Uluslararası HastaDuyurularİletişim
HACETTEPE ÜNİVERSİTESİHASTANELERİ
Randevu Al
TR
  1. Ana Sayfa
  2. Doktorlar
  3. Doç. Dr. Doğuş Vurallı Karaoğlan
DK

Doç. Dr.

Doğuş Vurallı Karaoğlan

Çocuk Endokrinoloji · Çocuk Hastanesi

Randevu Al

Yayınlar

Kaynak: Hacettepe Üniversitesi Akademik Veri Yönetim Sistemi (AVESİS) · Tüm yayınlar (47) ↗

Makaleler 38

  1. The First-Year Outcomes of the Nationwide Neonatal CAH Screening in Türkiye: High Rate of False Positives for 21-Hydroxylase Deficiency and a Higher Detection Rate of Non-Classical CasesGURAN T., Yuruker E., ANIK A., Atar M., çamtosun e., Eviz E., et al.Journal of Clinical Research in Pediatric Endocrinology, cilt.17, sa.4, ss.488-493, 2025 (SCI-Expanded, Scopus, TRDizin)
  2. A Rare Kidney Involvement of Lysinuric Protein Intolerance: Membranoproliferative GlomerulonephritisBALTU D., SERİN O., AKSU T., HIZARCIOĞLU GÜLŞEN H., ORHAN D., YILDIZ Y., et al.PEDIATRIC NEPHROLOGY, sa.1, 2024 (SCI-Expanded, Scopus)
  3. Epidemiology of type 1 diabetes mellitus in children and adolescents: A 50-year, single-center experienceKANDEMİR N., VURALLI KARAOĞLAN D., Ozon A., Gonc N., ARDIÇLI D., Jalilova L., et al.JOURNAL OF DIABETES, cilt.16, sa.5, 2024 (SCI-Expanded, Scopus)
  4. Severe Early-Onset Obesity and Diabetic Ketoacidosis due to a Novel Homozygous c.169C>T p.Arg57*Variant in CEP19 GeneCayir A., TÜRKYILMAZ A., Rabenstein H., Guven F., Karagoz Y. S., VURALLI KARAOĞLAN D., et al.MOLECULAR SYNDROMOLOGY, cilt.15, sa.2, ss.104-113, 2023 (SCI-Expanded, Scopus)
  5. Effects of insulin therapy on respiratory functions, pulmonary exacerbation and nutritional status in cystic fibrosis-related diabetesVURALLI KARAOĞLAN D., Alboga D., ŞENKALFA B., GÖZMEN O., Yalcin E., DOĞRU ERSÖZ D., et al.HORMONE RESEARCH IN PAEDIATRICS, ss.182, 2023 (SCI-Expanded, Scopus)
  6. Priming with sex steroids increases the specificity of GH tests in the diagnosis of "True" isolated growth hormone deficiencyVURALLI KARAOĞLAN D., Ozon A., Gonc N.HORMONE RESEARCH IN PAEDIATRICS, ss.293, 2023 (SCI-Expanded, Scopus)
  7. Adult heights of the cases whose GH treatment was discontinued at early retesting reached their target heightsVURALLI KARAOĞLAN D., Ozon A., Gonc N.HORMONE RESEARCH IN PAEDIATRICS, ss.284, 2023 (SCI-Expanded, Scopus)
  8. Clinical characteristics, molecular genetics analysis results and long-term follow-up of a large cohort of congenital hyperinsulinism from Turkey: A nationwide cross-sectional studyDEMİRBİLEK H., Ozbek M. N., Yildiz M., Houghton J. L. A., Onal H., GÜRBÜZ F., et al.HORMONE RESEARCH IN PAEDIATRICS, ss.589, 2023 (SCI-Expanded, Scopus)
  9. Evaluation Of Long-term Height and Pubertal Outcome Of Boys Presented With Delayed Puberty Due To Constitutional Delay In Growth And Puberty And Isolated Hypogonadotropic HypogonadismDOĞAN Ö., VURALLI KARAOĞLAN D., DEMİRBİLEK H.HORMONE RESEARCH IN PAEDIATRICS, ss.387, 2023 (SCI-Expanded, Scopus)
  10. Does premature adrenarche affect adult height in girls?VURALLI KARAOĞLAN D., DEMİR O. O., CELEP İ., Gonc N., Ozon A.HORMONE RESEARCH IN PAEDIATRICS, ss.372-373, 2023 (SCI-Expanded, Scopus)
  11. Serum kisspeptin, neurokinin B and inhibin B levels can be used as an auxiliary parameter to distinguish idiopathic CPP from premature thelarche in the early stages of pubertyVURALLI KARAOĞLAN D., Ciftci N., DEMİRBİLEK H.HORMONE RESEARCH IN PAEDIATRICS, cilt.95, sa.SUPPL 2, ss.62-63, 2022 (SCI-Expanded, Scopus)
