Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Hideaki Onda"'
Publikováno v:
PLoS ONE, Vol 17, Iss 3 (2022)
Background Intracranial aneurysms (IAs) cause subarachnoid hemorrhage, which has high rates of mortality and morbidity when ruptured. Recently, the role of rare variants in the genetic background of complex diseases has been increasingly recognized.
Externí odkaz:
https://doaj.org/article/651425cce0964a19ab964229cd302f90
Autor:
Yosuke Moteki, Hideaki Onda, Hidetoshi Kasuya, Taku Yoneyama, Yoshikazu Okada, Kengo Hirota, Maki Mukawa, Tadashi Nariai, Shohei Mitani, Hiroyuki Akagawa
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 4, Iss 5, Pp n/a-n/a (2015)
Background A founder variant of RNF213, p.R4810K (c.14429G>A, rs112735431), was recently identified as a major genetic risk factor for moyamoya disease (MMD) in Japan. Although the association of p.R4810K was reported to be highly significant and rep
Externí odkaz:
https://doaj.org/article/6a2ea7b878e2401fbdf509c2bbfc70f0
Autor:
Hiroyuki Akagawa, Hidetoshi Kasuya, Taku Yoneyama, Asami Kikuchi, Tatsuya Maegawa, Yasuhiro Kuroi, Hideaki Onda
Publikováno v:
Journal of the Neurological Sciences. 399:183-185
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8f4625a138cd4b9a92a4a774f058769
https://doi.org/10.1016/j.jns.2019.02.033
https://doi.org/10.1016/j.jns.2019.02.033
Autor:
Hiroyuki Akagawa, Hideaki Onda, Hidetoshi Kasuya, Kengo Hirota, Takakazu Kawamata, Taku Yoneyama
Publikováno v:
Journal of Stroke and Cerebrovascular Diseases. 25:2900-2906
Background Autosomal dominant polycystic kidney disease (ADPKD) caused by deleterious mutations in PKD1 (16p13.3) and PKD2 (4q21) often coexists with intracranial aneurysms (IAs). In this study, we investigated whether IAs without obvious renal disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebf70812e428b5c96223dff1258dfcde
https://doi.org/10.1016/j.jstrokecerebrovasdis.2016.08.002
https://doi.org/10.1016/j.jstrokecerebrovasdis.2016.08.002
Autor:
Hiroyuki Akagawa, Makoto Shibuya, Hideaki Onda, Hidetoshi Kasuya, Tatsuya Maegawa, Yasuhiro Kuroi
Publikováno v:
Neuro-oncology Advances
Background Angiomatous and microcytic meningiomas are classified as rare subtypes of grade I meningiomas by World Health Organization (WHO). They typically exhibit distinct histopathological features as indicated by their WHO titles; however, these a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16c140f1037324638fe8d550cd6088a9
https://doi.org/10.1093/noajnl/vdz028
https://doi.org/10.1093/noajnl/vdz028
Autor:
Taku Yoneyama, Tadashi Nariai, Takumi Kudo, Shunsuke Nomura, Hidetoshi Kasuya, Takakazu Kawamata, Yasuo Aihara, Taketoshi Maehara, Hideaki Onda, Maki Mukawa, Hiroyuki Akagawa, Kazutaka Sumita
Publikováno v:
Human Genome Variation. 5
Moyamoya disease is a progressive steno-occlusive condition of the main intracranial arteries that results in the compensatory formation of fragile moyamoya vessels at the base of the brain. RNF213 is the most significant susceptibility gene and is o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::048c65b43b536a65101f441c0f7a04fb
https://doi.org/10.1038/hgv.2017.60
https://doi.org/10.1038/hgv.2017.60
Autor:
Hideaki Onda, Hiroyuki Akagawa, Toyoaki Shinohara, Hiroyuki Kinouchi, Hidetoshi Kasuya, Toru Tateoka, Kengo Hirota
Publikováno v:
Journal of the Neurological Sciences. 362:144-146
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd01f48e3eaad67f68f8216f36a67123
https://doi.org/10.1016/j.jns.2016.01.037
https://doi.org/10.1016/j.jns.2016.01.037
Autor:
Hiroyuki, Akagawa, Maki, Mukawa, Tadashi, Nariai, Shunsuke, Nomura, Yasuo, Aihara, Hideaki, Onda, Taku, Yoneyama, Takumi, Kudo, Kazutaka, Sumita, Taketoshi, Maehara, Takakazu, Kawamata, Hidetoshi, Kasuya
Publikováno v:
Human Genome Variation
Moyamoya disease is a progressive steno-occlusive condition of the main intracranial arteries that results in the compensatory formation of fragile moyamoya vessels at the base of the brain. RNF213 is the most significant susceptibility gene and is o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5d47b764375219a31b47514730a24e50
https://pubmed.ncbi.nlm.nih.gov/29387438
https://pubmed.ncbi.nlm.nih.gov/29387438
Autor:
Asami Kikuchi, Kengo Hirota, Takakazu Kawamata, Toshiyuki Sasaki, Hiroyuki Akagawa, Akihiko Hino, Hidetoshi Kasuya, Hideki Oka, Hideaki Onda, Tetsuryu Mitsuyama
Publikováno v:
Human Genome Variation
Cerebral cavernous malformation is a neurovascular abnormality that can cause seizures, focal neurological deficits and intracerebral hemorrhage. Familial forms of this condition are characterized by de novo formation of multiple lesions and are auto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4a94161f72cea428b45542624e4ebab
https://doi.org/10.1038/hgv.2016.32
https://doi.org/10.1038/hgv.2016.32
Autor:
Hideaki Onda, Kazutaka Sumita, Maki Mukawa, Hiroyuki Akagawa, Taketoshi Maehara, Takakazu Kawamata, Yasuo Aihara, Tadashi Nariai, Takumi Kudo, Kengo Hirota, Hidetoshi Kasuya, Taku Yoneyama
Publikováno v:
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. 26(1)
The etiology of Moyamoya disease (MMD) is still largely unclear, despite identification of RNF213 as the most significant susceptibility gene in East Asian patients. Following up our previous study confirming genetic heterogeneity in Japanese patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3a31142e02f2a293f660fc9e24ce882
https://pubmed.ncbi.nlm.nih.gov/27717682
https://pubmed.ncbi.nlm.nih.gov/27717682