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

 

Complete List of Published Work in MyBibliography:

 

https://www.ncbi.nlm.nih.gov/pubmed/?term=Yuksel+Bilgin

 

1: Kendir OT, Yilmaz HL, Ozkaya AK, Turan I, Gokay SS, Bilen S, Yildizdas RD,Yuksel B. Determination of cerebral edema with serial measurement of optic nerve sheath diameter during treatment in children with diabetic ketoacidosis: alongitudinal study. J Pediatr Endocrinol Metab. 2019 Jul 12. pii:/j/jpem.ahead-of-print/jpem-2019-0016/jpem-2019-0016.xml. doi:10.1515/jpem-2019-0016. [Epub ahead of print] PubMed PMID: 31299007.

 

2: 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, BrainCE, 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-LeoAM, Drui D, Cariou B, Lopez-Siguero JP, Harris M, Duncan EL, Hindmarsh PC, AuchusRJ, Donaldson MD, Achermann JC, Metherell LA. Predicted Benign and SynonymousVariants in 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.

 

3: 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.

 

4: Gürbüz F, Taştan M, Turan İ, Yüksel B. Efficiency of Single Dose of Tolvaptan Treatment During the Triphasic Episode After Surgery for Craniopharyngioma. JClin ResPediatr Endocrinol. 2019 May 28;11(2):202-206. doi:10.4274/jcrpe.galenos.2018.2018.0182. Epub 2018 Sep 27. PubMed PMID: 30257818;PubMed Central PMCID: PMC6571528.

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 Novel

Mutation 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, Topaloglu AK, Yuksel B. The Authors' Reply: In systemicpseudohypoaldosteronism type 1 skin manifestations are not rare and the diseaseis not transient. Clin Endocrinol (Oxf). 2018 May 17. doi: 10.1111/cen.13742.[Epub ahead of print] PubMed PMID: 29772605.

 

7: Mengen E, Kotan LD, Ucakturk SA, Topaloglu AK, Yuksel B. A Novel FrameshiftMutation in ESCO2 Gene in Roberts Syndrome. J Coll Physicians Surg Pak. 2018May;28(5):403-405. doi: 10.29271/jcpsp.2018.05.403. PubMed PMID: 29690975.

 

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

29582446.

 

9: Çelik G, Taş D, Tahiroğlu A, Avci A, Yüksel B, Çam P. Vitamin D Deficiency in Obsessive-Compulsive Disorder Patients with Pediatric Autoimmune NeuropsychiatricDisorders Associated with Streptococcal Infections: A Case Control Study. NoroPsikiyatr Ars. 2016 Mar;53(1):33-37. doi: 10.5152/npa.2015.8763. Epub 2016 Mar 1.PubMed PMID: 28360763; PubMed Central PMCID: PMC5353234.

 

10: Turan I, Hutchins BI, Hacihamdioglu B, Kotan LD, Gurbuz F, Ulubay A, MengenE, Yuksel B, Wray S, Topaloglu AK. CCDC141 Mutations in IdiopathicHypogonadotropic Hypogonadism. J Clin Endocrinol Metab. 2017 Jun1;102(6):1816-1825. doi: 10.1210/jc.2016-3391. PubMed PMID: 28324054; PubMedCentral PMCID: PMC5470764.

 

11: Şeker-Yılmaz B, Kör D, Bulut FD, Yüksel B, Karabay-Bayazıt A, Topaloğlu AK,Ceylaner G, Önenli-Mungan N. Impaired glucose tolerance in Fanconi-Bickelsyndrome: Eight patients with two novel mutations. Turk J Pediatr.2017;59(4):434-441. doi: 10.24953/turkjped.2017.04.010. PubMed PMID: 29624224.

 

12: 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.

 

13: 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.

 

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: 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.

 

17: 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.

 

18: 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.

 

19: 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 karyotpye

distribution in Turkish girls with Turner syndrome. Am J Med Genet A. 2016

Apr;170A(4):942-8. doi: 10.1002/ajmg.a.37498. Epub 2016 Jan 20. PubMed PMID:

26788866.

