ACADEMIC POSITIONS:

 

 

·        2016-2018 Assistant Professor, Department of Pediatrics, Cukurova University, Adana, Turkey

 

·        2018- Associate Professor, Department of Pediatrics, Cukurova University, Adana, Turkey

 

 

 

PEER-REVIEWED ARTICLES:(In Journals Indexed by SCI or SCIE)

 

Times cited:432(webofknowledge)

h-index: 8

Complete List of Published Work in MyBibliography:

https://www.ncbi.nlm.nih.gov/pubmed/?term=G%C3%BCrb%C3%BCz+f

 

 

1: Maharaj A, Buonocore F, Meimaridou E, Ruiz-Babot G, Guasti L, Peng HM, Capper CP, Burgos-Tirado N, Prasad R, Hughes CR, Maudhoo A, Crowne E, Cheetham TD, Brain CE, Suntharalingham JP, Striglioni N, Yuksel B, Gurbuz F, Gupta S, Lindsay R, Couch R, Spoudeas HA, Guran T, Johnson S, Fowler DJ, Conwell LS, McInerney-Leo AM, Drui D, Cariou B, Lopez-Siguero JP, Harris M, Duncan EL, Hindmarsh PC, Auchus RJ, Donaldson MD, Achermann JC, Metherell LA. Predicted Benign and SynonymousVariantsin CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing. JEndocr Soc. 2018 Oct 30;3(1):201-221. doi: 10.1210/js.2018-00130. eCollection2019 Jan 1. PubMed PMID: 30620006; PubMed Central PMCID: PMC6316989.

 

2: Kotan LD, Isik E, Turan I, Mengen E, Akkus G, Tastan M, Gurbuz F, Yuksel B,Topaloglu AK. Prevalence and associated phenotypes of PLXNA1 variants innormosmic and anosmic idiopathic hypogonadotropic hypogonadism. Clin Genet. 2019 Feb;95(2):320-324. doi: 10.1111/cge.13482. Epub 2018 Dec 26. PubMed PMID: 30467832.

 

3: Gürbüz F, Taştan M, Turan İ, Yüksel B. Efficiency of Single Dose of Tolvaptan Treatment During the Triphasic Episode After Surgery for Craniopharyngioma. J Clin Res Pediatr Endocrinol. 2018 Sep 27. doi: 10.4274/jcrpe.0182. [Epub ahead ofprint] PubMed PMID: 30257818.

 

4: Güran T, Tezel B, Gürbüz F, Selver Eklioğlu B, Hatipoğlu N, Kara C, Şimşek E, Çizmecioğlu FM, Ozon A, Baş F, Aydın M, Darendeliler F. Neonatal Screening forCongenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants. JClin Res Pediatr Endocrinol. 2019 Feb 20;11(1):13-23. doi:10.4274/jcrpe.galenos.2018.2018.0117. Epub 2018 Aug 14. PubMed PMID: 30111524;PubMed Central PMCID: PMC6398187.

 

5: Kışla Ekinci RM, Gürbüz F, Balcı S, Bişgin A, Taştan M, Yüksel B, Yılmaz M.Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a NovelMutation in GALNT3 Gene: Experience from Southern Turkey. J Clin Res Pediatr Endocrinol. 2019 Feb 20;11(1):94-99. doi: 10.4274/jcrpe.galenos.2018.2018.0134. Epub 2018 Jul 17. PubMed PMID: 30015621; PubMed Central PMCID: PMC6398194.

 

6: Turan I, Kotan LD, Tastan M, Gurbuz F, Topaloglu AK, Yuksel B. Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance. Clin Endocrinol (Oxf). 2018 Jun;88(6):799-805. doi: 10.1111/cen.13603. Epub 2018 Apr 18. PubMed PMID: 29582446.

 

7: Gurbuz F, Desai S, Diao F, Turkkahraman D, Wranitz F, Wood-Trageser M, Shin YH, Kotan LD, Jiang H, Witchel S, Gurtunca N, Yatsenko S, Mysliwec D, Topaloglu K, Rajkovic A. Novel inactivating mutations of the DCAF17 gene in American and Turkish families cause male infertility and female subfertility in the mouse model. Clin Genet. 2018 Apr;93(4):853-859. doi: 10.1111/cge.13183. Epub 2018 Jan24. PubMed PMID: 29178422.

