Bilimsel çalışmalar

Prof. Dr. Zeynep Atay

105 yayın. Her yayının yanında bilginin kaynağı yazar.

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  1. Premature Pubarche, Hyperinsulinemia and Hypothyroxinemia: Novel Manifestations of Congenital Portosystemic Shunts (Abernethy Malformation) in Children

    Hormone Research in Paediatrics, 2015

    DOI 10.1159/000369395 PMID 25676144 24 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  2. Risk factors for mortality caused by hypothalamic obesity in children with hypothalamic tumours

    Pediatric Obesity, 2015

    DOI 10.1111/ijpo.12076 PMID 26463004 14 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  3. Dysosteosclerosis from a unique mutation in SLC29A3

    Bone Abstracts, 2015

    DOI 10.1530/boneabs.4.p97 7 atıf (OpenAlex) Kaynak: OpenAlex

  4. Growth without growth hormone syndrome in a patient with craniopharyngioma

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2015

    1 atıf (OpenAlex) Kaynak: OpenAlex

  5. Factors Effecting Response to Growth Hormone Treatment in Children with Turner Syndrome

    54th ESPE Meeting (ESPE 2015), 2015

    Kaynak: OpenAlex

  6. Hereditary Vitamin D-Resistant Rickets: Report of Four Cases with Successful Use of Intermittent Intravenous Calcium Via Peripheral Route

    54th ESPE Meeting (ESPE 2015), 2015

    Kaynak: OpenAlex

  7. Friedreich's Ataxia Presenting with Diabetes Mellitus in an Adolescent

    2015

    Kaynak: OpenAlex

  8. The Growth Characteristics of Patients with Noonan Syndrome, and First 2 Years Results of GH Treatment: A Nationwide Multicentre Study

    54th ESPE Meeting (ESPE 2015), 2015

    Kaynak: OpenAlex

  9. Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

    Journal of Clinical Research in Pediatric Endocrinology, 2015

    DOI 10.4274/jcrpe.1794 PMID 25800474 11 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  10. Aetiological Spectrum and Clinical Characteristics of 129 Children with Gonadotropin Independent Precocious Puberty: A Nationwide Cohort Study

    54th Annual ESPE, 2015

    Kaynak: OpenAlex

  11. Primary Adrenal Insufficiency in Children without Congenital Adrenal Hyperplasia: Molecular and Clinical Characterisation of a Nationwide Cohort

    54th ESPE Meeting (ESPE 2015), 2015

    Kaynak: OpenAlex

  12. Comparison of Treatment Alternatives for Hypercalcemia due to Vitamin D Intoxication in Children

    54th ESPE Meeting (ESPE 2015), 2015

    Kaynak: OpenAlex

  13. Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

    The Journal of Clinical Endocrinology & Metabolism, 2015

    DOI 10.1210/jc.2015-3250 PMID 26523528 130 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  14. Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism

    Journal of Clinical Endocrinology and Metabolism, 2015

    DOI 10.1210/jc.2015-1150 PMID 25774885 28 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  15. H Syndrome: A Multifaceted Histiocytic Disorder with Hyperpigmentation and Hypertrichosis

    Acta Dermato Venereologica, 2015

    DOI 10.2340/00015555-2145 PMID 26015165 26 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  16. Response to GH Treatment in the Very Young with GH Deficiency

    54th Annual ESPE, 2015

    Kaynak: OpenAlex

  17. Effects of leukemia inhibitory receptor gene mutations on human hypothalamo–pituitary–adrenal function

    Pituitary, 2014

    DOI 10.1007/s11102-014-0594-5 PMID 25145448 6 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  18. Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS

    Bone, 2014

    DOI 10.1016/j.bone.2014.10.006 PMID 25464124 25 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  19. Novel homozygous inactivating mutation of the calcium-sensing receptor gene (CASR) in neonatal severe hyperparathyroidism—lack of effect of cinacalcet

    Bone, 2014

    DOI 10.1016/j.bone.2014.04.010 PMID 24735972 30 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  20. Higher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus

    Pediatric Diabetes, 2014

    DOI 10.1111/pedi.12167 PMID 25039448 16 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  21. Final Height in Girls with Idiopathic Central Precocious Puberty Treated with GNRH Analog: Comparison with Untreated Controls

    53rd ESPE Meeting, 2014

    1 atıf (OpenAlex) Kaynak: OpenAlex

  22. Hypoglycemia: An unrecognized problem in cystic fibrosis (CF) patients unmasked by continues glucose monitorisation (CGM)

    European Respiratory Journal, 2014

    DOI 10.1183/13993003/erj.44.suppl_58.p1216 1 atıf (OpenAlex) Kaynak: OpenAlex

  23. Department of Pediatric Endocrinology, Marmara University

    Dspace Repository (Marmara Üniversitesi), 2014

    Kaynak: OpenAlex

  24. Younger Age and BMI [gt]3SD are Risk Factors for Mortality in Children with Hypothalamic Obesity

    ESPE 2014, 2014

    Kaynak: OpenAlex

  25. Papillary Thyroid Cancer with Diffuse Pulmonary Metastasis: How to Manage?

    53rd ESPE Meeting, 2014

    Kaynak: OpenAlex

  26. Eleven Years of Letrozole Treatment in a Child with 11-[beta] Hydroxylase Deficiency: Effect on Bone Age and Height Prognosis

