المؤلفون: H. Vestergaard, Júlio César Rocha, Joanna Gribben, Sylvain Dubois, Clara Vasconcelos, H. Zweers, U. Meyer, C. Maritz, M. Heddrich-Ellerbrok, S.M. Bernabei, K. Va nde Kerckhove, F.J. White, S. Adam, C. Jankowski, I. Saruggia, S. Bigot, A. van Teeffelen-Heithoff, R. Link, A. Terry, J. Wildgoose, J. Baruteau, François Eyskens, K. van Wyk, R.G. Janssen-Regelink, C. Ferguson, A.M.J. van Wegberg, M. Robert, C. Laguerre, K. Luyten, Marjorie Dixon, R. Thom, Louise Robertson, S. Dawson, Anne Daly, Katharina Dokoupil, Carolyn Dunlop, Anita MacDonald, A. Faria, S. Lowry, M.F. Almeida, E. Favre, M. van Rijn, M. Dassy, E. Sjoqvist, H. Champion, C. Jouault, S. McDowell, Carmen Rohde, S. Le Verge, Sharon Evans, J. Stafford, M. Assoun, Carolina Gonçalves, D. Webster, A. Micciche

المساهمون: Faculteit Medische Wetenschappen/UMCG

المصدر: Molecular Genetics and Metabolism, 110, 4, pp. 439-45
Molecular genetics and metabolism
Molecular Genetics and Metabolism, 110, 439-45
Molecular Genetics and Metabolism, 110(4), 439-445. ACADEMIC PRESS INC ELSEVIER SCIENCE

مصطلحات موضوعية: Adult, medicine.medical_specialty, Pediatrics, Adolescent, Endocrinology, Diabetes and Metabolism, Amino-Acid N-Acetyltransferase, Argininosuccinic Aciduria, MULTICENTER, Branch chain amino acids (BCAA), Body weight, DIAGNOSIS, Biochemistry, THERAPY, Endocrinology, Urea cycle disorders (UCD), Internal medicine, Surveys and Questionnaires, Genetics, medicine, Diet, Protein-Restricted, Humans, Molecular gastro-enterology and hepatology [IGMD 2], Child, Molecular Biology, Urea Cycle Disorders, Inborn, Ornithine Carbamoyltransferase, Total protein, Citrullinemia, Arginase, business.industry, Metabolic disorder, Dietary management, Infant, Newborn, Protein restricted diet, Infant, medicine.disease, Europe, Treatment Outcome, Argininosuccinic aciduria, Dietary treatment, Urea cycle, Child, Preschool, Amino Acids, Essential, Carbon-Nitrogen Ligases with Glutamine as Amide-N-Donor, Human medicine, Metabolic, business, Essential amino acids (EAA)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84d9716cdbd9a1401c49ce1ff816e99e
https://research.rug.nl/en/publications/a306aca2-d245-490e-845a-3b27cb76ff7b

المؤلفون: M. van Rijn, M. E. Rubio-Gozalbo, R.G. Janssen-Regelink, H.E.E. Zweers-van Essen, M.R. Heiner-Fokkema, N.A. van der Herberg-van de Wetering, C. C. Boelen, M.C. de Vries, C. E. M. Hollak, G. Venema, Annet M. Bosch, E.M.C. van der Ploeg, F. J. van Spronsen, N.M. Ter Horst, C. Jonkers, F.C. Hofstede, E. C. Carbasius Weber, Mirian C. H. Janssen, Karen Anjema

المساهمون: Amsterdam Gastroenterology Endocrinology Metabolism, Paediatric Metabolic Diseases, Endocrinology, Extramural researchers, Center for Liver, Digestive and Metabolic Diseases (CLDM), Kindergeneeskunde, RS: GROW - School for Oncology and Reproduction

المصدر: Molecular genetics and metabolism, 104(Suppl), S60-S63. Academic Press Inc.
Molecular Genetics and Metabolism, 104 Suppl, pp. S60-3
Molecular Genetics and Metabolism, 104, S60-S63. ACADEMIC PRESS INC ELSEVIER SCIENCE
Molecular Genetics and Metabolism, 104 Suppl, S60-3
Molecular Genetics and Metabolism, 104, S60-S63. Academic Press Inc.

