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Items: 1 to 50 of 162

1.

Near final height in patients with idiopathic growth hormone deficiency: A single-centre experience.

Kurnaz E, Çetinkaya S, Aycan Z.

J Paediatr Child Health. 2018 May 28. doi: 10.1111/jpc.14061. [Epub ahead of print]

PMID:
29806866
2.

Evaluation of the Ovarian Reserve in Adolescents with Hashimoto's Thyroiditis Using Serum anti- Müllerian Hormone Levels.

Özalp Akın E, Aycan Z.

J Clin Res Pediatr Endocrinol. 2018 May 16. doi: 10.4274/jcrpe.0047. [Epub ahead of print]

3.

Subnormal Growth Velocity And Related Factors During GnRH Analog Therapy For Idiopathic Central Precocious Puberty.

Muratoğlu Şahin N, Uğraş Dikmen A, Çetinkaya S, Aycan Z.

J Clin Res Pediatr Endocrinol. 2018 Apr 24. doi: 10.4274/jcrpe.0023. [Epub ahead of print]

4.

Reply.

Yoldas T, Orun UA, Sağsak E, Aycan Z, Kaya Ö, Ozgur S, Karademir S.

Echocardiography. 2018 Apr;35(4):580. doi: 10.1111/echo.13889. No abstract available.

PMID:
29679448
5.

Abnormal Uterine Bleeding In Adolescents.

Elmaoğulları S, Aycan Z.

J Clin Res Pediatr Endocrinol. 2018 Feb 28. doi: 10.4274/jcrpe.0014. [Epub ahead of print]

6.

Investigation of MKRN3 mutation in patients with familial central precocious puberty.

Aycan Z, Savaş-Erdeve Ş, Çetinkaya S, Kurnaz E, Keskin M, Muratoğlu Şahin N, Bayramoğlu E, Ceylaner G.

J Clin Res Pediatr Endocrinol. 2018 Feb 28. doi: 10.4274/jcrpe.5506. [Epub ahead of print]

7.

Quantitative evaluation of early retinal changes in children with type 1 diabetes mellitus without retinopathy.

Tekin K, Inanc M, Kurnaz E, Bayramoglu E, Aydemir E, Koc M, Kiziltoprak H, Aycan Z.

Clin Exp Optom. 2018 Feb 28. doi: 10.1111/cxo.12667. [Epub ahead of print]

PMID:
29488254
8.

Clinical follow-up data and the rate of development of precocious and rapidly progressive puberty in patients with premature thelarche.

Çiçek D, Savas-Erdeve S, Cetinkaya S, Aycan Z.

J Pediatr Endocrinol Metab. 2018 Mar 28;31(3):305-312. doi: 10.1515/jpem-2017-0247.

PMID:
29373318
9.

Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty.

Çetinkaya S, Poyrazoğlu Ş, Baş F, Ercan O, Yıldız M, Adal E, Bereket A, Abalı S, Aycan Z, Erdeve ŞS, Berberoğlu M, Şıklar Z, Tayfun M, Darcan Ş, Mengen E, Bircan İ, Jones FMÇ, Şimşek E, Papatya ED, Özbek MN, Bolu S, Abacı A, Büyükinan M, Darendeliler F.

J Pediatr Endocrinol Metab. 2018 Jan 26;31(2):175-184. doi: 10.1515/jpem-2017-0123.

PMID:
29353264
10.

Evaluation of anterior segment parameters in patients with Turner syndrome using Scheimpflug imaging.

Inanc M, Tekin K, Kurnaz E, Citirik M, Altas G, Aycan Z.

J AAPOS. 2018 Feb;22(1):56-60. doi: 10.1016/j.jaapos.2017.10.007. Epub 2017 Dec 27.

PMID:
29288835
11.

Clinical and genetic characterisation of a series of patients with triple A syndrome.

Kurnaz E, Duminuco P, Aycan Z, Savaş-Erdeve Ş, Muratoğlu Şahin N, Keskin M, Bayramoğlu E, Bonomi M, Çetinkaya S.

Eur J Pediatr. 2018 Mar;177(3):363-369. doi: 10.1007/s00431-017-3068-8. Epub 2017 Dec 19.

PMID:
29255950
12.

Vaginal bleeding and a giant ovarian cyst in an infant with 21-hydroxylase deficiency.