 

20: Gürbüz F, Özalp Yüreğir Ö, Ceylaner S, Topaloğlu AK, Yüksel B. Coexistence ofKabuki 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.

 

21: Önenli-Mungan N, Kör D, Karabay-Bayazıt A, Cengiz N, Yavuz S, Noyan A,

Ceylaner G, Şeker-Yılmaz B, Topaloğlu AK, Yüksel B, Anarat A. Genotypic and

phenotypic features of the cystinosis patients from the South Eastern part of

Turkey. Turk J Pediatr. 2016;58(4):362-370. PubMed PMID: 28276207.

 

22: Mengen E, Tunc S, Kotan LD, Nalbantoglu O, Demir K, Gurbuz F, Turan I, Seker

G, 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.

 

23: Guran T, Buonocore F, Saka N, Ozbek MN, Aycan Z, Bereket A, Bas F, Darcan S,

Bideci A, Guven A, Demir K, Akinci A, Buyukinan M, Aydin BK, Turan S, Agladioglu

SY, Atay Z, Abali ZY, Tarim O, Catli G, Yuksel B, Akcay T, Yildiz M, Ozen S,

Doger E, Demirbilek H, Ucar A, Isik E, Ozhan B, Bolu S, Ozgen IT, Suntharalingham

JP, Achermann JC. Rare Causes of Primary Adrenal Insufficiency: Genetic and

Clinical Characterization of a Large Nationwide Cohort. J Clin Endocrinol Metab.

2016 Jan;101(1):284-92. doi: 10.1210/jc.2015-3250. Epub 2015 Nov 2. PubMed PMID:

26523528; PubMed Central PMCID: PMC4701852.

 

24: Gurbuz F, Gurbuz BB, Celik GG, Yildirim V, Ucakturk SA, Seydaoglu G, Ucakturk

EM, Topaloglu AK, Yuksel B. Effects of methylphenidate on appetite and growth in

children diagnosed with attention deficit and hyperactivity disorder. J Pediatr

Endocrinol Metab. 2016 Jan;29(1):85-92. doi: 10.1515/jpem-2015-0171. PubMed PMID:

26352086.

 

25: Poyrazoğlu Ş, Akçay T, Arslanoğlu İ, Atabek ME, Atay Z, Berberoğlu M, Bereket

A, Bideci A, Bircan İ, Böber E, Can Ş, Cesur Y, Darcan Ş, Demir K, Dündar B,

Ersoy B, Esen İ, Güven A, Kara C, Keskin M, Kurtoğlu S, Memioğlu N, Özbek MN,

Özgen T, Sarı E, Şıklar Z, Şimşek E, Turan S, Yeşilkaya E, Yüksel B, Darendeliler

F. Current practice in diagnosis and treatment of growth hormone deficiency in

childhood: a survey from Turkey. J Clin Res Pediatr Endocrinol. 2015

Mar;7(1):37-44. doi: 10.4274/jcrpe.1794. PubMed PMID: 25800474; PubMed Central

PMCID: PMC4439890.

 

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, Selver

Eklioğlu 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, Pirgon

Ö, Çatlı G, Can HD, Gürbüz F, Binay Ç, Baş VN, Fidancı K, Polat A, Gül D, Açıkel

C, Demirbilek H, Cinaz P, Bondy C. Turner syndrome and associated problems in

Turkish children: a multicenter study. J Clin Res Pediatr Endocrinol. 2015

Mar;7(1):27-36. doi: 10.4274/jcrpe.1771. PubMed PMID: 25800473; PubMed Central

PMCID: PMC4439889.

 

27: Baş F, Uyguner ZO, Darendeliler F, Aycan Z, Çetinkaya E, Berberoğlu M, Şiklar

Z, Öcal G, Darcan Ş, Gökşen D, Topaloğlu AK, Yüksel B, Özbek MN, Ercan O,

Evliyaoğlu O, Çetinkaya S, Şen Y, Atabek E, Toksoy G, Aydin BK, Bundak R.

Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with

combined pituitary hormone deficiency: a multicenter study. Endocrine. 2015

Jun;49(2):479-91. doi: 10.1007/s12020-014-0498-1. Epub 2014 Dec 11. PubMed PMID:

25500790.

