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1دورية أكاديمية
المؤلفون: Sharon Evans, Anne Daly, Satnam Chahal, Catherine Ashmore, John MacDonald, Anita MacDonald
المصدر: Molecular Genetics and Metabolism Reports, Vol 14, Iss C, Pp 10-14 (2018)
مصطلحات موضوعية: Metabolic disorders, Phenylketonuria (PKU), Neophobia, Taste preferences, Food frequency questionnaire, L-amino acid supplements, Medicine (General), R5-920, Biology (General), QH301-705.5
وصف الملف: electronic resource
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المؤلفون: Anita MacDonald, Catherine Ashmore, S Chahal, John MacDonald, Anne Daly, Sharon Evans
المصدر: Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 14, Iss C, Pp 10-14 (2018)مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Taste, Food frequency questionnaire, Metabolic disorders, Phenylketonuria (PKU), Food preference, 03 medical and health sciences, chemistry.chemical_compound, Endocrinology, Food choice, Genetics, medicine, lcsh:QH301-705.5, Molecular Biology, lcsh:R5-920, 030109 nutrition & dietetics, Aspartame, Taste preferences, business.industry, digestive, oral, and skin physiology, Neophobia, food and beverages, nutritional and metabolic diseases, medicine.disease, Preference, lcsh:Biology (General), chemistry, L-amino acid supplements, lcsh:Medicine (General), business, Research Paper, Clinical psychology
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المؤلفون: Aguiar, A., Ahring, K., Almeida, M. F., Assoun, M., Belanger Quintana, A., Bigot, S., Bihet, G., Malmberg, Karin Blom, Burlina, A., Bushueva, T., Caris, A., Chan, H., Clark, A., Clark, S., Cochrane, B., Corthouts, K., Dalmau, J., Dassy, M., De Meyer, A., Didycz, B., Diels, M., Dokupil, K., Dubois, S., Eftring, K., Ekengren, J., Ellerton, C., Evans, S., Faria, A., Fischer, A., Ford, S., Freisinger, P., Gizewska, M., Gokmen-Ozel, H., Gribben, J., Gunden, F., Heddrich-Ellerbrok, M., Heiber, S., Heidenborg, C., Jankowski, C., Janssen-Regelink, R., Jones, I., Jonkers, C., Joerg-Streller, M., Kaalund-Hansen, K., Kiss, E., Lammardo, A. M., Lang, K., Lier, D., Lilje, R., Lowry, S., Luyten, K., MacDonald, A., Meyer, U., Moor, D., Pal, A., Robert, M., Robertson, L., Rocha, J. C., Rohde, C., Ross, K., Saruhan, S., Sjoqvist, E., Skeath, R., Stoelen, L., Ter Horst, N. M., Terry, A., Timmer, C., Tuncer, N., Vande Kerckhove, K., van der Ploeg, L., van Rijn, M., van Spronsen, F. J., van Teeffelen-Heithoff, A., van Wegberg, A., van Wyk, K., Vasconcelos, C., Vitoria, I., Wildgoose, J., Webster, D., White, F. J., Zweers, H.
المصدر: Molecular Genetics and Metabolism. 115(1):17-22
مصطلحات موضوعية: Phenylketonuria, Protein substitute, L-Amino acid supplements, Glycomacropeptide
وصف الملف: print
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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
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5دورية أكاديمية
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6مورد إلكتروني
المؤلفون: UCL - (SLuc) Service d'endocrinologie et de nutrition, Aguiar, A., Ahring, K., Almeida, M.F., Assoun, M., Belanger Quintana, A., Bigot, S., Bihet, G., Blom Malmberg, K., Burlina, A., Bushueva, T., Caris, A., Chan, H., Clark, A., Clark, S., Cochrane, B., Corthouts, K., Dalmau, J., Dassy, Martine, De Meyer, A., Didycz, B., Diels, M., Dokupil, K., Dubois, S., Eftring, K., Ekengren, J., Ellerton, C., Evans, S., Faria, A., Fischer, A., Ford, S., Freisinger, P., Gizewska, M., Gokmen-Ozel, H., Gribben, J., Gunden, F., Heddrich-Ellerbrok, M., Heiber, S., Heidenborg, C., Jankowski, C., Janssen-Regelink, R., Jones, I., Jonkers, C., Joerg-Streller, M., Kaalund-Hansen, K., Kiss, E., Lammardo, A.M., Lang, K., Lier, D., Lilje, R., Lowry, S., Luyten, K., MacDonald, A., Meyer, U., Moor, D., Pal, A., Robert, M., Robertson, L., Rocha, J.C., Rohde, C., Ross, K., Saruhan, S., Sjöqvist, E., Skeath, R., Stoelen, L., Ter Horst, N.M., Terry, A., Timmer, C., Tuncer, N., Vande Kerckhove, K., van der Ploeg, L., van Rijn, M., van Spronsen, F.J., van Teeffelen-Heithoff, A., van Wegberg, A., van Wyk, K., Vasconcelos, C., Vitoria, I., Wildgoose, J., Webster, D., White, F.J., Zweers, H.
المصدر: Molecular Genetics and Metabolism, Vol. 115, no. 1, p. 17-22 (2015)
مصطلحات الفهرس: Phenylketonuria, Protein substitute, l-Amino acid supplements, Glycomacropeptide, info:eu-repo/semantics/article
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7دورية أكاديمية
المؤلفون: Evans S; Birmingham Women's and Children's Hospital NHS Foundation Trust, United Kingdom., Daly A; Birmingham Women's and Children's Hospital NHS Foundation Trust, United Kingdom., Chahal S; Birmingham Women's and Children's Hospital NHS Foundation Trust, United Kingdom., Ashmore C; Birmingham Women's and Children's Hospital NHS Foundation Trust, United Kingdom., MacDonald J; Birmingham Women's and Children's Hospital NHS Foundation Trust, United Kingdom., MacDonald A; Birmingham Women's and Children's Hospital NHS Foundation Trust, United Kingdom.
المصدر: Molecular genetics and metabolism reports [Mol Genet Metab Rep] 2017 Oct 31; Vol. 14, pp. 10-14. Date of Electronic Publication: 2017 Oct 31 (Print Publication: 2018).
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Elsevier Inc Country of Publication: United States NLM ID: 101624422 Publication Model: eCollection Cited Medium: Print ISSN: 2214-4269 (Print) Linking ISSN: 22144269 NLM ISO Abbreviation: Mol Genet Metab Rep Subsets: PubMed not MEDLINE