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Items: 1 to 50 of 92

1.

Restoration of Height after 11 Years of Letrozole Treatment in 11β-Hydroxylase Deficiency.

Atay Z, Turan S, Buğdaycı O, Guran T, Bereket A.

Horm Res Paediatr. 2019 Aug 27:1-6. doi: 10.1159/000501456. [Epub ahead of print]

PMID:
31454824
2.

Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease.

Jolly A, Bayram Y, Turan S, Aycan Z, Tos T, Abali ZY, Hacihamdioglu B, Coban Akdemir ZH, Hijazi H, Bas S, Atay Z, Guran T, Abali S, Bas F, Darendeliler F, Colombo R, Barakat TS, Rinne T, White JJ, Yesil G, Gezdirici A, Gulec EY, Karaca E, Pehlivan D, Jhangiani SN, Muzny DM, Poyrazoglu S, Bereket A, Gibbs RA, Posey JE, Lupski JR.

J Clin Endocrinol Metab. 2019 Aug 1;104(8):3049-3067. doi: 10.1210/jc.2019-00248.

PMID:
31042289
3.

PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans.

Guran T, Yesil G, Turan S, Atay Z, Bozkurtlar E, Aghayev A, Gul S, Tinay I, Aru B, Arslan S, Koroglu MK, Ercan F, Demirel GY, Eren FS, Karademir B, Bereket A.

Eur J Endocrinol. 2019 May 1;180(5):291-309. doi: 10.1530/EJE-19-0067.

PMID:
30893644
4.

Comparison of Treatment Regimens in Management of Severe Hypercalcemia Due to Vitamin D Intoxication in Children

Demir K, Döneray H, Kara C, Atay Z, Çetinkaya S, Çayır A, Anık A, Eren E, Uçaktürk A, Can Yılmaz G, Törel Ergür A, Kendirci M, Aycan Z, Bereket A, Aydın M, Orbak Z, Özkan B.

J Clin Res Pediatr Endocrinol. 2019 May 28;11(2):140-148. doi: 10.4274/jcrpe.galenos.2018.2018.0131. Epub 2018 Nov 5.

5.

Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey

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.

J Clin Res Pediatr Endocrinol. 2019 May 28;11(2):149-156. doi: 10.4274/jcrpe.galenos.2018.2018.0206. Epub 2018 Nov 5.

6.

Evaluation of vitamin D status and its correlation with gonadal function in children at mini-puberty.

Kılınç S, Atay E, Ceran Ö, Atay Z.

Clin Endocrinol (Oxf). 2019 Jan;90(1):122-128. doi: 10.1111/cen.13856. Epub 2018 Oct 17.

PMID:
30229999
7.

Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey

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, Sağsak 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.

J Clin Res Pediatr Endocrinol. 2018 Nov 29;10(4):336-342. doi: 10.4274/jcrpe.0025. Epub 2018 May 23.

8.

Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development.

Baetens D, Güran T, Mendonca BB, Gomes NL, De Cauwer L, Peelman F, Verdin H, Vuylsteke M, Van der Linden M; ESR2 STUDY GROUP, Atay Z, Bereket A, de Krijger RR, Preter K, Domenice S, Turan S, Stoop H, Looijenga LH, De Bosscher K, Cools M, De Baere E.

Genet Med. 2018 Jul;20(7):717-727. doi: 10.1038/gim.2017.163. Epub 2017 Oct 26.

PMID:
29261182
9.

The Distribution of Different Types of Diabetes in Childhood: A Single Center Experience

Haliloğlu B, Abalı S, Buğrul F, Çelik E, Baş S, Atay Z, Güran T, Turan S, Bereket A.

J Clin Res Pediatr Endocrinol. 2018 Jun 1;10(2):125-130. doi: 10.4274/jcrpe.5204. Epub 2017 Nov 24.

10.

Hypoglycemia is common in children with cystic fibrosis and seen predominantly in females.

Haliloglu B, Gokdemir Y, Atay Z, Abali S, Guran T, Karakoc F, Ersu R, Karadag B, Turan S, Bereket A.

Pediatr Diabetes. 2017 Nov;18(7):607-613. doi: 10.1111/pedi.12470. Epub 2016 Nov 22.

