Keywords: فنیل کتونوری; AUC; Area under the curve; CNS; Central nervous system; CSF; Cerebrospinal fluid; LAT1; Large neutral amino acid transporter 1; LNAA; Large neutral amino acid; Phe; Phenylalanine; PKU; Phenylketonuria; TAT1; T-type amino acid transporter 1; Trp; Tryptopha
مقالات ISI فنیل کتونوری (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: فنیل کتونوری; Phenylketonuria; Cost of living; Time burden;
Keywords: فنیل کتونوری; BH4; 6R-tetrahydrobiopterin; ECT; early and continuously treated; HPA; hyperphenylalaninemia; IDC; index of dietary control; IQ; intelligence quotient; LNAA; large neutral amino acid; PAH; phenylalanine hydroxylase; PKU; phenylketonuria; SD; standard devi
Keywords: فنیل کتونوری; Phenylketonuria; White matter; Executive; Brain; Cognition;
Keywords: فنیل کتونوری; IEM; inborn errors of metabolism; NIH; National Institutes of Health; ODS; Office of Dietary Supplements; ORDR; Office of Rare Diseases Research; HRSA; Health Resources and Services Administration; PKU; phenylketonuria; PAH; phenylalanine hydroxylase; PHE
Keywords: فنیل کتونوری; DAH7PS; 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase; IEC; ion exchange chromatography; MBP; maltose binding protein; PS; Phenyl Sepharose; Phe; phenylalanine; PAH; phenylalanine hydroxylase; PKU; phenylketonuria; PAGE; polyacrylamide gel electrop
Keywords: فنیل کتونوری; Mass spectrometry; Method validation; Phenylketonuria; Phenylalanine
Late-diagnosed phenylketonuria mimicking x-linked adrenoleukodystrophy with heterozygous mutations of the PAH Gene: A case report and literature review
Keywords: فنیل کتونوری; Late diagnosis; Heterozygous mutations; Leukoencephalopathy; Phenylketonuria;
The impact of phenylketonuria on PKU patients' quality of life: Using of the phenylketonuria-quality of life (PKU-QOL) questionnaires
Keywords: فنیل کتونوری; Phenylketonuria; Quality of life; Metabolic disorders; Nutrition;
BH4 deficiency identified in a neonatal screening program for hyperphenylalaninemia
Keywords: فنیل کتونوری; Phenylketonuria; Neonatal screening; Intellectual disability; Rare diseases; Fenilcetonúria; Triagem neonatal; Deficiência intelectual; Doenças raras;
BH4 deficiency identified in a neonatal screening program for hyperphenylalaninemia
Keywords: فنیل کتونوری; Phenylketonuria; Neonatal screening; Intellectual disability; Rare diseases; Fenilcetonúria; Triagem neonatal; Deficiência intelectual; Doenças raras;
The Anorexia Nervosa Genetics Initiative (ANGI): Overview and methods
Keywords: فنیل کتونوری; AN; anorexia nervosa; ANGI; Anorexia Nervosa Genetics Initiative; ANGI-ANZ(AUS); Study recruitment for Australia/New Zealand from Australia; ANGI-ANZ(NZ); Study recruitment for Australia/New Zealand from New Zealand; ANGI-DK; Study recruitment for Denmark
Pegvaliase for the treatment of phenylketonuria: Results of a long-term phase 3 clinical trial program (PRISM)
Keywords: فنیل کتونوری; ACMG; American College of Medical Genetics and Genomics; ADHD RS-IV IA; Attention Deficit Hyperactivity Disorder Rating Scale IV inattention subscale; AE; adverse event; CTCAE; Common Terminology Criteria for Adverse Events; DMC; Data Monitoring Committee
Phenylalanine ammonia lyase (PAL): From discovery to enzyme substitution therapy for phenylketonuria
