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Author/Creator Aoyama, Yuka

1. Characterization and outcome of 41 patients with beta‐ketothiolase deficiency: 10 years' experience of a medical center in northern Vietnam. Issue 3 (20th February 2017)

Authors:
Nguyen, Khanh Ngoc; Abdelkreem, Elsayed; Colombo, Roberto; Hasegawa, Yuki; Can, Ngoc Thi Bich; Bui, Thao Phuong; Le, Hai Thanh; Tran, Mai Thi Chi; Nguyen, Hoan Thi; Trinh, Hung Thanh; Aoyama, Yuka; Sasai, Hideo; Yamaguchi, Seiji; Fukao, Toshiyuki; Vu, Dung Chi
Journal:
Journal of inherited metabolic disease
Issue:
Volume 40:Issue 3(2017)
Page Start:
395
Record Type:
Journal Article
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4. Deficiency of 3‐hydroxybutyrate dehydrogenase (BDH1) in mice causes low ketone body levels and fatty liver during fasting. Issue 5 (23rd April 2020)

Authors:
Otsuka, Hiroki; Kimura, Takeshi; Ago, Yasuhiko; Nakama, Mina; Aoyama, Yuka; Abdelkreem, Elsayed; Matsumoto, Hideki; Ohnishi, Hidenori; Sasai, Hideo; Osawa, Masatake; Yamaguchi, Seiji; Mitchell, Grant A.; Fukao, Toshiyuki
Journal:
Journal of inherited metabolic disease
Issue:
Volume 43:Issue 5(2020)
Page Start:
960
Record Type:
Journal Article
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5. Heterozygous carriers of succinyl‐CoA:3‐oxoacid CoA transferase deficiency can develop severe ketoacidosis. Issue 6 (10th July 2017)

Authors:
Sasai, Hideo; Aoyama, Yuka; Otsuka, Hiroki; Abdelkreem, Elsayed; Naiki, Yasuhiro; Kubota, Mitsuru; Sekine, Yuji; Itoh, Masatsune; Nakama, Mina; Ohnishi, Hidenori; Fujiki, Ryoji; Ohara, Osamu; Fukao, Toshiyuki
Journal:
Journal of inherited metabolic disease
Issue:
Volume 40:Issue 6(2017)
Page Start:
845
Record Type:
Journal Article
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8. Single‐nucleotide substitution T to A in the polypyrimidine stretch at the splice acceptor site of intron 9 causes exon 10 skipping in the ACAT1 gene. Issue 2 (8th February 2017)

Authors:
Sasai, Hideo; Aoyama, Yuka; Otsuka, Hiroki; Abdelkreem, Elsayed; Nakama, Mina; Hori, Tomohiro; Ohnishi, Hidenori; Turner, Lesley; Fukao, Toshiyuki
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 5:Issue 2(2017)
Page Start:
177
Record Type:
Journal Article
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