T. Yamada

发表

Investigating the relationship between stroke and obstructive sleep apnea.

V. Somers, Thoru Yamada, M. Dyken, 1996, Stroke.

13.5-Tb/s (135 × 111-Gb/s/ch) no-guard-interval coherent OFDM transmission over 6,248 km using SNR maximized second-order DRA in the extended L-band

E. Yamazaki, S. Matsuoka, Y. Miyamoto, 2009, 2009 Conference on Optical Fiber Communication - incudes post deadline papers.

Central achromatopsia

A. Damasio, H. Damasio, H. Damasio, 1980, Neurology.

Diagnosing rhythmic movement disorder with video-polysomnography.

M. Dyken, T. Yamada, D. Lin-Dyken, 1997, Pediatric neurology.

Three novel mutations (G27E, insAAC, R179X) in the ORNT1 gene of Japanese patients with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome

J. Kira, S. Tsujino, Y. Eto, 2000, Annals of neurology.

[A case of neuro-Behçet's disease presenting as chronic progressive cerebellar ataxia].

J. Kira, T. Taniwaki, T. Yamada, 2000, Rinsho shinkeigaku = Clinical neurology.

Amplification of JC virus regulatory DNA sequences from cerebrospinal fluid: diagnostic value for progressive multifocal leukoencephalopathy

Y. Itoyama, K. Fujihara, J. Kira, 1998, Archives of Virology.

Effect of swallowing training on swallowing disorders in Parkinson's disease.

T. Kachi, T. Yamada, M. Nagaya, 2000, Scandinavian journal of rehabilitation medicine.

Selective increase in cellular A beta 42 is related to apoptosis but not necrosis.

A. Tomlinson, Stephen Naylor, S. Younkin, 2000, Neuroreport.

[Hepatic involvement in a case of lysosomal glycogen storage disease with normal acid maltase].

J. Kira, I. Nonaka, T. Yamada, 1999, Rinsho shinkeigaku = Clinical neurology.

Familial Creutzfeldt-Jakob disease with D178N-129M mutation ofPRNP presenting as cerebellar ataxia without insomnia

H. Shigeto, T. Iwaki, J. Kira, 2000, Journal of Neurology Neurosurgery & Psychiatry.

Increased CSF C4d in demyelinating neuropathy indicates the radicular involvement

K. Hirayama, T. Yamada, S. Kuwabara, 1995, Acta neurologica Scandinavica.

Lovastatin does not correct the accumulation of very long-chain fatty acids in tissues of adrenoleukodystrophy protein-deficient mice

J. Kira, T. Taniwaki, T. Yamada, 2000, Journal of Inherited Metabolic Disease.

[Diaphragmatic myoclonus of spinal origin].

K. Hirayama, T. Yamada, H. Shinotoh, 1986, Rinsho shinkeigaku = Clinical neurology.

Autosomal dominant limb‐girdle muscular dystrophy with ankle joint contracture

J. Kira, K. Tanaka, T. Yamada, 1999, Acta neurologica Scandinavica.

Periodic alternating nystagmus in a patient with MS

T. Yamada, Y. Ohyagi, T. Nakagawa, 2001, Neurology.

[Osteoporosis and fractures in Parkinson's disease].

T. Kachi, T. Yamada, K. Ando, 1995, Nihon Ronen Igakkai zasshi. Japanese journal of geriatrics.

Sensory conduction study of cisplatin neuropathy: preservation of small myelinated fibers.

T. Kachi, G. Sobue, T. Yamada, 1997, Internal medicine.

Increased concentration of C4d complement protein in the cerebrospinal fluids in progressive supranuclear palsy

K. Hirayama, T. Yamada, M. Asahina, 1994, Acta neurologica Scandinavica.

[A patient with motor neuron syndrome clinically similar to amyotrophic lateral sclerosis, presenting spontaneous recovery].

