Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Izumi Aida"'
Autor:
Akiyoshi Kakita, Takanori Nozawa, Takashi Nakajima, Yasuko Toyoshima, Takashi Tani, Naoyuki Kojima, Izumi Aida, Shinnichi Katada, Mari Tada, Hitoshi Takahashi, Ryoko Koike, Osamu Onodera
Publikováno v:
Neuropathology. 41:450-456
Parkinson's disease (PD) is one of the most common neurodegenerative disorders. The cardinal neuropathological features of PD include selective and progressive loss of pigmented neurons in the substantia nigra, deficiencies in dopaminergic signaling
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::253947ff835270199c6f7b2c7da8c662
https://doi.org/10.1111/neup.12777
https://doi.org/10.1111/neup.12777
Publikováno v:
Internal Medicine
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a rare progressive neurodegenerative disease caused by either homozygous or compound heterozygous mutations in the SACS gene. The original ARSACS cases found in Quebec showed very
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8082bdc4378eaa97193846c8ec113839
http://europepmc.org/articles/PMC8758457
http://europepmc.org/articles/PMC8758457
Autor:
Riki Matsumoto, Yasuko Toyoshima, Akinori Miyashita, Akio Yokoseki, Izumi Aida, Atsushi Ishikawa, Tetsuhiko Ikeda, Hitoshi Takahashi, Osamu Onodera, Masato Kanazawa, Takashi Nakajima, Kento Saito, Takeshi Ikeuchi, Tatsushi Toda, Masatoshi Wakabayashi, Ryoko Takeuchi, Hiroaki Miyahara, Naohiko Seike, Akiyoshi Kakita
Publikováno v:
Movement Disorders. 36:1634-1643
BACKGROUND Mutations in PRKN are the most common cause of autosomal recessive juvenile parkinsonism. The objective of this study was to investigate the association between genotype and pathology in patients with PRKN mutations. METHODS We performed a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::934f892b020d03fa837b67d0e455d1b1
https://doi.org/10.1002/mds.28521
https://doi.org/10.1002/mds.28521
Autor:
Makoto Sainouchi, Mari Tada, Yusran Ady Fitrah, Norikazu Hara, Kou Tanaka, Jiro Idezuka, Izumi Aida, Takashi Nakajima, Akinori Miyashita, Kohei Akazawa, Takeshi Ikeuchi, Osamu Onodera, Akiyoshi Kakita
Publikováno v:
Neuropathology and Applied Neurobiology. 48
Neuronal and glial inclusions comprising transactive response DNA-binding protein of 43 kDa (TDP-43) have been identified in the brains of patients with corticobasal degeneration (CBD), and a possible correlation between the presence of these inclusi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a00fca0645268855596f22f4d2de05e2
https://doi.org/10.1111/nan.12786
https://doi.org/10.1111/nan.12786
Publikováno v:
Internal Medicine; 2022, Vol. 61 Issue 16, p2517-2521, 5p
Publikováno v:
Muscle & Nerve. 55:591-595
Introduction: We sought to: (1) determine the distribution of GABAA receptors (GABAA-Rs) in the brain of Duchenne muscular dystrophy (DMD) patients; and (2) ascertain if the distribution pattern correlates with cognitive dysfunction. Methods: Fourtee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25a8c01b0ce1a243efce690f4e3c22da
https://doi.org/10.1002/mus.25383
https://doi.org/10.1002/mus.25383
Publikováno v:
Internal Medicine; 12/15/2021, Vol. 60 Issue 24, p3963-3967, 5p
Autor:
Yasuko Toyoshima, Takayoshi Shimohata, Akira Satoh, Mutsuo Oyake, Mitsuhiro Tsujihata, Haruka Ouchi, Mari Tada, Hitoshi Takahashi, Itsuro Tomita, Izumi Aida, Masatoyo Nishizawa
Publikováno v:
Movement Disorders. 29:238-244
The aim of this study was to investigate corticobasal syndrome with respect to underlying pathologies, the ability of current clinical criteria to detect early stages of disease, and symptoms and signs predicting background pathologies. We retrospect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34f554d22969c6deb35147f69f30bcf9
https://doi.org/10.1002/mds.25746
https://doi.org/10.1002/mds.25746
Publikováno v:
Musclenerve. 55(4)
In this study we sought to: (1) determine the distribution of GABAFourteen DMD patients [young adult (n = 7, 18-25 years old) and older adult (n = 7, 30-37 years old) groups] and 16 age-matched normal volunteers participated. GABAAll DMD patients sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7457b0198f60659393f481cefa9c8b83
https://pubmed.ncbi.nlm.nih.gov/27543743
https://pubmed.ncbi.nlm.nih.gov/27543743
Autor:
H. Shimizu, H. Endo, Hoyu Takahashi, M. Tobinaga, Izumi Aida, T. Ikeda, Y. Yonemoti, Takashi Nakajima, Tetsuo Ozawa, J. Ito, Akiyoshi Kakita, K. Ohta
Publikováno v:
Journal of the Neurological Sciences. 381:593-594
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f80878cacf5a7f055b459202370398a7
https://doi.org/10.1016/j.jns.2017.08.1674
https://doi.org/10.1016/j.jns.2017.08.1674