PMID:
27873431
11.

GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey.

Haliloglu B, Hysenaj G, Atay Z, Guran T, Abalı S, Turan S, Bereket A, Ellard S.

Clin Endocrinol (Oxf). 2016 Sep;85(3):393-9. doi: 10.1111/cen.13121. Epub 2016 Jul 5.

12.

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study.

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, Bolu S, Korkmaz HA, Şimşek E, Çatlı G, Büyükinan M, Çayır A, Evliyaoğlu O, İşgüven P, Özgen T, Hatipoğlu N, Elhan AH, Berberoğlu M.

J Clin Res Pediatr Endocrinol. 2016 Sep 1;8(3):305-12. doi: 10.4274/jcrpe.3013. Epub 2016 Apr 29.

13.

The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study.

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.

J Clin Endocrinol Metab. 2016 May;101(5):1980-8. doi: 10.1210/jc.2015-3500. Epub 2016 Mar 10. Erratum in: J Clin Endocrinol Metab. 2018 May 1;103(5):2075.

PMID:
26964727
14.

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort.

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.

J Clin Endocrinol Metab. 2016 Jan;101(1):284-92. doi: 10.1210/jc.2015-3250. Epub 2015 Nov 2.

15.

Risk factors for mortality caused by hypothalamic obesity in children with hypothalamic tumours.

Haliloglu B, Atay Z, Guran T, Abalı S, Bas S, Turan S, Bereket A.

Pediatr Obes. 2016 Oct;11(5):383-8. doi: 10.1111/ijpo.12076. Epub 2015 Oct 14.

PMID:
26463004
16.

H syndrome: a multifaceted histiocytic disorder with hyperpigmentation and hypertrichosis.

Tekin B, Atay Z, Ergun T, Can M, Tuney D, Babay S, Turan S, Bereket A, Zlotogorski A, Molho-Pessach V.

Acta Derm Venereol. 2015 Nov;95(8):1021-3. doi: 10.2340/00015555-2145. No abstract available.

17.

Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey.

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.

J Clin Res Pediatr Endocrinol. 2015 Mar;7(1):37-44. doi: 10.4274/jcrpe.1794.

18.

Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism.

Bayram Y, Gulsuner S, Guran T, Abaci A, Yesil G, Gulsuner HU, Atay Z, Pierce SB, Gambin T, Lee M, Turan S, Bober E, Atik MM, Walsh T, Karaca E, Pehlivan D, Jhangiani SN, Muzny D, Bereket A, Buyukgebiz A, Boerwinkle E, Gibbs RA, King MC, Lupski JR.

J Clin Endocrinol Metab. 2015 May;100(5):E808-14. doi: 10.1210/jc.2015-1150. Epub 2015 Mar 16.

19.

Premature pubarche, hyperinsulinemia and hypothyroxinemia: novel manifestations of congenital portosystemic shunts (Abernethy malformation) in children.

Bas S, Guran T, Atay Z, Haliloglu B, Abalı S, Turan S, Bereket A.

Horm Res Paediatr. 2015;83(4):282-7. doi: 10.1159/000369395. Epub 2015 Feb 7.

PMID:
25676144
20.

Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS.

Turan S, Thiele S, Tafaj O, Brix B, Atay Z, Abali S, Haliloglu B, Bereket A, Bastepe M.

Bone. 2015 Feb;71:53-7. doi: 10.1016/j.bone.2014.10.006. Epub 2014 Oct 18.

21.

Effects of leukemia inhibitory receptor gene mutations on human hypothalamo-pituitary-adrenal function.

Guran T, Guran O, Paketci C, Kipoglu O, Firat I, Turan S, Atay Z, Haliloglu B, Bereket A.

Pituitary. 2015 Aug;18(4):456-60. doi: 10.1007/s11102-014-0594-5.

PMID:
25145448
22.

Higher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus.

Abalı S, Turan S, Atay Z, Güran T, Haliloğlu B, Bereket A.

Pediatr Diabetes. 2015 Aug;16(5):361-6. doi: 10.1111/pedi.12167. Epub 2014 Jul 11.

PMID:
25039448
23.

Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features.

