Keywords: بیماری ادرار شربت افرا; fluid resuscitation; cerebral edema; renal-replacement therapy; anticoagulation; branched chain amino acids; BCAA; Branched chain amino acid; ED; Emergency department; IVF; Intravenous fluid; MSUD; Maple syrup urine disease; PN; Parenteral nutrition;
مقالات ISI بیماری ادرار شربت افرا (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: بیماری ادرار شربت افرا; Amino acid metabolism; Low protein products; Phenylketonuria; Tyrosinemia; Maple Syrup Urine Disease; Homocystinuria; Saudi Arabia;
Keywords: بیماری ادرار شربت افرا; Neuro-metabolic disorder; Maple syrup urine disease; BCKDHA; BCKDHB; DBT; Southwest Iran;
Keywords: بیماری ادرار شربت افرا; genetic testing; maple syrup urine disease; metabolic disorders; newborn screening;
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; Branched-chain α-ketoacid dehydrogenase complex; BCKDHA; DBT; Jordan;
Keywords: بیماری ادرار شربت افرا; acrodermatitis enteropathica; DBT gene; maple syrup urine disease; myelopathy; zinc deficiency;
Keywords: بیماری ادرار شربت افرا; DHT; digital health technology; GMDI; Genetic Metabolic Dietitians International; IEMs; inborn errors of metabolism; Leu; leucine; Lys; lysine; MSUD; maple syrup urine disease; MNT; metabolic nutrition therapy; Phe; phenylalanine; PKU; phenylketonuria; PD
Keywords: بیماری ادرار شربت افرا; Branched chain amino acids; Maple syrup urine disease; Brain; Cytokines
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; Branched chain ketoacid dehydrogenase; Living related donor liver transplantation; Domino transplantation;
Keywords: بیماری ادرار شربت افرا; glutaric aciduria type I; homocystinuria; isovaleric aciduria; maple syrup urine disease; medium chain acyl-CoA dehydrogenase deficiency; newborn screening; phenylketonuria; tandem mass spectrometry
Keywords: بیماری ادرار شربت افرا; gLE; genetic leukoencephalopathy; CNS; central nervous system; MRI; magnetic resonance imaging; MSUD; Maple Syrup Urine Disease; ClC-2; Chloride Ion Channel 2; MLC; Megalencephalic Leukoencephalopathy with subcortical cysts; X-ALD; X-linked Adrenoleukodys
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; MSUD; Inborn errors of metabolism; DiagnosisDoença da urina de xarope de bordo; DXB; Erros inatos do metabolismo; Diagnóstico
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; BCKDHA; BCKDHB; DBT; Mutation; Genotype–phenotype; Prenatal diagnosis; Modeling; Genetics; Indian
Keywords: بیماری ادرار شربت افرا; Glutaric aciduria; Maple syrup urine disease; Epileptic encephalopathy; West syndrome
Keywords: بیماری ادرار شربت افرا; NaPBA; sodium phenylbutyrate; UCD; urea cycle disorder; BCAA; branched-chain amino acids; RDCRN; Rare Diseases Clinical Research Network; GLM; generalized linear model; OTCD; ornithine transcarbamylase deficiency; BCKDK; branched-chain ketoacid dehydrogen
Keywords: بیماری ادرار شربت افرا; carrier frequency; dihydrolipoyl transacetylase gene; gene preference; maple syrup urine disease; Taiwanese Aboriginal Austronesian tribe
Keywords: بیماری ادرار شربت افرا; Allo-ILE; alloisoleucine; BCAA; branched-chain amino acids; BCKA; branched-chain α-ketoacids; BCKD; branched-chain α-ketoacid dehydrogenase; CoA; coenzyme A; DRI; dietary reference intake; GMDI; Genetic Metabolic Dietitians International; HRSA; health r
Keywords: بیماری ادرار شربت افرا; MSUD; maple syrup urine disease; BCAA; branched chain amino acids; BCKD; branched chain a ketoacid dehydrogenase complex; BCKDK; branched chain ketoacid dehydrogenase kinase; PPM1K/PP2Cm; protein phosphatase 2Cm; Maple syrup urine disease; Branched-chain
Keywords: بیماری ادرار شربت افرا; Branched-chain α-keto acid; Ultra fast liquid chromatography-mass spectrometry; Maple syrup urine disease; 2-Keto-3-methylvalerate; 2-Ketoisocaproate; 2-Ketoisovalerate;
Keywords: بیماری ادرار شربت افرا; 3-MT; 3-methoxytyramine; 5-HIAA; 5-hydroxyindoleacetic acid; 5-HT; serotonin, 5-hydroxytryptamine; ACoA; acetyl-CoA; α-KG; alpha-ketoglutarate; ANOVA; analysis of variance; AEC; amnion epithelial cells; BCAA; branched chain amino acid; BCKA; branched cha
Keywords: بیماری ادرار شربت افرا; BCAA; branched-chain amino acids; BCATc or BCATm; the cytosolic or mitochondrial isoform of branched-chain amino acid transaminase respectively (gene names: BCAT1 for BCATc, BCAT2 for BCATm); BCKA; branched chain keto acids; BCKD; branched-chain keto acid
Keywords: بیماری ادرار شربت افرا; 15-F2t-IsoP; 15-F2t-isoprostane; ADP; adenosine 5ʹ-diphosphate; Arg-1; arginase-1; BCAAs; branched-chain amino acids; BME; basal Eagle's medium; IGF-1; insulin-like growth factor-1; IL; interleukin; iNOS; inducible nitric oxide synthase; KPBS; potassium-
