المؤلفون: E J Schroor, Wilma Oostdijk, Roel J. Odink, Maria A. J. de Ridder, Danielle C. M. van der Kaay, Willie M. Bakker-van Waarde, Anita C. S. Hokken-Koelega, Ciska Westerlaken, Annemieke J. Lem, Cees Noordam, Eric J. Sulkers, Flip J. P. C. M. van der Hulst, Jaap Mulder

المساهمون: Pediatrics, Erasmus MC other, Medical Informatics, Surgery

المصدر: Journal of Clinical Endocrinology and Metabolism, 97(11), 4096-4105
Journal of Clinical Endocrinology and Metabolism, 97(11), 4096-4105. ENDOCRINE SOC
Journal of Clinical Endocrinology and Metabolism, 97(11), 4096-4105. Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 97, 4096-105
Journal of Clinical Endocrinology and Metabolism, 97, 11, pp. 4096-105

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Context (language use), Biochemistry, Short stature, PUBERTAL DEVELOPMENT, law.invention, Gonadotropin-Releasing Hormone, DOUBLE-BLIND, Follicle-stimulating hormone, Endocrinology, Randomized controlled trial, law, Internal medicine, FOR-GESTATIONAL-AGE, medicine, Humans, PRECOCIOUS PUBERTY, Precocious puberty, Longitudinal Studies, AGONIST TREATMENT, Child, SHORT STATURE, FOLLOW-UP DATA, Intention-to-treat analysis, Dose-Response Relationship, Drug, business.industry, Biochemistry (medical), Infant, Newborn, CATCH-UP, FOLLICLE-STIMULATING-HORMONE, medicine.disease, Body Height, Somatropin, Mitochondrial medicine [IGMD 8], Treatment Outcome, FINAL HEIGHT, Growth Hormone, Infant, Small for Gestational Age, Small for gestational age, Female, medicine.symptom, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b169283cdf550281b441172aa48974fTest
https://doi.org/10.1210/jc.2012-1987Test

المؤلفون: Elbrich P. C. Siemensma, Roderick F. A. de Lind van Wijngaarden, Frank H. de Jong, Barto J. Otten, Anita C. S. Hokken-Koelega

المساهمون: Pediatrics, Internal Medicine

المصدر: Journal of Clinical Endocrinology and Metabolism, 97, E452-9
Journal of Clinical Endocrinology and Metabolism, 97, 3, pp. E452-9
Journal of Clinical Endocrinology and Metabolism, 97(3), E452-E459. Endocrine Society

مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, endocrine system, medicine.medical_specialty, Adolescent, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Context (language use), Biochemistry, Endocrinology, Hypogonadotropic hypogonadism, Internal medicine, Prepuberty, Testis, medicine, Humans, Inhibins, Testosterone, Longitudinal Studies, Young adult, Child, business.industry, Hormonal regulation [IGMD 6], Puberty, Biochemistry (medical), Age Factors, Infant, nutritional and metabolic diseases, Luteinizing Hormone, medicine.disease, Pathophysiology, nervous system diseases, Mitochondrial medicine [IGMD 8], Child, Preschool, Follicle Stimulating Hormone, business, Prader-Willi Syndrome, hormones, hormone substitutes, and hormone antagonists, Cohort study, Hormone

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6720f6d40a3d7594ff381fe977344097Test
https://doi.org/10.1210/jc.2011-1954Test

المؤلفون: Jan M. Wit, Barto J. Otten, Bert Elvers, Hetty J. van der Kamp, Paul H. Verkerk, Caren G. M. Oudshoorn, Maja van Baarle

المصدر: Journal of Clinical Endocrinology and Metabolism, 90, 3904-7
Journal of Clinical Endocrinology and Metabolism, 90, 7, pp. 3904-7

مصطلحات موضوعية: medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, Coefficient of variation, Birth weight, Clinical Biochemistry, Gestational Age, Sensitivity and Specificity, Biochemistry, Neonatal Screening, Endocrinology, Internal medicine, medicine, Birth Weight, Humans, Cutoff, Congenital adrenal hyperplasia, Newborn screening, Adrenal Hyperplasia, Congenital, Endocrinology and reproduction [UMCN 5.2], business.industry, 17-alpha-Hydroxyprogesterone, Hormonal regulation [IGMD 6], Biochemistry (medical), Infant, Newborn, Gestational age, Liter, medicine.disease, Mitochondrial medicine [IGMD 8], Regression Analysis, business, Blood sampling

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a509bda319634e8e9e92695a0bc3b68bTest
https://doi.org/10.1210/jc.2004-2136Test

المؤلفون: Carl-Joachim Partsch, Pierre Déchelotte, Thierry Brue, Begüm Atasay, Dominique Beckers, Anne Barlier, Leo Dunkel, Patricia A. Donohoue, Monique De Vroede, Jacques Weill, M. Gueydan, Georges Malpuech, Marc Nicolino, Jennifer H. Kyllo, Christie Riddell, B. Pigeon, Bruno Allolio, C. Noordam, Cheri Deal, Juan J. Heinrich, Sophie Vallette-Kasic, Anne-Marie Pulichino, Michel David, Felix G. Riepe, Jacques Drouin, Raja Brauner, Merih Berberoğlu, Matti Hero, Stefanie Hahner, Martin Fassnacht, Guy Van Vliet, Alain Enjalbert, Francis de Zegher, Elizabeth A. Cummings, Wolfgang G. Sippell, Sevket Yigit

المساهمون: UCL - SSS/IREC/MONT - Pôle Mont Godinne, UCL - (MGD) Service de pédiatrie, Interactions cellulaires neuroendocriniennes (ICN), Université de la Méditerranée - Aix-Marseille 2-Centre National de la Recherche Scientifique (CNRS), Gautron, Conception

المصدر: The Journal of clinical endocrinology and metabolism, Vol. 90, no.3, p. 1323-31 (2005)
Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, 2005, 90, pp.1323-1331
Journal of Clinical Endocrinology and Metabolism, 90, 3, pp. 1323-31
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2005, 90, pp.1323-1331
Journal of Clinical Endocrinology and Metabolism, 90, 1323-31

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Health aging / healthy living [IGMD 5], Adolescent, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Genes, Recessive, 030209 endocrinology & metabolism, Prenatal diagnosis, Adrenocorticotropic hormone, Biology, Gene mutation, Compound heterozygosity, medicine.disease_cause, Biochemistry, Infant, Newborn, Diseases, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, Adrenocorticotropic Hormone, Cause of Death, Internal medicine, medicine, Adrenal insufficiency, Humans, Age of Onset, Child, 030304 developmental biology, Cause of death, Homeodomain Proteins, 0303 health sciences, Mutation, Endocrinology and reproduction [UMCN 5.2], Biochemistry (medical), Infant, Newborn, medicine.disease, Pedigree, 3. Good health, Mitochondrial medicine [IGMD 8], Female, T-Box Domain Proteins, Adrenocorticotropic hormone deficiency, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d838a81f80b753f3e94c77571d41bb52Test
https://doi.org/10.1210/jc.2004-1300Test