Search Results - "Furiya, Y"

Construction and Quality Evaluation of the Japanese Sarcopenic Dysphagia Database by Mizuno, S., Wakabayashi, Hidetaka, Fujishima, I., Kishima, M., Itoda, M., Yamakawa, M., Wada, F., Kato, R., Furiya, Y., Nishioka, S., Momosaki, R.

“…Objectives To describe the activity and evaluate the quality of the Japanese sarcopenic dysphagia database. Design Cohort registry study. Setting 19 hospitals…”
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Sarcopenia Is Associated with Fecal Incontinence in Patients with Dysphagia: Implication for Anal Sarcopenia by Mizuno, S., Wakabayashi, Hidetaka, Yamakawa, M., Wada, F., Kato, R., Furiya, Y., Nishioka, S., Momosaki, R.

“…Objectives To examine the relationship between sarcopenia and fecal incontinence in patients with dysphagia. Design Cross-sectional study using the Japanese…”
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Global and Region-Specific Analyses of Apparent Diffusion Coefficient in Dentatorubral-Pallidoluysian Atrophy by Kin, T, Hirano, M, Taoka, T, Furiya, Y, Kataoka, H, Kichikawa, K, Ueno, S

“…Dentatorubral-pallidoluysian atrophy (DRPLA) is an autosomal dominant spinocerebellar ataxia. Techniques for the quantitative assessment of neurodegenerative…”
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Peripheral neuropathy in chromosome16q22.1 linked autosomal dominant cerebellar ataxia by Furiya, Yoshiko, Hirano, Makito, Nomura, Masami, Asai, Hidehiro, Kiriyama, Takao, Ueno, Satoshi

“…Autosomal dominant cerebellar ataxia (ADCA) includes heterogeneous neurodegenerative diseases with or without various neurological signs and symptoms. Ishikawa…”
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Rivastigmine improves patients’ appetite by increasing serum active ghrelin and cortisol in Alzheimer’s disease by Furiya, Y., Tomiyama, T., Oba, N., Ikeda, M., Ueno, S.

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ALADIN^{I482S}$Causes Selective Failure of Nuclear Protein Import and Hypersensitivity to Oxidative Stress in Triple A Syndrome by Hirano, Makito, Furiya, Yoshiko, Asai, Hirohide, Yasui, Akira, Ueno, Satoshi

“…Triple A syndrome is an autosomal recessive neuroendocrinological disease caused by mutations in a gene that encodes 546 amino acid residues. The encoded…”
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Racemization of Asp23 residue affects the aggregation properties of Alzheimer amyloid beta protein analogues by TOMIYAMA, T, ASANO, S, FURIYA, Y, SHIRASAWA, T, ENDO, N, MORI, H

“…The beta proteins in amyloid deposits of Alzheimer's disease have been found to be racemized and/or isomerized at their Asp residues (Roher, A. E., Lowenson,…”
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Restoration of nuclear-import failure caused by triple A syndrome and oxidative stress by Kiriyama, Takao, Hirano, Makito, Asai, Hirohide, Ikeda, Masanori, Furiya, Yoshiko, Ueno, Satoshi

“…Triple A syndrome is an autosomal recessive neurological disease, mimicking motor neuron disease, and is caused by mutant ALADIN, a nuclear-pore complex…”
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Humanin detected in skeletal muscles of MELAS patients: a possible new therapeutic agent by Kariya, Shingo, Hirano, Makito, Furiya, Yoshiko, Sugie, Kazuma, Ueno, Satoshi

“…Humanin (HN) was originally identified as an endogenous peptide that protects neuronal cells from apoptosis induced by various types of Alzheimer's…”
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A case of Fisher syndrome showing pharyngeal-cervical-brachial weakness with an elevation of anti-GQ 1 b and anti-GT 1 a antibodies by Furiya, Y, Murakami, N, Kataoka, H, Suzumura, A, Takayanagi, T

“…A 15-year-old boy developed ataxic gait, diplopia and hoarseness. Within 3 days after the onset, he had additional symptoms of dysphagia and dysarthria. He was…”
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Effect of humanin on decreased ATP levels of human lymphocytes harboring A3243G mutant mitochondrial DNA by Kariya, Shingo, Hirano, Makito, Furiya, Yoshiko, Ueno, Satoshi

