Bilimsel çalışmalar

Prof. Dr. Cengiz Kara

323 yayın. Her yayının yanında bilginin kaynağı yazar.

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  1. Noonan sendromlu hastalarda büyüme özellikleri (Çok merkezli çalışma)

    Kaynak: livhospital.com profil sayfası

  2. GCK Gen Mutasyonuna Bağlı Diyabeti Olan Olguların Klinik ve Moleküler Özellikleri ile Dokuz Yeni Mutasyonun Tanımlanması (Çok merkezli çalışma)

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  3. Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi

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  4. YAYINLARKuyucu N, Kara C, Bakırtaş A, Teziç T. Successful treatment of visceral leishmaniasis with allopurinol plus ketoconasole in an infant who developed pancreatitis caused by meglumine antimonate. Pediatr Infect Dis J 2001; 20 (4): 455-457

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  5. Karakurt C, Kara C, Akgün D, Sipahi T. Spondylocostal Dysostosis: Presentation of Two Cases. Int Pediatr 2001;16 (3):173-175

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  6. Sipahi T, Kara C, Tavil B, İnci A, Oksal A. Alpha-1 antityripsin deficiency: an overlooked cause of late hemorrhagic disease of the newborn. J Pediatr Hematol Onkol 2003; 25(3): 274-275

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  7. Kara C, Kutlu AO, Tosun MS, Apaydın S, Şenel F. Sertoli cell tumor causing prepubertal gynecomastia in a boy with Peutz-Jeghers syndrome: The outcome of 1-year treatment with aromatase inhibitor testolactone. Horm Res 2005; 63 (5): 252-256 Epub 2005 Jun 9.

    Kaynak: livhospital.com profil sayfası

  8. Kara C, Öcal G, Berberoğlu M, Şıklar Z, Adıyaman P. Persistently Raised TSH in Adequately Treated Congenital Hypothyroidism Followed-up for a Long Time. J Pediatr Endocrinol Metab. 2008;21(3):251-6

    Kaynak: livhospital.com profil sayfası

  9. Sadeghi F, Yürür Kutlay N, Berberoğlu M, Çetinkaya E, Aycan Z, Kara C, Ilgın Ruhi H, Öçal G, Şıklar Z, Elhan A, and Tükün A.Identification of Frequency and Distribution of the 9 Most Frequent Mutations among Patients with 21-OHD in Turkey. J Pediatr Endocrinol Metab. 2008;21(8):781-7.

    Kaynak: livhospital.com profil sayfası

  10. Oguz Kutlu A, Akbiyik F, Kara C. Postnatal testicular regression mircopenis and microcephaly: Conformation of anew syndrome?Am J Med Genet A.2009; 149A(4):742–5doi: 10.1002/ajmg.a.32542.

    Kaynak: livhospital.com profil sayfası

  11. Çetinkaya S, Kunak B, Kara C, Demirçeken F, Yaralı N, Polat E, Aycan Z. Response to the letter by Drs Vanden Eijnden and Martinovici. J Pediatr Endocrinol Metab 2010;23(11):1208

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  12. Erdoğan S, Kara C, Uçaktürk A, Aydın M. Etiological classification and clinical assessment of children and adolescents with disorders of sex development. J Clin Res Pediatr Endocrinol 2011;3(2):77-83 doi:10.4274/jcrpe.v3i2.16. Epub 2011 Aug 6

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  13. Kutlu AO. Kara C. Iodine deficiency in pregnant women in the apparently iodine-sufficient capital city of Turkey. Clin Endocrinol (Oxf). 2012;77(4):615-20doi: 10.1111/j.1365-2265.2012.04440.x.

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  14. Simsek DG, Aycan Z, Ozen S, Cetinkaya S, Kara C, Abalı S, Demir K, Tunç O, Uçaktürk A, Asar G, Baş F, Cetinkaya E, Aydın M, Karagüzel G, Orbak Z, Sıklar Z, Altıncık A, Okten A, Ozkan B, Ocal G, Semiz S, Arslanoğlu I, Evliyaoğlu O, Bundak R, Darcan S. Diabetes Care, Glycemic Control, Complications and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study. J Clin Res Pediatr Endocrinol. 2013;5(1):20-26doi: 10.4274/Jcrpe.893. Epub 2013 Feb 19.

