87 results on '"Baş, Firdevs"'
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2. THE INFLUENCE OF GROWTH HORMONE TREATMENT ON INSULIN SENSITIVITY IN CHILDREN AND ADOLESCENTS
3. In response to: “Letter to: “Endocrinological Approach to Adolescents with Gender Dysphoria: Experience of a Pediatric Endocrinology Department in a Tertiary Center in Turkey””
4. Endocrinological Approach to Adolescents with Gender Dysphoria: Experience of a Pediatric Endocrinology Department in a Tertiary Center in Turkey
5. Endokrin Bozucuların Ergen Sağlığı Üzerine Etkileri
6. Evaluation of Children with Secondary Osteoporosis: A Single-center Experience
7. Body proportions in patients with Turner syndrome on growth hormone treatment
8. Severe Hypercalcemia in an Infant with Subcutaneous Fat Necrosis: Successful Management with Bisphosphonate Treatment
9. Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor
10. Gender Dysphoria in Adolescents
11. Adolesan Çağındaki Çocuklarda Otoimmün Tiroiditte Parvovirus B19’un Rolü
12. Comparison of National Growth Standards for Turkish Infants and Children with World Health Organization Growth Standards
13. Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD
14. A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High IGF-I Values at Transition to Adult Care
15. COMPARISON OF SINGLE DOSE AND MULTI-DOSE hCG STIMULATION TESTS
16. Growth and Pubertal Features in a Cohort of 83 Patients with Osteogenesis Imperfecta
17. BONE HEALTH AND GROWTH IN SPINAL MUSCULAR ATROPHY TYPE 2 AND 3
18. BONE HEALTH AND GROWTH IN SPINAL MUSCULAR ATROPHY TYPE 2 AND 3
19. Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome
20. Recommendations for Clinical Decision-making in Children with Type 1 Diabetes and Celiac Disease: Type 1 Diabetes and Celiac Disease Joint Working Group Report
21. Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia
22. Long-term Follow-up of a Toddler with Papillary Thyroid Carcinoma: A Case Report with a Literature Review of Patients Under 5 Years of Age
23. Clinical Alteration of Sleep Related Dissociative Disorder into Psychogenic Nonepileptic Seizure in an Adolescent Girl with The History of Physical Abuse in Early Childhood
24. BASELINE CHARACTERISTICS OF PATIENTS WITH GROWTH HORMONE DEFICIENCY
25. Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants
26. Nationwide Turkish Cohort Study of Hypophosphatemic Rickets
27. A Novel Homozygous Mutation of the Acid-Labile Subunit (IGFALS) Gene in a Male Adolescent
28. Determination of insulin resistance and its relationship with hyperandrogenemia,anti-Müllerian hormone, inhibin A, inhibin B, and insulin-like peptide-3 levels in adolescent girls with polycystic ovary syndrome
29. Measurement of serum vitamin B12-related metabolites in newborns: implications for new cutoff values to detect B12 deficiency
30. Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey
31. Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants
32. A Rare Cause of Adrenal Insufficiency – Isolated ACTH Deficiency Due to TBX19 Mutation: Long-Term Follow-Up of Two Cases and Review of the Literature
33. Precocious or early puberty in patients with combined pituitary hormone deficiency due to POU1F1 gene mutation: case report and review of possible mechanisms
34. Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey
35. Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants
36. A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations
37. Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene
38. Glycemic control and health behaviors in adolescents with type 1 diabetes
39. Incidence of Type 1 Diabetes in Children Aged Below 18 Years During 2013-2015 in Northwest Turkey
40. Klinefelter Syndrome in Childhood: Variability in Clinical and Molecular Findings
41. Determinants of Increased Aortic Diameters in Young Normotensive Patients With Turner Syndrome Without Structural Heart Disease
42. Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty
43. Two novel mutations in XYLT2 cause spondyloocular syndrome
44. Clinicopathological Characteristics of Papillary Thyroid Cancer in Children with Emphasis on Pubertal Status and Association with BRAFV600E Mutation
45. Cleidocranial dysplasia: Clinical, endocrinologic and molecular findings in 15 patients from 11 families
46. Prevelance of vitamin D and B12 deficiency in adolescence
47. Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height
48. The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study
49. Anti-Müllerian Hormone and Inhibin-A, but not Inhibin-B or Insulin-Like Peptide-3, may be Used as Surrogates in the Diagnosis of Polycystic Ovary Syndrome in Adolescents: Preliminary Results
50. Diagnosis and management of pediatric adrenal insufficiency
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