 

8: Elmaoğulları S, Uçaktürk SA, Elbeg Ş, Döğer E, Tayfun M, Gürbüz F, Bideci A.Prevalence of ZnT8 Antibody in Turkish Children and Adolescents with New OnsetType 1 Diabetes. J Clin Res Pediatr Endocrinol. 2018 Jun 1;10(2):108-112. doi: 10.4274/jcrpe.5020. Epub 2017 Sep 25. PubMed PMID: 28943512; PubMed Central PMCID: PMC5985378.

 

9: Turan I, Hutchins BI, Hacihamdioglu B, Kotan LD, Gurbuz F, Ulubay A, Mengen E, Yuksel B, Wray S, Topaloglu AK. CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism. J Clin Endocrinol Metab. 2017 Jun 1;102(6):1816-1825. doi: 10.1210/jc.2016-3391. PubMed PMID: 28324054; PubMed Central PMCID: PMC5470764.

 

10: Akkuş G, Kotan LD, Durmaz E, Mengen E, Turan İ, Ulubay A, Gürbüz F, Yüksel B,Tetiker T, Topaloğlu AK. Hypogonadotropic Hypogonadism due to Novel FGFR1Mutations. J Clin Res Pediatr Endocrinol. 2017 Jun 1;9(2):95-100. doi:10.4274/jcrpe.3908. Epub 2016 Dec 23. PubMed PMID: 28008864; PubMed CentralPMCID: PMC5463295.

11: Gürbüz F, Ceylaner S, Topaloğlu AK, Yüksel B. Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis. J Clin Res PediatrEndocrinol. 2016 Sep 1;8(3):373-4. doi: 10.4274/jcrpe.3343. Epub 2016 May 16.PubMed PMID: 27181494; PubMed Central PMCID: PMC5096508.

 

12: Ünal S, Gönülal D, Uçaktürk A, Siyah Bilgin B, Flanagan SE, Gürbüz F, Tayfun M, Elmaoğulları S, Araslı A, Demirel F, Ellard S, Hussain K. A Novel HomozygousMutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism andSuccessful Management with Sirolimus. J Clin Res Pediatr Endocrinol. 2016 Dec1;8(4):478-481. doi: 10.4274/jcrpe.2773. Epub 2016 May 16. PubMed PMID: 27181099;PubMed Central PMCID: PMC5198009.

 

13: Dimitri P, De Franco E, Habeb AM, Gurbuz F, Moussa K, Taha D, Wales JK, HogueJ, Slavotinek A, Shetty A, Balasubramanian M. An emerging, recognizable facialphenotype in association with mutations in GLI-similar 3 (GLIS3). Am J Med GenetA. 2016 Jul;170(7):1918-23. doi: 10.1002/ajmg.a.37680. Epub 2016 May 5. PubMedPMID: 27148679.

 

14: Gürbüz F, Yüksel B, Topaloğlu AK. Wolcott-Rallison Syndrome with NovelEIF2AK3 Gene Mutation. J Clin Res Pediatr Endocrinol. 2016 Dec 1;8(4):496-497.doi: 10.4274/jcrpe.3065. Epub 2016 Jun 4. PubMed PMID: 27145240; PubMed CentralPMCID: PMC5198013.

 

15: Gurbuz F, Ceylaner S, Erdogan S, Topaloglu AK, Yuksel B. Sertoli cell onlysyndrome with ambiguous genitalia. J Pediatr Endocrinol Metab. 2016 Jul1;29(7):849-52. doi: 10.1515/jpem-2015-0458. PubMed PMID: 27124672.

 

16: Gurbuz F, Uzunmehmetoğlu OY, Diler Ö, Metcalf JS, Codd GA. Occurrence ofmicrocystins in water, bloom, sediment and fish from a public water supply. SciTotal Environ. 2016 Aug 15;562:860-868. doi: 10.1016/j.scitotenv.2016.04.027.Epub 2016 Apr 23. PubMed PMID: 27115623.

 

17: Kotan LD, Cooper C, Darcan Ş, Carr IM, Özen S, Yan Y, Hamedani MK, Gürbüz F, Mengen E, Turan İ, Ulubay A, Akkuş G, Yüksel B, Topaloğlu AK, Leygue E.Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations inSRA1. J Clin Res Pediatr Endocrinol. 2016 Jun 5;8(2):125-34. doi: 10.4274/jcrpe.3248. Epub 2016 Apr 18. PubMed PMID: 27086651; PubMed CentralPMCID: PMC5096466.

 

18: Hutchins BI, Kotan LD, Taylor-Burds C, Ozkan Y, Cheng PJ, Gurbuz F, Tiong JD,Mengen E, Yuksel B, Topaloglu AK, Wray S. CCDC141 Mutation Identified in Anosmic Hypogonadotropic Hypogonadism (Kallmann Syndrome) Alters GnRH Neuronal Migration.Endocrinology. 2016 May;157(5):1956-66. doi: 10.1210/en.2015-1846. Epub 2016 Mar 25. PubMed PMID: 27014940; PubMed Central PMCID: PMC4870868.

