T. Nagashima

发表

Respiratory Abnormalities in Neuromuscular Disorders

T. Nagashima, 1991 .

Ocular Motor Disorders in Mitochondrial Encephalopathy With Lactic Acid and Stroke-Like Episodes With the 3271 (T-C) Point Mutation in Mitochondrial DNA

Y. Shinmei, M. Kase, Kazuhiko Yoshida, 2007, Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.

Meningeal large granular lymphocyte lymphoma

K. Kazumata, K. Nagashima, H. Hasegawa, 1998 .

Wernicke encephalopathy-like symptoms as an early manifestation of Creutzfeldt–Jakob disease in a chronic alcoholic

M. Okawa, Hidehiro Takahashi, K. Nagashima, 1999, Journal of the Neurological Sciences.

Adult T‐cell lymphoma involving the leptomeninges associated with a spinal cord schwannoma

A. Stan, T. Itoh, Y. Okada, 2001, Neuropathology : official journal of the Japanese Society of Neuropathology.

Clinicopathological studies of peripheral neuropathy in Churg–Strauss syndrome

T. Oshikiri, T. Chuma, Y. Orba, 2002, Neuropathology : official journal of the Japanese Society of Neuropathology.

Clinicopathological and virological analyses of familial human T-lymphotropic virus type I-associated polyneuropathy

T. Chuma, N. Tachi, W. Hall, 2005, Journal of NeuroVirology.

Chronic demyelinating polyneuropathy in graft‐versus‐host disease following allogeneic bone marrow transplantation

T. Chuma, Y. Orba, K. Nagashima, 2002, Neuropathology : official journal of the Japanese Society of Neuropathology.

Familial bulbo-spinal muscular atrophy associated with testicular atrophy and sensory neuropathy (Kennedy-Alter-Sung syndrome) Autopsy case report of two brothers

T. Nagashima, Y. Morimatsu, K. Hirose, 1988, Journal of the Neurological Sciences.

Pseudopseudohypoparathyroidism with recurrent polyneuropathy: an autopsy report with special reference to the peripheral nervous system

T. Kanda, M. Oda, T. Nagashima, 1991, Journal of the Neurological Sciences.

Clinical classification of 103 Japanese patients with Guillain-Barré syndrome

K. Hirata, N. Kokubun, N. Yuki, 2016, Journal of the Neurological Sciences.

Creatine kinase (CK)-linked IgA in Isaacs' syndrome An immune complex disease?

K. Nagashima, T. Nagashima, K. Hirose, 1985, Journal of the Neurological Sciences.

Cerebral vasculitis in chronic mucocutaneous candidiasis: autopsy case report.

A. Stan, Y. Sakiyama, K. Nagashima, 2000 .

Cerebral vasculitis in chronic mucocutaneous candidiasis: Autopsy case report

A. Stan, Y. Sakiyama, K. Nagashima, 2000, Neuropathology : official journal of the Japanese Society of Neuropathology.

MYOGLOBIN IMMUNOHISTOCHEMICAL STUDIES ON RHABDOMYOLYSIS WITH ACUTE RENAL FAILURE

K. Nagashima, T. Nagashima, H. Tanabe, 1987 .

" Retinal Migraine " is an Oxymoron

N. Newman, M. Kase, R. Daroff, 2019 .

P‐ANCA‐positive Wegener’s granulomatosis presenting with hypertrophic pachymeningitis and multiple cranial neuropathies: Case report and review of literature

T. Itoh, K. Nagashima, T. Seki, 2000, Neuropathology : official journal of the Japanese Society of Neuropathology.

Cortical deafness in multiple sclerosis

S. Tsuji, T. Tabira, T. Nagashima, 1981, Journal of neurology, neurosurgery, and psychiatry.

Anti‐Hu paraneoplastic syndrome presenting with brainstem‐cerebellar symptoms and Lambert–Eaton myasthenic syndrome

T. Chuma, T. Itoh, Y. Orba, 2003, Neuropathology : official journal of the Japanese Society of Neuropathology.

Adult Leigh syndrome with mitochondrial DNA mutation at 8993

K. Nagashima, H. Nishihara, T. Nagashima, 1999, Acta Neuropathologica.

Dysferlinopathy associated with rigid spine syndrome

I. Nonaka, Y. Hayashi, I. Nishino, 2004, Neuropathology : official journal of the Japanese Society of Neuropathology.

A mitochondrial encephalo-myo-neuropathy with a nucleotide position 3271 (T-C) point mutation in the mitochondrial DNA

I. Nonaka, T. Chuma, K. Nagashima, 2001, Neuromuscular Disorders.

Oculopharyngeal muscular dystrophy in a Japanese family with a short GCG expansion (GCG)11 in PABP2 gene

M. Kase, I. Nonaka, T. Chuma, 2000, Neuromuscular Disorders.

IMMUNOHISTOCHEMICAL LOCALIZATION OF PROTEIN KINASE C ISOZYMES IN HUMAN CEREBELLUM, HIPPOCAMPUS AND SPINAL CORD

H. Hidaka, K. Nagashima, Y. Fujioka, 1991 .

Multiple sclerosis co-existent with myxedema An autopsy case report

K. Nagashima, T. Nagashima, Katsuhiro Yamada, 1984, Journal of the Neurological Sciences.

[Congenital facioscapulohumeral muscular dystrophy associated with tongue atrophy and sensorineural hearing disturbance].

T. Shimizu, H. Hayashi, T. Nagashima, 1991, Rinsho shinkeigaku = Clinical neurology.

DEMONSTRATION OF NEURONAL LOCALIZATION IN ONUFROWCZ'S GROUP-X IN RABBIT BY DOUBLE LABELING METHOD

H. Yamada, T. Nagashima, H. Beppu, 1979 .

REAPPRAISAL FOR PHRENIC MOTOR INNERVATION IN KITTENS BY HRP AND FLUORESCENT DUAL LABELING STUDIES

H. Yamada, T. Nagashima, H. Beppu, 1980 .

[Adrenomyeloneuropathy associated with congenital cataract--report of a family with MRI study].

T. Komori, T. Nagashima, K. Hirose, 1988, Rinshō shinkeigaku Clinical neurology.

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein.

I. Kanazawa, S. Tsuji, Koichiro Nakamura, 2001, Human molecular genetics.

[Postpolio late progressive muscular atrophy--clinical and epidemiologic analyses in 4 Japanese cases].

T. Komori, M. Sakurai, T. Nagashima, 1990, Rinshō shinkeigaku Clinical neurology.

[Ocular motor abnormalities in progressive supranuclear palsy].

T. Nagashima, K. Hirose, H. Tanabe, 1989, No to shinkei = Brain and nerve.