  12. Feminizing Adrenocortical Tumors as a Rare Etiology of Isosexual/Contrasexual PseudopubertyVURALLI KARAOĞLAN D., Gonc N., Ozon A., EKİNCİ S., Dogan H. S., TEKGÜL S., et al.JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.14, sa.1, ss.17-28, 2022 (SCI-Expanded, Scopus, TRDizin)
  13. Clinical, biochemical, and echocardiographic evaluation of neonates with vitamin D deficiency due to maternal vitamin D deficiencyCayir A., Akyigit A., Gullu U. U., Kahveci H., Yildiz D., Kurnaz E., et al.CARDIOLOGY IN THE YOUNG, cilt.32, sa.1, ss.88-93, 2022 (SCI-Expanded, Scopus)
  14. Epidemiology of type 1 diabetes in children and adolescents: a 50-year, single center experienceKANDEMİR N., VURALLI KARAOĞLAN D., ÖZÖN Z. A., GÖNÇ E. N., ARDIÇLI D., Jalilova L., et al.HORMONE RESEARCH IN PAEDIATRICS, cilt.94, sa.SUPPL 1, ss.99, 2021 (SCI-Expanded, Scopus)
  15. Clinical features and long-term follow up of childhood papillary thyroid cancer (PTC): a single reference-center experienceOzon A., Emet D. C., Gonc N., VURALLI KARAOĞLAN D., Buyukyilmaz G., KANDEMİR N., et al.HORMONE RESEARCH IN PAEDIATRICS, cilt.94, sa.SUPPL 1, ss.62-63, 2021 (SCI-Expanded, Scopus)
  16. Cardiovascular risk factors in adolescents with type 1 diabetes: Prevalence and gender differencesVURALLI KARAOĞLAN D., Jalilova L., ALİKAŞİFOĞLU A., ÖZÖN Z. A., GÖNÇ E. N., KANDEMİR N.HORMONE RESEARCH IN PAEDIATRICS, cilt.94, sa.SUPPL 1, ss.236, 2021 (SCI-Expanded, Scopus)
  17. Which parameters predict the beneficial effect of GnRHa treatment on height in girls with central precocious puberty?VURALLI KARAOĞLAN D., Gonc N. E., ÖZÖN Z. A., KANDEMİR N., ALİKAŞİFOĞLU A.CLINICAL ENDOCRINOLOGY, cilt.94, sa.5, ss.804-810, 2021 (SCI-Expanded, Scopus)
  18. Kawasaki-like disease in children with COVID-19.Akca Ü., KESİCİ S., ÖZSÜREKCİ Y., AYKAN H. H., Batu E. D., ATALAY E., et al.Rheumatology international, cilt.40, ss.2105-2115, 2020 (SCI-Expanded, Scopus)
  19. Central nervous system imaging in girls with central precocious puberty: when is necessary?VURALLI KARAOĞLAN D., GÖNÇ E. N., ALİKAŞİFOĞLU A., KANDEMİR N., ÖZÖN Z. A.ARCHIVES OF ENDOCRINOLOGY METABOLISM, cilt.64, sa.5, ss.591-596, 2020 (SCI-Expanded, Scopus)
  20. Gender-related differences in etiology of organic central precocious pubertyVURALLI KARAOĞLAN D., Ozon A., GÖNÇ E. N., Oguz K. K., KANDEMİR N., ALİKAŞİFOĞLU A.TURKISH JOURNAL OF PEDIATRICS, cilt.62, sa.5, ss.763-769, 2020 (SCI-Expanded, Scopus, TRDizin)
  21. Treatment with Depot Leuprolide Acetate in Girls with Idiopathic Precocious Puberty: What Parameter should be Used in Deciding on the Initial Dose?VURALLI KARAOĞLAN D., ALİKAŞİFOĞLU A., İYİGÜN İ., Canoruc D., Ozon A., Gonc N., et al.JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.12, sa.1, ss.37-44, 2020 (SCI-Expanded, Scopus, TRDizin)
  22. Long-term effects of GnRH agonist treatment on body mass index in girls with idiopathic central precocious pubertyVURALLI KARAOĞLAN D., ÖZÖN Z. A., GÖNÇ E. N., ALİKAŞİFOĞLU A., KANDEMİR N.JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.33, sa.1, ss.99-105, 2020 (SCI-Expanded, Scopus)
  23. HDAC4 mutations cause diabetes and induce beta-cell FoxO1 nuclear exclusionGong M., Yu Y., VURALLI KARAOĞLAN D., Froehler S., Kuehnen P., Du Bois P., et al.HORMONE RESEARCH IN PAEDIATRICS, cilt.91, ss.66, 2019 (SCI-Expanded, Scopus)
  24. Improvement of final height in idiopathic central precocious puberty is associated with delay of bone maturation with GnRH agonist therapy under the age of 7 yearsVURALLI KARAOĞLAN D., GÖNÇ E. N., ÖZÖN Z. A., KANDEMİR N., ALİKAŞİFOĞLU A.HORMONE RESEARCH IN PAEDIATRICS, cilt.91, ss.330, 2019 (SCI-Expanded, Scopus)