S. Tsuji, J. Kira, T. Yamada, 2000, Rinsho shinkeigaku = Clinical neurology.

Juvenile Parkinsonism with Marked Diurnal Fluctuation

K. Hirayama, T. Yamada, Y. Koguchi, 1989, The Japanese journal of psychiatry and neurology.

[An autopsy case with lower motor neuron disease showing a transient-appearance of anti-GM1 antibody and an improvement of conduction block after gamma-globulin administration].

T. Iwaki, J. Kira, T. Taniwaki, 1999, No to shinkei = Brain and nerve.

Occipital hypoperfusion in Parkinson’s disease without dementia: correlation to impaired cortical visual processing

Takashi Kato, Kengo Ito, Y. Abe, 2003, Journal of neurology, neurosurgery, and psychiatry.

[Serial MRI findings in patients with CNS cryptococcosis].

T. Yamada, S. Terao, T. Mitsuma, 1998, Rinsho shinkeigaku = Clinical neurology.

Congenital myopathy with myasthenic features and congenital cataract in two siblings

T. Yamada, T. Kitaguchi, T. Kobayashi, 1989, Journal of Neurology.

Nonhaemorrhagic thalamic infarction. Clinical, neuropsychological and electrophysiological findings in four anatomical groups defined by computerized tomography.

A. Damasio, H. Damasio, P. Eslinger, 1985, Brain : a journal of neurology.

Pontine lesion in opsoclonus-myoclonus syndrome shown by MRI.

K. Hirayama, T. Yamada, T. Hattori, 1988, Journal of neurology, neurosurgery, and psychiatry.

Histopathology of the nonrefluxing megaloureter: a clue to its pathogenesis.

T. Koyanagi, T. Yamada, S. Tokunaka, 1982, The Journal of urology.

Adrenoleukodystrophy protein-deficient mice represent abnormality of very long chain fatty acid metabolism.

T. Yamada, Takurou Kobayashi, A. Kondo, 1997, Biochemical and biophysical research communications.

HLA-DPB1*0501-associated opticospinal multiple sclerosis: clinical, neuroimaging and immunogenetic studies.

F. Mihara, J. Kira, Y. Nishimura, 1999, Brain : a journal of neurology.

A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1

H Furuya, T Sasazuki, J. Kira, 2001, Neurology.

Adrenoleukodystrophy protein enhances association of very long-chain acyl-coenzyme A synthetase with the peroxisome

J. Kira, T. Taniwaki, T. Yamada, 1999, Neurology.

Adrenoleukodystrophy gene encodes an 80 kDa membrane protein.

T. Iwaki, T. Yamada, I. Goto, 1994, Biochemical and biophysical research communications.

Focal cervical poliopathy causing juvenile muscular atrophy of distal upper extremity: a pathological study.

K. Hirayama, T. Yamada, M. Tomonaga, 1987, Journal of neurology, neurosurgery, and psychiatry.

Cavernous haemangioma in the oculomotor nerve

S. Nishio, M. Fukui, T. Yamada, 1986, Journal of Neurology.

Diagnosing narcolepsy through the simultaneous clinical and electrophysiologic analysis of cataplexy.

M. Dyken, T. Yamada, M. Yeh, 1996, Archives of neurology.

[An adult case of peripheral facial nerve palsy following acute cerebellitis associated with high antibody titers against varicella-zoster virus].

J. Kira, T. Taniwaki, T. Yamada, 1998, Rinsho shinkeigaku = Clinical neurology.

[A case of Gerstmann-Sträussler-Scheinker syndrome (GSS) with late onset--a haplotype analysis of Glu219Lys polymorphism in PrP gene].

T. Iwaki, J. Kira, K. Doh-ura, 2001, Rinsho shinkeigaku = Clinical neurology.

POEMS syndrome with necrotizing vasculitis: A novel feature of vascular abnormalities

Y. Fukuuchi, T. Yamada, A. Koto, 2000, Neurology.

Nonhemorrhagic infarction of the thalamus

A. Damasio, P. Eslinger, N. Graff-Radford, 1984, Neurology.

Covert orienting attention in Parkinson's disease.

