T. Morita

发表

Spinocerebellar ataxia type 2 (SCA2) is associated with TDP-43 pathology

A. Kakita, Hitoshi Takahashi, Y. Toyoshima, 2011, Acta Neuropathologica.

Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions

A. Kakita, Hitoshi Takahashi, M. Yamada, 2008, Acta Neuropathologica.

Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology

A. Kakita, Hitoshi Takahashi, M. Yamada, 2008, Acta Neuropathologica.

Depletion of medullary serotonergic neurons in patients with multiple system atrophy who succumbed to sudden death

A. Kakita, Hitoshi Takahashi, M. Nishizawa, 2009, Brain : a journal of neurology.

Venous congestive myelopathy: Three autopsy cases showing a variety of clinicopathologic features

A. Kakita, Hitoshi Takahashi, T. Morita, 2008, Neuropathology : official journal of the Japanese Society of Neuropathology.

Widespread vertebral and epidural venous plexus metastasis of prostatic carcinoma presenting wedge‐shaped radial lesions in the spinal cord

S. Takeda, K. Oyanagi, T. Morita, 2003, Neuropathology : official journal of the Japanese Society of Neuropathology.

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.

Transportin 1 accumulates in FUS inclusions in adult‐onset ALS without FUS mutation

A. Kakita, H. Takahashi, M. Nishizawa, 2013, Neuropathology and applied neurobiology.

Widespread occurrence of alpha-synuclein/NACP-immunoreactive neuronal inclusions in juvenile and adult-onset Hallervorden-Spatz disease with Lewy bodies.

K. Wakabayashi, M. Yoshimoto, H. Takahashi, 1999, Neuropathology and applied neurobiology.

Sporadic motor neuron disease with severe sensory neuronopathy

Hitoshi Takahashi, K. Wakabayashi, T. Morita, 1998, Acta Neuropathologica.

Suprachiasmatic nucleus in a patient with multiple system atrophy with abnormal circadian rhythm of arginine-vasopressin secretion into plasma

S. Tsuji, Hitoshi Takahashi, K. Oyanagi, 1998, Journal of the Neurological Sciences.

Spinal anterior horn cells in sporadic amyotrophic lateral sclerosis show ribosomal detachment from, and cisternal distention of the rough endoplasmic reticulum

T. Komori, T. Mizutani, K. Oyanagi, 2008, Neuropathology and applied neurobiology.

Oncogenic osteomalacia: Pre- and postoperative histomorphometric studies

N. Endo, T. Tanizawa, T. Morita, 2006, Journal of Bone and Mineral Metabolism.

Familial juvenile parkinsonism

S. Tsuji, H. Takahashi, E. Ohama, 1994, Neurology.

Demyelination and remyelination in spinal cord lesions of human lymphotropic virus type I-associated myelopathy

T. Shimizu, E. Ohama, T. Morita, 2004, Acta Neuropathologica.

Eosinophilic esophagitis: a case report. Effective treatment with systemic corticosteroids for the relapse of the disease

K. Kamimura, K. Kimura, T. Morita, 2008, Clinical journal of gastroenterology.

Lung carcinoma metastasis presenting as a pineal region tumor

A. Kakita, Hitoshi Takahashi, T. Morita, 2003, Neuropathology : official journal of the Japanese Society of Neuropathology.

Alteration of midkine expression in the ischemic brain of humans

K. Oyanagi, T. Morita, M. Wada, 2002, Journal of the Neurological Sciences.

Survival motor neuron (SMN) protein in the spinal anterior horn cells of patients with sporadic amyotrophic lateral sclerosis

A. Kakita, T. Mizutani, Hitoshi Takahashi, 2011, Brain Research.

Widespread ischemic brain lesions caused by vasculopathy associated with neurofibromatosis type 1

A. Kakita, Hitoshi Takahashi, Hajime Tanaka, 2010, Neuropathology : official journal of the Japanese Society of Neuropathology.

Cerebellar involvement in progressive supranuclear palsy: A clinicopathological study

A. Kakita, Hitoshi Takahashi, T. Shimohata, 2009, Movement disorders : official journal of the Movement Disorder Society.

Pursuit of the origin of the large myelinated fibers of the anterolateral funiculus in the spinal cord in humans in relation to the pathomechanism in amyotrophic lateral sclerosis

Hitoshi Takahashi, K. Oyanagi, T. Morita, 1999, Acta Neuropathologica.

Mutation-induced loss of APP function causes GABAergic depletion in recessive familial Alzheimer’s disease: analysis of Osaka mutation-knockin mice

T. Miyakawa, A. Takashima, H. Mori, 2017, Acta Neuropathologica Communications.

The phenotype spectrum of Japanese multiple system atrophy

A. Kakita, T. Shimohata, K. Wakabayashi, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

Primary progressive aphasia with focal glial tauopathy

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

Lewy bodies in the lower sacral parasympathetic neurons of a patient with Parkinson's disease

S. Takeda, K. Oyanagi, K. Wakabayashi, 2004, Acta Neuropathologica.

Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and Lewy body pathology

T. Iwatsubo, M. Hasegawa, K. Wakabayashi, 2000, Acta Neuropathologica.

Widespread occurrence of α‐synuclein/NACP‐immunoreactive neuronal inclusions in juvenileand adult‐onset Hallervorden–Spatz diseasewith Lewy bodies

K. Wakabayashi, M. Yoshimoto, T. Morita, 1999 .

Malignant potential of hepatic angiomyolipoma: case report and literature review

K. Kamimura, K. Kimura, T. Morita, 2010, Clinical journal of gastroenterology.