Keywords: فنیل کتونوری; Phenylketonuria; PKU; Phenylalanine ammonia lyase; PAL; Phenylalanine hydroxylase; Phenylalanine; Enzyme substitution therapy;
Aptamer-based assay for monitoring genetic disorder phenylketonuria (PKU)
Keywords: فنیل کتونوری; Aptamer; Genetic disorder; Biomarker; Phenylketonuria; Gold nanostructure;
Brain bioenergetics in rats with acute hyperphenylalaninemia
Keywords: فنیل کتونوری; Bioenergetics; Brain; HyperphenylalanineMia; Mitochondria; Phenylalanine; Phenylketonuria;
First-year metabolic control guidelines and their impact on future metabolic control and neurocognitive functioning in children with PKU
Keywords: فنیل کتونوری; Phenylketonuria; Children; PKU; Guidelines; Blood phenylalanine; Neurocognitive function;
Class enzyme-based motors for “on the fly” enantiomer analysis of amino acids
Keywords: فنیل کتونوری; Class-enzyme motors; Millimeter motors; Enantiomers; Phenylketonuria; Vibrio Cholerae;
MinireviewNew protein structures provide an updated understanding of phenylketonuria
Keywords: فنیل کتونوری; PAH; Phenylalanine hydroxylase; PKU; phenylketonuria; Phenylketonuria; Phenylalanine hydroxylase; Allostery; Conformational selection; Pharmacological chaperones;
Production of human recombinant phenylalanine hydroxylase in Lactobacillus plantarum for gastrointestinal delivery
Keywords: فنیل کتونوری; Phenylketonuria; Lactobacilli; Phenylalanine hydroxylase; Caco-2 cells;
80-lecie fenyloketonurii. CzÄÅÄ II: pierwszy literacki oraz inne niemedyczne opisy choroby
Keywords: فنیل کتونوری; fenyloketonuria; literatura; humanistyczne umiejÄtnoÅci w zawodzie lekarza; historia medycyny; Phenylketonuria; Literary texts; Human competencies of doctoring; History of medicine;
Construction of different calibration models by FTIR/ATR spectra and their application in screening of phenylketonuria
Keywords: فنیل کتونوری; Kernel function partial least squares; Consensus; Attenuated total reflectance Fourier transform infrared spectroscopy; Phenylketonuria;
Phenylketonuria (PKU): A problem solved?
Keywords: فنیل کتونوری; ACMG, American College of Medical Genetics and Genomics; NPKUA, National PKU Alliance; PAH, phenylalanine hydroxylase; Phe, phenylalanine; PKU, phenylketonuriaPhenylalanine; Phenylketonuria; Phenylalanine hydroxylase deficiency
80-lecie fenyloketonurii. CzÄÅÄ I: historia nazwy i nietuzinkowi pionierzy badaÅ nad chorobÄ
Keywords: فنیل کتونوری; fenyloketonuria; fenylopirogronianowa amencja; wrodzone bÅÄdy metabolizmu; historia medycyny; Phenylketonuria; Phenylpyruvic amentia; Inborn errors of metabolism; History of medicine;
DNA methylation in the pathophysiology of hyperphenylalaninemia in the PAHenu2 mouse model of phenylketonuria
Keywords: فنیل کتونوری; PAHenu2; DNA methylation; Phenylketonuria; Toxicity;
Badania IQ u pacjentów z fenyloketonuriÄ
w latach piÄÄdziesiÄ
tych i szeÅÄdziesiÄ
tych XX wieku
Keywords: فنیل کتونوری; historia medycyny; fenyloketonuria; IQ; DQ; History of medicine; Phenylketonuria; IQ; DQ;
A novel common large genomic deletion and two new missense mutations identified in the Romanian phenylketonuria population
Keywords: فنیل کتونوری; PAH, phenylalanine hydroxylase; HPA, hyperphenylalaninemia; PKU, phenylketonuria; BH4, tetrahydrobiopterin; L-Phe, phenylalanine; MLPA, multiplex ligation-dependent probe amplification; NGS, next generation sequencingHyperphenylalaninemia; Phenylketonuria