Keywords: بیماری ادرار شربت افرا; HTx; hepatocyte transplant; OLT; orthotopic liver transplantation; CYP; cytochrome P450; DLT; domino liver transplantation; OD; organ donor; MD; metabolic and diseased livers; MMA; methylmalonic acidemia; PHO; primary hyperoxaluria; MSUD; Maple Syrup Urin
Natural history of children and adults with maple syrup urine disease in the NBS-MSUD Connect registry
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; Inherited metabolic disorder; Inborn error of metabolism; Natural history; Registry;
Fourteen new mutations of BCKDHA, BCKDHB and DBT genes associated with maple syrup urine disease (MSUD) in Malaysian population
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; Autosomal recessive; Mutation; BCKDH; BCAAs; MSUD;
In silico prediction of the pathogenic effect of a novel variant of BCKDHA leading to classical maple syrup urine disease identified using clinical exome sequencing
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; Branched-chain alpha-keto acid dehydrogenase complex; BCKDH complex E1b subunit assembly; Amino acid residues interactions; Clinical exome sequencing;
Human dihydrolipoamide dehydrogenase (E3) deficiency: Novel insights into the structural basis and molecular pathomechanism
Keywords: بیماری ادرار شربت افرا; E3-deficiency; Dihydrolipoamide dehydrogenase; Alpha-ketoglutarate dehydrogenase complex; Pyruvate dehydrogenase complex; Pathogenic mutation; KGDHc; alpha-ketoglutarate (also known as 2-oxoglutarate) dehydrogenase complex; KG; alpha-ketoglutarate; PDHc;
Correction of hyperleucinemia in MSUD patients on leucine-free dietary therapy
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; Leucine; Clinical presentation; Emergency management; Hyperleucinemia;
Profiles of amino acids and biogenic amines in the plasma of Cri-du-Chat patients
Keywords: بیماری ادرار شربت افرا; 5-HT; serotonin; 5p; chromosome 5; AcOrn; acetyl ornitine; ADMA; dimethylarginine asymmetric; ADP; adenosine diphosphate; AGAT; glycine amidinotransferase; Ala; alanine; Alpha AAA; alpha-aminoadipic acid; Arg; arginine; ASL; argininosuccinate lyase; Asn;
Identification of a novel BCKDHA deletion causing maple syrup urine disease
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; BCKDHA; branched-chain amino acids; newborn screening;
A three-tier algorithm for guanidinoacetate methyltransferase (GAMT) deficiency newborn screening
Keywords: بیماری ادرار شربت افرا; GAMT; guanidinoacetate methyltransferase; BC; British Columbia; GAA; guanidinoacetate; LC-MS/MS; liquid chromatography tandem mass spectrometry; MSUD; maple syrup urine disease; AGAT; arginine:glycine amidinotransferase; ddH20; distilled deionized water;
Plasma amino acid and urine organic acid profiles of Filipino patients with maple syrup urine disease (MSUD) and correlation with their neurologic features
Keywords: بیماری ادرار شربت افرا; MSUD; maple syrup urine disease; BCAA; branched chain amino acids; LNAA; large neutral amino acids; BCKAD; branched chain keto acid dehydrogenase; MSUD; Plasma amino acids; Urine organic acids; Neurologic features;
Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach
Keywords: بیماری ادرار شربت افرا; ACMG; American College of Medical Genetics; AGREE II; Appraisal of Guidelines for Research and Evaluation; BH4; tetrahydrobiopterin; BMD; bone mineral disease; DRI; dietary reference intake; DXA; dual x-ray absorptiometry; EF; executive function; FFM; fat
Joint SOGC-CCMG Opinion for Reproductive Genetic Carrier Screening: An Update for All Canadian Providers of Maternity and Reproductive Healthcare in the Era of Direct-to-Consumer Testing
Keywords: بیماری ادرار شربت افرا; Carrier screening; prenatal screening; autosomal recessive disorder; autosomal dominant disorder; X-linked disorder; thalassemia; hemoglobinopathy; cystic fibrosis; Duchenne/Becker muscular dystrophy; Fragile X; spinal muscular atrophy; Tay-Sachs disease;
Opinion commune de la SOGC et du CCGM sur le dépistage génétique en contexte de procréation : Mise à jour à l'intention de l'ensemble des prestataires canadiens de soins de santé maternelle et de services en procréation, à l'ère des tests offerts dire
Keywords: بیماری ادرار شربت افرا; Carrier screening; prenatal screening; autosomal recessive disorder; autosomal dominant disorder; X-linked disorder; thalassemia; hemoglobinopathy; cystic fibrosis; Duchenne/Becker muscular dystrophy; Fragile X; spinal muscular atrophy; Tay-Sachs disease;
