal of the Neurological Sciences.

Aprosencephaly: histopathological features of the rudimentary forebrain and retina

A. Kakita, Hitoshi Takahashi, S. Hayashi, 2001, Acta Neuropathologica.

Apolipoprotein E epsilon4 allele and progression of cortical Lewy body pathology in Parkinson's disease.

S. Tsuji, A. Kakita, S. Hayashi, 1998, Acta neuropathologica.

An autopsy case of autosomal‐recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene

Hitoshi Takahashi, S. Hayashi, K. Wakabayashi, 2000, Movement disorders : official journal of the Movement Disorder Society.

Autosomal dominant diffuse Lewy body disease

S. Tsuji, Hitoshi Takahashi, S. Hayashi, 1998, Acta Neuropathologica.

Neuropathology with Clinical Correlations of Sporadic Amyotrophic Lateral Sclerosis: 102 Autopsy Cases Examined Between 1962 and 2000

A. Kakita, Hitoshi Takahashi, Y. Piao, 2003, Brain pathology.

A 76‐year‐old woman presenting with adult‐onset, slowly progressive cerebellar symptoms

S. Hayashi, Toshiya Sato, Hitoshi Takahashi, 2002, Neuropathology : official journal of the Japanese Society of Neuropathology.

NACP/alpha-synuclein-positive filamentous inclusions in astrocytes and oligodendrocytes of Parkinson's disease brains.

S. Hayashi, K. Wakabayashi, M. Yoshimoto, 2000, Acta neuropathologica.

Novel mutations, pseudo‐dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism

S. Tsuji, T. Yuasa, Hitoshi Takahashi, 2000, Annals of neurology.

Cerebellar cortical tau pathology in progressive supranuclear palsy and corticobasal degeneration

A. Kakita, Hitoshi Takahashi, Y. Piao, 2002, Acta Neuropathologica.

A case of hereditary diffuse leukoencephalopathy with axonal spheroids caused by a de novo mutation in CSF1R masquerading as primary progressive multiple sclerosis

T. Iwaki, J. Kira, Kunihiro Yoshida, 2013, Multiple sclerosis.

Expression of calbindin D-28k and parvalbumin in cerebral cortical dysgenesis induced by administration of ethylnitrosourea to rats at the stage of neurogenesis

A. Kakita, S. Hayashi, M. Yamada, 2001, Acta Neuropathologica.

Pick’s disease: selective occurrence of apolipoprotein E-immunoreactive Pick bodies in the limbic system

S. Tsuji, A. Kakita, Hitoshi Takahashi, 1997, Acta Neuropathologica.

Animal model of axonal Guillain‐Barré syndrome induced by sensitization with GM1 ganglioside

K. Hirata, Hitoshi Takahashi, A. Ohnishi, 2001, Annals of neurology.

Animal model of axonal Guillain-Barré syndrome induced by sensitization with GM1 ganglioside.

K. Hirata, Hitoshi Takahashi, A. Ohnishi, 2001 .

A case of severe chronic inflammatory demyelinating polyradiculoneuropathy with monoclonal gammopathy of undetermined significance with alternating immunoglobulin class to IgM from IgA.

S. Kusunoki, K. Okamoto, S. Hayashi, 2016, Rinsho shinkeigaku = Clinical neurology.

Nonapoptotic cell death caused by the inhibition of RNA polymerase disrupts organelle distribution

K. Okamoto, S. Hayashi, T. Yamazaki, 2007, Journal of the Neurological Sciences.

Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation

S. Tsuji, Hitoshi Takahashi, Y. Piao, 2004, Acta Neuropathologica.

Loss of calretinin- and parvalbumin-immunoreactive axons in anterolateral columns beyond the corticospinal tracts of amyotrophic lateral sclerosis spinal cords

K. Okamoto, M. Amari, S. Hayashi, 2013, Journal of the Neurological Sciences.

A case of adult-onset reducing body myopathy presenting a novel clinical feature, asymmetrical involvement of the sternocleidomastoid and trapezius muscles