 

19: Uslu B, Gurbuz F, Temiz F, Yuksel B, Mungan N, Topaloglu AK. TheInvestigation of Plasma Glucagon-like Peptide-1 Levels in Newly Diagnosed Type 1 DiabeticChildren. West Indian Med J. 2015 Sep 3;65(1):141-146. doi:10.7727/wimj.2014.134. PubMed PMID: 26901603.

 

20: Darendeliler F, Yeşilkaya E, Bereket A, Baş F, Bundak R, Sarı E, KüçükemreAydın B, Darcan Ş, Dündar B, Büyükinan M, Kara C, Mazıcıoğlu MM, Adal E, AkıncıA, 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, ÖktenA, 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, AbalıS, Akın L, Eklioğlu BS, Kaba S, Anık A, Baş S, Ünüvar 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, Sağlam C, Gül D, Polat A,Açıkel C, Cinaz P. Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group. J Clin Res Pediatr Endocrinol. 2015Sep;7(3):183-91. doi: 10.4274/jcrpe.2023. PubMed PMID: 26831551; PubMed CentralPMCID: PMC4677552.

 

21: Sari E, Bereket A, Yeşilkaya E, Baş F, Bundak R, Aydın BK, Darcan Ş, DündarB, 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,ErcanO, HatunŞ, Şimşek E, Ökten A, Abacı A, Döneray H, Özbek MN, Keskin M, ÖnalH, Akyürek N, Bulan K, Tepe D, Emeksiz HC, Demir K, Kızılay D, Topaloğlu AK, ErenE, 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,ÇizmecioğluF, 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. 2016Apr;170A(4):942-8. doi: 10.1002/ajmg.a.37498. Epub 2016 Jan 20. PubMed PMID: 26788866.

 

 

22: Gürbüz F, Özalp Yüreğir Ö, Ceylaner S, Topaloğlu AK, Yüksel B. Coexistence of Kabuki Syndrome and Autoimmune Thyroiditis. J Clin Res Pediatr Endocrinol. 2016Mar 5;8(1):105-6. doi: 10.4274/jcrpe.2686. Epub 2015 Dec 18. PubMed PMID:26757828; PubMed Central PMCID: PMC4805041.

 

23: Mengen E, Tunc S, Kotan LD, Nalbantoglu O, Demir K, Gurbuz F, Turan I, SekerG, Yuksel B, Topaloglu AK. Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide. Horm Res Paediatr. 2016;85(2):107-11. doi: 10.1159/000441977.Epub 2015 Nov 24. PubMed PMID: 26595427.

 

24: Gurbuz F, Gurbuz BB, Celik GG, Yildirim V, Ucakturk SA, Seydaoglu G, UcakturkEM, Topaloglu AK, Yuksel B. Effects of methylphenidate on appetite and growth in children diagnosed with attention deficit and hyperactivity disorder. J PediatrEndocrinol Metab. 2016 Jan;29(1):85-92. doi: 10.1515/jpem-2015-0171. PubMed PMID:26352086.

 

25: Dimitri P, Habeb AM, Gurbuz F, Millward A, Wallis S, Moussa K, Akcay T, TahaD, Hogue J, Slavotinek A, Wales JK, Shetty A, Hawkes D, Hattersley AT, Ellard S, De Franco E. Expanding the Clinical Spectrum Associated With GLIS3 Mutations. JClin Endocrinol Metab. 2015 Oct;100(10):E1362-9. doi: 10.1210/jc.2015-1827. Epub 2015 Aug 10. Erratum in: J Clin Endocrinol Metab. 2015 Dec;100(12):4685. Garbuz,F [corrected to Gurbuz, F]. PubMed PMID: 26259131; PubMed Central PMCID:PMC4596041.

 

26: Yeşilkaya E, Bereket A, Darendeliler F, Baş F, Poyrazoğlu Ş, Küçükemre Aydın B, Darcan Ş, Dündar B, Büyükinan M, Kara C, Sarı E, 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, Abalı S, Akın L, SelverEklioğlu B, Kaba S, Anık A, Baş S, Ünüvar T, Sağlam H, Bolu S, Özgen T, Doğan D, Deniz Çakır E, Şen Y, Andıran N, Çizmecioğlu F, Evliyaoğlu O, Karagüzel G, PirgonÖ, Çatlı G, Can HD, Gürbüz F, Binay Ç, Baş VN, Fidancı K, Polat A, Gül D, AçıkelC, Demirbilek H, Cinaz P, Bondy C. Turner syndrome and associated problems inTurkish children: a multicenter study. J Clin Res Pediatr Endocrinol. 2015 Mar;7(1):27-36. doi: 10.4274/jcrpe.1771. PubMed PMID: 25800473; PubMed CentralPMCID: PMC4439889.