Şahin NM, Bayramoğlu E, Çetinkaya S, Erdeve ŞŞ, Karaman A, Akdoğan MP, Aycan Z.

J Pediatr Endocrinol Metab. 2018 Jan 26;31(2):229-233. doi: 10.1515/jpem-2017-0235.

PMID:
29252197
13.

Subclinical left ventricular systolic and diastolic dysfunction in type 1 diabetic children and adolescents with good metabolic control.

Yoldaş T, Örün UA, Sagsak E, Aycan Z, Kaya Ö, Özgür S, Karademir S.

Echocardiography. 2018 Feb;35(2):227-233. doi: 10.1111/echo.13764. Epub 2017 Dec 3.

PMID:
29205484
14.

Novel mutations in the LRP5 gene in patients with Osteoporosis-pseudoglioma syndrome.

Pekkinen M, Grigelioniene G, Akin L, Shah K, Karaer K, Kurtoğlu S, Ekbote A, Aycan Z, Sağsak E, Danda S, Åström E, Mäkitie O.

Am J Med Genet A. 2017 Dec;173(12):3132-3135. doi: 10.1002/ajmg.a.38491. Epub 2017 Oct 21. No abstract available.

PMID:
29055141
15.

Effects of 1-year growth hormone replacement therapy on thyroid volume and function of the children and adolescents with idiopathic growth hormone deficiency.

Keskin M, Bayramoglu E, Aycan Z.

J Pediatr Endocrinol Metab. 2017 Oct 26;30(11):1187-1190. doi: 10.1515/jpem-2017-0210.

PMID:
29040069
16.

Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation.

Muratoğlu Şahin N, Bilici ME, Kurnaz E, Pala Akdoğan M, Ceylaner S, Aycan Z.

J Pediatr Endocrinol Metab. 2017 Aug 28;30(8):889-892. doi: 10.1515/jpem-2016-0315.

PMID:
28742517
17.

A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make.

Çetinkaya S, Güran T, Kurnaz E, Keskin M, Sağsak E, Savaş Erdeve S, Suntharalingham JP, Buonocore F, Achermann JC, Aycan Z.

J Clin Res Pediatr Endocrinol. 2018 Mar 1;10(1):68-73. doi: 10.4274/jcrpe.4638. Epub 2017 Jul 24.

18.

Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height.

Savaş-Erdeve Ş, Çetinkaya S, Abalı ZY, Poyrazoğlu Ş, Baş F, Berberoğlu M, Sıklar Z, Korkmaz Ö, Buluş D, Akbaş ED, Güran T, Böber E, Akın O, Yılmaz GC, Aycan Z.

J Pediatr Endocrinol Metab. 2017 Jul 26;30(7):759-766. doi: 10.1515/jpem-2017-0088.

PMID:
28672743
19.

Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism.

Aycan Z, Cangul H, Muzza M, Bas VN, Fugazzola L, Chatterjee VK, Persani L, Schoenmakers N.

J Clin Endocrinol Metab. 2017 Sep 1;102(9):3085-3090. doi: 10.1210/jc.2017-00529.

20.

Objective Evaluation of Corneal and Lens Clarity in Children With Type 1 Diabetes Mellitus.

Tekin K, Inanc M, Kurnaz E, Bayramoglu E, Aydemir E, Koc M, Aycan Z.

Am J Ophthalmol. 2017 Jul;179:190-197. doi: 10.1016/j.ajo.2017.05.010. Epub 2017 May 17.

PMID:
28528120
21.

Cardiac MRI and 3D contrast-enhanced MR angiography in pediatric and young adult patients with Turner syndrome.

Yiğit H, Önder A, Özgür S, Aycan Z, Karademir S, Doğan V.

Turk J Med Sci. 2017 Feb 27;47(1):127-133. doi: 10.3906/sag-1511-3.

PMID:
28263479
22.

The variable clinical phenotype of three patients with hepatic glycogen synthase deficiency.

Kasapkara ÇS, Aycan Z, Açoğlu E, Senel S, Oguz MM, Ceylaner S.

J Pediatr Endocrinol Metab. 2017 Apr 1;30(4):459-462. doi: 10.1515/jpem-2016-0317.

PMID:
28245189
23.

AMH levels in girls with various pubertal problems.

Savas-Erdeve S, Sagsak E, Keskin M, Cetinkaya S, Aycan Z.

J Pediatr Endocrinol Metab. 2017 Mar 1;30(3):333-335. doi: 10.1515/jpem-2016-0217.

