Slide 1 Catabolism of the Carbon Skeletons of Amino Acids Excess amino acids are catabolized to amphibolic intermediates used as sources of energy or for carbohydrate and…
High Incidence of Lipid Deposition in the Liver of Rats Fed a Diet Supplemented with Branched-Chain Amino Acids under Vitamin B6 Deficiency High Incidence of Lipid Deposition…
MRI and clinical features of maple syrup urine disease: preliminary results in 10 cases Ailan Cheng* Lianshu Han* Yun Feng Huimin Li Rong Yao Dengbin Wang Biao Jin Maple
Case-5.pmdINDIAN PEDIATRICS 738 VOLUME 53__AUGUST 15, 2016 CCCCC AAAAA SSSSS E RE RE RE RE R EEEEE PPPPP OOOOO RRRRR TTTTT Isoleucine Deficiency in a Neonate Treated for
INVESTIGATION OF GENE AND CELLULAR THERAPIES TO CURE MAPLE SYRUP URINE DISEASE (MSUD) IN A GENETICALLY ENGINEERED MOUSE MODEL Submitted to the Graduate Faculty of The University
Molecular basis of various forms of maple syrup urine disease in Chilean patientswileyonlinelibrary.com/journal/mgg3 Received: 10 July 2020 | Revised: 5 January 2021 | Accepted:
Microsoft Word - Document3Title of the study:Phenylbutyrate Therapy in maple Syrup Urine Disease NCT01529060 Section C: Background Information Maple syrup urine disease (MSUD;