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Yoshihiro Takeuchi

Showing results (71-80 of 77) with videos related to

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Journal of Pediatric Gastroenterology and Nutrition|April 1, 2008
Conformational change of UGT1A1 by a novel missense mutation (p.L131P) causing Crigler-Najjar syndrome type IYoshihiro Maruo, Ishwar Chander Verma, Katsuyuki Matsui, et al.
The Journal of Pediatrics|March 22, 2014
Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundiceYoshihiro Maruo, Yoriko Morioka, Hiroshi Fujito, et al.
Current Psychiatry Reports|February 8, 2017
The Role of Nutritional Supplements in the Treatment of ADHD: What the Evidence SaysKlaus W Lange, Joachim Hauser, Katharina M Lange, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 4, 2006
Crigler-Najjar syndrome type II caused by a homozygous triple mutation [T-3279G, A(TA)7TAA, and H39D] of UGT1A1Yoshihiro Maruo, Ali K Topaloglu, Hiroko Takahashi, et al.
Brain & Development|February 10, 2006
Effect of additional auditory and visual stimuli on continuous performance test (noise-generated CPT) in AD/HD children -- usefulness of noise-generated CPTMasaaki Uno, Junko Abe, Chihiro Sawai, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 8, 2011
Compound heterozygote of a novel missense mutation (p.K402T) and a double missense mutation (p.[G71R;Y486D]) in type II Crigler-Najjar syndromeYoshihiro Maruo, Funda Ozgenc, Yu Mimura, et al.
Brain & Development|September 5, 2018
X-linked Charcot-Marie-Tooth disease type 5 with recurrent weakness after febrile illnessNoriko Nishikura, Takanori Yamagata, Takao Morimune, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
Journal of Pediatric Gastroenterology and Nutrition|April 1, 2008
Conformational change of UGT1A1 by a novel missense mutation (p.L131P) causing Crigler-Najjar syndrome type IYoshihiro Maruo, Ishwar Chander Verma, Katsuyuki Matsui, et al.
The Journal of Pediatrics|March 22, 2014
Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundiceYoshihiro Maruo, Yoriko Morioka, Hiroshi Fujito, et al.
Current Psychiatry Reports|February 8, 2017
The Role of Nutritional Supplements in the Treatment of ADHD: What the Evidence SaysKlaus W Lange, Joachim Hauser, Katharina M Lange, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 4, 2006
Crigler-Najjar syndrome type II caused by a homozygous triple mutation [T-3279G, A(TA)7TAA, and H39D] of UGT1A1Yoshihiro Maruo, Ali K Topaloglu, Hiroko Takahashi, et al.
Brain & Development|February 10, 2006
Effect of additional auditory and visual stimuli on continuous performance test (noise-generated CPT) in AD/HD children -- usefulness of noise-generated CPTMasaaki Uno, Junko Abe, Chihiro Sawai, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 8, 2011
Compound heterozygote of a novel missense mutation (p.K402T) and a double missense mutation (p.[G71R;Y486D]) in type II Crigler-Najjar syndromeYoshihiro Maruo, Funda Ozgenc, Yu Mimura, et al.
Brain & Development|September 5, 2018
X-linked Charcot-Marie-Tooth disease type 5 with recurrent weakness after febrile illnessNoriko Nishikura, Takanori Yamagata, Takao Morimune, et al.
Pageof 8