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Journal Article
Turk Pediatri Arsivi, ISSN 1306-0015, 2018, Volume 53, Issue Suppl 1, pp. S209 - S223
Thyroid functions in the fetus and newborn carry importance in terms of the baby's health and development of the central nervous system. Maternaliodine... 
Newborn | Congenital | Hypothyroidism | Maternal thyroid problems | Thyroid diseases
Journal Article
AJIC: American Journal of Infection Control, ISSN 0196-6553, 2015, Volume 43, Issue 9, pp. 1015 - 1017
Journal Article
Journal Article
Journal Article
Journal of Pediatric Endocrinology and Metabolism, ISSN 0334-018X, 07/2018, Volume 31, Issue 7, pp. 711 - 716
Background: Adolescents with type 1 diabetes mellitus (T1DM) are at an increased risk of eating disturbances. The aim of this study was to evaluate whether the... 
type 1 diabetes mellitus | adolescent | disordered eating | sibling | anorexia | ADOLESCENTS | INVOLVEMENT | ENDOCRINOLOGY & METABOLISM | PEDIATRICS | CHILDREN | Diabetes
Journal Article
Journal Article
The Journal of Steroid Biochemistry and Molecular Biology, ISSN 0960-0760, 01/2017, Volume 165, p. 57
11β-Hydroxylase deficiency is the second most frequent type of congenital adrenal hyperplasia and is more common in those of Turkish descent than in other... 
Nucleotide sequence | Exons | Genes | Hydroxylase | Hyperplasia | Aldosterone synthase | Insertion | Medical screening | Steroid 11ß-hydroxylase | Studies | Prenatal diagnosis | Gene frequency | Clonal deletion | Mutation | Deoxyribonucleic acid--DNA
Journal Article
Journal of Steroid Biochemistry and Molecular Biology, ISSN 0960-0760, 01/2017, Volume 165, p. 57
* Seventeen different CYP11B1 gene mutations (6 novel) were detected in 28 patients. * The novel mutation p.Gly446Ser causes the late-onset type of the... 
Gene mutations | Genes | Cytochrome P-450 | Genetic aspects | Children | Health aspects
Journal Article
Journal of clinical research in pediatric endocrinology, ISSN 1308-5727, 07/2019
Doses of GnRH analogues used to treat idiopathic central precocious puberty(iCPP) may vary with clinician preference. Aim of this study is to evaluate the... 
Journal Article
Turkish Journal of Pediatrics, ISSN 0041-4301, 03/2012, Volume 54, Issue 2, pp. 177 - 179
Journal Article
Proceedings of the National Academy of Sciences of the United States, ISSN 0027-8424, 03/2017, Volume 114, Issue 10, p. E1933
  Congenital adrenal hyperplasia (CAH), resulting from mutations in CYP11B1, a gene encoding 11β-hydroxylase, represents a rare autosomal recessive Mendelian... 
Physiological aspects | Genetic aspects | Genetic disorders | Gene expression | Health aspects | Hyperplasia | Genetics | Mutation | Gender | Steroids
Journal Article
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