Keywords: اسیدهای آلی; Organic acidemia; Fatty acid oxidation disorder; Amino acid disorder; Inherited metabolic disease; Expanded newborn screening; Incidence rate; GC/MS; gas chromatography-mass spectrometry; MS/MS; tandem mass spectrometry; OA; organic acidemia; FAOD; fatt
مقالات ISI اسیدهای آلی (ترجمه نشده)
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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: اسیدهای آلی; Organic acidemia; Ketone utilization; Pyruvate metabolism; Metabolic acidosis; Ketoacidosis; Inborn error of metabolism;
Keywords: اسیدهای آلی; Inborn errors of metabolism (IEM); Gas chromatography/mass spectrometry (GC/MS); Organic acidemia; Aminoacidopathies; Newborn screening;
Keywords: اسیدهای آلی; Propionic acidemia; Organic acidemia; Outcome; Sodium citrate; Anaplerosis; Clinical trial;
Keywords: اسیدهای آلی; protein metabolism; urea cycle disorder; organic acidemia; protein intake; calorie intake; protein/energy ratio; %fatmass; Percentage body fat mass; AAF; Amino acid-based formula; BIA; Bioelectrical impedance analysis; BMI; Body mass index; BMR; Basal m
Keywords: اسیدهای آلی; organic acidemia; newborn screening; C3 acylcarnitine; nonketotic; hyperglycinemia; hyperammonemia; longitudinal follow up; natural; history; GI; Gastrointestinal; IBEM-IS; Inborn Errors of Metabolism Information System; NBS; Newborn screening; PA; Propio
Keywords: اسیدهای آلی; Metabolic; Acidosis; Hypoglycemia; Hyperammonemia; Fatty acid oxidation; Urea cycle; Organic acidemia;
Keywords: اسیدهای آلی; Organic acidemia; Glutaric acidemia; Gas chromatography; Solid phase microextraction; Alkyl chloroformate; Urine
Keywords: اسیدهای آلی; Inborn errors of metabolism; Liver transplant; Hepatocyte transplant; Liver failure; Organic acidemia; Amino aciduria;
Recapitulation of metabolic defects in a model of propionic acidemia using patient-derived primary hepatocytes
Keywords: اسیدهای آلی; Organic acidemia; Propionic acidemia; Ammonia; Urea; Hepatocyte; Hemodynamic flow;
Ocular disease in the cobalamin C defect: A review of the literature and a suggested framework for clinical surveillance
Keywords: اسیدهای آلی; Cobalamin C defect; Organic acidemia; Homocystinuria; Ophthalmology; Maculopathy; Oxidative stress;
Inhibition of N-acetylglutamate synthase by various monocarboxylic and dicarboxylic short-chain coenzyme A esters and the production of alternative glutamate esters
Keywords: اسیدهای آلی; NAGS; N-acetylglutamate synthase; CoA; coenzyme A; UPLC-MS/MS; Ultraperformance liquid chromatography-tandem mass spectrometry; UCDs; urea cycle defects; CPS; carbamyl phosphate synthetase; CNS; central nervous system; NAG; N-acetylglutamate; GC-MS;
Natural history of propionic acidemia
Keywords: اسیدهای آلی; Propionic acidemia; Organic acidemia; Pancreatitis; Cardiomyopathy; Long QT interval; Long-term complications;
Chronic management and health supervision of individuals with propionic acidemia
Keywords: اسیدهای آلی; Propionic acidemia; Organic acidemia; Propionic aciduria; Organic aciduria; Chronic management; Health supervision;
Acute management of propionic acidemia
Keywords: اسیدهای آلی; Propionic acidemia; Inborn error of metabolism; Organic acidemia; Treatment; Acute management;
Clinical and molecular investigation of 19 Japanese cases of glutaric acidemia type 1
Keywords: اسیدهای آلی; Glutaric acidemia type 1 (GA1); Glutaryl-CoA dehydrogenase (GCDH); Organic acidemia; Genotype-phenotype correlation; Common mutation
Characterization of new ACADSB gene sequence mutations and clinical implications in patients with 2-methylbutyrylglycinuria identified by newborn screening
Keywords: اسیدهای آلی; Branched chain acyl coenzyme A dehydrogenase; 2-Methylbutyryl coenzyme A dehydrogenase; Organic acidemia; Isoleucine metabolism; Acyl-CoA dehydrogenase; Newborn screening
Urinary organic metabolite screening of children with influenza-associated encephalopathy for inborn errors of metabolism using GC/MS
Keywords: اسیدهای آلی; Fructose-1; 6-Diphosphatase deficiency; Organic acidemia; Convulsive disorder; Valproic acid
Clinical and molecular investigations of Japanese cases of glutaric acidemia type 2
Keywords: اسیدهای آلی; Glutaric acidemia type 2 (GA2); Electron transfer flavoprotein (ETF); Electron transfer flavoprotein dehydrogenase (ETFDH); Organic acidemia; Fatty acid metabolism disorder;
ESI–MS/MS study of acylcarnitine profiles in urine from patients with organic acidemias and fatty acid oxidation disorders
Keywords: اسیدهای آلی; Urine; Acylcarnitine; Newborn screening; Electrospray ionization tandem mass spectrometry; Organic acidemia; Fatty acid oxidation disorder; Screening; ESI–MS/MS; Carnitine deficiency; Pivoxil; Glutaric; Aciduria type 1; GA1
Acidified acetonitrile and methanol extractions for quantitative analysis of acylcarnitines in plasma by stable isotope dilution tandem mass spectrometry
Keywords: اسیدهای آلی; Acylcarnitine analysis; Organic acidemia; Defects of fatty acid oxidation; Inherited disorders; Tandem mass spectrometry;
Clinical onset and prognosis of Asian children with organic acidemias, as detected by analysis of urinary organic acids using GC/MS, instead of mass screening
Keywords: اسیدهای آلی; Organic acidemia; GC/MS; Clinical onset; Outcome; Newborn screening;