Badania IQ u chorych na fenyloketonuriÄ w latach siedemdziesiÄ
tych i osiemdziesiÄ
tych XX wieku
Keywords: فنیل کتونوری; historia medycyny; fenyloketonuria; IQ; DQ; History of medicine; Phenylketonuria; IQ; DQ;
Co-expression of phenylalanine hydroxylase variants and effects of interallelic complementation on in vitro enzyme activity and genotype-phenotype correlation
Keywords: فنیل کتونوری; Tetrahydrobiopterin; Phenylketonuria; PKU; Hyperphenylalaninemia;
Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach
Keywords: فنیل کتونوری; 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
Utilidad de los marcadores de remodelado óseo en la detección de enfermedad mineral ósea en pacientes con fenilcetonuria
Keywords: فنیل کتونوری; Fenilcetonuria; Osteopenia; Tetrahidrobiopterina; DensitometrÃa; Nutrición; Mineralización ósea; Phenylketonuria; Osteopenia; Tetrahydrobipterin; Densitometry; Nutrition; Bone mineralization;
Utility of bone turnover markers in metabolic bone disease detection in patients with phenylketonuria
Keywords: فنیل کتونوری; Phenylketonuria; Osteopenia; Tetrahydrobipterin; Densitometry; Nutrition; Bone mineralizationFenilcetonuria; Osteopenia; Tetrahidrobiopterina; Densitometría; Nutrición; Mineralización ósea
Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approach
Keywords: فنیل کتونوری; Phenylketonuria; Protein substitute; l-Amino acid supplements; Glycomacropeptide
Is BRIEF a useful instrument in day to day care of patients with phenylketonuria?
Keywords: فنیل کتونوری; PKU; phenylketonuria; PAH; phenylalanine hydroxylase; Phe; phenylalanine; Tyr; tyrosine; EF; executive functions; BRIEF; Behavior Rating Inventory of Executive Function; ANT; Amsterdam Neuropsychological Tasks; BRIEF-A; Behavior Rating Inventory of Execut
Altered DNA methylation in PAH deficient phenylketonuria
Keywords: فنیل کتونوری; Phenylketonuria; Methylome; Gene expression; Biomarker;
Long-term safety and efficacy of sapropterin: The PKUDOS registry experience
Keywords: فنیل کتونوری; AE; adverse event; PKU; phenylketonuria; Phe; phenylalanine; BH4; tetrahydrobiopterin; PKUDOS; phenylketonuria demographics, outcomes and safety; PAH; phenylalanine hydroxylase; Phenylketonuria; Phenylalanine; Sapropterin;
Neurocognitive and neuroimaging outcome of early treated young adult PKU patients: A longitudinal study
Keywords: فنیل کتونوری; PKU; phenylketonuria; Phe; phenylalanine; EF; executive function; WAIS-R; Wechsler Adult Intelligence Scale-Revised; EPMT; Elithorn's Perceptual Maze Test; WCST; Wisconsin Card Sorting Test; IDC; Index of Dietary Control; MRI; Magnetic Resonance Imaging;
Physiological competition of brain phenylalanine accretion: Initial pharmacokinetic analyses of aminoisobutyric and methylaminoisobutyric acids in Pahenu2 −/− mice
Keywords: فنیل کتونوری; Phenylketonuria; Large neutral amino acids; Phenylalanine; LAT-1 transporter; Aminoisobutyric acid; Methylaminoisobutyric acid; Pharmacokinetics
Evaluation of Neuropsychiatric Function in Phenylketonuria: Psychometric Properties of the ADHD Rating Scale-IV and Adult ADHD Self-Report Scale Inattention Subscale in Phenylketonuria
Keywords: فنیل کتونوری; attention deficit/hyperactivity disorder; inattention; metabolic disorder; phenylketonuria; psychometrics;