“…Humanin (HN) was originally identified as an endogenous peptide that protects neuronal cells from apoptosis by mutant Alzheimer’s disease genes. This…”
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Peripheral neuropathy in chromosome16q22.1 linked autosomal dominant cerebellar ataxia by Furiya, Yoshiko, Hirano, Makito, Nomura, Masami, Asai, Hirohide, Kiriyama, Takao, Ueno, Satoshi

“…Table 1 Data from nerve conduction study and test of autonomic nervous system in the two patients Patient No 1 (81 y) Patient No 2 (52 y) Normal range Elderly…”
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Humanin attenuates apoptosis induced by DRPLA proteins with expanded polyglutamine stretches by Kariya, Shingo, Hirano, Makito, Nagai, Yoshitaka, Furiya, Yoshiko, Fujikake, Nobuhiro, Toda, Tatsushi, Ueno, Satoshi

“…Dentatorubral-pallidoluysian atrophy (DRPLA) is an autosomal-dominant neurodegenerative disorder caused by expansion of CAG repeats in the DRPLA gene, which…”
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Cytoprotective effect of novel histone deacetylase inhibitors against polyglutamine toxicity by Kariya, Shingo, Hirano, Makito, Uesato, Shinichi, Nagai, Yoshitaka, Nagaoka, Yasuo, Furiya, Yoshiko, Asai, Hirohide, Fujikake, Nobuhiro, Toda, Tatsushi, Ueno, Satoshi

“…Dentatorubral-pallidoluysian atrophy (DRPLA) is an autosomal dominant neurological disorder caused by a CAG repeat expansion in the DRPLA gene encoding…”
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Lack of association between polymorphic microsatellites of the VMAT2 gene and Parkinson's disease in Japan by Kariya, Shingo, Hirano, Makito, Takahashi, Nobuyuki, Furiya, Yoshiko, Ueno, Satoshi

“…The etiology of Parkinson's disease (PD) remains unclear; however, generation of reactive oxygen species during oxidation of dopamine (DA) could be one of the…”
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Amyloid β protein 42(43) in cerebrospinal fluid of patients with Alzheimer's disease by Tamaoka, Akira, Sawamura, Naoya, Fukushima, Tetsuo, Shoji, Shin'ichi, Matsubara, Etsuro, Shoji, Mikio, Hirai, Shunsaku, Furiya, Yoshiko, Endoh, Riuko, Mori, Hiroshi

“…To investigate the pathomechanism of amyloid β protein (Aβ) deposition in brains with Alzheimer's disease (AD), cerebrospinal fluid (CSF) levels of Aβ species…”
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Loss of function mechanism in aprataxin-related early-onset ataxia by Hirano, Makito, Furiya, Yoshiko, Kariya, Shingo, Nishiwaki, Tomohisa, Ueno, Satoshi

“…Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is an autosomal recessive form of cerebellar ataxia that occurs most commonly in Japan but is…”
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A case of basilar artery occlusion associated with one-and-a-half syndrome, paralytic pontine exotropia and WEBINO-syndrome by Furiya, Y, Uchiyama, S, Shibagaki, Y, Yamamoto, K, Ichikawa, H, Iwata, M

“…We report a 79-year-old woman with basilar artery occlusion. She had a sudden onset of tetraplegia and disturbed consciousness, and within four days from the…”
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Novel splice variants increase molecular diversity of aprataxin, the gene responsible for early-onset ataxia with ocular motor apraxia and hypoalbuminemia by Hirano, Makito, Nishiwaki, Tomohisa, Kariya, Shingo, Furiya, Yoshiko, Kawahara, Makoto, Ueno, Satoshi

“…Early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH) is one of the most common forms of autosomal recessive cerebellar ataxia. We identified…”
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SPECT revealed cortical dysfunction in a patient who had genetically definite megalencephalic leukoencephalopathy with subcortical cysts by Kiriyama, Takao, Tanizawa, Emi, Hirano, Makito, Shinkai, Takayuki, Asai, Hirohide, Furiya, Yoshiko, Ueno, Satoshi

“…Abstract We describe the findings on single photon emission computed tomography (SPECT) in a patient who had genetically definite megalencephalic…”
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