Výsledky vyhledávání

Correlation of callosal angle at the splenium with gait and cognition in normal pressure hydrocephalus

Autor: Takaaki Hattori, Masahiro Ohara, Tatsuhiko Yuasa, Reo Azuma, Qingmeng Chen, Ryoichi Hanazawa, Akihiro Hirakawa, Satoshi Orimo, Takanori Yokota

Publikováno v: Journal of Neurosurgery. :1-11

OBJECTIVE Idiopathic normal pressure hydrocephalus (iNPH) is characterized by ventricular enlargement that deforms the corpus callosum, making the callosal angle (CA) small. The authors aimed to evaluate the clinical usefulness of the CA in different

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b55f25e49134b27e85cb8bee8c10bcb3
https://doi.org/10.3171/2022.12.jns221825

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Home Medical Care for Parkinson's Disease

Autor: Ryo Hattori, Reo Azuma, Seiko Shimada, Satoshi Orimo

Publikováno v: The Japanese Journal of Rehabilitation Medicine. 56:213-217

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::667a0ccfdd3aba7b3a053701ac699fa6
https://doi.org/10.2490/jjrmc.56.213

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A Case of an Elderly Diabetic Patient Developing Wernicke Encephalopathy without Alcohol Abuse or an Unbalanced Diet

Autor: Yuzo Mizuno, Satoshi Orimo, Yuya Tsurutani, Akira Sata, Yuji Kaneko, Naoko Sagawa, Mai Kondo, Mariko Miyao, Reo Azuma

Publikováno v: Nippon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics. 52:177-183

A 70-year-old man with a 28-year history of type 2 diabetes mellitus was admitted due to persistent vomiting and neurological abnormalities in Nov 2012. He had developed gait disturbance and diplopia for six months during antiplatelet therapy, which

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb54c2bce93a80c0d95ff72fd0bc7def
https://doi.org/10.3143/geriatrics.52.177

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A novel mutation of PDE8B Gene in a Japanese family with autosomal-dominant striatal degeneration

Autor: Reo, Azuma, Kinya, Ishikawa, Kosei, Hirata, Yuji, Hashimoto, Makoto, Takahashi, Kenji, Ishii, Akira, Inaba, Takanori, Yokota, Satoshi, Orimo

Publikováno v: Movement disorders : official journal of the Movement Disorder Society. 30(14)

Autosomal-dominant striatal degeneration is a rare autosomal-dominant neurodegenerative movement disorder characterized by slowly progressive parkinsonism. Recently, a mutation of the cyclic nucleotide phosphodiesterase 8B gene was reported to be a c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0b9b87462287b6048d7975f6afc4c67a
https://pubmed.ncbi.nlm.nih.gov/26769607

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Relationship and factor structure in multisystem neurodegeneration in Parkinson disease

Autor: Mark Hallett, Akira Inaba, Tianxia Wu, Reo Azuma, Takaaki Hattori, Satoshi Orimo, Hidehiro Mizusawa

Objectives Parkinson's disease (PD) is a multisystem neurodegenerative disease. We aimed to identify the relationship and factor structure among its different features. Materials & methods Motor, olfactory and cognitive function, and cardiac sympathe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7384dd7cbab05e2a72e4433bc78fff08
https://europepmc.org/articles/PMC4208945/