A randomized, placebo-controlled, double-blind study of sapropterin to treat ADHD symptoms and executive function impairment in children and adults with sapropterin-responsive phenylketonuria
Keywords: فنیل کتونوری; Phenylketonuria; PKU; Treatment; Sapropterin; Attention deficit-hyperactivity disorder; Mental health;
Overweight and obesity in PKU: The results from 8 centres in Europe and Turkey
Keywords: فنیل کتونوری; Phenylketonuria; Obesity; Overweight
WspóÅwystÄpowanie dwóch rzadkich chorób genetycznych: fenyloketonurii oraz zespoÅu Pradera i Williego. Opis przypadku
Keywords: فنیل کتونوری; fenyloketonuria; zespóÅ Pradera i Williego; hydroksylaza fenyloalaniny; tetrahydrobiopteryna; Phenylketonuria; Prader-Willi Syndrome; Phenylalanine hydroxylase; Tetrahydrobiopterin;
Variability in phenylalanine control predicts IQ and executive abilities in children with phenylketonuria
Keywords: فنیل کتونوری; Phenylketonuria; Phenylalanine; Variability; IQ; Executive abilities;
Sapropterin dihydrochloride use in pregnant women with phenylketonuria: An interim report of the PKU MOMS sub-registry
Keywords: فنیل کتونوری; AE; adverse event; Apgar; Appearance, Pulse, Grimace, Activity, Respiration; BH4; tetrahydrobiopterin; BMI; Body Mass Index; CDC; Centers for Disease Control and Prevention; ID; identification; LMP; last menstrual period; OFC; occipitofrontal circumferenc
Inborn Error of Metabolism (IEM) screening in Singapore by electrospray ionization-tandem mass spectrometry (ESI/MS/MS): An 8Â year journey from pilot to current program
Keywords: فنیل کتونوری; DBS; dried blood spot; ESI/MS/MS; electrospray ionization-tandem mass spectrometry; LC/MS/MS; liquid chromatography-tandem mass spectrometry; FAOD; fatty acid oxidation disorder; FPR; false positive rate; IEM; Inborn Errors of Metabolism; NBS; newborn scr
Anthropometric characteristics and nutrition in a cohort of PAH-deficient patients
Keywords: فنیل کتونوری; Phenylketonuria; Growth; Nutrition; Anthropometrics; PAH-deficient; BH4; (6R)-L-erythro-5,6,7,8-tetrahydrobiopterin; HPA; hyperphenylalaninaemia; GR; growth rate; PAH; phenylalanine-4-hydroxylase; Phe; phenylalanine; PKU; phenylketonuria; Ref.; reference;
Supplementation with a powdered blend of PUFAs normalizes DHA and AA levels in patients with PKU
Keywords: فنیل کتونوری; Phenylketonuria; Docosahexaenoic acid; Arachidonic acid; Fish oil; KeyOmega;
Simultaneous determination of phenylalanine and tyrosine in peripheral capillary blood by HPLC with ultraviolet detection
Keywords: فنیل کتونوری; High performance liquid chromatography; Ultraviolet detection; Phenylalanine; Tyrosine; Phenylketonuria;
Quantitation of gamma-hydroxybutyric acid in dried blood spots: Feasibility assessment for newborn screening of succinic semialdehyde dehydrogenase (SSADH) deficiency
Keywords: فنیل کتونوری; SSADH; succinic semialdehyde dehydrogenase; DBS; dried blood spots; IMDs; inherited metabolic disorders; PKU; phenylketonuria; PHE; phenylalanine; GABA; gamma aminobutyric acid; GHB; gamma-hydroxybutyric acid; α-HBA; alpha-hydroxybutyric acid; β-HBA; be
White matter integrity and executive abilities following treatment with tetrahydrobiopterin (BH4) in individuals with phenylketonuria
Keywords: فنیل کتونوری; Phenylketonuria; Tetrahydrobiopterin; Sapropterin; White matter; Diffusion tensor imaging; Executive;