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Journal of Clinical Research in Pediatric Endocrinology, ISSN 1308-5727, 06/2016, Volume 8, Issue 1
Journal Article
Journal Article
JCRPE Journal of Clinical Research in Pediatric Endocrinology, ISSN 1308-5727, 2017, Volume 9, Issue 2, pp. 182 - 184
On the main page (Auxology), standard deviation (SD) scores and percentile values can be calculated for weight, height, body mass index, and head circumference... 
Endocrinology - methods | Age Factors | Humans | Pediatrics - methods | Adolescent | Decision Support Techniques | Sex Factors | Child, Preschool | Female | Male | Child Development | Child | Pediatrics | Values | Thyroid gland | Insulin-like growth factors | Disease control | Girls | Children & youth | Variables | Body mass index | Insulin resistance | Bone density | Teenagers | Physical growth | Age | Endocrinology | Letter to the Editor
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2015, Volume 10, Issue 7, p. e0131376
Journal Article
JCRPE Journal of Clinical Research in Pediatric Endocrinology, ISSN 1308-5727, 06/2016, Volume 8
Journal Article
Journal of Pediatric Endocrinology and Metabolism, ISSN 0334-018X, 09/2016, Volume 29, Issue 9, pp. 1111 - 1114
Journal Article
Hormone Research in Paediatrics, ISSN 1663-2818, 03/2016, Volume 85, Issue 2, pp. 107 - 111
Introduction: Mutations of the human GNRH1 gene are an extremely rare cause of normosmic idiopathic hypogonadotropic hypogonadism (nIHH), with only 6 mutations... 
Original Paper | Puberty | GNRH1 | Idiopathic hypogonadotropic hypogonadism | GENE | TURKEY | HORMONE RECEPTOR | BIOLOGY | ENDOCRINOLOGY & METABOLISM | PEDIATRICS | PREVALENCE | Hypogonadism - genetics | Young Adult | Homozygote | Protein Precursors - genetics | DNA Mutational Analysis | Gonadotropin-Releasing Hormone - genetics | Humans | Adolescent | Female | Male | Cohort Studies
Journal Article
Journal of Pediatric Endocrinology and Metabolism, ISSN 0334-018X, 02/2016, Volume 29, Issue 2, pp. 133 - 138
Congenital hypothyroidism (CH) is the most frequent endocrine disorder during the neonatal period, and a delay in diagnosis and treatment leads to irreversible... 
L-thyroxine | congenital hypothyroidism | overtreatment | THERAPY | GROWTH | ENDOCRINOLOGY & METABOLISM | PEDIATRICS | CHILDREN | Dose-Response Relationship, Drug | Female | Male | Congenital Hypothyroidism - drug therapy | Humans | Thyroxine - administration & dosage | Care and treatment | Congenital hypothyroidism | Diagnosis
Journal Article
Journal of Clinical Research in Pediatric Endocrinology, ISSN 1308-5727, 06/2017, Volume 9, Issue 2, p. 12
Journal Article
Journal of Clinical Research in Pediatric Endocrinology, ISSN 1308-5727, 06/2017, Volume 9, Issue 1, p. 12
Mutations of PROP1 are the most frequent genetic defect in non-syndromic combined pituitary hormone insufficiency and are characterized by growth hormone (GH),... 
Adrenal glands | Mutation | Physical growth
Journal Article
Journal of clinical research in pediatric endocrinology, ISSN 1308-5727, 09/2019
Many new features have recently been incorporated to ÇEDD Çözüm / Child Metrics, an online and freely accessible scientific toolset. Various auxological... 
Journal Article
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