نتائج البحث - "J. Ekengren"

المساهمون: Ege Üniversitesi, HUS Children and Adolescents, Clinicum, University of Helsinki, HUS Internal Medicine and Rehabilitation, Children's Hospital, MUMC+: TPZ Dietetiek (9), RS: FHML non-thematic output, UCL - (SLuc) Unité d'endocrinologie pédiatrique

المصدر: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, 16, pp. 82-89
Molecular Genetics and Metabolism Reports, 16, 82. Elsevier BV
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Molecular Genetics and Metabolism Reports, 16, 82-89. Elsevier Science
Molecular Genetics and Metabolism Reports, Vol. 16, no. ?, p. 82-89 (2018)
Molecular Genetics and Metabolism Reports, 16, 82-89
Molecular Genetics And Metabolism Reports
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Molecular genetics and metabolism reports, 16, 82-89. ELSEVIER SCIENCE BV
Molecular Genetics and Metabolism Reports, Vol 16, Iss, Pp 82-89 (2018)

مصطلحات موضوعية: 0301 basic medicine, Pediatrics, PKU, Phenylketonuria, Breastfeeding, lnfectious Diseases and Global Health Radboud Institute for Molecular Life Sciences [Radboudumc 4], IMD, Inherited Metabolic Disorders, PROTEIN, 030105 genetics & heredity, Phe-Free Infant Formula, Endocrinology, IMD, Standard infant formula, HDE PED, Medicine, Phenylketonuria, lcsh:QH301-705.5, 2. Zero hunger, lcsh:R5-920, 1184 Genetics, developmental biology, physiology, Inherited Metabolic Disorders, 3. Good health, PKU, GROWTH, lcsh:Medicine (General), DIETARY-MANAGEMENT, Research Paper, Phe, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Phe, Phenylalanine, Phenylalanine, Breast milk, 03 medical and health sciences, Phe-free infant formula, Infant practices, Genetics, Weaning, Molecular Biology, Newborn screening, Infant Practices, business.industry, Dietary management, nutritional and metabolic diseases, lcsh:Biology (General), Infant formula, Human medicine, business, Breast feeding

وصف الملف: pdf; image/pdf; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d942c40638f6ca21973930945496c0c6

View record from ScienceDirect

5

Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approach

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