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  15. Sari E, Bereket A, Yeşilkaya E, Baş F, Bundak R, Aydın BK, Darcan Ş, Dündar B, Büyükinan M, Kara C, Adal E, Akıncı A, Atabek ME, Demirel F, Çelik N, Özkan B, Özhan B, Orbak Z, Ersoy B, Doğan M, Ataş A, Turan S, Gökşen D, Tarım Ö, Yüksel B, Ercan O, Hatun Ş, Şimşek E, Ökten A, Abacı A, Döneray H, Özbek MN, Keskin M, Önal H, Akyürek N, Bulan K, Tepe D, Emeksiz HC, Demir K, Kızılay D, Topaloğlu AK, Eren E, Özen S, Demirbilek H, Abalı S, Akın L, Eklioğlu BS, Kaba S, Anık A, Baş S, Unuvar T, Sağlam H, Bolu S, Özgen T, Doğan D, Çakır ED, Şen Y, Andıran N, Çizmecioğlu F, Evliyaoğlu O, Karagüzel G, Pirgon Ö, Çatlı G, Can HD, Gürbüz F, Binay Ç, Baş VN, Fidancı K, Gül D, Polat A, Acıkel C, Cinaz P, Darendeliler F. Anthropometric findings from birth to adulthood and their relation with karyotype distribution in Turkish girls with Turner syndrome. Am J Med Genet A. 2016 Apr;170(4):942-8. doi: 10.1002/ajmg.a.37498. Epub 2016 Jan 20.

    Kaynak: livhospital.com profil sayfası

  16. Atay Z, Yesilkaya E, Erdeve SS, Turan S, Akin L, Eren E, Doger E, Aycan Z,Abali ZY, Akinci A, Siklar Z, Ozen S, Kara C, Tayfun M, Sari E, Tutunculer F,Karabulut GS, Karaguzel G, Cetinkaya S, Saglam H, Bideci A, Kurtoglu S, Guran T, Bereket A. The Etiology and Clinical Features of Non-CAH Gonadotropin-IndependentPrecocious Puberty: A Multicenter Study. J Clin Endocrinol Metab. 2016May;101(5):1980-8. doi: 10.1210/jc.2015-3500. Epub 2016 Mar 10.

    Kaynak: livhospital.com profil sayfası

  17. Şıklar Z, Genens M, Poyrazoğlu Ş, Baş F, Darendeliler F, Bundak R, Aycan Z, Savaş Erdeve Ş, Çetinkaya S, Güven A, Abalı S, Atay Z, Turan S, Kara C, Can Yılmaz G, Akyürek N, Abacı A, Çelmeli G, Sarı E, Yeşilkaya E, Bolu S, Korkmaz HA, Şimşek E, Çatlı G, Büyükinan M, Çayır A, Evliyaoğlu O, İşgüven P, Özgen IT, Hatipoğlu N, Elhan AH, Berberoğlu M. The growth characteristics of patients with Noonan syndrome, and first 3 years results of GH treatment: A Nationwide multicenter study. J Clin Res Pediatr Endocrinol. 2016 Sep 1;8(3):305-12.doi: 10.4274/jcrpe.3013. Epub 2016 Apr 29.

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  18. Bayram N, Aydın ÖF, Şenbil N, Akçören Z, Öcal B, Oksal A, Rezaki B, Kara C, Gürer Y. Evaluation of 51 patients with Duchenne muscular dystrophy. 4th International Congress of the World Muscle Society, Antalya, Turkey, 14-16 October 1999. Neuromuscular Disorders 1999: 9: G.P.7.16

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  19. Kara C, Ocal G, Berberoglu M, Adiyaman P, Siklar Z. Persistently raised TSH in adequately treated congenital hypothyroidism followed-up for a long time. ESPE/LWPES 7th Joint Meeting Paediatric Endocrinology, Lyon, France, September 21-24, 2005. Hormone Research 2005; 64 (suppl 1): 106 (P1-353)

    Kaynak: livhospital.com profil sayfası

  20. Evliyaoglu O, Kutlu A, Kara C. Incidence of iodine deficiency in the etiology of congenital hypothyroidism. ESPE/LWPES 7th Joint Meeting Paediatric Endocrinology, Lyon, France, September 21-24, 2005. Hormone Research 2005; 64 (suppl 1): 119 (P1-403)

    Kaynak: livhospital.com profil sayfası

  21. Evliyaoglu O, Kutlu A, Kara C. Incomplete McCune-Albright syndrome associated with polycystic ovary. ESPE/LWPES 7th Joint Meeting Paediatric Endocrinology, Lyon, France, September 21-24, 2005. Hormone Research 2005; 64 (suppl 1): 214 (P2-733)

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  22. Akbıyık F, Oğuz Kutlu A, Kara C. Surgical timing in testicular adrenal tumors which are unresponsive to medical treatment. From Gene to Gender 2nd International Symposium on Disorders of Sex Development (DSD), Lübeck, Germany, August 31 – September 2, 2006. Abstracts and Programs P-1181, p12

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  23. Oğuz Kutlu A, Akbıyık F, Kara C. Monitoring plasma rennin activity in late diagnosed simple virilizing congenital adrenal hyperplasia patients. From Gene to Gender 2nd International Symposium on Disorders of Sex Development (DSD), Lübeck, Germany, August 31 – September 2, 2006. Abstracts and Programs P-1182, p46

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  24. Oğuz Kutlu A, Akbıyık F, Kara C. Infantile testicular regression syndrome: a rare case / a new syndrome? From Gene to Gender 2nd International Symposium on Disorders of Sex Development (DSD), Lübeck, Germany, August 31 – September 2, 2006. Abstracts and Programs P-1181, p1

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  25. Çetinkaya S, Kara C. The effects of glucocorticoid replacement therapy on bone mineral density in children with congenital adrenal hyperplasia. The Endocrine Society’s 89th Annual Meeting ENDO 07, Toronto, Canada, June 2-5, 2007. Program & Abstracts P4-288, p742

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  26. Darcan S, Arslanoğlu İ, İşgüven P et al. Etiological and auxological profile of short stature in pediatric endocrine clinics in the year of 2005: an attempt for a more accurate classification of short stature. 46th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Helsinki, Finland, June 27-30, 2007. Hormone Research 2007; 68 (suppl 1): 162 (PO1-518)

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  27. Kara C, Oğuz Kutlu A, Çetinkaya S. Sertoli cell tumor causing prepubertal gynecomastia in a boy with Peutz-Jeghers syndrome: the outcome of three-year treatment with aromatase inhibitors. 46th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Helsinki, Finland, June 27-30, 2007. Hormone Research 2007; 68 (suppl 1): 200 (PO2-643)

    Kaynak: livhospital.com profil sayfası

  28. Oğuz Kutlu A, Teziç T, Kara C. Jod-Basedow developed in a severe iodine deficiency related goiter in childhood. 46th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Helsinki, Finland, June 27-30, 2007. Hormone Research 2007; 68 (suppl 1): 255 (R-66)

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  29. Kara C, Usta B, Oğuz Kutlu A. Distinguishing features of thelarche variant: evaluation of 93 girls with premature breast development. 47th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), İstanbul, Turkey, September 20-23, 2008. Hormone Research 2008; 70 (suppl 1): 220 (P2-d3-739)

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  30. Ökten G, Pınarlı FA, Kara C, Tükün A, Kara N, Güneş SO. Congenital adrenal hyperplasia associated wirh agenesis of the finger and toe distal phalanges. 8th Balkan Meeting on Human Genetics, Cavtat-Dubrovnik, Crotia, May 14-17, 2009. Final Programme; p72 (42-MB)

