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1دورية أكاديمية
المؤلفون: Takeshi Ikeuchi, Toru Imamura, Yasuhiro Kawase, Yoshimi Kitade, Miyuki Tsuchiya, Takayoshi Tokutake, Kensaku Kasuga, Ryuji Yajima, Tamao Tsukie, Akinori Miyashita, Morihiro Sugishita, Ryozo Kuwano, Masatoyo Nishizawa
المصدر: Dementia and Geriatric Cognitive Disorders Extra, Vol 1, Iss 1, Pp 267-275 (2011)
مصطلحات موضوعية: Amnestic syndrome, Familial dementia, Founder effect, FTDP-17, MAPT mutation, Neurology. Diseases of the nervous system, RC346-429, Geriatrics, RC952-954.6
وصف الملف: electronic resource
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المؤلفون: Miyuki Tsuchiya
المصدر: Dynamiques du commun ISBN: 9791035106058
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::64fd22b0af3cae6e6bc284a2ab07d221
https://doi.org/10.4000/books.psorbonne.99902 -
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المؤلفون: Miyuki Tsuchiya
المصدر: Revue internationale de politique comparée. 24:51-75
مصطلحات موضوعية: Sociology and Political Science, Political Science and International Relations
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9a3c6d2f28fe1661963ecb9ca92fd734
https://doi.org/10.3917/ripc.241.0051 -
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المؤلفون: Ryozo Kuwano, Masatoyo Nishizawa, Toru Imamura, Tamao Tsukie, Takeshi Ikeuchi, Yoshimi Kitade, Ryuji Yajima, Morihiro Sugishita, Kensaku Kasuga, Miyuki Tsuchiya, Akinori Miyashita, Takayoshi Tokutake, Yasuhiro Kawase
المصدر: Dementia and Geriatric Cognitive Disorders EXTRA
Dementia and Geriatric Cognitive Disorders Extra, Vol 1, Iss 1, Pp 267-275 (2011)مصطلحات موضوعية: Genetics, Familial dementia, Anterograde amnesia, Genetic heterogeneity, Cognitive Neuroscience, Parkinsonism, Single-nucleotide polymorphism, lcsh:Geriatrics, Founder effect, Biology, medicine.disease, lcsh:RC346-429, FTDP-17, lcsh:RC952-954.6, MAPT mutation, Psychiatry and Mental health, Genotype, Mutation (genetic algorithm), medicine, Original Research Article, medicine.symptom, Amnestic syndrome, lcsh:Neurology. Diseases of the nervous system, Frontotemporal dementia
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d6ceebd74c71d2bf324363e2fc5ca8d
https://doi.org/10.1159/000331243 -
5Genotype–phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia
المؤلفون: Mitsunori Yamada, Masatoyo Nishizawa, Shoji Tsuji, Kyoko Maruta, Akihide Koyama, Yoshiki Sekijima, Miyuki Tsuchiya, Atsushi Shiga, Tatsuya Sato, Akio Yokoseki, Takeshi Ikeuchi, Chieko Suzuki, Tomohiko Ishihara, Osamu Onodera, Hidetoshi Date, Masayoshi Tada
المصدر: Brain. 134:1387-1399
مصطلحات موضوعية: medicine.medical_specialty, Pathology, Ataxia, Neural Conduction, Action Potentials, Kaplan-Meier Estimate, Biology, Transfection, Compound heterozygosity, Apraxia, Gastroenterology, Frameshift mutation, Ocular Motility Disorders, Internal medicine, Reflex, medicine, Humans, Missense mutation, RNA, Messenger, Age of Onset, Genetic Association Studies, Cell Line, Transformed, Family Health, Aprataxin, Nuclear Proteins, Tetracycline, medicine.disease, DNA-Binding Proteins, Gene Expression Regulation, Mutation, Regression Analysis, Neurology (clinical), Age of onset, medicine.symptom, Hypoalbuminemia
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a34efaed483426f65fbd82c4c0587d7
https://doi.org/10.1093/brain/awr069 -
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المؤلفون: Osamu Onodera, Hideki Ishizu, Kensaku Kasuga, Hiroaki Nozaki, Akinori Miyashita, Tamao Tsukie, Takeshi Ikeuchi, Miyuki Tsuchiya, Kenju Aoki, Hiroyuki Kaneko, Masatoyo Nishizawa, Toru Imamura, Ryozo Kuwano, Atsushi Ishikawa
