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Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences|October 27, 2021
Screening of multiple acyl-CoA dehydrogenase deficiency in newborns and follow-up of patientsDuo Zhou, Meiling Ye, Zhenzhen Hu, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 13, 2017
[Analysis of UQCRB gene mutation in a child with mitochondrial complex III deficiency]Ting Zhang, Fang Hong, Guling Qian, et al.Journal of the American Heart Association|May 2, 2025
Resolving Early Targets and Metabolomic Profile of Congenital Heart Disease Through Tandem Mass Spectrometry Screening in NeonatesJiayu Zhang, Wei Jiang, Die Li, et al.Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences|December 18, 2023
Results of neonatal screening for congenital hypothyroidism and hyperphenylalaninemia in Zhejiang province from 1999 to 2022Duo Zhou, Rulai Yang, Xinwen Huang, et al.Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences|January 5, 2020
[Genetic analysis of newborns with abnormal metabolism of 3-hydroxyisovalerylcarnitine]Dingwen Wu, Bin Lu, Jianbin Yang, et al.Journal of Inherited Metabolic Disease|November 10, 2012
Demographics, diagnosis and treatment of 256 patients with tetrahydrobiopterin deficiency in mainland China: results of a retrospective, multicentre studyJun Ye, Yanling Yang, Weimin Yu, et al.Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences|November 19, 2020
[Effects of delivery and storage conditions on concentrations of amino acids and carnitines in neonatal dried blood spots]Lingwei Hu, Zhenzhen Hu, Jianbin Yang, et al.Frontiers in Genetics|August 30, 2021
Case Report: Expanding the Digenic Variants Involved in Thyroid Hormone Synthesis-10 New Cases of Congenital Hypothyroidism and a Literature ReviewRulai Yang, Yijun Lu, Chenxi Yang, et al.Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences|November 21, 2023
Long-term follow-up of children with carbamoyl phosphate synthase 1 deficiency detected in newborn screeningZhanming Zhang, Fan Tong, Chi Chen, et al.Human Mutation|April 14, 2025
A Comprehensive LOVD Database for Fatty Acid Oxidation Disorders in Chinese PopulationsTing Zhang, Zinan Yu, Lingwei Hu, et al.Pageof 5