Arman A, Bereket A, Coker A, Kiper PÖ, Güran T, Ozkan B, Atay Z, Akçay T, Haliloglu B, Boduroglu K, Alanay Y, Turan S.

Orphanet J Rare Dis. 2014 Apr 26;9:60. doi: 10.1186/1750-1172-9-60.

24.

Novel homozygous inactivating mutation of the calcium-sensing receptor gene (CASR) in neonatal severe hyperparathyroidism-lack of effect of cinacalcet.

Atay Z, Bereket A, Haliloglu B, Abali S, Ozdogan T, Altuncu E, Canaff L, Vilaça T, Wong BY, Cole DE, Hendy GN, Turan S.

Bone. 2014 Jul;64:102-7. doi: 10.1016/j.bone.2014.04.010. Epub 2014 Apr 13.

PMID:
24735972
25.

A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo-cardiomyopathy.

Atay Z, Bereket A, Turan S, Haliloglu B, Memisoglu A, Khayat M, Shalev SA, Spiegel R.

Gene. 2013 Feb 15;515(1):197-9. doi: 10.1016/j.gene.2012.11.044. Epub 2012 Dec 9.

PMID:
23235116
26.

Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia.

Haliloglu B, Guran T, Atay Z, Abali S, Mornet E, Bereket A, Turan S.

Eur J Pediatr. 2013 Jun;172(6):851-3. doi: 10.1007/s00431-012-1868-4. Epub 2012 Oct 24.

PMID:
23093139
27.

Current status of childhood obesity and its associated morbidities in Turkey.

Bereket A, Atay Z.

J Clin Res Pediatr Endocrinol. 2012 Mar;4(1):1-7. doi: 10.4274/jcrpe.506.

28.

An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).

Turan S, Hughes C, Atay Z, Guran T, Haliloglu B, Clark AJ, Bereket A, Metherell LA.

J Clin Endocrinol Metab. 2012 May;97(5):E771-4. doi: 10.1210/jc.2011-2414. Epub 2012 Feb 15.

29.

The prevalence and risk factors of premature thelarche and pubarche in 4- to 8-year-old girls.

Atay Z, Turan S, Guran T, Furman A, Bereket A.

Acta Paediatr. 2012 Feb;101(2):e71-5. doi: 10.1111/j.1651-2227.2011.02444.x. Epub 2011 Sep 23.

PMID:
21854448
30.

Puberty and influencing factors in schoolgirls living in Istanbul: end of the secular trend?

Atay Z, Turan S, Guran T, Furman A, Bereket A.

Pediatrics. 2011 Jul;128(1):e40-5. doi: 10.1542/peds.2010-2267. Epub 2011 Jun 13.

PMID:
21669888
31.

Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes.

Guran T, Akcay T, Bereket A, Atay Z, Turan S, Haisch L, Konrad M, Schlingmann KP.

Nephrol Dial Transplant. 2012 Feb;27(2):667-73. doi: 10.1093/ndt/gfr300. Epub 2011 Jun 9.

PMID:
21669885
32.

Cognitive and psychosocial development in children with familial hypomagnesaemia.

Guran T, Arman A, Akcay T, Kayan E, Atay Z, Turan S, Bereket A.

Magnes Res. 2011 Mar;24(1):7-12. doi: 10.1684/mrh.2011.0278.

33.

Serum alkaline phosphatase levels in healthy children and evaluation of alkaline phosphatase z-scores in different types of rickets.

Turan S, Topcu B, Gökçe İ, Güran T, Atay Z, Omar A, Akçay T, Bereket A.

J Clin Res Pediatr Endocrinol. 2011;3(1):7-11. doi: 10.4274/jcrpe.v3i1.02. Epub 2011 Feb 23.

34.

Prevalence of type 1 diabetes mellitus in 6-18-yr-old school children living in Istanbul, Turkey.

Akesen E, Turan S, Güran T, Atay Z, Save D, Bereket A.

Pediatr Diabetes. 2011 Sep;12(6):567-71. doi: 10.1111/j.1399-5448.2010.00744.x. Epub 2011 Mar 21.

PMID:
21418453
35.

Radiologic and hormonal evaluation of pituitary abnormalities in patients with Bardet-Biedl syndrome.

Guran T, Ekinci G, Atay Z, Turan S, Akcay T, Bereket A.