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  31. Şensoy G, Elmalı M, Belet N, Kara C, Selçuk MB, Top A, Yıldıran A. Aspergillosis presenting as osteoarthritis in a child treated with voriconasole. 27th Annual Meeting of the European Society for Paediatric Infectious Diseases, Brussels, Belgium, June 9-13, 2009. The Pediatric Infectious Disease Journal 2009; 28(6): e90 (P265)

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  32. Gökşen Şimşek D, Aycan Z, Özen S, Çetinkaya S, Kara C, Abalı S, Demir K, Tunç Ö, Uçaktürk A, Asar G, Bas F, Çetinkaya E, Aydın M, Karagüzel G, Orbak Z, Şıklar Z, Altıncık A, Öktem A, Özkan B, Öcal G, Semiz S, Arslanoğlu A, Evliyaoğlu E, Bundak R & Darcan Ş. Type 1 diabetes mellitus: glycemic control and compliacations in Turkish children and adolescents. 35th Annual Meeting of the International Society for Pediatric and Adolescent Diabetes (ISPAD), Ljubljana, Slovenia, 2-5 September 2009. Pediatric Diabetes 2009; 10(Suppl 11): 76 (P143)

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  33. Uçaktürk A, Kara C, Aydın M. Gliclazide-induced hypoglycemia: delayed presentation and successful treatment with octreotide.LWPES/ESPE 8th Joint Meeting, New York, USA, September 9-12, 2009. Hormone Research 2009; 72 (Suppl 3): 489 (R16)

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  34. Genç G, Uçaktürk A, Kara C, Bek K, Açıkgöz Y, Özkaya O. Nephropathic cystinosis with nutritional rickets. 1st International Cystinosis Conference in East Mediterranean, Ankara, Turkey, October 1-4, 2009. Congress Book: 39

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  35. Uçaktürk A, Kara C, Işıklar F, Aydın M. Munchausen syndrome by proxy in a young girl presenting as apparent cyclic vaginal bleeding. 49th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Prague, Czech Republic, September 22-25, 2010. Hormone Researchin Pediatrics 2010; 74 (suppl 3): 87 (P1-d2-285)

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  36. Uçaktürk A, Kara C, Dinler G, Kalaycı AG, Aydın M. Metabolic syndrome presented with steroid induced hyperlipidemic pancreatitis in an adolescent girl. 49th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Prague, Czech Republic, September 22-25, 2010. Hormone Researchin Pediatrics 2010; 74 (suppl 3): 184 (P2-d2-616)

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  37. Erdoğan S, Kara C, Uçaktürk A, Aydın M. Etiological classification and clinical assessment of disorders of sex development (DSD) in 95 children and adolescents. 49th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Prague, Czech Republic, September 22-25, 2010. Hormone Researchin Pediatrics 2010; 74 (suppl 3): 205-6 (P2-d2-686)

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  38. Uçaktürk A, Kara C, Ceylaner S, Günindi F, Aydın M. A case report of Xp21 contiguous gene syndrome: adrenal hypoplasia congenita, glycerol kinase deficiency and Duchenne muscular dystrophy.50th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Glasgow, United Kingdom, September 25-28, 2011. Hormone Researchin Pediatrics 2011; 76 (suppl 2): 141-2 (P2-d2-450)

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  39. Uçaktürk A, Kara C, Günindi F, Aydın M. Low-dose, single day pamidronat treatment in osteogenesis imperfect. 50th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Glasgow, United Kingdom, September 25-28, 2011. Hormone Researchin Pediatrics 2011; 76 (suppl 2): 153 (P2-d2-487)

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  40. Günindi F, Kara C, Uçaktürk A, Akkuş L, Aydın M. Galactorrhea due to contact dermatitis of breast. 50th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Glasgow, United Kingdom, September 25-28, 2011. Hormone Researchin Pediatrics 2011; 76 (suppl 2): 211 (P2-d2-673)