27: Wood-Trageser MA, Gurbuz F, Yatsenko SA, Jeffries EP, Kotan LD, Surti U,Ketterer DM, Matic J, Chipkin J, Jiang H, Trakselis MA, Topaloglu AK, Rajkovic A.MCM9 mutations are associated with ovarian failure, short stature, andchromosomal instability. Am J Hum Genet. 2014 Dec 4;95(6):754-62. doi:10.1016/j.ajhg.2014.11.002. PubMed PMID: 25480036; PubMed Central PMCID:PMC4259971.

 

28: Gurbuz F, Gurbuz B, Çayir A, Tezer H. Epstein-barr virus encephalitis ininfancy. West Indian Med J. 2014 Mar;63(2):206-7. doi: 10.7727/wimj.2014.021.Epub 2014 Jun 10. PubMed PMID: 25303265; PubMed Central PMCID: PMC4655663.

 

29: Demirbilek H, Ozbek MN, Demir K, Kotan LD, Cesur Y, Dogan M, Temiz F, Mengen E, Gurbuz F, Yuksel B, Topaloglu AK. Normosmic idiopathic hypogonadotropichypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in theKISS1R gene in three unrelated families. Clin Endocrinol (Oxf). 2015 Mar;82(3):429-38. doi: 10.1111/cen.12618. Epub 2014 Nov 7. PubMed PMID: 25262569.

 

30: Çayır A, Turan Mİ, Gurbuz F, Kurt N, Yildirim A. The effect of lifestyle change and metformin therapy on serum arylesterase and paraoxonase activity in obese children. J Pediatr Endocrinol Metab. 2015 May;28(5-6):551-6. doi:10.1515/jpem-2013-0486. PubMed PMID: 25252747.

 

31: Kotan LD, Hutchins BI, Ozkan Y, Demirel F, Stoner H, Cheng PJ, Esen I, Gurbuz F, Bicakci YK, Mengen E, Yuksel B, Wray S, Topaloglu AK. Mutations in FEZF1 cause Kallmann syndrome. Am J Hum Genet. 2014 Sep 4;95(3):326-31. doi: 10.1016/j.ajhg.2014.08.006. PubMed PMID: 25192046; PubMed Central PMCID: PMC4157145.

 

32: Topaloglu AK, Lomniczi A, Kretzschmar D, Dissen GA, Kotan LD, McArdle CA, Koc AF, Hamel BC, Guclu M, Papatya ED, Eren E, Mengen E, Gurbuz F, Cook M, Castellano JM, Kekil MB, Mungan NO, Yuksel B, Ojeda SR. Loss-of-function mutations in PNPLA6 encoding neuropathy target esterase underlie pubertal failure and neurological deficits in Gordon Holmes syndrome. J Clin Endocrinol Metab. 2014Oct;99(10):E2067-75. doi: 10.1210/jc.2014-1836. Epub 2014 Jul 17. PubMed PMID:25033069; PubMed Central PMCID: PMC5393493.

 

33: Aslan TB, Gurbuz F, Temiz F, Yuksel B, Topaloglu AK. Etiological evaluationof patients presenting with isolated micropenis to an academic health carecenter. Indian J Pediatr. 2014 Aug;81(8):775-9. doi: 10.1007/s12098-013-1205-6. Epub 2013 Sep 5. PubMed PMID: 24005879.

 

34: Gürbüz F, Yağcı-Küpeli B, Kör Y, Yüksel B, Zorludemir S, Gürbüz BB, Küpeli S.The first report of cabergoline-induced immune hemolytic anemia in an adolescent with prolactinoma. J Pediatr Endocrinol Metab. 2014 Jan;27(1-2):159-63. doi:10.1515/jpem-2013-0151. PubMed PMID: 23945126.

 

35: Yüksel B, Kulle AE, Gürbüz F, Welzel M, Kotan D, Mengen E, Holterhus PM, Topaloğlu AK, Grötzinger J, Riepe FG. The novel mutation p.Trp147Arg of the steroidogenic acute regulatory protein causes classic lipoid congenital adrenal hyperplasia with adrenal insufficiency and 46,XY disorder of sex development. Horm Res Paediatr. 2013;80(3):163-9. doi: 10.1159/000354086. Epub 2013 Aug 1. PubMed PMID: 23920000.

 

36: Tolu-Kendir O, Kiriş N, Temiz F, Gürbüz F, Onenli-Mungan N, Topaloğlu AK,Yüksel B. Relationship between metabolic control and neurocognitive functions inchildren diagnosed with type I diabetes mellitus before and after 5 years of age.Turk J Pediatr. 2012 Jul-Aug;54(4):352-61. PubMed PMID: 23692715.

 

37: Gürbüz F, Kotan LD, Mengen E, Şıklar Z, Berberoğlu M, Dökmetaş S, Kılıçlı MF, Güven A, Kirel B, Saka N, Poyrazoğlu Ş, Cesur Y, Doğan M, Özen S, Özbek MN, Demirbilek H, Kekil MB, Temiz F, Önenli Mungan N, Yüksel B, Topaloğlu AK. Distribution of gene mutations associated with familial normosmic idiopathichypogonadotropic hypogonadism. J Clin Res Pediatr Endocrinol. 2012Sep;4(3):121-6. doi: 10.4274/jcrpe.725. Epub 2012 Jul 5. PubMed PMID: 22766261;PubMed Central PMCID: PMC3459159.

 

38: Azık FM, Akıncı A, Saylı TR, Culha VK, Teberik K, Teke MY, Gürbüz F.Unilateral exudative retinal detachment as the sole presentation of relapsingacute lymphoblastic leukemia. Turk J Haematol. 2012 Jun;29(2):181-4. doi:10.5505/tjh.2012.72623. Epub 2012 Jun 15. PubMed PMID: 24744652; PubMed CentralPMCID: PMC3986959.

 

 

39: Topaloglu AK, Tello JA, Kotan LD, Ozbek MN, Yilmaz MB, Erdogan S, Gurbuz F,Temiz F, Millar RP, Yuksel B. Inactivating KISS1 mutation and hypogonadotropichypogonadism. N Engl J Med. 2012 Feb 16;366(7):629-35. doi:10.1056/NEJMoa1111184. PubMed PMID: 22335740.

40: GürbüzF, Ağın M, Mengen E, Elçi H, Ünal İ, Tümgör G, Yüksel B. "Kronikkaraciğer hastalığı olan çocukların D vitamini düzeyleri". Cukurova Medical Journal 43(2018): 450-456

41: MunganN, Gürbüz F, Mengen E, Özgür Ö, Topaloğlu A, Yüksel B. "Osteogenezis İmperfekta Olan Çocuklarda İki Farklı Pamidronat Protokolünün Değerlendirilmesi". Cukurova Medical Journal 39 (2014): 532-539

42: Fatih GÜRBÜZ. Sağlıklı Çocuk İzlemi. Healthy Child Follow Up. Turkiye Klinikleri J Fam Med-Special Topics. 2017;8(5):305-10.

 

43: Yeni Tanımlanmış Bir Glukokinaz Gen Mutasyonuna Bağlı Mody Tip 2 Olgusu. Mody Type 2 Case Due to Newly Diagnosed Mutations in the Glucokinase. Yılmaz A, Elmaoğulları S, Tayfun M, Uçaktürk S.A, Gürbüz F,Demirel F, Topaloğlu A.K. Turkiye Klinikleri J Case Rep. 2016;24(2 Suppl 1):S 1-5

 

 

 

MEMBERSHIPS:

 

·        Member, Turkish Society for Pediatric Endocrinology and Diabetes 2010-present

·        Member, European Society for Paediatric Endocrinology 2012-present

 

 

 

 

EDUCATIONAL ACTIVITIES AS AN ASSOCIATE PROFESSOR

 

Classes taught at the Cukurova University Faculty of Medicine

 

·        Thyroid disorders in children and adolescents YEAR 3 and 4

 

·        Congenital hypothyroidism YEAR 3 and 4

 

·        Obesity in children and adolescents YEAR 3 and 4

 

·        Puberty and adolescence YEAR 3

 

·        Precoccious puberty YEAR 3

 

·        Delayed puberty YEAR 3

 

·        Water balance and its disorders  YEAR 4

 

·        Calcium Metabolism Disorders. YEAR 3 and 4

 

Classes taught at the Department of Pediatrics for residents

 

·        Growth and puberty

 

·        Pubertal disorders

 

·        Thyroid disorders

 

·        Water balance and its disorders

 

·        Childhood Obesity

 

·        Calcium Metabolism Disorders

 

·        Diabetes Mellitus