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1دورية أكاديمية
المؤلفون: Hales C., Taylor P. N., Channon S., Mcewan K., Thapar A., Langley K., Muller I., Draman M. S., Dayan C., Gregory J. W., Okosieme O., Lazarus J. H., Rees D. A., Ludgate M.
المساهمون: C. Hale, P.N. Taylor, S. Channon, K. Mcewan, A. Thapar, K. Langley, I. Muller, M.S. Draman, C. Dayan, J.W. Gregory, O. Okosieme, J.H. Lazaru, D.A. Ree, M. Ludgate
مصطلحات موضوعية: ADHD, autism, childhood, pregnancy, thyroid, thyroxine, Adult, Attention Deficit Disorder with Hyperactivity, Biomarker, Case-Control Studie, Child, Child Behavior, Preschool, Cohort Studie, Female, Follow-Up Studie, Human, Hypothyroidism, Male, Prenatal Diagnosi, Prenatal Exposure Delayed Effect, Prognosi, Surveys and Questionnaire, Thyroid Function Test, United Kingdom, Mothers, Settore MED/13 - Endocrinologia
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31665323; info:eu-repo/semantics/altIdentifier/wos/WOS:000525870500042; volume:105; issue:3; firstpage:e416; lastpage:e427; numberofpages:12; journal:THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM; http://hdl.handle.net/2434/806804Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85079203914
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المؤلفون: Irene Campi, Marcel M.A.M. Mannens, M.H. Breuning, Mehul T. Dattani, Marco Bonomi, Giorgio Radetti, W. Oostdijk, Daniel J. Bernard, Krishna Chatterjee, Nadia Schoenmakers, Joseph A M J L Janssen, H. Zhu, Paolo Beck-Peccoz, Sjoerd D. Joustra, Maria Paola Lombardi, J.M. Wit, Erik Endert, Raoul C.M. Hennekam, Nienke R. Biermasz, Natasha M. Appelman-Dijkstra, Yu Sun, Aimee J. Varewijck, Alberto M. Pereira, Charlotte A Heinen, A S P van Trotsenburg, Eleonora P M Corssmit, Luca Persani, Timothy M. E. Davis, Beata Bak
المساهمون: Endocrinology, Graduate School, Amsterdam Gastroenterology Endocrinology Metabolism, Laboratory for Endocrinology, Amsterdam Neuroscience, Amsterdam Public Health, Human Genetics, Paediatrics, Amsterdam Cardiovascular Sciences, Amsterdam Reproduction & Development (AR&D), Paediatric Endocrinology, Internal Medicine
المصدر: Journal of clinical endocrinology and metabolism, 98(12), 4942-4952. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 98(12), 4942-4952. Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 98(12), 4942-4952مصطلحات موضوعية: Delayed puberty, Adult, Male, medicine.medical_specialty, Aging, Heterozygote, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Immunoglobulins, Context (language use), Biochemistry, Testicular Diseases, Endocrinology, X Chromosome Inactivation, Internal medicine, medicine, Factor V Leiden, Congenital Hypothyroidism, Humans, Child, Aged, 80 and over, Family Health, Metabolic Syndrome, Puberty, Delayed, business.industry, Human Growth Hormone, Biochemistry (medical), Infant, Membrane Proteins, Genetic Diseases, X-Linked, Organ Size, medicine.disease, Congenital hypothyroidism, Hypoprolactinemia, Prolactin, Female, Metabolic syndrome, medicine.symptom, business, Body mass index, Weight gain
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17eb6e22e0801827994fba2a88dfa2d8Test
https://pure.eur.nl/en/publications/51ed2254-11a0-4202-8c57-63351e3c7191Test -
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المؤلفون: Sabrina Corbetta, Patrizia Porazzi, Mariacarolina Salerno, Paolo Prontera, Gabriella Nebbia, Natascia Tiso, Mohamad Maghnie, Roberto Gastaldi, Giovanna Weber, Daniela Frizziero, Laura Fugazzola, Luana Mandarà, Roberta Biffanti, Federica Marelli, Giorgio Radetti, Maria Cristina Vigone, Luca Persani, Tiziana de Filippis
المساهمون: De Filippis, Tiziana, Marelli, Federica, Nebbia, Gabriella, Porazzi, Patrizia, Corbetta, Sabrina, Fugazzola, Laura, Gastaldi, Roberto, Vigone, Maria Cristina, Biffanti, Roberta, Frizziero, Daniela, Mandarà, Luana, Prontera, Paolo, Salerno, Mariacarolina, Maghnie, Mohamad, Tiso, Natascia, Radetti, Giorgio, Weber, Giovanna, Persani, Luca, de Filippis, T, Marelli, F, Nebbia, G, Porazzi, P, Corbetta, S, Fugazzola, L, Gastaldi, R, Vigone, Mc, Biffanti, R, Frizziero, D, Mandarà, L, Prontera, P, Salerno, M, Maghnie, M, Tiso, N, Radetti, G, Persani, L.