  25. To whom should central nervous system imaging be performed in girls with central precocious puberty (CPP)?VURALLI KARAOĞLAN D., GÖNÇ E. N., ALİKAŞİFOĞLU A., KANDEMİR N., ÖZÖN Z. A.HORMONE RESEARCH IN PAEDIATRICS, cilt.91, ss.465, 2019 (SCI-Expanded, Scopus)
  26. Long term effects of GnRH agonist therapy on BMI in girls with idiopathic central precocious pubertyVURALLI KARAOĞLAN D., ÖZÖN Z. A., GÖNÇ E. N., ALİKAŞİFOĞLU A., KANDEMİR N.HORMONE RESEARCH IN PAEDIATRICS, cilt.91, ss.464, 2019 (SCI-Expanded, Scopus)
  27. Spondyloocular syndrome: Presentation of two siblings diagnosed with the rare disease and the results of Pamidronate TherapyVURALLI KARAOĞLAN D., ŞİMŞEK KİPER P. Ö., Utine E., ÜNSAL Y., ALİKAŞİFOĞLU A., KANDEMİR N.HORMONE RESEARCH IN PAEDIATRICS, cilt.91, ss.387, 2019 (SCI-Expanded, Scopus)
  28. Growth Hormone Deficiency in the Transition PeriodVURALLI KARAOĞLAN D.TURKISH JOURNAL OF ENDOCRINOLOGY AND METABOLISM, cilt.23, sa.3, ss.181-186, 2019 (ESCI, Scopus, TRDizin)
  29. HDAC4 mutations cause diabetes and induce -cell FoxO1 nuclear exclusionGong M., Yu Y., Liang L., VURALLI KARAOĞLAN D., Froehler S., Kuehnen P., et al.MOLECULAR GENETICS & GENOMIC MEDICINE, cilt.7, sa.5, 2019 (SCI-Expanded, Scopus)
  30. Ion Transporters, Channelopathies, and Glucose DisordersDEMİRBİLEK H., Galcheva S., VURALLI KARAOĞLAN D., Al-Khawaga S., Hussain K.INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, cilt.20, sa.10, 2019 (SCI-Expanded, Scopus)
  31. Systemic Pseudohypoaldosteronism Type 1 due to 3 Novel Mutations in SCNN1A and SCNN1B GenesCayir A., Demirelli Y., Yildiz D., Kahveci H., Yarali O., Kurnaz E., et al.HORMONE RESEARCH IN PAEDIATRICS, cilt.91, sa.3, ss.175-185, 2019 (SCI-Expanded, Scopus)
  32. Clinical Approach to Hypocalcemia in Newborn Period and Infancy: Who Should Be Treated?VURALLI KARAOĞLAN D.INTERNATIONAL JOURNAL OF PEDIATRICS, cilt.2019, 2019 (ESCI, Scopus)
  33. What Is the Best Parameter to Decide the Initial Dose of Depot Leuprolide Acetate in Girls with Idiopathic Central Precocious Puberty?VURALLI KARAOĞLAN D., ALİKAŞİFOĞLU A., Lyigun I., Canoruc D., Ozon A., Gonc N., et al.HORMONE RESEARCH IN PAEDIATRICS, cilt.90, ss.102-103, 2018 (SCI-Expanded, Scopus)
  34. A Rare Cause of Hyperinsulinemic Hypoglycemia: Costello SyndromeVURALLI KARAOĞLAN D., KOŞUKCU C., Taskiran E., Simsek P. O., ÜTİNE G. E., BODUROĞLU O. K., et al.HORMONE RESEARCH IN PAEDIATRICS, cilt.90, ss.363, 2018 (SCI-Expanded, Scopus)
  35. Gender-Related Differences in Etiological Distribution of Organic Causes of Central Precocious PubertyVURALLI KARAOĞLAN D., Ozon A., Gonc N., KANDEMİR N., ALİKAŞİFOĞLU A.HORMONE RESEARCH IN PAEDIATRICS, cilt.90, ss.518-519, 2018 (SCI-Expanded, Scopus)
  36. ESTABLISHMENT OF HORMONE CONTROL WITH DEXAMETHASONE IN PATIENTS WITH CLASSICAL CONGENITAL ADRENAL HYPERPLASIA AFTER FINAL HEIGHTGonc N., Ozon A., ALİKAŞİFOĞLU A., VURALLI KARAOĞLAN D., KANDEMİR N.HORMONE RESEARCH IN PAEDIATRICS, cilt.88, ss.252, 2017 (SCI-Expanded, Scopus)
  37. Vitamin A status and factors associated in healthy school-age childrenVURALLI KARAOĞLAN D., TÜMER L., Hasanoglu A., BİBEROĞLU G., PAŞAOĞLU H.CLINICAL NUTRITION, cilt.33, sa.3, ss.509-512, 2014 (SCI-Expanded, Scopus)
  38. Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiencyKANDEMİR N., VURALLI KARAOĞLAN D., Taskiran E., Gonc N., Ozon A., ALİKAŞİFOĞLU A., et al.TURKISH JOURNAL OF PEDIATRICS, cilt.54, sa.6, ss.570-575, 2012 (SCI-Expanded, Scopus)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 9

