Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Mao, Mukai"'
Autor:
Mao Mukai, Ai Hamano, Ikuko Mizuta, Isao Yokota, Akiko Watanabe-Hosomi, Hiraku Matsuura, Takashi Koizumi, Jun Matsuura, Tomoyuki Ohara, Shigenori Matsushima, Satoshi Teramukai, Kei Yamada, Toshiki Mizuno
Publikováno v:
Frontiers in Neurology, Vol 13 (2023)
BackgroundImpaired cerebrovasoreactivity is thought to play an important role in the pathophysiology of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). We aimed to clarify the association between
Externí odkaz:
https://doaj.org/article/8d5c042e35784a6a86b53058552e7ae3
Publikováno v:
Frontiers in Aging Neuroscience, Vol 12 (2020)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a hereditary cerebral small vessel disease caused by mutations in NOTCH3, is characterized by recurrent stroke without vascular risk factors, mood d
Externí odkaz:
https://doaj.org/article/d1618f9321554437bb1370feb1d20e3b
Autor:
Akiko Watanabe-Hosomi, Ai Hamano, Toshiki Mizuno, Ikuko Mizuta, Mao Mukai, Jun Matsuura, Hidekazu Tomimoto, Takashi Koizumi
Publikováno v:
Journal of Human Genetics. 65:637-646
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8eea4eeadd16f0a29492ec1502a66f2d
https://doi.org/10.1038/s10038-020-0751-9
https://doi.org/10.1038/s10038-020-0751-9
Autor:
Toshiki Mizuno, Ai Hamano, Tomoyuki Ohara, Ikuko Mizuta, Akiko Watanabe-Hosomi, Jun Matsuura, Mao Mukai, Takashi Koizumi
Publikováno v:
Journal of Stroke and Cerebrovascular Diseases. 28:1431-1439
Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is definitely diagnosed by genetic testing. Such testing involves the analysis of exons 2-24 of NOTCH3, which encode the epidermal growth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19ff30f7aade15d11825308a40b2c3ce
https://doi.org/10.1016/j.jstrokecerebrovasdis.2019.03.026
https://doi.org/10.1016/j.jstrokecerebrovasdis.2019.03.026
Autor:
Masaki Kondo, Ikuko Mizuta, Masaru Matsui, Toshiki Mizuno, Isao Yokota, Koushun Matsuo, Keita Ito, Ai Hamano, Kei Yamada, Takashi Koizumi, Masanori Nakagawa, Akihiro Fujii, Akiko Watanabe-Hosomi, Satoshi Teramukai, Mao Mukai
Publikováno v:
Clinical neuropharmacology. 43(5)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an orphan disease clinically characterized by migraine, recurrent strokes, and dementia. Currently, there are no disease-modifying therapies, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fced71c6c8b511fdc79f4d3eb1e9237
https://pubmed.ncbi.nlm.nih.gov/32947425
https://pubmed.ncbi.nlm.nih.gov/32947425
Autor:
Akiyoshi Yokote, Mao Mukai, Masako Kinoshita, Toshiki Mizuno, Ikuko Mizuta, Wing Tung Esther Yeung, Takashi Koizumi, Tomoyuki Ohara, Akiko Watanabe-Hosomi
Publikováno v:
Journal of Human Genetics. 63:687-690
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), caused by NOTCH3, primarily affects small cerebral arteries; however, stenosis of major intracranial arteries has occasionally been reported. Recent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4d05ad7ff1bcc931e30dd5586c90ee1
https://doi.org/10.1038/s10038-018-0428-9
https://doi.org/10.1038/s10038-018-0428-9
Autor:
Akiko Watanabe-Hosomi, Takashi Koizumi, Yasuhiro Tomii, Ai Hamano, Masanori Nakagawa, Hidekazu Tomimoto, Osamu Onodera, Teruyuki Hirano, Masaki Kondo, Ikuko Mizuta, Makoto Uchino, Toshiki Mizuno, Mao Mukai
Publikováno v:
Journal of the Neurological Sciences. 381:62-67
Purpose Definite diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukocencephalopathy (CADASIL) is mostly done by identification of NOTCH3 mutations. We aimed to develop criteria for selecting patients suspected fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::377de05b7c1afd415103b29a9b47cdf9
https://doi.org/10.1016/j.jns.2017.08.009
https://doi.org/10.1016/j.jns.2017.08.009
Autor:
Kyoko Itoh, Tomoyuki Ohara, Yu-ichi Noto, Yukie Kushimura, Daisuke Nakashima, Toshiki Mizuno, Yukio Ando, Mao Mukai, Ikuko Mizuta, Akihiko Ueda
Publikováno v:
Journal of the Neurological Sciences. 394:38-40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a076dee971de5e49799f6002990170fe
https://doi.org/10.1016/j.jns.2018.08.029
https://doi.org/10.1016/j.jns.2018.08.029
Autor:
Mao, Mukai, Ikuko, Mizuta, Akiko, Watanabe-Hosomi, Takashi, Koizumi, Jun, Matsuura, Ai, Hamano, Hidekazu, Tomimoto, Toshiki, Mizuno
Publikováno v:
Journal of human genetics. 65(8)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary cerebral small vessel disease caused by NOTCH3, and characterized by recurrent cerebral ischemic events without vascular risk factors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8bbbb0456708a0a738aeb65249291456
https://pubmed.ncbi.nlm.nih.gov/32277177
https://pubmed.ncbi.nlm.nih.gov/32277177
Autor:
Ryo Inoue, Toshiki Mizuno, Takashi Koizumi, Yuji Naito, Mao Mukai, Sayori Wada, Tomohisa Takagi, Akiko Watanabe, Ikuko Mizuta, Jun Matsuura
Publikováno v:
Journal of Clinical Biochemistry and Nutrition
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a major hereditary small vessel disease caused by mutations in NOTCH3. The variations in progression and severity among patients suggest that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::419294156c6eb89f64e7aa7170b88ee6
https://pubmed.ncbi.nlm.nih.gov/31777426
https://pubmed.ncbi.nlm.nih.gov/31777426