Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Shuichi Yatsuga"'
Autor:
Makoto Okada, Yugo Nagayama, Hitomi Saiki, Kazutoshi Ito, Shuichi Yatsuga, Shinichiro Nagamitsu
Publikováno v:
BMC Nutrition, Vol 9, Iss 1, Pp 1-4 (2023)
Abstract Background There have been reports of isolated trace elements or vitamin deficiencies due to imbalanced diets, but no cases of selenium deficiency combined with scurvy have been reported. Case presentation A 7 year-old boy diagnosed with aut
Externí odkaz:
https://doaj.org/article/cb1970baf99a4b82bf3fb9ff53995ca7
Autor:
Cameron Young, Dominyka Batkovskyte, Miyuki Kitamura, Maria Shvedova, Yutaro Mihara, Jun Akiba, Wen Zhou, Anna Hammarsjö, Gen Nishimura, Shuichi Yatsuga, Giedre Grigelioniene, Tatsuya Kobayashi
Publikováno v:
HGG Advances, Vol 4, Iss 1, Pp 100148- (2023)
Summary: Mitochondrial diseases are a heterogeneous group of genetic disorders caused by pathogenic variants in genes encoding gene products that regulate mitochondrial function. These genes are located either in the mitochondrial or in the nuclear g
Externí odkaz:
https://doaj.org/article/d0f69c7ad5b442daa8ce8c143d8685b9
Publikováno v:
Clinical Case Reports, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract A severe Angelman syndrome (AS) patient with a very large deletion (19.3 Mb) at 15q11.2‐q14 required laryngotracheal separation, which is not a common surgery in AS. Comparative genomic hybridization‐based microarrays can be useful to co
Externí odkaz:
https://doaj.org/article/afd5a81735ec47e7adc463124626543a
Autor:
Miyuki Kitamura, Junko Nishioka, Takako Matsumoto, Satoko Umino, Atsuko Kawano, Reo Saiki, Yukari Tanaka, Shuichi Yatsuga
Publikováno v:
Endocrine and Metabolic Science, Vol 7, Iss , Pp 100119- (2022)
Objective: This study provided a rough estimate incidence of primary pediatric central diabetes insipidus (CDI) and examines the diagnostic factors between pediatric CDI and primary polydipsia (PP). Methods: We collected 27 patients with chief compla
Externí odkaz:
https://doaj.org/article/505944f2f4a447c1a499001fe82c3582
Autor:
Satoko Umino, Miyuki Kitamura, Yuko Katoh‐Fukui, Maki Fukami, Takeshi Usui, Shuichi Yatsuga, Yasutoshi Koga
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
Abstract Background 21‐hydroxylase deficiency (21‐OHD) is caused due to CYP21A2 gene variant. In males, the excess androgens produce varying degrees of penile enlargement and small testes. CHARGE syndrome (CS) has a broad spectrum of symptoms. In
Externí odkaz:
https://doaj.org/article/4428caf4579a46e280f486144f5f214f
Publikováno v:
久留米大学心理学研究 = Kurume University psychological research. 22:51-59
本研究の目的は,子どもの肥満治療に対する母親のモチベーション(動機)の推移や動機に影響を与える要因を明らかにすることであった。複線経路・等至性モデル(Trajectory Equifinality M
Autor:
田中 友規 (Tomoki Tanaka), 嘉村 拓朗 (Takuro Kamura), 近藤 里香子 (Rikako Kondo), 八ツ賀 秀一 (Shuichi Yatsuga), 岡松 由記 (Yuki Okamatsu)
Publikováno v:
Nihon Kyukyu Igakukai Zasshi: Journal of Japanese Association for Acute Medicine. 33:173-177
Autor:
Kikumi Ushijima-Fuchino, Yuko Koga, Satoko Umino, Junko Nishioka, Junichiro Araki, Shuichi Yatsuga, Yushiro Yamashita
Publikováno v:
Clinical Pediatric Endocrinology. 31:199-204
Autor:
Masahiro Kinoshita, Eimei Harada, Sachiko Iwata, Kennosuke Tsuda, Yushiro Yamashita, Hisayoshi Okamura, Naoko Hara, Ryota Shindo, Toshihiro Morisaki, Shuichi Yatsuga, Yasutoshi Koga, Mamoru Saikusa, Osuke Iwata
Publikováno v:
Mitochondrion. 61:25-30
Serum growth differentiation factor 15 (GDF15) is a useful biomarker of mitochondrial diseases; its utility in newborns remains unknown. To investigate the temporal change in GDF15 within the first week of life, and to identify its potential control
Autor:
Shingo Niimi, Takuro Kimura, Reo Saiki, Hiroshi Kanda, Yuki Okamatsu, Maki Goto, Shuichi Yatsuga
Publikováno v:
Cureus.