 

28: Demirbilek H, Ozbek MN, Demir K, Kotan LD, Cesur Y, Dogan M, Temiz F, Mengen

E, Gurbuz F, Yuksel B, Topaloglu AK. Normosmic idiopathic hypogonadotropic

hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the

KISS1R 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.

 

29: 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.

 

30: 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. 2014

Oct;99(10):E2067-75. doi: 10.1210/jc.2014-1836. Epub 2014 Jul 17. PubMed PMID:

25033069; PubMed Central PMCID: PMC5393493.

 

31: Raimondo A, Chakera AJ, Thomsen SK, Colclough K, Barrett A, De Franco E,

Chatelas A, Demirbilek H, Akcay T, Alawneh H; International NDM Consortium,

Flanagan SE, Van De Bunt M, Hattersley AT, Gloyn AL, Ellard S; International NDM

Consortium. Phenotypic severity of homozygous GCK mutations causing neonatal or

childhood-onset diabetes is primarily mediated through effects on protein

stability. Hum Mol Genet. 2014 Dec 15;23(24):6432-40. doi: 10.1093/hmg/ddu360.

Epub 2014 Jul 11. PubMed PMID: 25015100; PubMed Central PMCID: PMC4240195.

 

32: Aslan TB, Gurbuz F, Temiz F, Yuksel B, Topaloglu AK. Etiological evaluation

of patients presenting with isolated micropenis to an academic health care

center. Indian J Pediatr. 2014 Aug;81(8):775-9. doi: 10.1007/s12098-013-1205-6.

Epub 2013 Sep 5. PubMed PMID: 24005879.

 

33: Gul Mert G, Horoz OO, Herguner MO, Incecik F, Yildizdas RD, Onenli Mungan N,

Yuksel B, Altunbasak S. Hashimoto's encephalopathy: four cases and review of

literature. Int J Neurosci. 2014 Apr;124(4):302-6. doi:

10.3109/00207454.2013.836706. Epub 2013 Oct 2. Review. PubMed PMID: 23967879.

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 in children 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: Karagun BS, Temiz F, Ozer G, Yuksel B, Topaloglu AK, Mungan NO, Mazman M,

Karagun GM. Chromium levels in healthy and newly diagnosed type 1 diabetic

children. Pediatr Int. 2012 Dec;54(6):780-5. doi:

10.1111/j.1442-200X.2012.03696.x. Epub 2012 Oct 9. PubMed PMID: 22783884.

 

38: 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.

 

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: Yüksel B, Özbek MN, Mungan NÖ, Darendeliler F, Budan B, Bideci A, ÇetinkayaE, Berberoğlu M, Evliyaoğlu O, Yeşilkaya E, Arslanoğlu İ, Darcan Ş, Bundak R,Ercan O.Serum IGF-1 and IGFBP-3 levels in healthy children between 0 and 6 yearsof age. J Clin Res Pediatr Endocrinol. 2011;3(2):84-8. doi:10.4274/jcrpe.v3i2.17. Epub 2011 Jun 8. PubMed PMID: 21750637; PubMed CentralPMCID: PMC3119446.

 

41: Temiz F, Ozbek MN, Kotan D, Sangun O, Mungan NO, Yuksel B, Topaloglu AK. Ahomozygous recurring mutation in WISP3 causing progressive pseudorheumatoidarthropathy. J Pediatr Endocrinol Metab. 2011;24(1-2):105-8. PubMed PMID:21528827.

 

42: Tasci E, Ozbek MN, Onenli-Mungan N, Temiz F, Topaloglu AK, Yuksel B. Lowserum adiponectin levels in children and adolescents with diabetic retinopathy.Eurasian J Med. 2011 Apr;43(1):18-22. doi: 10.5152/eajm.2011.04. PubMed PMID:25610154; PubMed Central PMCID: PMC4261362.

 

43: Gençaslan M, Bilgin Y, Keskin M. Systematic investigation of global phasebehavior of polymer mixtures in the pressure-temperature plane. J Chem Phys. 2010Dec 21;133(23):234112. doi: 10.1063/1.3518977. PubMed PMID: 21186863.