المصدر: Europe PubMed Central
مصطلحات موضوعية: 0301 basic medicine, Male, endocrine system diseases, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Fluorescent Antibody Technique, Biochemistry, Pathogenesis, 0302 clinical medicine, Endocrinology, Alagille syndrome, Serrate-Jagged Proteins, Child, Zebrafish, Thyroid, Penetrance, Congenital hypothyroidism, Alagille Syndrome, Diabetes and Metabolism, medicine.anatomical_structure, Adult, Animals, Calcium-Binding Proteins, Child, Preschool, Computational Biology, Female, Humans, Intercellular Signaling Peptides and Proteins, Jagged-1 Protein, Membrane Proteins, Thyroid Dysgenesis, Zebrafish Proteins, Biochemistry (medical), endocrine system, JAG1, medicine.medical_specialty, JAG1 Loss-Of-Function Variations, Novel Predisposing Event, Pathogenesis of Congenital Thyroid Defects, congenital hypothyroidism, 030209 endocrinology & metabolism, Context (language use), Biology, Thyroid dysgenesis, 03 medical and health sciences, Internal medicine, medicine, Preschool, medicine.disease, 030104 developmental biology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c503b84fc2252c736abc88a8c8b591cdTest
http://hdl.handle.net/11567/876561Test -
4دورية أكاديمية
المؤلفون: Á. Lábadi, B. Gellén, G. Kleinau, H. Biebermann, B. Ruzsa, O. Rideg, A. Miseta, G. L. Kovács, A. Patócs, E. Felszeghy, E. V. Nagy, E. Mezősi, E.S. Grassi, G. Gelmini, L. Persani
المساهمون: Á. Lábadi, E.S. Grassi, B. Gellén, G. Kleinau, H. Biebermann, B. Ruzsa, G. Gelmini, O. Rideg, A. Miseta, G.L. Kovác, A. Patóc, E. Felszeghy, E.V. Nagy, E. Mezősi, L. Persani
مصطلحات موضوعية: adolescent, adult, animal, COS cell, cercopithecus aethiop, child, cohort studie, congenital hypothyroidism, human, Hungary, infant, newborn, middle aged, models, molecular, pedigree, protein conformation, protein processing, post-translational, receptors, thyrotropin, signal transduction, structure-activity relationship, mutation, missense, medicine (all), Settore MED/13 - Endocrinologia, Settore MED/38 - Pediatria Generale e Specialistica
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/25978107; info:eu-repo/semantics/altIdentifier/wos/WOS:000360840600012; volume:100; issue:7; firstpage:E1039; lastpage:E1045; numberofpages:7; journal:THE JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM; http://hdl.handle.net/2434/335453Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84944153415
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المؤلفون: Osnat Admoni, Gianluigi Caltabiano, Dallasheh Kawthar, Alexandra M. Dumitrescu, Samuel Refetoff, Chutintorn Sriphrapradang, Marla S. Barkoff, Mia C. Weiss, Yardena Tenenbaum-Rakover, Leonardo Pardo
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, endocrine system, endocrine system diseases, Adolescent, Genotype, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Mutant, Thyroid Gland, Gene mutation, Biology, Thyroid Function Tests, Biochemistry, Iodide Peroxidase, Thyrotropin receptor, TSHR Gene Mutation, Endocrinology, Thyroid peroxidase, Internal medicine, medicine, Congenital Hypothyroidism, Humans, Allele, Child, Gene, Alleles, Genetic Association Studies, Genetics, Analysis of Variance, Biochemistry (medical), food and beverages, Infant, Receptors, Thyrotropin, JCEM Online: Brief Reports, Middle Aged, eye diseases, Arabs, Pedigree, Hyperthyroxinemia, Child, Preschool, embryonic structures, biology.protein, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebb3e73075906006b5bc4240e90b3632Test
https://europepmc.org/articles/PMC3100752Test/