T. Imai

发表

Motor neuron disease with slow eye movements and vertical gaze palsy

B. Okuda, T. Yamamoto, M. Yamasaki, 1992, Acta neurologica Scandinavica.

Acute ventilatory failure in multiple sclerosis

M. Yamasaki, T. Imai, Toru Yamamoto, 1989, Journal of the Neurological Sciences.

Marked increase in cerebrospinal fluid ubiquitin in Creutzfeldt-Jakob disease

Takeo Kato, K. Kujirai, T. Kawanami, 1992, Neuroscience Letters.

Ataxic variant of adrenoleukodystrophy: MRI and CT findings

H. Kusaka, T. Imai, 1992, Journal of Neurology.

A Case of Diffuse Lewy Body and Alzheimer's Diseases with Periodic Synchronous Discharges

T. Imai, Toru Yamamoto, 1988, Journal of neuropathology and experimental neurology.

Hidefumi Ito, T. Imai, Junichiro Kawamura, 1998, Journal of neurology, neurosurgery, and psychiatry.

Exon skipping caused by a base substitution at a splice site in the GTP cyclohydrolase I gene in a Japanese family with hereditary progressive dystonia dopa responsive dystonia.

H. Ito, Y. Nagai, T. Imai, 1995, Biochemical and biophysical research communications.

Ubiquitin-positive inclusion in anterior horn cells in subgroups of motor neuron diseases: A comparative study of adult-onset amyotrophic lateral sclerosis, juvenile amyotrophic lateral sclerosis and werdnig-hoffmann disease

H. Kusaka, S. Goto, T. Imai, 1993, Journal of the Neurological Sciences.

IgM M‐protein with antibody activity against gangliosides with disialosyl residue in sensory neuropathy binds to sensory neurons

J. Kimura, S. Kusunoki, R. Kaji, 1996, Muscle & nerve.

Adult-onset motor neuron disease with basophilic intraneuronal inclusion bodies.

H. Kusaka, T. Imai, S. Matsumoto, 1993, Clinical neuropathology.

Mutant GTP cyclohydrolase I mRNA levels contribute to dopa‐responsive dystonia onset

H. Ito, T. Imai, S. Ueno, 1996, Annals of neurology.

Spontaneous remission of a massive CNS inflammation with eosinophilic infiltrate.

Hidefumi Ito, T. Imai, S. Matsumoto, 2003, Internal medicine.

α-Tocopherol transfer protein gene: Exon skipping of all transcripts causes ataxia

H. Ito, H. Kusaka, T. Imai, 1997, Neurology.

Expression and Translocation of Aquaporin‐2 in the Endolymphatic Sac in Patients with Meniere’s Disease

H. Inohara, H. Kiyama, T. Kitahara, 2010, Journal of neuroendocrinology.

[A case of cerebral paragonimiasis with intracerebral hemorrhage as initial finding].

B. Okuda, M. Yamasaki, K. Maya, 1985, Rinsho shinkeigaku = Clinical neurology.

Intraductal mucin-producing tumors of the pancreas.

T. Imai, T. Yamamoto, Y. Kawarada, 1992, The American journal of gastroenterology.

[Adenoid cystic carcinoma presenting as cavernous sinus syndrome: a clinico-pathological study of two cases].

T. Yamamoto, T. Imai, 1989, No to shinkei = Brain and nerve.

Epithelium-lined cyst of the pretectal region: case report and electron microscope study.

H. Kusaka, T. Imai, T. Nishioka, 1989, Surgical neurology.

Intracisternal inclusions in Schwann cells of the sural nerve

H. Kusaka, T. Imai, 1992, Acta Neuropathologica.

Anaphylactoid purpura with cardiac involvement.

T. Imai, S. Matsumoto, 1970, Archives of disease in childhood.

Golgi apparatus and intraneuronal inclusions of anterior horn cells in amyotrophic lateral sclerosis: an immunohistochemical study

H. Kusaka, Hidefumi Ito, T. Imai, 1996, Acta Neuropathologica.

Striatal efferent involvement and its correlation to levodopa efficacy in patients with multiple system atrophy

H. Kusaka, T. Imai, H Ito, 1996, Neurology.

Clinicopathologic investigation of a family with expanded SCA8 CTA/CTG repeats

H. Ito, H. Kusaka, H. Kawakami, 2006, Neurology.

A sensory level on the trunk in lower lateral brainstem lesions

B. Okuda, T. Imai, S. Matsumoto, 1988, Neurology.

Retrograde pyramidal tract degeneration in a patient with cervical haematomyelia.

T. Yamamoto, M. Yamasaki, T. Imai, 1989, Journal of neurology, neurosurgery, and psychiatry.

Cheiro-oral syndrome with bilateral oral involvement: a study of pontine lesions by high-resolution magnetic resonance imaging.

S. Kaku, M. Yamasaki, T. Imai, 1989, Journal of neurology, neurosurgery, and psychiatry.

Ultrastructural study of chromatolytic neurons in an adult-onset sporadic case of amyotrophic lateral sclerosis

H. Kusaka, T. Yamamoto, M. Yamasaki, 2004, Acta Neuropathologica.

Retrograde pyramidal tractdegeneration inapatient withcervical haematomyelia

M. Yamasaki, T. Imai, Toru Yamamoto, 2017 .

Topographic involvement of the striatal efferents in basal ganglia of patients with adult-onset motor neuron disease with basophilic inclusions

H. Kusaka, Hidefumi Ito, T. Imai, 2004, Acta Neuropathologica.

An adult-onset case of sporadic motor neuron disease with basophilic inclusions

H. Kusaka, T. Imai, S. Matsumoto, 2004, Acta Neuropathologica.

[A comparative immunohistochemical study of ubiquitin-positive skein-like inclusions in anterior horn neurons in subgroups of adult-onset motor neuron diseases].

H. Ito, H. Kusaka, M. Yamasaki, 1993, Rinsho shinkeigaku = Clinical neurology.

Pathology of motor neurons in amyotrophic lateral sclerosis with dementia.

H. Kusaka, T. Imai, 1993, Clinical Neuropathology.

Sporadic amyotrophic lateral sclerosis with dementia and Cu/Zn superoxide dismutase-positive Lewy body-like inclusions.

N. Shibata, H. Ito, H. Kusaka, 1996, Clinical neuropathology.

Synaptic pathology of spinal anterior horn cells in amyotrophic lateral sclerosis: An immunohistochemical study

H. Kusaka, S. Goto, Hidefumi Ito, 1994, Journal of the Neurological Sciences.