المصدر: Dementia and Geriatric Cognitive Disorders. 26:43-49
مصطلحات موضوعية: Pathology, medicine.medical_specialty, biology, business.industry, Cognitive Neuroscience, Point mutation, Tau protein, medicine.disease, Bioinformatics, Psychiatry and Mental health, mental disorders, PSEN2, medicine, biology.protein, PSEN1, Dementia, Missense mutation, Geriatrics and Gerontology, Alzheimer's disease, Age of onset, business
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المؤلفون: Akio Kawakami, Reiji Koide, Naoki Nakao, Akio Kimura, Yuusaku Nakmura, Tatsuro Mutoh, Osamu Onodera, Hiroko Yamamoto, Takeshi Ikeuchi, Miyuki Tsuchiya, Ko Sahashi, Hiroaki Nozaki, Masatoyo Nishizawa
المصدر: Movement Disorders. 22:857-862
مصطلحات موضوعية: Male, Untranslated region, Ataxia, Disease, Biology, Polymorphism, Single Nucleotide, Atrophy, Gene Frequency, Japan, medicine, Guanine Nucleotide Exchange Factors, Humans, Spinocerebellar Ataxias, Age of Onset, Gene, Aged, Genes, Dominant, Genetics, Genetic heterogeneity, Chromosome Mapping, Spectrin, Chromosome, DNA, Middle Aged, medicine.disease, Neurology, Spinocerebellar ataxia, Female, Neurology (clinical), medicine.symptom, Chromosomes, Human, Pair 16
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المؤلفون: Shinichi Katada, Masatoyo Nishizawa, Osamu Onodera, Hiroyuki Kaneko, Satoshi Naruse, Tomokatsu Yoshida, Takeshi Ikeuchi, Miyuki Tsuchiya, Masaki Hirose, Masanori Nakagawa, Toshiaki Takahashi
المصدر: Movement Disorders. 24:1393-1395
مصطلحات موضوعية: Pathology, medicine.medical_specialty, Ataxia, Glial fibrillary acidic protein, biology, medicine.diagnostic_test, business.industry, Magnetic resonance imaging, medicine.disease, Alexander disease, Neurology, Mutation (genetic algorithm), medicine, biology.protein, In patient, Neurology (clinical), Spastic ataxia, medicine.symptom, business
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المؤلفون: Takeshi Ikeuchi, Jiro Idezuka, Osamu Onodera, Masatoyo Nishizawa, Miyuki Tsuchiya, Ryoko Koike, Nae Matsubara, Atsushi Homma, Arika Hasegawa, Hiroaki Nozaki
المصدر: Movement disorders : official journal of the Movement Disorder Society. 25(11)
مصطلحات موضوعية: Adult, Male, Pediatrics, medicine.medical_specialty, Disease onset, Adolescent, Nerve Tissue Proteins, Disease, Kaplan-Meier Estimate, Statistics, Nonparametric, Correlation, Young Adult, Atrophy, Japan, medicine, Humans, Genetic Predisposition to Disease, Age of Onset, Child, Aged, Aged, 80 and over, Dentatorubral-pallidoluysian atrophy, Movement Disorders, business.industry, Age Factors, Long term disability, Middle Aged, medicine.disease, Myoclonic Epilepsies, Progressive, Prognosis, Surgery, Natural history, Neurology, Child, Preschool, Female, Neurology (clinical), business, Trinucleotide repeat expansion, Trinucleotide Repeat Expansion
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المؤلفون: Takeshi, Ikeuchi, Hiroyuki, Kaneko, Akinori, Miyashita, Hiroaki, Nozaki, Kensaku, Kasuga, Tamao, Tsukie, Miyuki, Tsuchiya, Toru, Imamura, Hideki, Ishizu, Kenju, Aoki, Atsushi, Ishikawa, Osamu, Onodera, Ryozo, Kuwano, Masatoyo, Nishizawa
المصدر: Dementia and geriatric cognitive disorders. 26(1)
مصطلحات موضوعية: Male, DNA Mutational Analysis, Molecular Sequence Data, tau Proteins, Middle Aged, Kidney, Pedigree, Asian People, Japan, Presenilin-2, Presenilin-1, Humans, Point Mutation, Dementia, Female, Genetic Predisposition to Disease, Amino Acid Sequence, Genetic Testing, Age of Onset, Cells, Cultured