l-Carnitine supplementation decreases DNA damage in treated MSUD patients
Keywords: بیماری ادرار شربت افرا; MSUD; maple syrup urine disease; BCAAs; branched-chain amino acids; l-car; l-carnitine; DI; damage index; MDA; malondialdehyde; BCKDH; branched-chain α-keto acid dehydrogenase; BCKA; branched-chain α-keto acids; KIC; α-ketoisocaproate; Leu; leucine; Il
Maple syrup urine disease in Brazil: a panorama of the last two decades
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; MSUD; Inborn errors of metabolism; DiagnosisDoença da urina de xarope de bordo; DXB; Erros inatos do metabolismo; Diagnóstico
Eleven novel mutations of the BCKDHA, BCKDHB and DBT genes associated with maple syrup urine disease in the Chinese population: Report on eight cases
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; Branched chain amino acids; BCKDHA gene; BCKDHB gene; DBT gene; Prenatal diagnosis
Newborn screening for dihydrolipoamide dehydrogenase deficiency: Citrulline as a useful analyte
Keywords: بیماری ادرار شربت افرا; DLD deficiency; Maple syrup urine disease; Newborn screening; Second-tier testing; Citrulline
Identification of three novel mutations by studying the molecular genetics of Maple Syrup Urine Disease (MSUD) in the Lebanese population
Keywords: بیماری ادرار شربت افرا; Maple Syrup Urine Disease; MSUD; Mutation; Lebanon; Lebanese population; Lebanon MSUD; MSUD novel mutations
Protein and lipid damage in maple syrup urine disease patients: l-carnitine effect
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; Lipid peroxidation; Antioxidant; l-Carnitine
Keto acid profiling analysis as ethoxime/tert-butyldimethylsilyl derivatives by gas chromatography-mass spectrometry
Keywords: بیماری ادرار شربت افرا; TCA; tricarboxylic acid; MSUD; maple syrup urine disease; GC-MS; gas chromatography-mass spectrometry; MO/TMS; methoxime/trimethylsilyl; EO; ethoxime; TBDMS; tert-butyldimethylsilyl; SIM; selected ion monitoring; IS; internal standard; TDPA; 3,3â²-th
Amino acid disorders detected by quantitative amino acid HPLC analysis in Thailand: An eight-year experience
Keywords: بیماری ادرار شربت افرا; ASL; argininosuccinate lyase; ASS; argininosuccinate synthetase; CPS1; carbamoylphosphate synthetase I; HCY; homocystinuria; HPA; hyperphenylalaninemia; HPLC; high-performance liquid chromatography; IEM; inborn error of metabolism; MSUD; maple syrup urine
Antioxidant administration prevents memory impairment in an animal model of maple syrup urine disease
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; Antioxidants; Cognitive impairment; SHIRPA; Inborn errors of metabolism
DNA damage in an animal model of maple syrup urine disease
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; Branched-chain amino acids; DNA damage; Comet assay; Oxidative stress; Antioxidant treatment
Liver Transplantation for Classical Maple Syrup Urine Disease: Long-Term Follow-Up in 37 Patients and Comparative United Network for Organ Sharing Experience
Keywords: بیماری ادرار شربت افرا; BCAA; Branched-chain amino acid; BCKDH; Branched-chain ketoacid dehydrogenase complex; MSUD; Maple syrup urine disease; UNOS; United Network for Organ Sharing;
Analysis of gene mutations in Chinese patients with maple syrup urine disease
Keywords: بیماری ادرار شربت افرا; Maple syrup urine disease; Branched-chain α-keto acid dehydrogenase complex; Gene mutation;
Chromatographic diagnosis of maple syrup urine disease by measuring the l-alloisoleucine/l-phenylalanine ratio in dried blood spots
Keywords: بیماری ادرار شربت افرا; Neonatal screening; Branched-chain amino acids; Alloisoleucine/phenylalanine ratio; Maple syrup urine disease; Phenylketonuria; High-performance ligand-exchange chromatography
Evaluation and long-term follow-up of infants with inborn errors of metabolism identified in an expanded screening programme
Keywords: بیماری ادرار شربت افرا; BD; biotinidase deficiency; CIT 1; type I citrullinaemia; FFA; free fatty acid; GA-1; type I glutaric aciduria; GALE; classical galactosaemia; GALK; galactokinase deficiency; HPA; hyperphenylalaninaemia; IEM; inborn errors of metabolism; IQ; Intellectual
An Ethical and Policy Analysis of Elective Transplantation for Metabolic Conditions Diagnosed by Newborn Screening
Keywords: بیماری ادرار شربت افرا; CoA; Coenzyme A; DDLT; Deceased donor liver transplant; DPR; Doctor-patient relationship; LDLT; Living donor liver transplantation; LT; Liver transplantation; MELD; Model for End-stage Liver Disease; MESSAGE; MELD Exceptional Case Study Group; MMA; Methyl