Asymmetrical enhancement of middle-latency auditory evoked fields with aging (2003)
Yamada,T., Nakamura,A., Horibe,K., Washimi,Y., Bundo,M., Kato,T., ...
We studied the effects of aging on middle-latency auditory evoked fields (P50m), and analyzed their interhemispheric differences. Magnetic responses following tone-burst stimuli to the right ear were...
Asymmetrical enhancement of middle-latency auditory evoked fields with aging (2003)
Yamada,T., Nakamura,A., Horibe,K., Washimi,Y., Bundo,M., Kato,T., ...
We studied the effects of aging on middle-latency auditory evoked fields (P50m), and analyzed their interhemispheric differences. Magnetic responses following tone-burst stimuli to the right ear were...
Asymmetrical enhancement of middle-latency auditory evoked fields with aging (2003)
Yamada, T., Nakamura, A., Horibe, K., Washimi, Y., Bundo, M., Kato, T., ...
We studied the effects of aging on middle-latency auditory evoked fields (P50m), and analyzed their interhemispheric differences. Magnetic responses following tone-burst stimuli to the right ear were...
Asymmetrical enhancement of middle-latency auditory evoked fields with aging (2003)
Yamada, T., Nakamura, Akinori, Horibe, K., Washimi, Y., Bundo, M., Kato, T., ...
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Sato, T, Oyake, M, Nakamura, K, Nakao, K, Fukusima, Y, Onodera, O, ...
Mismatched nucleotides may facilitate expansion of trinucleotide repeats in genetic diseases (1998)
Nakayabu, M, Miwa, S, Suzuki, M, Izuta, S, Sobue, G, Yoshida, S
Founder effect in spinal and bulbar muscular atrophy (SBMA) (1996)
Tanaka, F, Doyu, M, Ito, Y, Matsumoto, M, Mitsuma, T, Abe, K, ...
Mismatched nucleotides may facilitate expansion of trinucleotide repeats in genetic diseases.
Nakayabu, M, Miwa, S, Suzuki, M, Izuta, S, Sobue, G, Yoshida, S
We have studied the contribution of mismatch sequences to the trinucleotide repeat expansion that causes hereditary diseases. Using an oligonucleotide duplex, (CAG)5/(CTG)5, as a template-primer, DNA...
Mismatched nucleotides may facilitate expansion of trinucleotide repeats in genetic diseases.
Nakayabu, M, Miwa, S, Suzuki, M, Izuta, S, Sobue, G, Yoshida, S
We have studied the contribution of mismatch sequences to the trinucleotide repeat expansion that causes hereditary diseases. Using an oligonucleotide duplex, (CAG)5/(CTG)5, as a template-primer, DNA...
Central motor and sensory conduction in X-linked recessive bulbospinal neuronopathy.
Central conduction was studied in 12 patients with X-linked recessive bulbospinal neuronopathy (XBSN) using percutaneous electrical cortical, cervical and lumbar stimulation and somatosensory evoked...
Sensory conduction study in chronic sensory ataxic neuropathy.
Kachi, T, Sobue, G, Yamamoto, M, Igata, A
Sensory conduction was studied in six patients with chronic sensory ataxic neuropathy of an idiopathic type and associated with Sjögren's syndrome. Motor nerve conduction velocities were normal in...
Homozygosity for Machado-Joseph disease gene enhances phenotypic severity.
Sobue, G, Doyu, M, Nakao, N, Shimada, N, Mitsuma, T, Maruyama, H, ...
Charcot-Marie-Tooth families in Japan with MPZ Thr124Met mutation
Kurihara, S, Adachi, Y, Imai, C, Araki, H, Hattori, N, Numakura, C, ...
Ohmori, H, Ando, Y, Makita, Y, Onouchi, Y, Nakajima, T, Saraiva, M, ...
Axonal and perikaryal involvement in chronic inflammatory demyelinating polyneuropathy
Nagamatsu, M, Terao, S, Misu, K, Li, M, Hattori, N, Ichimura, M, ...
OBJECTIVES—To assess the extent of loss of myelinated nerve fibres and spinal motor neuron loss in chronic inflammatory demyelinating polyneuropathy (CIDP), a clinicopathological study was...
Course and distribution of facial corticobulbar tract fibres in the lower brain stem
Terao, S, Miura, N, Takeda, A, Takahashi, A, Mitsuma, T, Sobue, G
The course and distribution of the facial corticobulbar tract (CBT) was examined by correlating MRI of brain stem lesions with neurological symptoms and signs including central (C-FP) or peripheral...
Coexisting vertical and horizontal one and a half syndromes
TERAO, S, OSANO, Y, FUKUOKA, T, MIURA, N, MITSUMA, T, SOBUE, G
Misu, K, Yoshihara, T, Shikama, Y, Awaki, E, Yamamoto, M, Hattori, N, ...