  1. Spondyloocular syndrome: Presentation of two siblings diagnosed with the rare disease and the results of Pamidronate TherapyVURALLI KARAOĞLAN D., ŞİMŞEK KİPER P. Ö., UTİNE G. E., ÜNSAL Y., ALİKAŞİFOĞLU A., KANDEMİR N.The 58th Annual ESPE Meeting, VİYANA, Avusturya, 19 - 21 Eylül 2019, cilt.91, ss.387, (Özet Bildiri)
  2. SOX9 gene dublication-related 46,XX ovotesticular disorder of sex developmentÖZÖN Z. A., ALİKAŞİFOĞLU A., GÖNÇ E. N., VURALLI KARAOĞLAN D., BÜYÜKYILMAZ G., ŞİMŞEK KİPER P. Ö., et al.10th International Meeting of Pediatric Endocrinolgy, 14 - 17 Eylül 2017, (Özet Bildiri)
  3. Tiroid Meduller Karsinomlu Çocukların Sağaltımında Cerrahi StratejilerBOYBEYİ Ö., KARNAK İ., YALÇIN E. Ş., VURALLI D., GÖNÇ E. N., ORHAN D., et al.33. Ulusal Çocuk Cerrahisi Kongresi, Çocuk Cerrahisi Dergisi, Türkiye, 28 - 31 Ekim 2015
  4. Unusual Presentation of Autoimmune Polyglandular Syndrome Type 1 (Aps1)VURALLI KARAOĞLAN D., TAN Ç., ÇAĞDAŞ AYVAZ D. N., TEZCAN F. İ., DEMİR H., HIZARCIOĞLU GÜLŞEN H., et al.
  5. A Rare Cause of Hyperinsulinemic Hypoglycemia: Costello SyndromeVURALLI KARAOĞLAN D., KOŞUKCU C., TAŞKIRAN Z. E., ŞİMŞEK KİPER P. Ö., UTİNE G. E., BODUROĞLU O. K., et al.
  6. Sox9 gene duplication-related 46, XX ovotesticular disorder of sex developmentÖZÖN Z. A., ALİKAŞİFOĞLU A., GÖNÇ E. N., VURALLI KARAOĞLAN D., BÜYÜKYILMAZ G., ŞİMŞEK KİPER P. Ö., et al.
  7. Erişkin boya erişen klasik konjenital adrenal hiperplazili olgularda hormon kontrolünün deksametazonla sağlanması.GÖNÇ E. N., ÖZÖN Z. A., ALİKAŞİFOĞLU A., VURALLI KARAOĞLAN D., KANDEMİR N.
  8. SOX9 gen duplikasyonuna bağlı 46,XX ovotestiküler cinsel farklılaşma bozukluğuÖZÖN Z. A., ALİKAŞİFOĞLU A., GÖNÇ E. N., VURALLI KARAOĞLAN D., Büyükyılmaz G., ŞİMŞEK KİPER P. Ö., et al.
  9. SOX9 gen dublikasyonuna bağlı 46,XX ovotestiküler cinsel farklılaşma bozukluğu.ÖZÖN Z. A., ALİKAŞİFOĞLU A., GÖNÇ E. N., VURALLI KARAOĞLAN D., Büyükyılmaz G., ŞİMŞEK KİPER P. Ö., et al.

İletişim

Bölüm
Çocuk Endokrinoloji, Çocuk Hastanesi

Son güncelleme: