Doç. Dr. Hüseyin Anıl Korkmaz
Branşı: Çocuk Sağlığı ve Hastalıkları, Çocuk Endokrinoloji
Yabancı Diller: İngilizce
İletişim adresi: …..@saglik.gov.tr
Klinik: Çocuk Endokrinoloji ve Metabolizma Hastalıkları Kliniği
Tıbbi ilgi ve uzmanlık alanları:
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Eğitimi:
2017 Doçentlik, Ankara Üniversitesi (sınav yeri)
2014 Yan Dal Uzmanlık, Dr. Behçet Uz Çocuk Hastalıkları Eğitim ve Araştırma Hastanesi, İzmir
2010 Uzmanlık, Dokuz Eylül Üniversitesi Tıp Fakültesi Pediatri ABD, İzmir
2004 Lisans, Ege Üniversitesi Tıp Fakültesi, İzmir
Çalışılan Kurumlar:
2005/2010 Dokuz Eylül Üniversitesi Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Arş. Gör., Doktor
2010/2011 Bitlis Adilcevaz Onkoloji Hastanesi, Uzman Doktor
2011/2011 Uludağ Üniversitesi Tıp Fakültesi Çocuk Nefroloji Bilim Dalı, Uzman Doktor
2011/2015 Dr. Behçet Uz Çocuk Hastalıkları ve Cerrahisi Eğitim ve Araştırma Hastanesi Çocuk Endokrinolojisi Bölümü, Uzman Doktor
2015/2015 Manchester Royal Children Hospital, Çocuk Endokrinolojisi Bölümü, Uzman Doktor
2015/2017 Balıkesir Atatürk Devlet Hastanesi Çocuk Endokrinolojisi Bölümü, Uzman Doktor
2017/2018 Manisa Merkezefendi Devlet Hastanesi Çocuk Endokrinolojisi Bölümü, Uzman Doktor
2018/2019 Manisa Şehir Hastanesi, Doçent Doktor
2019/2019 King’s College Hospital (London), Çocuk Endokrinolojisi Bölümü
2019/2021 Manisa Şehir Hastanesi, Doçent Doktor
2021/…. S.B.Ü. Dr. Behçet Uz Çocuk Sağlığı ve Cerrahisi Eğitim ve Araştırma Hastanesi, Doçent Doktor
Yayınlar:
A. Uluslararası hakemli dergilerde yayımlanan makaleler :
A1. Erbas O, Yılmaz M, Korkmaz HA, Bora S, Evren V, Peker G. Oxytocin inhibits pentylentetrazol-induced seizures in the rat. Peptides 2013;40:141-4.
A2. Dizdarer C, Korkmaz HA, Büyükocak ÖM, Tarancı SM, Coban A. Impact of insulin resistance on insulin-like growth factor-1/insulin like growth factor-binding protein-3 axis and on early weight gain in small for gestational age infants. J Clin Res Pediatr Endocrinol 2013;5:104-9.
A3. Korkmaz HA, Aydin A, Unal B. Comparison of acellular pertussis-tetanus-diphtheria vaccines and whole-cell pertussis-tetanus-diphtheria vaccines in infancy. Paediatr Int Child Health 2014;34:198-202.
A4. Yılmaz U, Yılmaz TS, Akıncı G, Korkmaz HA, Tekgül H. The effect of antiepileptic drugs on thyroid function in children. Seizure 2014;23:29-35.
A5. Eren E, Edgunlu T, Korkmaz HA, Cakir ED, Demir K, Cetin ES, Celik SK. Genetic variants of estrogen beta and leptin receptors may cause gynecomastia in adolescent. Gene 2014;541:101-6.
A6. Pala HG, Pala EE, Artunc Ulkumen B, Aktug H, Yavasoglu A, Korkmaz HA, Erbas O. The protective effect of granulocyte colony-stimulating factor on endometrium and ovary in a rat model of diabetes mellitus. Gynecol Obstet Invest 2014;78:94-100.
A7. Korkmaz HA, Demir K, Kılıç FK, Terek D, Arslanoğlu S, Dizdarer C, Ozkan B.Management of central diabetes insipidus with oral desmopressin lyophilisate in infants. J Pediatr Endocrinol Metab 2014;27:923-7.
A8. Bayır O, Korkmaz HA, Dizdarer C, Meşe T, Tavlı V. Carotid artery intima-media thickness in pediatric type 1 diabetic patients. Anadolu Kardiyol Derg 2014;14:464-70.
A9. Erbas O, Korkmaz HA, Oltulu F, Aktug H, Yavasoglu A, Akman L, Solmaz V, Taskiran D. Oxytocin alleviates cisplatin-induced renal damage in rats. Iran J Basic Med Sci 2014;17:747-52.
A10. Korkmaz HA, Edgünlü T, Eren E, Demir K, Çakir ED, Çelik SK, Özkan B. GPR30 Gene Polymorphisms Are Associated with Gynecomastia Risk in Adolescents. Horm Res Paediatr 2015;83:177-82.
A11. Dönmez O, Korkmaz HA, Yıldız N, Ediz B. Comparison of serum cystatin C and creatinine levels in determining glomerular filtration rate in children with stage I to III chronic renal disease. Ren Fail 2015;37:784-90.
A12. Anık A, Çatlı G, Abacı A, Sarı E, Yeşilkaya E, Korkmaz HA, Demir K, Altıncık A, Tuhan HÜ, Kızıldağ S, Özkan B, Ceylaner S, Böber E. Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing. J Pediatr Endocrinol Metab 2015;28:1265-71.
A13. Gülez P, Korkmaz HA, Özkök D, Can D, Özkan B. Factors Influencing Serum Vitamin D Concentration in Turkish Children Residing in İzmir: A Single-Center Experience. J Clin Res Pediatr Endocrinol 2015;7:294-300.
A14. Temur M, Yilmaz Ö, Aksun S, Özün ÖP, Calan M, Küme T, Karakulak M, Korkmaz HA. Increased circulating urocortin-3 levels is associated with polycystic ovary syndrome. Gynecol Endocrinol 2016;32:218-22.
A15. Nacaroglu T, Isguder R, Bahceci S, Ceylan G, Korkmaz HA, Karaman S, Karkiner CSU, Can D. Can Mean Platelet Volume be Used as a Biomarker for Asthma? Advances in Dermatology and Allergology 2016;33:182-7.
A16. Korkmaz HA, Hazan F, Dizdarer C, Tükün A. Hypochondroplasia in a child with 1620C>G (Asn540Lys) mutation in FGFR3. J Clin Res Pediatr Endocrinol 2012;4:220-2.
A17. Korkmaz HA, Özkan B, Hazan F, Büyükinan M, Çelik T. A case of Turner syndrome with concomitant transient hypogammaglobulinaemia of infancy and centraldiabetes insipidus. J Clin Res Pediatr Endocrinol 2013;5:62-4.
A18. Korkmaz HA,Dizdarer C, Hazan F, Karaarslan U.Attempted suicide with levothyroxine in an adolescent girl. J Pediatr Endocrinol Metab 2013;26:129-31.
A19. Korkmaz HA, Ozkan B, Terek D, Dizdarer C, Arslanoğlu S. Neonatal seizure as a manifestation of unrecognized maternal hyperparathyroidism. J Clin Res Pediatr Endocrinol 2013;5(3):206-8.
A20. Korkmaz HA,Dizdarer C, Ecevit CO. Hypocalcemic seizure in an adolescent with Down syndrome: a manifestation of unrecognized celiac disease. Turk J Pediatr 2013;55:536-8.
A21. Hazan F, Karaca E, Koker SA, Korkmaz HA, Mese T, Onay H, Ozkinay F. A Novel Missense Mutation in BRAF Caused Cardio-Facio-Cutaneous Syndrome. Iran J Pediatr 2013;23:608-9.