PMID:
28245188
24.

Cross-cultural industrial organizational psychology and organizational behavior: A hundred-year journey.

Gelfand MJ, Aycan Z, Erez M, Leung K.

J Appl Psychol. 2017 Mar;102(3):514-529. doi: 10.1037/apl0000186. Epub 2017 Feb 16. Review.

PMID:
28206774
25.

Bone mineral density and growth in children with coeliac disease on a gluten free-diet.

Tuna Kırsaçlıoğlu C, Kuloğlu Z, Tanca A, Küçük NÖ, Aycan Z, Öcal G, Ensari A, Kalaycı AG, Girgin N.

Turk J Med Sci. 2016 Dec 20;46(6):1816-1821. doi: 10.3906/sag-1508-52.

PMID:
28081333
26.

Ambivalent stereotypes link to peace, conflict, and inequality across 38 nations.

Durante F, Fiske ST, Gelfand MJ, Crippa F, Suttora C, Stillwell A, Asbrock F, Aycan Z, Bye HH, Carlsson R, Björklund F, Dagher M, Geller A, Larsen CA, Latif AA, Mähönen TA, Jasinskaja-Lahti I, Teymoori A.

Proc Natl Acad Sci U S A. 2017 Jan 24;114(4):669-674. doi: 10.1073/pnas.1611874114. Epub 2017 Jan 9.

27.
28.

A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene.

Keskin M, Muratoğlu Şahin N, Kurnaz E, Bayramoğlu E, Savaş Erdeve Ş, Aycan Z, Çetinkaya S.

J Clin Res Pediatr Endocrinol. 2017 Mar 1;9(1):91-94. doi: 10.4274/jcrpe.3238. Epub 2016 Oct 31.

29.

Comparison of anterior segment parameters in juvenile diabetes mellitus and healthy eyes.

Uzel MM, Elgin U, Sen E, Keskin M, Sağsak E, Aycan Z.

Eur J Ophthalmol. 2016 Nov 4;26(6):618-622. doi: 10.5301/ejo.5000764. Epub 2016 Mar 5.

PMID:
26951536
30.

Is Chromosomal Study Necessary for Girls with Inguinal Hernia?

Kurnaz E, Savas-Erdeve S, Aycan Z.

J Clin Diagn Res. 2016 Aug;10(8):SL01. doi: 10.7860/JCDR/2016/18948.8235. Epub 2016 Aug 1. No abstract available.

31.

Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ.

Nicholas AK, Serra EG, Cangul H, Alyaarubi S, Ullah I, Schoenmakers E, Deeb A, Habeb AM, Almaghamsi M, Peters C, Nathwani N, Aycan Z, Saglam H, Bober E, Dattani M, Shenoy S, Murray PG, Babiker A, Willemsen R, Thankamony A, Lyons G, Irwin R, Padidela R, Tharian K, Davies JH, Puthi V, Park SM, Massoud AF, Gregory JW, Albanese A, Pease-Gevers E, Martin H, Brugger K, Maher ER, Chatterjee VK, Anderson CA, Schoenmakers N.

J Clin Endocrinol Metab. 2016 Dec;101(12):4521-4531. Epub 2016 Aug 15.

32.

Treatment experience and long-term follow-up data in two severe neonatal hyperparathyroidism cases.

Savas-Erdeve S, Sagsak E, Keskin M, Magdelaine C, Lienhardt-Roussie A, Kurnaz E, Cetinkaya S, Aycan Z.

J Pediatr Endocrinol Metab. 2016 Sep 1;29(9):1103-10. doi: 10.1515/jpem-2015-0261.

PMID:
27390877
33.

Optic Nerve Parameters in Obese Children as Measured by Spectral Domain Optical Coherence Tomography.

Koca S, Keskin M, Saricaoglu MS, Koca SB, Duru N, Şahin Hamurcu M, Şahin Muratoğlu N, Aycan Z.

Semin Ophthalmol. 2017;32(6):743-747. doi: 10.1080/08820538.2016.1177095. Epub 2016 Jul 1.

PMID:
27367416
34.
35.

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.

36.

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.

PMID:
26964727
37.

Co-Existence of Thyroid Nodule and Thyroid Cancer in Children and Adolescents with Hashimoto Thyroiditis: A Single-Center Study.

Keskin M, Savas-Erdeve S, Aycan Z.