J. Kira, Y. Hayashi, I. Nishino, 2014, Journal of the Neurological Sciences.

Ganglioglioma with a tanycytic ependymoma as the glial component

S. Kameyama, S. Hayashi, H. Takahashi, 2000, Acta Neuropathologica.

Variable expression of microglial DAP12 and TREM2 genes in Nasu-Hakola disease

A. Kakita, Kunihiro Yoshida, S. Hayashi, 2015, Neurogenetics.

A case of neuromyelitis optica harboring both anti-aquaporin-4 antibodies and a pathogenic mitochondrial DNA mutation for Leber’s hereditary optic neuropathy

J. Kira, S. Hayashi, R. Yamasaki, 2014, Multiple sclerosis.

Immunotherapy‐refractory vacuolar myopathy with mucin deposition in scleromyxedema: A possible role of fibroblast growth factor 2

T. Iwaki, J. Kira, Y. Oda, 2020, Neuropathology : official journal of the Japanese Society of Neuropathology.

Hopkins syndrome following the first episode of bronchial asthma associated with enterovirus D68: a case report

J. Kira, S. Hayashi, R. Yamasaki, 2018, BMC Neurology.

Alpha-synuclein pathology affecting Bergmann glia of the cerebellum in patients with alpha-synucleinopathies.

A. Kakita, Hitoshi Takahashi, Y. Piao, 2003, Acta neuropathologica.

Diffuse Mallory Bodies in the Liver, Diffuse Lewy Bodies in the Brain and Diffuse Fat Replacement (Lipomatous Pseudohypertrophy) of the Pancreas in a Patient with Juvenile Parkinson's Disease

S. Hayashi, N. Yoshimura, Y. Fukushima, 1992, Acta pathologica japonica.

Aggregation of alpha-synuclein/NACP in the neuronal and glial cells in diffuse Lewy body disease: a survey of six patients.

Y. Piao, S. Hayashi, K. Wakabayashi, 2000, Clinical neuropathology.

Heterogeneity of presenile dementia with bone cysts (Nasu–Hakola disease):: Three genetic forms

S. Hayashi, H. Takahashi, Y. Takahashi, 2002, Neurology.

Case of white‐eyed shunt carotid‐cavernous sinus fistula mimicking optic neuritis

K. Okamoto, S. Hayashi, K. Mashio, 2018, Clinical and Experimental Neuroimmunology.

Author response: Pilocytic astrocytoma with anaplasia arising from the optic chiasm in a very elderly patient

S. Hayashi, 2018, Neurology.

Spinocerebellar ataxia type 17-digenic TBP/STUB1 disease: neuropathologic features of an autopsied patient

A. Kakita, M. Nakashima, S. Hayashi, 2022, Acta Neuropathologica Communications.

[A case of chronic progressive motor-dominant multiple mononeuritis associated with primary Sjögren's syndrome].

J. Kira, S. Hayashi, B. Saitoh, 2015, Rinsho shinkeigaku = Clinical neurology.

Bilateral periventricular nodular heterotopia due to filamin 1 gene mutation: widespread glomeruloid microvascular anomaly and dysplastic cytoarchitecture in the cerebral cortex

Renzo Guerrini, Hitoshi Takahashi, Christopher A. Walsh, 2002, Acta Neuropathologica.

Ubiquitinated neuronal inclusions in the neostriatum in patients with amyotrophic lateral sclerosis with and without dementia--a study of 60 patients 31 to 87 years of age.

A. Kakita, M. Yamada, Y. Piao, 2001, Clinical neuropathology.

Light- and electron-microscopic studies of intracytoplasmic acidophilic granules in the human locus ceruleus and substantia nigra

S. Hayashi, S. Oyanagi, S. Sekiya, 2004, Acta Neuropathologica.

Ectopic germinoma involving multiple midline and paramedian structures outside the pineal gland or hypophyseal region of the brain prior to tumor development

K. Okamoto, S. Hayashi, 2015, Journal of the Neurological Sciences.

[A case of neuromyelitis optica spectrum disorder associated with a limited cutaneous systemic sclerosis and Sjögren syndrome].