Clin Dysmorphol. 2011 Jan;20(1):26-31. doi: 10.1097/MCD.0b013e32833fd528.

PMID:
20966747
36.

Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor.

Guran T, Tolhurst G, Bereket A, Rocha N, Porter K, Turan S, Gribble FM, Kotan LD, Akcay T, Atay Z, Canan H, Serin A, O'Rahilly S, Reimann F, Semple RK, Topaloglu AK.

J Clin Endocrinol Metab. 2009 Oct;94(10):3633-3639. doi: 10.1210/jc.2009-0551. Epub 2009 Sep 15.

37.

Actinomycotic suppurative thyroiditis in a child.

Karatoprak N, Atay Z, Erol N, Goksugur SB, Ceran O.

J Trop Pediatr. 2005 Dec;51(6):383-5. Epub 2005 Jun 9.

PMID:
15947015
38.

Predictive value of image cytometry for diagnosis of lung cancer in heavy smokers.

Xing S, Khanavkar B, Nakhosteen JA, Atay Z, Jöckel KH, Marek W; RIDTELC Lung Study Group.

Eur Respir J. 2005 Jun;25(6):956-63.

39.

A neonatal case of citrullinemia with urolithiasis.

Ozkozaci T, Akin M, Atay Z, Uyanik B, Nuhoglu C, Ceran O.

Ann Saudi Med. 2004 Sep-Oct;24(5):399-400. No abstract available.

40.

Effect of BCG vaccine on tuberculin skin tests in 7-11-year-old children.

Bozaykut A, Atay E, Sevim H, Atay Z, Ceran O.

Acta Paediatr. 2004 Aug;93(8):1033-5.

PMID:
15456191
41.

Hypernatraemic dehydration in exclusively breastfed neonates.

Atay Z, Akin M, Goksugur SB, Ozkozaci T, Ceran O.

Ann Trop Paediatr. 2004 Jun;24(2):185-6. No abstract available.

PMID:
15186549
42.
43.

The effects of iron therapy on thyroid function tests in children with iron deficiency anemia.

Ceran O, Akin M, Yavrucu C, Ozkozaci T, Atay Z.

J Pediatr Endocrinol Metab. 2003 Feb;16(2):238-9. No abstract available.

PMID:
12713265
44.

Postpartum maternal levels of hemoglobin A1c and cord C-peptide in macrosomic infants of non-diabetic mothers.

Akin M, Ceran O, Atay E, Atay Z, Akin F, Akturk Z.

J Matern Fetal Neonatal Med. 2002 Oct;12(4):274-6.

PMID:
12572597
45.

Effect of BCG vaccine on tuberculin skin tests in 1-6-year-old children.

Bozaykut A, Ipek IO, Ozkars MY, Seren LP, Atay E, Atay Z.

Acta Paediatr. 2002;91(2):235-8.

PMID:
11952015
46.

Acute infantile haemorrhagic oedema associated with hepatitis A.

Bozaykut A, Atay E, Atay Z, Ipek IO, Akin M, Dursun E.

Ann Trop Paediatr. 2002 Mar;22(1):59-61.

PMID:
11926052
47.
48.

Detection of pancreatic metastases by EUS-guided fine-needle aspiration.

Fritscher-Ravens A, Sriram PV, Krause C, Atay Z, Jaeckle S, Thonke F, Brand B, Bohnacker S, Soehendra N.

Gastrointest Endosc. 2001 Jan;53(1):65-70.

PMID:
11154491
49.

[Automated quantitative image cytometry of bronchial washings in suspected lung cancer: comparison with cytology, histology and clinical diagnosis].

Marek W, Krampe S, Dickgreber NJ, Nielsen L, Muti A, Khanavkar B, Müller KM, Atay Z, Topalidis T, Nakhosteen JA.

Pneumologie. 1999 Dec;53(12):583-95. German.

PMID:
10684237
50.

[Endosonographically controlled fine needle aspiration cytology--indications and results in routine diagnosis].

Fritscher-Ravens A, Schirrow L, Atay Z, Petrasch S, Brand B, Bohnacker S, Soehendra N.

Z Gastroenterol. 1999 May;37(5):343-51. German.

PMID:
10413842

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