    53rd ESPE Meeting, 2014

    Kaynak: OpenAlex

  27. Sleep-related Breathing Disorders in Pycnodysostosis

    53rd ESPE Meeting, 2014

    Kaynak: OpenAlex

  28. Is There a Change in the Presentation of Childhood Type-1 Diabetes Mellitus in the Last 15 Years? Data from a Tertiary Care Center in Turkey

    ESPE 2014, 2014

    Kaynak: OpenAlex

  29. Hyperthyroidism Due to TSH Secreting Pituitary Adenoma in a 7-Year-Old Boy

    53rd ESPE Meeting, 2014

    Kaynak: OpenAlex

  30. GAD Antibody Positivity is Associated with Higher Prevalence of Autoimmune Thyroiditis in Children with Type 1 Diabetes Mellitus

    53rd ESPE Meeting, 2014

    Kaynak: OpenAlex

  31. Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features

    Orphanet Journal of Rare Diseases, 2014

    DOI 10.1186/1750-1172-9-60 PMID 24767306 31 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  32. Sleep disordered breathing in pycnodysostosis patients

    European Respiratory Journal, 2014

    DOI 10.1183/13993003/erj.44.suppl_58.p2277 1 atıf (OpenAlex) Kaynak: OpenAlex

  33. 10. The influence of body mass index and socioeconomic status on pubertal development

    Wageningen Academic Publishers eBooks, 2014

    DOI 10.3920/978-90-8686-767-7.010 1 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  34. Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia

    European Journal of Pediatrics, 2012

    DOI 10.1007/s00431-012-1868-4 PMID 23093139 7 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  35. Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: Novel mutations in TRPM6 and CLDN16 genes

    Nephrology Dialysis Transplantation, 2012

    DOI 10.1093/ndt/gfr300 PMID 21669885 25 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  36. An Atypical Case of Familial Glucocorticoid Deficiency without Pigmentation Caused by Coexistent Homozygous Mutations inMC2R(T152K) andMC1R(R160W)

    The Journal of Clinical Endocrinology & Metabolism, 2012

    DOI 10.1210/jc.2011-2414 PMID 22337906 31 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  37. A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo-cardiomyopathy

    Gene, 2012

    DOI 10.1016/j.gene.2012.11.044 PMID 23235116 20 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  38. The prevalence and risk factors of premature thelarche and pubarche in 4- to 8-year-old girls

    Acta Paediatrica, International Journal of Paediatrics, 2012

    DOI 10.1111/j.1651-2227.2011.02444.x PMID 21854448 37 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  39. Current Status of Childhood Obesity and its Associated Morbidities in Turkey

    Journal of Clinical Research in Pediatric Endocrinology, 2012

    DOI 10.4274/jcrpe.506 PMID 22394698 103 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  40. Vitamin D ve Güncel Öneriler

    Turkiye Klinikleri Pediatric Sciences - Special Topics, 2012

    1 atıf (OpenAlex) Kaynak: OpenAlex

  41. Cognitive and psychosocial development in children with familial hypomagnesaemia

    Magnesium Research, 2011

    DOI 10.1684/mrh.2011.0278 PMID 21489917 3 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  42. Radiologic and hormonal evaluation of pituitary abnormalities in patients with Bardet-Biedl syndrome

    Clinical Dysmorphology, 2011

    DOI 10.1097/mcd.0b013e32833fd528 PMID 20966747 16 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  43. Serum alkaline phosphatase levels in healthy children and evaluation of alkaline phosphatase z-scores in different types of rickets

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2011

    DOI 10.4274/jcrpe.v3i1.02 PMID 21448327 98 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  44. Prevalence of type 1 diabetes mellitus in 6-18-yr-old school children living in Istanbul, Turkey

    Pediatric Diabetes, 2011

    DOI 10.1111/j.1399-5448.2010.00744.x PMID 21418453 12 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  45. Puberty and influencing factors in schoolgirls living in Istanbul: End of the secular trend?

    Pediatrics, 2011

    DOI 10.1542/peds.2010-2267 PMID 21669888 43 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  46. An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W)

    Society for Endocrinology BES 2011, 2011

    1 atıf (OpenAlex) Kaynak: OpenAlex

  47. Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor

    Journal of Clinical Endocrinology and Metabolism, 2009

    DOI 10.1210/jc.2009-0551 PMID 19755480 100 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  48. Actinomycotic Suppurative Thyroiditis in a Child

    Journal of Tropical Pediatrics, 2005

    DOI 10.1093/tropej/fmi030 PMID 15947015 14 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex

  49. Effect of BCG vaccine on tuberculin skin tests in 7-11-year-old children

    Acta Paediatrica, 2004

    DOI 10.1080/08035250410024970 PMID 15456191 Kaynak: OpenAlex

  50. Hypernatraemic dehydration in exclusively breastfed neonates

    Annals of Tropical Paediatrics, 2004

    DOI 10.1179/027249304225013484 PMID 15186549 2 atıf (OpenAlex) Kaynak: OpenAlex