K. Hirayama, M. Schulzer, T. Yamada, 1990, Journal of neurology, neurosurgery, and psychiatry.

Hyperprolactinemia in optico-spinal multiple sclerosis.

J. Kira, T. Yamada, Y. Ohyagi, 2000, Internal medicine.

Violent sleep-related behavior leading to subdural hemorrhage.

Thoru Yamada, M. Dyken, T. Yamada, 1995, Archives of neurology.

[A case of MELAS presenting complex partial status epilepticus].

T. Yamada, K. Ishido, K. Kamikaseda, 2001, Rinsho shinkeigaku = Clinical neurology.

[An adult case of primary antiphospholipid syndrome presenting recurrent anterior spinal artery syndrome].

J. Kira, T. Yamada, Y. Ohyagi, 2001, Rinsho shinkeigaku = Clinical neurology.

Inclusion body myositis associated with hepatitis C virus infection.

T Yamamoto, H Furuya, J. Kira, 2001, Fukuoka igaku zasshi = Hukuoka acta medica.

Acute measles encephalitis in adults

Z. Wszolek, H. Inoue, T. Yamada, 2005, Journal of Neurology.

Narcolepsy: Unequivocal diagnosis after split‐screen, video‐polysomnographic analysis of a prolonged cataplectic attack

M. Dyken, T. Yamada, D. Lin-Dyken, 1994, Neurology.

[Central motor conduction time in the pseudopolyneuritic form of amyotrophic lateral sclerosis].

T. Kachi, G. Sobue, T. Yamada, 1991, Rinshō shinkeigaku Clinical neurology.

Anti-Ri-associated paraneoplastic cerebellar degeneration without opsoclonus in a patient with a neuroendocrine carcinoma of the stomach.

H. Shigeto, T. Iwaki, J. Kira, 2000, Fukuoka igaku zasshi = Hukuoka acta medica.

Striatonigral degeneration with motor neuron disease

J. Kira, T. Taniwaki, T. Yamada, 2000, Journal of Neurology.

A novel mutation of the GTP‐cyclohydrolase I gene in a patient with hereditary progressive dystoniddopa‐responsive dystonia

J. Kira, T. Taniwaki, T. Yamada, 1998, Neurology.

Erratum: Increased HTLV-I proviral DNA in HTLV-I-associated myelopathy: A quantitative polymerase chain reaction study (Ann Neurol (Feb. 1991) 29 (194-201))

Y. Sakaki, Y. Itoyama, J. Kira, 1991 .

Autosomal dominant familial spinal and bulbar muscular atrophy with gynecomastia

K Ikezoe, H Furuya, J. Kira, 1999, Neurology.

[A case of spinal myoclonus associated with epidural block for lumbago].

J. Kira, T. Taniwaki, T. Yamada, 1999, Rinsho shinkeigaku = Clinical neurology.

[A case of cervical myelopathy due to dural arteriovenous fistula at the craniocervical junction].

J. Kira, T. Taniwaki, T. Yamada, 1999, Rinsho shinkeigaku = Clinical neurology.

Raymond syndrome (alternating abducent hemiplegia) caused by a small haematoma at the medial pontomedullary junction.

J. Kira, T. Yamada, M. Satake, 1995, Journal of neurology, neurosurgery, and psychiatry.

[Myelopathy due to vitamin B12 deficiency presenting only sensory disturbances in upper extremities: a case report].

J. Kira, T. Taniwaki, T. Yamada, 1997, Rinsho shinkeigaku = Clinical neurology.

Adult‐onset hereditary sensory and autonomic neuropathy accompanied by anosmia but without skin ulceration

J. Kira, T. Taniwaki, A. Ohnishi, 2001, Acta neurologica Scandinavica.

Occipital hypoperfusion in Parkinson’s disease without dementia: correlation to impaired cortical visual processing

Takashi Kato, Kengo Ito, Y. Abe, 2003, Journal of neurology, neurosurgery, and psychiatry.

Fourteen and six c/sec positive bursts in comatose patients.

K. A. Kooi, R. Tucker, T. Yamada, 1976, Electroencephalography and clinical neurophysiology.