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Time Factors, Health aging / healthy living [IGMD 5], Adolescent, Phenylalanine hydroxylase, Phenylalanine, Endocrinology, Diabetes and Metabolism, HYDROXYLASE DEFICIENCY, Sapropterin, Blood phenylalanine, Biochemistry, MOLECULAR-GENETICS, Endocrinology, Phenylketonurias, Internal medicine, Genetics, medicine, Humans, Phenylketonuria, In patient, Child, Molecular Biology, Diagnostic Techniques and Procedures, Demography, RESPONSIVE PHENYLKETONURIA, BH4, Tetrahydrobiopterin, biology, Hydroxylase deficiency, business.industry, Infant, Middle Aged, Biopterin, Child, Preschool, PKU, biology.protein, Female, business, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff825ac137c9868dd923afda1cb7bdb7
https://doi.org/10.1016/j.ymgme.2011.09.024

المؤلفون: J. Wildgoose, K. Kaalund-Hansen, K. Eftring, C. Jankowski, D. Lier, S. Saruhan, S. Bigot, M. van Rijn, I. Jones, A. Clark, A. De Meyer, K. Luyten, Carmen Rohde, K. Lang, N. Tuncer, Sharon Evans, E. Sjoqvist, K. Vande Kerckhove, F.J. White, M. Heddrich-Ellerbrok, K. Blom Malmberg, R.G. Janssen-Regelink, H. Zweers, Hulya Gokmen-Ozel, A. Terry, Karen Corthouts, A.M. Lammardo, Júlio César Rocha, Clara Vasconcelos, Maria Gizewska, C. Ellerton, Martine Dassy, H. Chan, S. Lowry, K. van Wyk, N.M. Ter Horst, S. Clark, K. Dokupil, A. Faria, K. Ahring, C. Timmer, A. Belanger Quintana, Isidro Vitoria, F. Gunden, M. Diels, Sylvain Dubois, A. van Teeffelen-Heithoff, M. Joerg-Streller, S. Heiber, T. Bushueva, L. Stoelen, Alessandro P. Burlina, M. Assoun, Bozena Didycz, Abhijit Ricky Pal, D. Webster, C. Jonkers, L. van der Ploeg, G. Bihet, D. Moor, R. Skeath, J. Ekengren, U. Meyer, A. Aguiar, Jaime Dalmau, Anita MacDonald, Kathleen Ross, A. Fischer, M. Robert, F. J. van Spronsen, A.M.J. van Wegberg, Joanna Gribben, Carina Heidenborg, Suzanne Ford, Barbara Cochrane, M.F. Almeida, R. Lilje, L. Robertson, Peter Freisinger, A. Caris, E. Kiss

المساهمون: Extramural researchers, Endocrinology, Center for Liver, Digestive and Metabolic Diseases (CLDM)

المصدر: Molecular genetics and metabolism, 115(1), 17-22. Academic Press Inc.
Molecular genetics and metabolism
MOLECULAR GENETICS AND METABOLISM
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Molecular Genetics and Metabolism, 115(1), 17-22. ACADEMIC PRESS INC ELSEVIER SCIENCE
Molecular Genetics and Metabolism, 115, 1, pp. 17-22
Molecular Genetics and Metabolism, 115, 17-22
Molecular Genetics and Metabolism, 115(1), 17. Academic Press Inc.

مصطلحات موضوعية: Male, Pediatrics, age distribution, Southern Europe, Turkey, phenylalanine, Phenylketonurias, Cross-sectional study, patient monitoring, Endocrinology, Diabetes and Metabolism, lnfectious Diseases and Global Health Radboud Institute for Molecular Life Sciences [Radboudumc 4], INFANTS, METABOLIC-CONTROL, casein, preschool child, Biochemistry, Endocrinology, newborn, Surveys and Questionnaires, infant disease, Phenylketonuria, ADULT PATIENTS, Amino Acids, Child, Protein substitute, administration and dosage, GLYCOMACROPEPTIDE, education.field_of_study, L-Amino acid supplements, childhood disease, adult, Northern European, Caseins, Protein intake, clinical practice, Europe, AMINO-ACID MIXTURE, Chemistry, female, priority journal, Child, Preschool, OBESITY, Western europe, GROWTH, world health organization, Adult, Dietary Proteins, DIETARY-MANAGEMENT, amino acid, medicine.medical_specialty, Diet therapy, Population, Western Europe, Eastern Europe, World Health Organization, Article, caseinomacropeptide, Genetics, medicine, cross-sectional study, Humans, human, Preschool, education, Molecular Biology, Biology, prescription, business.industry, questionnaire, Infant, Newborn, Dietary management, Infant, school child, medicine.disease, protein intake, major clinical study, Obesity, Peptide Fragments, NITROGEN, protein intake, age distribution, diet therapy, peptide fragment, consensus, dietary supplement, Dietary Supplements, Human medicine, business, Glycomacropeptide

وصف الملف: image/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31964a57eca445eead65d48acda5743b
https://doi.org/10.1016/j.ymgme.2015.03.006

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