Tatsuro Oda

发表

Effects of aging on behavioral symptoms in Alzheimer's disease

K. Konishi, K. Hori, Tatsuro Oda, 2009 .

Identification of amino‐terminally cleaved tau fragments that distinguish progressive supranuclear palsy from corticobasal degeneration

H. Akiyama, M. Hasegawa, A. Mochizuki, 2004, Annals of neurology.

Glial tau-positive structures lack the sequence encoded by exon 3 of the tau protein gene

Masanori Kato, H. Akiyama, M. Okochi, 1997, Neuroscience Letters.

Basal ganglia lesions in corticobasal degeneration differ from those in Pick's disease and progressive supranuclear palsy: A topographic neuropathological study of six autopsy cases

K. Arima, T. Uchihara, H. Shimada, 1997 .

First episodes of behavioral symptoms in Alzheimer's disease patients at age 90 and over, and early‐onset Alzheimer's disease: Comparison with senile dementia of Alzheimer's type

T. Inada, K. Hori, Tatsuro Oda, 2005, Psychiatry and clinical neurosciences.

Phosphorylated TDP-43 in frontotemporal lobar degeneration and ALS

M. Morita, T. Beach, H. Akiyama, 2009 .

Neuronal and glial inclusions in frontotemporal dementia with or without motor neuron disease are immunopositive for p62

H. Akiyama, M. Hasegawa, T. Nonaka, 2003, Neuroscience Letters.

Pick’s disease with Pick bodies: An unusual autopsy case showing degeneration of the pontine nucleus, dentate nucleus, Clarke’s column, and lower motor neuron

A. Lees, H. Akiyama, R. de Silva, 2007, Neuropathology : official journal of the Japanese Society of Neuropathology.

Pathological Heterogeneity of the Precentral Gyrus in Pick’s Disease: A Study of 16 Autopsy Cases

K. Arima, A. Kakita, H. Akiyama, 2006, Acta Neuropathologica.

Donepezil‐responsive alcohol‐related prolonged delirium

M. Onaya, T. Inada, S. Hirai, 2003, Psychiatry and clinical neurosciences.

[Frontotemporal dementia (FTD) and genetic mutations including progranulin gene].

M. Morita, T. Beach, H. Akiyama, 2008, Rinsho shinkeigaku = Clinical neurology.

Different immunoreactivities of the microtubule-binding region of tau and its molecular basis in brains from patients with Alzheimer's disease, Pick's disease, progressive supranuclear palsy and corticobasal degeneration

H. Akiyama, K. Ishiguro, K. Ikeda, 2003, Acta Neuropathologica.

Degeneration of the inferior olive in spinocerebellar ataxia 6 may depend on disease duration: Report of two autopsy cases and statistical analysis of autopsy cases reported to date

H. Akiyama, Mari Yoshida, H. Sasaki, 2005, Neuropathology : official journal of the Japanese Society of Neuropathology.

Prion disease with 144 base pair insertion in a Japanese family line

E. Oguni, H. Kashima, T. Kitamoto, 2004, Acta Neuropathologica.

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

H. Akiyama, M. Hasegawa, H. Mori, 2006, Biochemical and biophysical research communications.

Occurrence of T cells in the brain of Alzheimer's disease and other neurological diseases

Masanori Kato, H. Akiyama, K. Kosaka, 2002, Journal of Neuroimmunology.

Activation of vascular endothelial cells and perivascular cells by systemic inflammation—an immunohistochemical study of postmortem human brain tissues

Masanori Kato, H. Akiyama, K. Kosaka, 2004, Acta Neuropathologica.

Phosphorylated TDP‐43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

M. Morita, H. Akiyama, F. Kametani, 2008, Annals of neurology.

Clinical Aspects of ‘Senile Dementia of the Tangle Type’ – A Subset of Dementia in the Senium Separable from Late-Onset Alzheimer’s Disease

Masanori Kato, H. Akiyama, Hitoshi Takahashi, 1998, Dementia and Geriatric Cognitive Disorders.

Methamphetamine psychosis in which tardive dystonia was successfully treated with clonazepam

T. Inada, Tatsuro Oda, N. Yamamoto, 2007, Psychiatry and clinical neurosciences.

Argyrophilic thread-like structure in corticobasal degeneration and supranuclear palsy

Kenji Ikeda, Hiromi Kondo, Kunimasa Arima, 1994, Neuroscience Letters.

Discrepancy between tau immunoreactivity and argyrophilia by the Bodian method in neocortical neurons of corticobasal degeneration

T. Uchihara, H. Mizusawa, K. Ikeda, 1998, Acta Neuropathologica.

Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy cases

M. Mimura, K. Arima, H. Akiyama, 2005, Acta Neuropathologica.

Distribution of cerebral cortical lesions in corticobasal degeneration: a clinicopathological study of five autopsy cases in Japan

T. Uchihara, H. Shimada, K. Ikeda, 1997, Acta Neuropathologica.

[Significance of the TDP-43 deposition in FTLD-U and ALS].

M. Morita, T. Beach, H. Akiyama, 2008, Rinsho shinkeigaku = Clinical neurology.

Argyrophilic grain disease with delusions and hallucinations: a pathological study.

H. Akiyama, M. Hasegawa, M. Onaya, 2010, Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society.

Corticobasal degeneration presenting with nonfluent primary progressive aphasia: a clinicopathological study

M. Mimura, H. Kashima, Motoichiro Kato, 2001, Journal of the Neurological Sciences.

‘Awakenings’ in demented patients

T. Inada, K. Hori, Tatsuro Oda, 2003, Psychiatry and clinical neurosciences.

Amyotrophic lateral sclerosis with dementia: an autopsy case showing many Bunina bodies, tau-positive neuronal and astrocytic plaque-like pathologies, and pallido-nigral degeneration

A. Lees, R. Silva, H. Akiyama, 2006, Acta Neuropathologica.

[Argyrophilic grain disease clinically mimicking Parkinson's disease with dementia: report of an autopsy case].

Y. Hirayasu, H. Akiyama, K. Ikeda, 2004, No to shinkei = Brain and nerve.

Ubiquitin-positive frontotemporal lobar degeneration presenting with progressive Gogi (word-meaning) aphasia. A neuropsychological, radiological and pathological evaluation of a Japanese semantic dementia patient

Y. Sakurai, H. Akiyama, M. Iwata, 2006, Journal of the Neurological Sciences.

SCA6 mutation analysis in a large cohort of the Japanese patients with late-onset pure cerebellar ataxia

A. Ohnishi, K. Tashiro, H. Sasaki, 1998, Journal of the Neurological Sciences.

Molecular features of the CAG repeats and clinical manifestation of Machado-Joseph disease.

G. Sobue, I. Nishino, M. Seto, 1995, Human molecular genetics.

Pacing Rhythms of “Wanderers” with Dementia

H. Kashima, T. Inada, K. Hori, 2001 .

Three cases of schizophrenia for which olanzapine was effective after early acute phase

T. Inada, Tatsuro Oda, Nobutomo Yamamoto, 2008, Psychiatry and clinical neurosciences.