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Section of Biostatistics, Department of Public Health, University of Copenhagen, Copenhagen, Denmark
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remaining 15 patients, 6 had compensated Leydig cell dysfunction. Figure 5 Testosterone and LH patterns in patients who were prepubertal at HSCT and had spontaneous onset of puberty ( n = 20, panel A and B), and patients who were pubertal
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Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK
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Malendowicz LK . Effects of sex hormones on the steroidogenic activity of dispersed adrenocortical cells of the rat adrenal cortex. Life Sciences 1995 57 833 – 837. ( https://doi.org/10.1016/0024-3205(95)02015-b ) 24 Oyola MG Handa RJ
Department of Pediatrics, Federal University of Uberlandia (UFU), Uberlandia, Minas Gerais, Brazil
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Department of Pediatrics, Federal University of Rio Grande do Sul (UFRGS), Porto Alegre, Rio Grande do Sul, Brazil
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Poison Control Center, FCM, UNICAMP, Campinas, Sao Paulo, Brazil
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Laboratory of Human Molecular Genetics, Center for Molecular Biology and Genetics Engineering (CBMEG), UNICAMP, Campinas, Sao Paulo, Brazil
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Department of Medical Genetics and Genomic Medicine, FCM, UNICAMP, Campinas, Sao Paulo, Brazil
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Department of Pediatrics, FCM, UNICAMP, Campinas, Sao Paulo, Brazil
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. ( https://doi.org/10.1186/s12610-016-0039-2 ) 18 Cailleux-Bounacer A Reznik Y Cauliez B Menard JF Duparc C Kuhn JM Evaluation of endocrine testing of Leydig cell function using extractive and recombinant human chorionic gonadotropin and
Department of Paediatric Endocrinology, Gynaecology, and Diabetology, AP-HP, Necker-Enfants Malades University Hospital, IMAGINE Institute affiliate, Paris, France
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Department of Paediatric Endocrinology, Gynaecology, and Diabetology, AP-HP, Necker-Enfants Malades University Hospital, IMAGINE Institute affiliate, Paris, France
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Department of Paediatric Endocrinology, Gynaecology, and Diabetology, AP-HP, Necker-Enfants Malades University Hospital, IMAGINE Institute affiliate, Paris, France
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Department of Paediatric Endocrinology, Gynaecology, and Diabetology, AP-HP, Necker-Enfants Malades University Hospital, IMAGINE Institute affiliate, Paris, France
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Department of Endocrinology and Reproductive Medicine, AP-HPIE3M, Hôpital Pitié-Salpêtrière, ICAN, Paris, France
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Department of Endocrinology and Reproductive Medicine, AP-HPIE3M, Hôpital Pitié-Salpêtrière, ICAN, Paris, France
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Centre for Rare Gynecological Disorders, Hospital Universitaire Necker-Enfants Malades, Paediatric Endocrinology, Gynaecology and Diabetology, AP-HP, Université de Paris, Paris, France
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Department of Paediatric Endocrinology, Gynaecology, and Diabetology, AP-HP, Necker-Enfants Malades University Hospital, IMAGINE Institute affiliate, Paris, France
Centre for Rare Gynecological Disorders, Hospital Universitaire Necker-Enfants Malades, Paediatric Endocrinology, Gynaecology and Diabetology, AP-HP, Université de Paris, Paris, France
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initial gonadal pool of germ cells in rats . Human Reproduction 2003 18 276 – 282 . ( https://doi.org/10.1093/humrep/deg058 ) 18 Menezo YJR Lescaille M Nicollet B Servy EJ Pregnancy and delivery after stimulation with rFSH of a galatosemia
Faculty of Medicine, University of Belgrade, Belgrade, Serbia
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Institute of Medical Statistics and Informatics, Belgrade, Serbia
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University Children’s Clinic, Belgrade, Serbia
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Mother and Child Health Care Institute of Serbia ‘Dr Vukan Cupic’, Belgrade, Serbia
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Mother and Child Health Care Institute of Serbia ‘Dr Vukan Cupic’, Belgrade, Serbia
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Clinic for Neurosurgery, University Clinical Center of Serbia, Belgrade, Serbia
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syndromes were classified as congenital (CONG) COGHD accounting for more than half of all included patients (86/170; 50.6%) ( Fig. 1 ). Patients with a history of cranial tumor, hematological malignancies, or pituitary TSH hyperplasia (non-tumoral TSH cell
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Academic Centre for Growth, Erasmus University Medical Centre, Rotterdam, the Netherlands
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Diabeter, National Diabetes Care and Research Centre, Rotterdam, the Netherlands
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Department of Paediatric Endocrinology, Leiden University Medical Centre, Leiden, the Netherlands
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Academic Centre for Growth, Erasmus University Medical Centre, Rotterdam, the Netherlands
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bowel disease, sickle cell disease, kidney diseases or common endocrine disorders such as diabetes mellitus ( 5 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 ). For example, Monaghan et al. ( 22 ) provide an overview of best
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–208) Inadequately iodized b 361 (6.5) 239 (159–349) Adequately iodized 5094 (91.9) 221 (150–312) Excessively iodized 65 (1.2) 189 (119–261) Wilcoxon test was used to compare UIC between genders. Kruskal–Wallis test was
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Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Setagaya, Tokyo, Japan
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Research Center for Environment and Developmental Medical Sciences, Kyushu University, Higashi-ku, Fukuoka, Japan
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Research Center for Environment and Developmental Medical Sciences, Kyushu University, Higashi-ku, Fukuoka, Japan
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Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Setagaya, Tokyo, Japan
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://doi.org/10.1016/s0022-3476(9570254-7 ) 18 Hobeika E Armouti M Kala H Fierro MA Winston NJ Scoccia B Zamah AM Stocco C . Oocyte-secreted factors synergize with FSH to promote aromatase expression in primary human cumulus cells . Journal of
Department of Pediatrics, China-Japan Friendship Hospital, Beijing, China
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Department of Pediatrics, China-Japan Friendship Hospital, Beijing, China
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Department of Pediatrics, China-Japan Friendship Hospital, Beijing, China
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β-cell function, insulin resistance, glycemia, and type 2 diabetes in finnish men . Journal of Clinical Endocrinology and Metabolism 2017 102 443 – 450 . ( https://doi.org/10.1210/jc.2016-2933 ). 9 Yuan Y Zhou B Wang S Ma J Dong F
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data were obtained from our databases: family history of diabetes, age of menarche, weight, BMI, waist circumference (WC), and Ferriman–Gallwey (FG) score. At the time of diagnosis of PP, girls were tested for FSH, LH, 17b-estradiol (E2), 17OH