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  41. Kara C, Gündüz, Çetinkaya S, Günindi F.Efficacy of bisphosphonates in the treatment of vitamin D intoxication.51st Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Leipzig, Germany, September 20-23, 2012. Hormone Research in Pediatrics 2012; 78 (suppl 1): 58 (P1-d1-197)

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  42. Kara C, Günindi, Üstyol A, Aydin M. Vitamin D intoxication associated with fish oil supplement in young children.51st Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Leipzig, Germany, September 20-23, 2012. Hormone Research in Pediatrics 2012; 78 (suppl 1): 58 (P1-d1-198)

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  43. Kutlu AO, Kara C.Iodine deficiency in pregnant women living in the capital city of Turkey, who appear to be iodine-sufficient.51st Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Leipzig, Germany, September 20-23, 2012. Hormone Research in Pediatrics 2012; 78 (suppl 1): 125 (P1-d3-397)

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  44. Uçakturk A, Kara C, Avcı B, Genç G, ÖzkayaO, Aydin M. Can kidney injury molecule-1 (KIM-1) and neutrophil gelatinase associated lipocalin (NGAL) be markers for early findings of diabetic nephropathy? 51st Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Leipzig, Germany, September 20-23, 2012. Hormone Research in Pediatrics 2012; 78 (suppl 1): 158 (P2-d1-507)

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  45. Kara C, Aydın T, Günindi F, Üstyol A, Aydın M. Prevalence and incidence of type 1 diabetes among children aged 0–18 years in Samsun, Turkey. 38th Annual Meeting of the International Society for Pediatric and Adolescent Diabetes (ISPAD), 10-13 October 2012, Istanbul, Turkey. Pediatric Diabetes 2012:13(suppl. 17):53 (P-474-169)

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  46. Aydın OF, Kara C, Jones J, Wood TC, May MM, Friez MJ, Schwartz CE. Allan-Herndon-Dudley syndrome caused by a novel MCT8/SLC16A2 mutation in a Turkish family. 9th Joint Meeting of Paediatric Endocrinology, September 19-22, 2013, Milan, Italy. Abstract Book (P2-d1-1143)

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  47. Günindi F, Kara C, Üstyol A, Aydın M.Assessment of the current iodine status via determination of the frequency of transient congenital hypothyroidism in the Central Black Sea Region of Turkey. 9th Joint Meeting of Paediatric Endocrinology, September 19-22, 2013, Milan, Italy. Abstract Book (P3-d1-1463)

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  48. Kara C, Can Yılmaz G, Demirbilek H, Flanagan SE, Ellard S, Hussain K, Aydın M. Efficacy and Safety of Sirolimus(mTOR Inhibitor) in Two Patients withDiazoxide-Unresponsive Hyperinsulinemic Hypoglycemia. I. Ege Endocrinology abd Genetics Symposium 25-27 February 2015, İzmir. J Clin Res Pediatr Endocrinol 2015; 7(Suppl 2): 86 (Poster Bildirisi, Üçüncülük Ödülü)

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  49. Can Yılmaz G, Kara C, Onay H, Aydın M. Growth Hormone Treatment in an Adolescent with Pycnodysostosis I. Ege Endocrinology abd Genetics Symposium 25-27 February 2015, İzmir. J Clin Res Pediatr Endocrinol 2015; 7 (Suppl 2): 87

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  50. Atay Z, Yeşilkaya E, Erdeve ŞS, Akin L, Eren E, Döger E, Aycan Z, Abali ZY, Akinci A, Siklar Z, Özen S, Kara C, Tayfun M, Tutunculer F, Karabulut GS, Karagüzel G, Saglam H, Bideci A, Kurtoglu S, Bereket A, Turan S, Sari E, Cetinkaya S, Güran T. Aetiological Spectrum and Clinical Characteristicsof 129 Children with Gonadotropin IndependentPrecocious Puberty: A Nationwide Cohort Study. 54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Barcelona, Spain, October 1-3, 2015. Hormone Research in Pediatrics 2015; 84 (suppl 1): 115-116 (P1-112)

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