OBJECTIVES AND METHODS—Seven families were studied with an axonal form of Charcot-Marie-Tooth disease (CMT) associated with mutations in the peripheral myelin protein zero (MPZ) gene—Thr124Met or...
Watanabe, H, Ieda, T, Katayama, T, Takeda, A, Aiba, I, Doyu, M, ...
Cardiac 123I-meta-iodobenzylguanidine (MIBG) uptake was measured in 11 patients with dementia with Lewy bodies (DLB), 10 patients with Alzheimer's disease (AD), and 10 age matched control subjects....
Postgastrectomy polyneuropathy with thiamine deficiency
Koike, H, Misu, K, Hattori, N, Ito, S, Ichimura, M, Ito, H, ...
OBJECTIVE—Polyneuropathy has been reported after gastrectomy performed to treat various lesions. Although thiamine deficiency is a possible cause of this neuropathy, the pathogenesis still remains...
Hamada, K, Hirayama, M, Watanabe, H, Kobayashi, R, Ito, H, Ieda, T, ...
Objectives: To elucidate the factors associated with severity of cardiac sympathetic nerve involvement in idiopathic Parkinson's disease (PD).
Abe, Y, Kachi, T, Kato, T, Arahata, Y, Yamada, T, Washimi, Y, ...
Objective: The purpose of this study was to analyse changes in regional cerebral blood flow (rCBF) in Parkinson's disease (PD) without dementia.
Hirayama, M, Fukatsu, H, Watanabe, H, Koike, Y, Noda, A, Ito, H, ...
Sjögren's syndrome associated painful sensory neuropathy without sensory ataxia
Mori, K, Iijima, M, Sugiura, M, Koike, H, Hattori, N, Ito, H, ...
Charcot-Marie-Tooth families in Japan with MPZ Thr124Met mutation
Kurihara, S, Adachi, Y, Imai, C, Araki, H, Hattori, N, Numakura, C, ...
Objective: To investigate the clinical manifestations of the axonal or demyelinating forms of the Japanese MPZ Thr124Met mutation originating in four different areas: Tottori, Nara, Aichi, and...
Primary lateral sclerosis presenting parkinsonian symptoms without nigrostriatal involvement
Mabuchi, N, Watanabe, H, Atsuta, N, Hirayama, M, Ito, H, Fukatsu, H, ...
Relationship between stridor and sleep apnoea syndrome: is it as simple as that?
Ghorayeb, I, Bioulac, B, Tison, F, Hirayama, M, Sobue, G, Fukatsu, H, ...
Interferon alfa treatment for Sjögren's syndrome associated neuropathy
Yamada, S, Mori, K, Matsuo, K, Inukai, A, Kawagashira, Y, Sobue, G
An unusual phenotype of McLeod syndrome with late onset axonal neuropathy
Wada, M, Kimura, M, Daimon, M, Kurita, K, Kato, T, Johmura, Y, ...
Watanabe, H, Fukatsu, H, Katsuno, M, Sugiura, M, Hamada, K, Okada, Y, ...
Objective: We performed 1H-MR spectroscopy (1H-MRS) on multiple brain regions to determine the metabolite pattern and diagnostic utility of 1H-MRS in multiple system atrophy (MSA).
Mori, K, Koike, H, Misu, K, Hattori, N, Ichimura, M, Sobue, G
OBJECTIVES—To determine spinal cord MRI findings in neuronopathy associated with Sjögren's syndrome and their correlation with severity of sensory impairment. METHODS—Clinical and...
Terao, S, Takatsu, S, Izumi, M, Takagi, J, Mitsuma, T, Takahashi, A, ...
Two patients are reported with contralateral hemiparesis including a face of supranuclear type, caused by an infarct of the unilateral ventromedial part of the upper medulla. Data from these patients...
Skin sympathetic nerve activity in Guillain-Barré syndrome: a microneurographic study
Yamamoto, K., Sobue, G., Iwase, S., Nagamatsu, M., Mano, T., Mitsuma, T.
To assess autonomic dysfunction, skin sympathetic nerve activity (SSNA) of four patients with Guillain-Barré syndrome was microneurographically studied in the acute and remission phase. Autonomic...
TERAO, S, IZUMI, M, TAKATSU, S, TAKAGI, J, MITSUMA, T, TAKEDA, A, ...
Progression and prognosis in pure autonomic failure (PAF): comparison with multiple system atrophy
Mabuchi, N, Hirayama, M, Koike, Y, Watanabe, H, Ito, H, Kobayashi, R, ...
Objective: To clarify the progression of autonomic symptoms and functional deterioration in pure autonomic failure (PAF), particularly in comparison with multiple system atrophy (MSA).
Age associated axonal features in HNPP with 17p11.2 deletion in Japan
Koike, H, Hirayama, M, Yamamoto, M, Ito, H, Hattori, N, Umehara, F, ...
Objective: To clarify age related changes in the clinicopathological features of hereditary neuropathy with liability to pressure palsy (HNPP) in Japanese patients with deletion of 17p11.2,...