J. Kira, S. Hayashi, Y. Ohyagi, 2013, Rinsho shinkeigaku = Clinical neurology.

NACP/α-synuclein-positive filamentous inclusions in astrocytes and oligodendrocytes of Parkinson’s disease brains

S. Hayashi, K. Wakabayashi, M. Yoshimoto, 2000, Acta Neuropathologica.

Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein

S. Tsuji, Hitoshi Takahashi, S. Hayashi, 2004, Annals of neurology.

Involvement of the cerebral cortex and autonomic ganglia in Machado-Joseph disease

S. Tsuji, S. Hayashi, M. Yamada, 2001, Acta Neuropathologica.

A case of synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome presenting with hypertrophic pachymeningitis

J. Kira, S. Hayashi, H. Murai, 2015, Journal of Neurological Sciences.

Meningeal plasma cell granuloma in the early stage of relapsing polychondritis.

K. Okamoto, S. Hayashi, Norihiko Akao, 2017, Rinsho shinkeigaku = Clinical neurology.

Widespread occurrence of intranuclear atrophin‐1 accumulation in the central nervous system neurons of patients with dentatorubral‐pallidoluysian atrophy

C. Ross, S. Tsuji, Hitoshi Takahashi, 2001, Annals of neurology.

Morvan’s syndrome and myasthenia gravis related to familial Mediterranean fever gene mutations

J. Kira, S. Hayashi, H. Takashima, 2016, Journal of Neuroinflammation.

Pathologic features of dysplasia and accompanying alterations observed in surgical specimens from patients with intractable epilepsy.

Hiroshi Masuda, Hitoshi Takahashi, Shigeki Kameyama, 2004, Journal of child neurology.

Morphometric and topographical studies of small neurons in sporadic amyotrophic lateral sclerosis spinal gray matter

K. Okamoto, M. Amari, M. Takatama, 2007, Neuropathology : official journal of the Japanese Society of Neuropathology.

Multiple cerebral infarcts with a few vasculitic lesions in the chronic stage of cerebral amyloid angiopathy‐related inflammation

Hitoshi Takahashi, S. Hayashi, M. Yamada, 2012, Neuropathology : official journal of the Japanese Society of Neuropathology.

Immune-mediated spastic paraparesis accompanied with high titres of voltage-gated potassium channel complex antibodies and myokymia/fasciculation

J. Kira, S. Hayashi, K. Ogata, 2016, Journal of the Neurological Sciences.

Alpha-synuclein accumulates in Purkinje cells in Lewy body disease but not in multiple system atrophy.

Hideo Fujiwara, Takeshi Iwatsubo, Masato Hasegawa, 2003, Journal of neuropathology and experimental neurology.

Subcellular localization of growth inhibitory factor in rat brain: light and electron microscopic immunohistochemical studies

Hitoshi Takahashi, T. Inuzuka, S. Hayashi, 1996, Brain Research.

Decreased CCR2 and CD62L expressions on peripheral blood classical monocytes in amyotrophic lateral sclerosis

J. Kira, S. Hayashi, T. Tateishi, 2014 .

Accumulation of α-synuclein/NACP is a cytopathological feature common to Lewy body disease and multiple system atrophy

Hitoshi Takahashi, Shintaro Hayashi, Akiyoshi Kakita, 1998, Acta Neuropathologica.

Accumulation of alpha-synuclein/NACP is a cytopathological feature common to Lewy body disease and multiple system atrophy.