A22. Demir K, Yıldız M, Elmas ÖN, Korkmaz HA, Tunç S, Olukman Ö, Hazan F, Özkan KU, Özkan B. Two different patterns of mini-puberty in two 46,XY newborns with 17β-hydroxysteroid dehydrogenase type 3 deficiency. J Pediatr Endocrinol Metab 2015;28:961-5.
A23. Nalbantoğlu Ö, Demir K, Korkmaz HA, Büyükinan M, Yıldız M, Tunç S, Özkan B. A novel mutation of AMH in three siblings with persistent Mullerian duct syndrome. J Pediatr Endocrinol Metab 2015;28:1379-82.
A24. Demir K, Nalbantoğlu Ö, Karaer K, Korkmaz HA, Yıldız M, Tunç S, Özkan B. Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy. J Clin Res Pediatr Endocrinol 2015;7:356-7.
A25. Erdem SB, Nacaroglu HT, Bag O, Karkiner CS, Korkmaz HA, Can D. DRESS syndrome associated with type 2 diabetes in a child. Cent Eur J Immunol 2015;40:493-6.
A26. Korkmaz HA, Demir K, Hazan F, Yıldız M, Elmas ON, Özkan B. Association of Wolfram syndrome with Fallot tetralogy in a girl. Archivos Argentinos de Pediatría 2016;114:163-5.
A27. Korkmaz HA, Karadaş N, Karadaş U. Is Hashimoto's Thyroiditis Associated with Chronic Immune Thrombocytopenic Purpura? Hong Kong Journal of Paediatrics 2016;21:133.
A28. Korkmaz HA. Are vitamin D drops containing 400 IU daily adequate for preventing vitamin D deficiency? J Clin Res Pediatr Endocrinol 2016;8:372.
A29. Nacaroglu T, Isguder R, Bahceci S, Ceylan G, Korkmaz HA, Karaman S, Karkiner CSU, Can D. Can Mean Platelet Volume be Used as a Biomarker for Asthma? Advances in Dermatology and Allergology 2016;33:182-7.
A30. Şıklar Z, Genens M, Poyrazoğlu Ş, B Firdevs, Darendeliler F, Bundak R, Aycan Z, Erdeve ŞS, Çetinkaya S, Güven A, Abalı S, Atay Z, Turan S, Kara C, Yılmaz GC, Akyürek N, Abacı A, Çelmeli G, Sarı E, Yeşilkaya E, Bolu S, Korkmaz HA, Şimşek E, Çatlı G, Büyükinan M, Çayır A, Evliyaoğlu O. 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;8:305-12.
A31. Hazan F, Korkmaz HA, Yararbaş K, Wuyts W, Tükün A. Trichorhinophalangeal syndrome type II presenting with short stature in a child. Archivos Argentinos de Pediatría 2016;114:e403-e407.
A32. Nacaroglu T, Isguder R, Bent S, Bahceci SE, Ceylan G, Korkmaz HA, Karaman S, Karkiner CSU, Can D. Can neutrophil/lymphocyte ratio be a novel biomarker of inflammation in children with asthma? European Journal of Inflammation 2016;14:109-12.
A33. Yildiz M, İşleten F, Demir K, Çelik N, Korkmaz HA, Tuğlu B, Elmas ÖN, Özkan B. Anti-Cyclic Citrullinated Peptide Antibodies are not Frequent in Children with Type 1 Diabetes. The Turkish Journal of Pediatrics 2016;58: 395-399.
A34. Isguder R, Ceylan G, Ağın H, Nacaroglu HT, Korkmaz HA, Devrim İ, Vergin C. Increased Mean Platelet Volume in Children with Sepsis as a Predictor of Mortality. The Turkish Journal of Pediatrics 2016;58:503-511.
A35. Özdemir R, Korkmaz HA, Küçük M, Karadeniz C, Meşe T, Özkan B. Assessment of early atherosclerosis and left ventricular dysfunction in children with 21-hydroxylase deficiency. Clin Endocrinol (Oxf) 2017;86:473-479.