 

44: Arman A, Yüksel B, Coker A, Sarioz O, Temiz F, Topaloglu AK. Novel growthhormone receptor gene mutation in a patient with Laron syndrome. J PediatrEndocrinol Metab. 2010 Apr;23(4):407-14. PubMed PMID: 20583548.

 

45: Ozbek MN, Senée V, Aydemir S, Kotan LD, Mungan NO, Yuksel B, Julier C,Topaloglu AK. Wolcott-Rallison syndrome due to the same mutation (W522X) inEIF2AK3 in two unrelated families and review of the literature. Pediatr Diabetes.2010 Jun;11(4):279-85. doi: 10.1111/j.1399-5448.2009.00591.x. Epub 2010 Feb 25.Review. PubMed PMID: 20202148.

 

46: Ozbek MN, Uslu AB, Onenli-Mungan N, Yuksel B, Pohlenz J, Topaloglu AK.Thyroid peroxidase gene mutations causing congenital hypothyroidism in threeTurkish families. J Pediatr Endocrinol Metab. 2009 Nov;22(11):1033-9. PubMedPMID: 20101889.

 

47: Bens S, Mohn A, Yüksel B, Kulle AE, Michalek M, Chiarelli F, Nuri Ozbek M,Leuschner I, Grötzinger J, Holterhus PM, Riepe FG. Congenital lipoid adrenalhyperplasia: functional characterization of three novel mutations in the STARgene. J ClinEndocrinol Metab. 2010 Mar;95(3):1301-8. doi: 10.1210/jc.2009-1176. Epub 2010 Jan 15. PubMed PMID: 20080861.

 

48: Horoz OO, Yuksel B, Bayazit AK, Attila G, Sertdemir Y, Mungan NO, TopalogluAK, Ozer G. Ambulatory blood pressure monitoring and serum nitric oxideconcentration in type 1 diabetic children. Endocr J. 2009;56(3):477-85. Epub 2009Feb 18. PubMed PMID: 19225212.

 

49: Topaloglu AK, Reimann F, Guclu M, Yalin AS, Kotan LD, Porter KM, Serin A,Mungan NO, Cook JR, Imamoglu S, Akalin NS, Yuksel B, O'Rahilly S, Semple RK. TAC3and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key rolefor Neurokinin B in the central control of reproduction. Nat Genet. 2009Mar;41(3):354-358.doi: 10.1038/ng.306. Epub 2008 Dec 11. PubMed PMID: 19079066; PubMed Central PMCID: PMC4312696.

 

50: Berberoğlu M, Sıklar Z, Darendeliler F, Poyrazoğlu S, Darcan S, Işgüven P,Bideci A, Ocal G, Bundak R, Yüksel B, Arslanoğlu I. Evaluation of permanentgrowth hormone deficiency (GHD) in young adults with childhood onset GHD: amulticenter study. J Clin Res Pediatr Endocrinol. 2008;1(1):30-7. doi:10.4008/jcrpe.v1i1.7. Epub 2008 Aug 5. PubMed PMID: 21318062; PubMed Central

PMCID: PMC3005632.

 

51: Yildizdas D, Erdem S, Küçükosmanoglu O, Yilmaz M, Yüksel B. Pulmonaryhypertension, heart failure and neutropenia due to diazoxide therapy. Adv Ther.2008 May;25(5):515-9. doi: 10.1007/s12325-008-0049-3. PubMed PMID: 18512033.

52: Topaloglu AK, Lu ZL, Farooqi IS, Mungan NO, Yuksel B, O'Rahilly S, Millar RP.Molecular genetic analysis of normosmic hypogonadotropic hypogonadism in aTurkish population: identification and detailed functional characterization of a novel mutation in the gonadotropin-releasing hormone receptor gene.Neuroendocrinology. 2006;84(5):301-8. Epub 2006 Dec 19. PubMed PMID: 17179725.

 

53: Erdogan S, Ergin M, Cevlik F, Yuksel B, Tuncer R, Tunali N, Polat S.Testicular adrenal rest hyperplasia due to 21-hydroxylase deficiency: a casereport. Endocr Pathol. 2006 Spring;17(1):83-7. PubMed PMID: 16760584.

