Keywords: اسید معده ایسووالریک; Isovaleric acidemia; Glycine; l-carnitine; Isovalerylcarnitine; Isovalerylglycine;
مقالات ISI اسید معده ایسووالریک (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: اسید معده ایسووالریک; Isovaleric acidemia; Protein restricted diet; Leucine; Leucine free l-amino acids; Natural protein;
Keywords: اسید معده ایسووالریک; Ebstein anomaly; Isovaleric acidemia; Congenital heart disease; Metabolic disorder
Keywords: اسید معده ایسووالریک; Isovaleric acidemia; IVD gene; Mutation screening; Genotype–phenotype correlation
A novel method for quantitation of acylglycines in human dried blood spots by UPLC-tandem mass spectrometry
Keywords: اسید معده ایسووالریک; Newborn screening; Inborn errors of metabolism; Tandem mass spectrometry; 2MBG; 2-methylbutyrylglycine; 3MCC; 3-methylcrotonyl-CoA carboxylase deficiency; 3MCG; 3-methylcrotonylglycine; AG; acetylglycine; BG; butyrylglycine; BKTD; beta ketothiolase defici
Selective and accurate C5 acylcarnitine quantitation by UHPLC-MS/MS: Distinguishing true isovaleric acidemia from pivalate derived interference
Keywords: اسید معده ایسووالریک; IVA; isovaleric acidemia; SCADD; short chain acyl-CoA dehydrogenase deficiency; GAI; glutaric acidemia type I; SCX; strong cation exchange; SPE; solid-phase extraction; LLOQ; lower limit of quantitation; ULOQ; upper limit of quantitation; CAP; College of
Prevalence and mutation analysis of short/branched chain acyl-CoA dehydrogenase deficiency (SBCADD) detected on newborn screening in Wisconsin
Keywords: اسید معده ایسووالریک; SBCADD; short/branched chain acyl-CoA dehydrogenase deficiency; 2-MBCD; 2-methylbutyryl CoA dehydrogenase deficiency; C2; acetylcarnitine; C3; propionylcarnitine; C5; 2-methylbutyrylcarnitine or isovalerylcarnitine; IVA; isovaleric acidemia; MS/MS; tandem
Clinical and molecular analysis of isovaleric acidemia patients in the United Arab Emirates reveals remarkable phenotypes and four novel mutations in the IVD gene
Keywords: اسید معده ایسووالریک; Isovaleric acidemia; Isovaleryl-CoA dehydrogenase; IVA; IVD
2-Methylbutyryl-coenzyme A dehydrogenase deficiency: Functional and molecular studies on a defect in isoleucine catabolism
Keywords: اسید معده ایسووالریک; 2-Methylbutyryl-CoA dehydrogenase; Methylbutyrylglycinuria; Isovaleryl-CoA dehydrogenase; Isovaleric acidemia; Organic acids; Newborn screening; Acylcarnitines; Valproic acid; Branched-chain amino acids; Fibroblasts
A sensitive liquid chromatographic method for the analysis of isovaleric and valeric acids in urine as fluorescent derivatives
Keywords: اسید معده ایسووالریک; Isovaleric and valeric acids; Isovaleric acidemia; Biomarker; Urine; Liquid chromatography
Genetic mutation profile of isovaleric acidemia patients in Taiwan
Keywords: اسید معده ایسووالریک; Isovaleric acidemia; Gene mutation; Tandem mass spectrometry
Different spectrum of mutations of isovaleryl-CoA dehydrogenase (IVD) gene in Korean patients with isovaleric acidemia
Keywords: اسید معده ایسووالریک; Isovaleric acidemia; IVD; Isovaleryl-CoA dehydrogenase; Acyl-CoA dehydrogenase; Mutation; Korean
Newborn screening for metabolic disorders
Keywords: اسید معده ایسووالریک; FAOD; Fatty acid oxidation disorders; GA-I; Glutaric acidemia type I; GALT; Galactose-1-phosphate uridyltransferase; IVA; Isovaleric acidemia; MCADD; Medium chain acyl-CoA dehydrogenase deficiency; 3-MCCD; 3-Methylcrotonyl-CoA carboxylase deficiency; MS/M