Pages that link to "Q37570443"
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The following pages link to Recommendations for the nutrition management of phenylalanine hydroxylase deficiency (Q37570443):
Displaying 50 items.
- Bone health in phenylketonuria: a systematic review and meta-analysis (Q27008288) (← links)
- Amino Acid Medical Foods Provide a High Dietary Acid Load and Increase Urinary Excretion of Renal Net Acid, Calcium, and Magnesium Compared with Glycomacropeptide Medical Foods in Phenylketonuria. (Q33701791) (← links)
- Diet History Is a Reliable Predictor of Suboptimal Docosahexaenoic Acid Levels in Adult Patients with Phenylketonuria (Q35752491) (← links)
- Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management (Q35889337) (← links)
- Phenylketonuria and Gut Microbiota: A Controlled Study Based on Next-Generation Sequencing (Q36060094) (← links)
- Phenylketonuria (PKU): A problem solved? (Q36680623) (← links)
- Phone-based motivational interviewing to increase self-efficacy in individuals with phenylketonuria (Q36680654) (← links)
- Clinical relevance of the discrepancy in phenylalanine concentrations analyzed using tandem mass spectrometry compared with ion-exchange chromatography in phenylketonuria (Q36680661) (← links)
- Nutritional status of patients with phenylketonuria in Japan (Q37198978) (← links)
- Phenylketonuria patients' and their parents' acceptance of the disease: multi-centre study. (Q37341947) (← links)
- Development of the US English version of the phenylketonuria - quality of life (PKU-QOL) questionnaire (Q37690085) (← links)
- National Institutes of Health (NIH) review of evidence in phenylalanine hydroxylase deficiency (phenylketonuria) and recommendations/guidelines for therapy from the American College of Medical Genetics (ACMG) and Genetics Metabolic Dietitians Intern (Q38205531) (← links)
- The relationship between dietary intake, growth and body composition in Phenylketonuria. (Q38664025) (← links)
- Adherence to clinic recommendations among patients with phenylketonuria in the United States (Q38761359) (← links)
- Protein intake and physical activity are associated with body composition in individuals with phenylalanine hydroxylase deficiency. (Q38808205) (← links)
- Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach (Q38841227) (← links)
- Neuropsychiatric comorbidities in adults with phenylketonuria: A retrospective cohort study (Q38912660) (← links)
- New protein structures provide an updated understanding of phenylketonuria (Q39394897) (← links)
- Modeling correlates of low bone mineral density in patients with phenylalanine hydroxylase deficiency (Q39992743) (← links)
- Special low protein foods for phenylketonuria: availability in Europe and an examination of their nutritional profile. (Q40181778) (← links)
- Long-term safety and efficacy of sapropterin: the PKUDOS registry experience (Q40260147) (← links)
- Sapropterin Dihydrochloride Mixed With Common Foods and Beverages (Q42153164) (← links)
- First-year metabolic control guidelines and their impact on future metabolic control and neurocognitive functioning in children with PKU. (Q42269076) (← links)
- The complete European guidelines on phenylketonuria: diagnosis and treatment. (Q42376686) (← links)
- Glycomacropeptide for nutritional management of phenylketonuria: a randomized, controlled, crossover trial. (Q42401605) (← links)
- Phenylketonuria Scientific Review Conference: state of the science and future research needs (Q45298394) (← links)
- Impact of Dietary Intake on Bone Turnover in Patients with Phenylalanine Hydroxylase Deficiency (Q47116443) (← links)
- Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations (Q47137137) (← links)
- Serum ischemia modified albumin is a possible new marker of oxidative stress in phenylketonuria (Q47899947) (← links)
- Host conditioning and rejection monitoring in hepatocyte transplantation in humans (Q47906882) (← links)
- Metabolomic Insights into the Nutritional Status of Adults and Adolescents with Phenylketonuria Consuming a Low-Phenylalanine Diet in Combination with Amino Acid and Glycomacropeptide Medical Foods. (Q49787227) (← links)
- A facile method for urinary phenylalanine measurement on paper-based lab-on-chip for PKU therapy monitoring (Q50014427) (← links)
- Metabolomic Markers of Essential Fatty Acids, Carnitine, and Cholesterol Metabolism in Adults and Adolescents with Phenylketonuria. (Q51246317) (← links)
- A new therapy prevents intellectual disability in mouse with phenylketonuria. (Q52584890) (← links)
- Metabolomic changes demonstrate reduced bioavailability of tyrosine and altered metabolism of tryptophan via the kynurenine pathway with ingestion of medical foods in phenylketonuria. (Q54839680) (← links)
- Optimising amino acid absorption: essential to improve nitrogen balance and metabolic control in phenylketonuria (Q57030358) (← links)
- Clinical and neuropsychological outcomes for children with phenylketonuria in Upper Egypt; a single-center study over 5 years (Q57483196) (← links)
- Diagnostic and therapeutic recommendations for the treatment of hyperphenylalaninemia in patients 0-4 years of age (Q58795807) (← links)
- The Use of Glycomacropeptide in Patients with Phenylketonuria: A Systematic Review and Meta-Analysis (Q59797027) (← links)
- Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians' current practices (Q60917781) (← links)
- Phenylketonuria Diet Promotes Shifts in Firmicutes Populations (Q64107955) (← links)
- Development of a Whole Blood Paper-Based Device for Phenylalanine Detection in the Context of PKU Therapy Monitoring. (Q64907934) (← links)
- Strategies to engage lost to follow-up patients with phenylketonuria in the United States: Best practice recommendations (Q90094497) (← links)
- Sex differences in body composition and bone mineral density in phenylketonuria: A cross-sectional study (Q90330656) (← links)
- The financial and time burden associated with phenylketonuria treatment in the United States (Q90980531) (← links)
- The effects of low protein products availability on growth parameters and metabolic control in selected amino acid metabolism disorders patients (Q91915666) (← links)
- The molecular epidemiology of hyperphenylalaninemia in Uygur population: incidence from newborn screening and mutational spectra (Q92243255) (← links)
- Simplified Diet for nutrition management of phenylketonuria: A survey of U.S. metabolic dietitians (Q94571369) (← links)
- Nutrient intake, body composition, and blood phenylalanine control in children with phenylketonuria compared to healthy controls (Q95259829) (← links)
- Prospects for Cell-Directed Curative Therapy of Phenylketonuria (PKU) (Q96306729) (← links)