Zobrazeno 1 - 10
of 163
pro vyhledávání: '"Noriko, Aida"'
Autor:
Eiji Nishio, Takanori Hayashi, Masashi Nakatani, Noriko Aida, Risa Suda, Takuma Fujii, Toru Wakatsuki, Shinichiro Honda, Nobuhiro Harada, Yohei Shimono
Publikováno v:
Biochemistry and Biophysics Reports, Vol 20, Iss , Pp - (2019)
Obesity commonly occurs in postmenopausal women, increasing the risk of various diseases. Estrogen can prevent obesity by activating lipid metabolism and suppressing depressive behavior. However, the reasons for obesity in postmenopausal women are no
Externí odkaz:
https://doaj.org/article/5c0d424796d74c4eb2bf1b2a23ecdd71
Autor:
Tetsuhiko Okabe, Taiki Nozaki, Noriko Aida, Jay Starkey, Mikako Enokizono, Tetsu Niwa, Atsuhiko Handa, Yuji Numaguchi, Yasuyuki Kurihara
Publikováno v:
Insights into Imaging, Vol 9, Iss 3, Pp 313-324 (2018)
Abstract Neurological complications of paediatric cancers are a substantial problem. Complications can be primary from central nervous system (CNS) spread or secondary from indirect or remote effects of cancer, as well as cancer treatments such as ch
Externí odkaz:
https://doaj.org/article/a3f16a85321648969234a1fe7ec4e08d
Autor:
Mikako Enokizono, Noriko Aida, Akira Yagishita, Yasuhiro Nakata, Reiko Ideguchi, Ryo Kurokawa, Tatsuo Kono, Toshio Moritani, Harushi Mori
Publikováno v:
Japanese Journal of Radiology.
Although there are many types of inborn errors of metabolism (IEMs) affecting the central nervous system, also referred to as neurometabolic disorders, individual cases are rare, and their diagnosis is often challenging. However, early diagnosis is m
Autor:
Noriko Aida
Publikováno v:
Magnetic Resonance in Medical Sciences. 21:9-28
MRI interpretations of the pediatric brain are often challenging for general radiologists and clinicians because MR signals and morphology are continuously changing in the developing brain. Furthermore, the developing brain reacts differently to inju
Autor:
Shibasaki, Jun, Niwa, Tetsu, Aurélie, Piedvache, Tomiyasu, Moyoko, Morisaki, Naho, Fujii, Yuta, Toyoshima, Katsuaki, Aida, Noriko, Tetsu, Niwa, Moyoko, Tomiyasu, Noriko, Aida
Publikováno v:
The Journal of pediatrics. 239:101-109
Objective: To determine the optimal quantitative magnetic resonance (MR) biomarker in neonatal encephalopathy following therapeutic hypothermia based on scan timing. Study design: This retrospective study included 98 neonates (35-41 weeks of gestatio
Autor:
Yukiko Kuroda, Mizuki Asano, Noriko Aida, Hiroaki Murakami, Kenjiro Kosaki, Tatsuro Kumaki, Naoto Nishimura, Kenji Kurosawa, Tomoko Uehara, Yumi Enomoto
Publikováno v:
Mol Syndromol
Okur-Chung neurodevelopmental syndrome is a rare autosomal dominant disorder caused by pathogenic variants in CSNK2A1, which encodes the alpha 1 catalytic subunit of casein kinase II. This syndrome is characterized by intellectual disability, devel
Autor:
Hiroko Shimbo, Mariko Takagi, Mitsuko Okuda, Yu Tsuyusaki, Kyoko Takano, Mizue Iai, Sumimasa Yamashita, Kei Murayama, Akira Ohtake, Yu-ichi Goto, Noriko Aida, Hitoshi Osaka
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 133-138 (2014)
Large numbers of genes are responsible for Leigh syndrome (LS), making genetic confirmation of LS difficult. We screened our patients with LS using a limited set of 21 primers encompassing the frequently reported gene for the respiratory chain comple
Externí odkaz:
https://doaj.org/article/0d4c921bb06e4469a5d305eaf92eb63b
Autor:
Katsuaki Toyoshima, Hiroshi Kawaguchi, Noriko Aida, Jun Shibasaki, Moyoko Tomiyasu, Mikako Enokizono, Takayuki Obata
Publikováno v:
Pediatric Research
Background A very-low-birth-weight (VLBW) preterm infants is associated with an increased risk of impaired neurodevelopmental outcomes. In this study, we investigated how neonatal brain metabolite concentrations changed with postmenstrual age and exa
Autor:
Yoshinori Tsurusaki, Yukiko Kuroda, Kenjiro Kosaki, Kenji Kurosawa, Tomoko Uehara, Hiroaki Murakami, Noriko Aida, Yumi Enomoto
Publikováno v:
Brain and Development. 42:289-292
Atypical phenotype of an imprinting disease can develop with a recessive homozygous variant due to uniparental isodisomy. We present a girl with severe intellectual disability, developmental delay, distinctive facial features, and other neuropsychiat
Publikováno v:
Pediatrics International. 64