 

54: Topaloglu AK, Yildizdas D, Yilmaz HL, Mungan NO, Yuksel B, Ozer G. Bonecalcium changes during diabetic ketoacidosis: a comparison with lactic acidosisdue to volume depletion. Bone. 2005 Jul;37(1):122-7. PubMed PMID: 15869925.

 

55: Yildizdas D, Topaloglu AK, Mungan NO, Yuksel B, Ozer G. Bone mineral changes in acute metabolic acidosis due to acute gastroenteritis. Calcif Tissue Int. 2004Nov;75(5):380-3. Epub 2004 Jul 30. PubMed PMID: 15592794.

 

56: Yildizdaş D, Onenli-Mungan N, Yapicioğlu H, Topaloğlu AK, Sertdemir Y, YükselB. Thyroid hormone levels and their relationship to survival in children withbacterial sepsis and septic shock. J Pediatr Endocrinol Metab. 2004Oct;17(10):1435-42. PubMed PMID: 15526723.

 

57: Borck G, Topaloglu AK, Korsch E, Martiné U, Wildhardt G, Onenli-Mungan N,Yuksel B, Aumann U, Koch G, Ozer G, Pfäffle R, Scherberg NH, Refetoff S, Pohlenz J. Four new cases of congenital secondary hypothyroidism due to a splice sitemutation in the thyrotropin-beta gene: phenotypic variability and founder effect.J Clin Endocrinol Metab. 2004 Aug;89(8):4136-41. PubMed PMID: 15292359.

 

58: Onenli-Mungan N, Yüksel B, Ozer G, Denli G, Topaloğlu AK, Teker Z. Familialthyroxin-binding globulin excess with ichthyosis: a case report. Turk J Pediatr. 2004 Apr-Jun;46(2):174-6. PubMed PMID: 15214750.

 

59: Onenli-Mungan N, Ozer G, Altunbaşak S, Besley G, Yüksel B, Topaloğlu AK,Soyupak S. Fucosidosis with hypothyroidism: a case report. Turk J Pediatr. 2004Apr-Jun;46(2):170-3. PubMed PMID: 15214749.

 

60: Onenli-Mungan N, Yüksel B, Elkay M, Topaloğlu AK, Baykal T, Ozer G. Type IIhyperprolinemia: a case report. Turk J Pediatr. 2004 Apr-Jun;46(2):167-9. PubMed PMID: 15214748.

 

61: Chong B, Hegde M, Fawkner M, Simonet S, Cassinelli H, Coker M, Kanis J,Seidel J, Tau C, Tüysüz B, Yüksel B, Love D; International HyperphosphatasiaCollaborative Group. Idiopathic hyperphosphatasia and TNFRSF11B mutations:relationships between phenotype and genotype. J Bone Miner Res. 2003Dec;18(12):2095-104. PubMed PMID: 14672344.

 

62: Yuksel B, Braun R, Topaloglu AK, Mungan NO, Ozer G, Huebner A. Three childrenwith triple A syndrome due to a mutation (R478X) in the AAAS gene. Horm Res.2004;61(1):3-6. Epub 2003 Nov 27. PubMed PMID: 14646395.

 

63: Bayazit AK, Yüksel B, Noyan A, Onenli N, Gönlüşen G, Ozer G, Anarat A. Early onset of diabetic nephropathy in a child with type 1 diabetes mellitus. Turk JPediatr. 2003 Jan-Mar;45(1):55-8. PubMed PMID: 12718374.

 

64: Ozer G, Teker Z, Cetiner S, Yilmaz M, Topaloglu AK, Onenli-Mungan N, YükselB. Serum IL-1, IL-2, TNFalpha and INFgamma levels of patients with type 1diabetes mellitus and their siblings. J Pediatr Endocrinol Metab. 2003Feb;16(2):203-10. PubMed PMID: 12713258.

MEMBERSHIPS:

 

·        Member, Turkish Society for Pediatric Endocrinology and Diabetes

·        International  Society for Pediatric and Adolescent Diabetes ( ISPAD)

·        National Pediatric Association

·        Member, European Society for Paediatric Endocrinology