A. Kakita, S. Hayashi, M. Yamada, 1998, Acta neuropathologica.

Variable expression of microglial DAP12 and TREM2 genes in Nasu-Hakola disease

A. Kakita, Kunihiro Yoshida, S. Hayashi, 2015, neurogenetics.

Autosomal dominant cerebellar ataxia (SCA6): clinical, genetic and neuropathological study in a family

S. Tsuji, S. Hayashi, H. Takahashi, 1998, Acta Neuropathologica.

Downregulation of Neuronal and Dendritic Connexin36-Made Electrical Synapses Without Glutamatergic Axon Terminals in Spinal Anterior Horn Cells From the Early Stage of Amyotrophic Lateral Sclerosis

J. Kira, K. Okamoto, S. Hayashi, 2018, Front. Neurosci..

Patients with temporal lobe epilepsy show an increase in brain-derived neurotrophic factor protein and its correlation with neuropeptide Y

Hitoshi Takahashi, Shigeki Kameyama, Shintaro Hayashi, 1999, Brain Research.

Extensive dysregulations of oligodendrocytic and astrocytic connexins are associated with disease progression in an amyotrophic lateral sclerosis mouse model

Satoshi O. Suzuki, J. Kira, S. Hayashi, 2014, Journal of Neuroinflammation.

Primary progressive aphasia with focal glial tauopathy

Y Shibasaki, T. Iwatsubo, M. Hasegawa, 2000, Neuropathology and applied neurobiology.

[Leber's hereditary optic neuropathy after head trauma: a case report].

K. Okamoto, S. Hayashi, 2011, Rinsho shinkeigaku = Clinical neurology.

Apolipoprotein E ε4 allele and progression of cortical Lewy body pathology in Parkinson’s disease

S. Tsuji, A. Kakita, Hitoshi Takahashi, 1998, Acta Neuropathologica.

TAR DNA-binding protein 43 pathology in a case clinically diagnosed with facial-onset sensory and motor neuronopathy syndrome: An autopsied case report and a review of the literature

T. Iwaki, J. Kira, S. Hayashi, 2013, Journal of the Neurological Sciences.

A possible variant of neuro-Behçet disease presenting chronic progressive ataxia without mucocutaneo-ocular symptoms

A. Kakita, Hitoshi Takahashi, S. Hayashi, 2006, Rheumatology International.

Pick's disease: alpha- and beta-synuclein-immunoreactive Pick bodies in the dentate gyrus.

Hitoshi Takahashi, S. Yagihashi, S. Hayashi, 2002, Acta neuropathologica.

Shower embolism‐like brain lesions in Churg–Strauss syndrome

J. Kira, S. Hayashi, Y. Ohyagi, 2013 .

Discriminative clinical and neuroimaging features of motor-predominant hereditary diffuse leukoencephalopathy with axonal spheroids and primary progressive multiple sclerosis: A preliminary cross-sectional study.

A. Hiwatashi, J. Kira, Kunihiro Yoshida, 2019, Multiple sclerosis and related disorders.

Pathologic Features of Dysplasia and Accompanying Alterations Observed in Surgical Specimens From Patients With Intractable Epilepsy

A. Kakita, S. Kameyama, Hitoshi Takahashi, 2004 .

Novel mutations, pseudo‐dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism

S. Tsuji, T. Yuasa, S. Hayashi, 2000, Annals of neurology.

Impaired Cytoplasmic–Nuclear Transport of Hypoxia‐Inducible Factor‐1α in Amyotrophic Lateral Sclerosis

T. Iwaki, J. Kira, S. Hayashi, 2013, Brain pathology.

Morvan’s syndrome and myasthenia gravis related to familial Mediterranean fever gene mutations

J. Kira, S. Hayashi, H. Takashima, 2016, Journal of Neuroinflammation.

[Acutely developed reversible posterior leukoencephalopathy syndrome following a prompt physical activity to avoid a traffic accident: a case report].

K. Okamoto, S. Hayashi, Y. Mizuno, 2009, Rinsho shinkeigaku = Clinical neurology.