Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Nodoka Adachi"'
Autor:
Eisuke Suganuma, Akira Oka, Hideaki Sakata, Nodoka Adachi, Satoshi Asanuma, Eiji Oguma, Akira Yamaguchi, Mihoko Furuichi, Yoji Uejima, Satoshi Sato, Tadamasa Takano, Yutaka Kawano, Risa Tanaka, Takashi Arai, Tsutomu Oh-Ishi
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background Congenital cytomegalovirus (cCMV) infection leads to sensorineural hearing loss (SNHL) and neurodevelopmental delays. However, the long-term outcomes of cCMV infection with severe neurological manifestations in infancy remain uncl
Externí odkaz:
https://doaj.org/article/ae7020382c884b29828217710fd0c0e2
Autor:
Hideaki Sakata, Ryohei Takahashi, Satoshi Sato, Eisuke Suganuma, Nodoka Adachi, Mihoko Furuichi, Tsutomu Oh-ishi, Sachi Yamamoto, Takashi Arai, Yutaka Kawano, Satoshi Asanuma, Yoji Uejima, Daigo Matsumoto, Tomoya Abe
Publikováno v:
Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy. 27(2)
Objectives Valganciclovir (VGCV) has been shown to improve sensorineural hearing loss (SNHL) and neurological outcomes in patients with neonatal symptomatic congenital cytomegalovirus (cCMV) infection. However, reports on the pharmacokinetics, effica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f50c81a8ddd65eb00dde8fd6f4283882
https://pubmed.ncbi.nlm.nih.gov/32907793
https://pubmed.ncbi.nlm.nih.gov/32907793
Autor:
Hideaki Sakata, Mihoko Furuichi, Takashi Arai, Eisuke Suganuma, Tsutomu Oh-ishi, Risa Tanaka, Satoshi Sato, Eiji Oguma, Yutaka Kawano, Akira Yamaguchi, Satoshi Asanuma, Nodoka Adachi, Yoji Uejima, Akira Oka, Tadamasa Takano
Publikováno v:
BMC Pediatrics
BMC Pediatrics, Vol 18, Iss 1, Pp 1-6 (2018)
BMC Pediatrics, Vol 18, Iss 1, Pp 1-6 (2018)
Background Congenital cytomegalovirus (cCMV) infection leads to sensorineural hearing loss (SNHL) and neurodevelopmental delays. However, the long-term outcomes of cCMV infection with severe neurological manifestations in infancy remain unclear. Case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e74dbcbaaf41c9c58dee6c26090b95c8
https://doi.org/10.1186/s12887-018-1348-8
https://doi.org/10.1186/s12887-018-1348-8
Autor:
Suganuma, Eisuke, Oka, Akira, Sakata, Hideaki, Nodoka Adachi, Asanuma, Satoshi, Oguma, Eiji, Yamaguchi, Akira, Furuichi, Mihoko, Uejima, Yoji, Sato, Satoshi, Takano, Tadamasa, Kawano, Yutaka, Tanaka, Risa, Arai, Takashi, Oh-Ishi, Tsutomu
Time line picture. (DOCX 56â kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cecf202f82a87d3b45811a18d3ba0664
Autor:
Jutaro Fujita, Takashi Arai, Hidetoshi Fujita, Jiro Matsumoto, Akira Yamaguchi, Tsutomu Oh-ishi, Tadashi Uesato, Hideaki Sakata, Hirofumi Kimoto, Nodoka Adachi, Ken Shirato, Takako Kizaki, Hideki Ohno, Satoshi Asanuma, Eiji Oguma
Publikováno v:
BMJ Open
Objective Approximately 8–10% of newborns with asymptomatic congenital cytomegalovirus (cCMV) infection develop sensorineural hearing loss (SNHL). However, the relationship between CMV load, SNHL and central nervous system (CNS) damage in cCMV infe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33cf666873824f186b7b0ab2bb2c37e2
http://europepmc.org/articles/PMC5253530
http://europepmc.org/articles/PMC5253530
Autor:
Nodoka Adachi, Akira Takagi, Yasuhide Okamoto, Satoko Ymaguchi, Hideaki Sakata, Atsuko Nakano, Ayako Kanno, Kimitaka Kaga, Kaoru Ogawa, Hidenobu Taiji, Tatsuo Matsunaga, Noriko Morimoto
Publikováno v:
AUDIOLOGY JAPAN. 53:164-170
前庭水管拡大症 (EVA: enlargement of the vestibular aqueduct) は最も頻度の高い内耳奇形である。EVAが認められる疾患としては, 先天性で発症し進行する難聴やめまいを呈し, ヨード有機化障害によ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1302c269c4f8eaf33c900a4b8ada2e24
https://doi.org/10.4295/audiology.53.164
https://doi.org/10.4295/audiology.53.164
Autor:
Hideaki Sakata, Nodoka Adachi, Manabu Tanaka, Shin-ichiro Hamano, Kimitaka Kaga, Kenji Kurosawa, Hitoshi Osaka
Publikováno v:
Auris Nasus Larynx. 35:404-407
We reported two cases of Pelizaeus-Merzbacher disease. Both cases visited our hospital manifesting horizontal nystagmoid movements present from birth, and delayed motor development. Magnetic resonance imaging of the brain showed diffuse dysmyelinatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::338818cee9dd61a6995112f57cfe8d20
https://doi.org/10.1016/j.anl.2007.09.002
https://doi.org/10.1016/j.anl.2007.09.002
Publikováno v:
Annals of Otology, Rhinology & Laryngology. 119:294-296
Objectives We sought to identify predictors for hearing loss in Japanese children with meningitis. Methods We analyzed 155 cases of pediatric meningitis without other entities causing hearing loss in children admitted to Saitama Children's Medical Ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::296a6461bbf5f3b3b9bd45871a756b06
https://doi.org/10.1177/000348941011900504
https://doi.org/10.1177/000348941011900504
Autor:
Naoko Yasui, Satoshi Asanuma, Hideaki Sakata, Motohiro Kato, Katsuyoshi Koh, Nodoka Adachi, Ryoji Hanada
Publikováno v:
Journal of pediatric hematology/oncology. 36(4)
Cisplatin is an effective chemotherapeutic agent against pediatric cancers; however, ototoxicity is a concern. This study describes the frequency, severity, and clinical course of hearing loss in Japanese pediatric patients treated with cisplatin-bas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::841737403b816a82baf82de103df98aa
https://pubmed.ncbi.nlm.nih.gov/24072246
https://pubmed.ncbi.nlm.nih.gov/24072246
Autor:
Shujiro Minami, Sawako Masuda, Hirokazu Sakamoto, Tatsuo Matsunaga, Hideaki Sakata, Haruo Yoshida, Nodoka Adachi, Yukiko Arimoto, Fujinobu Tanaka, Tomoko Sugiuchi, Hideki Mutai, Noriko Morita, Kimitaka Kaga, Hidenobu Taiji, Noriko Morimoto, Atsuko Nakano
Publikováno v:
Gene. 532(1)
The hearing loss caused by GJB2 mutations is usually congenital in onset, moderate to profound in degree, and non-progressive. The objective of this study was to study genotype/phenotype correlations and to document 14 children with biallelic GJB2 mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::857ec316d3a22ac0233a20073aac4710
https://pubmed.ncbi.nlm.nih.gov/24013081
https://pubmed.ncbi.nlm.nih.gov/24013081