A36. Katipoğlu N, Karapınar TH, Demir K, Aydin Köker S, Nalbantoğlu Ö, Ay Y, Korkmaz HA, Oymak Y, Yıldız M, Tunç S, Hazan F, Vergin C, Özkan B. Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report. Archivos Argentinos de Pediatría 2017;115:e153-e156.
A37. Korkmaz HA. A case of Marfan syndrome presenting with transverse striae of the back. Arch Argent Pediatr 2017;115(6):e491-e495.
A38. Poyrazoğlu Ş, Bundak R, Yavaş Abalı Z, Önal H, Sarıkaya S, Akgün A, Baş S, Abalı S, Bereket A, Eren E, Tarım Ö, Güven A, Yıldız M, Karaman Aksakal D, Yüksel A, Seymen Karabulut G, Hatun Ş, Özgen T, Cesur Y, Azizoğlu M, Dilek E, Tütüncüler F, Papatya Çakır E, Özcabı B, Evliyaoğlu O, Karadeniz S, Dursun F, Bolu S, Arslanoğlu İ, Yeşiltepe Mutlu G, Kırmızıbekmez H, İşgüven P, Üstyol A, Adal E, Uçar A, Cebeci N, Bezen D, Binay Ç, Semiz S, Korkmaz HA, Memioğlu N, Sagsak E, Peltek HN, Yıldız M, Akçay T, Turan S, Güran T, Atay Z, Akcan N, Çizmecioğlu F, Ercan O, Dağdeviren A, Baş F, İşsever H, Darendeliler F. Incidence of Type 1 Diabetes in Children Aged Below 18 Years During 2013-2015 in Northwest Turkey. J Clin Res Pediatr Endocrinol. 2018 May 23. doi: 10.4274/jcrpe.0025. [Epub ahead of print]
A39. Korkmaz HA. A case of Wolfram syndrome with chronic renal failure. Ann Pediatr Endocrinol Metab 2018;23:166-167.
A40. Eren E, Törel Ergür A, İşgüven ŞP, Çelebi Bitkin E, Berberoğlu M, Şıklar Z, Baş F, Yel S, Baş S, Söbü E, Bereket A, Turan S, Sağlam H, Atay Z, Ercan O, Güran T, Atabek ME, Korkmaz HA, Kılınç Uğurlu A, Akıncı A, Döğer E, Şimşek E, Akbaş ED, Abacı A, Gül Ü, Acar S, Mengen Uçaktürk E, Yıldız M, Ünal E, Tarım Ö. Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey. J Clin Res Pediatr Endocrinol. 2018 Nov 5. doi: 10.4274/jcrpe.0206. [Epub ahead of print]
A41. Korkmaz HA, Karaarslan U, Eraslan C, Atila D, Hazan F, Barisik V, Ata ES, Etlik O, Yildiz M, Ozkan B. Screening of PROP-1, LHX2 and POU1F1 Mutations in Patients with Ectopic Posterior Pituitary Gland. Acta Endo (Buc) 2018;14: 300-306.
A42. Korkmaz HA, Özdemir R, Küçük M, Karadeniz C, Meşe T, Özkan B. The Impact of 21-hydroxylase Deficiency on Cardiac Repolarization Changes in Children With 21-hydroxylase deficient Congenital Adrenal Hyperplasia. Turk J Pediatr 019;61:228-235.
A.43. Gürsoy S, Hazan F, Aykut A, Nalbantoğlu Ö, Korkmaz HA, Demir K, Özkan B, Çoğulu Ö. Detection of SHOX Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature. J Clin Res Pediatr Endocrinol. 2020 ;12:358-365.
A.44. Korkmaz HA. Letter to the Editor: Nutritional thrift can be associated with precocious puberty and premature adrenarche in children born small for gestational age. Clin Pediatr Endocrinol. 2020;29:131-132.