Horm Res Paediatr. 2016;85(3):181-7. doi: 10.1159/000443143. Epub 2016 Feb 25.

PMID:
26910846
38.

Ophthalmic Manifestations in Children With Congenital Hypothyroidism.

Kurtul BE, Ozer PA, Kabatas EU, Gürkan A, Aycan Z.

J Pediatr Ophthalmol Strabismus. 2016 Jan-Feb;53(1):29-34. doi: 10.3928/01913913-20160113-06.

PMID:
26836000
39.

Evaluation of Iodine Deficiency in Children with Attention Deficit/Hyperactivity Disorder.

Kanık Yüksek S, Aycan Z, Öner Ö.

J Clin Res Pediatr Endocrinol. 2016 Mar 5;8(1):61-6. doi: 10.4274/jcrpe.2406. Epub 2015 Dec 18.

40.

Complete androgen insensitivity syndrome associated with bilateral sertoli cell adenomas and unilateral paratesticular leiomyoma: A case report.

Savaş-Erdeve Ş, Aycan Z, Keskin M, Çetinkaya S, Karaman A, Apaydın S, Çakmakçı E.

Turk J Pediatr. 2016;58(6):654-657. doi: 10.24953/turkjped.2016.06.012.

41.

Gonadoblastoma in a patient with 46, XY complete gonadal dysgenesis.

Keskin M, Savaş-Erdeve Ş, Kurnaz E, Çetinkaya S, Karaman A, Apaydın S, Aycan Z.

Turk J Pediatr. 2016;58(5):538-540. doi: 10.24953/turkjped.2016.05.013.

42.

A case with atrophic autoimmune thyroiditis-related hypothyroidism causing multisystem involvement in early childhood.

Kurnaz E, Savaş-Erdeve Ş, Keskin M, Doğan V, Çetinkaya S, Aycan Z.

Turk J Pediatr. 2016;58(4):446-451.

43.

The first childhood case with coexisting Hashimoto thyroiditis, vitiligo and autoimmune hepatitis.

Keskin M, Savaş-Erdeve Ş, Özbay-Hoşnut F, Kurnaz E, Çetinkaya S, Aycan Z.

Turk J Pediatr. 2016;58(4):432-435.

44.

Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing.

Ağladıoğlu SY, Aycan Z, Çetinkaya S, Baş VN, Önder A, Peltek Kendirci HN, Doğan H, Ceylaner S.

J Pediatr Endocrinol Metab. 2016 Apr;29(4):487-96. doi: 10.1515/jpem-2015-0039.

PMID:
26669242
45.

Efficacy and safety of pamidronate in children with vitamin D intoxication.

Kara C, Çetinkaya S, Gündüz S, Can Yılmaz G, Aycan Z, Aydın M.

Pediatr Int. 2016 Jul;58(7):562-8. doi: 10.1111/ped.12875. Epub 2016 Feb 17.

PMID:
26646324
46.

Evaluating the Efficacy of Treatment with a GnRH Analogue in Patients with Central Precocious Puberty.

Kendirci HN, Ağladıoğlu SY, Baş VN, Önder A, Çetinkaya S, Aycan Z.

Int J Endocrinol. 2015;2015:247386. doi: 10.1155/2015/247386. Epub 2015 Oct 13.

47.

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.

48.

The evaluation of transient hypothyroidism in patients diagnosed with congenital hypothyroidism.

Peltek Kendirci HN, Aycan Z, Sağsak E, Keskin M, Çetinkaya S.

Turk J Med Sci. 2015;45(4):745-50.

PMID:
26422840
49.

Risk factors affecting the development of nephrocalcinosis, the most common complication of hypophosphatemic rickets.

Keskin M, Savaş-Erdeve Ş, Sağsak E, Çetinkaya S, Aycan Z.

J Pediatr Endocrinol Metab. 2015 Nov 1;28(11-12):1333-7. doi: 10.1515/jpem-2014-0447.

PMID:
26203600
50.

Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development.

Topcu V, Ilgin-Ruhi H, Siklar Z, Karabulut HG, Berberoglu M, Hacihamdioglu B, Savas-Erdeve S, Aycan Z, Peltek-Kendirci HN, Ocal G, Tukun FA.

J Pediatr Endocrinol Metab. 2015 Nov 1;28(11-12):1257-63. doi: 10.1515/jpem-2014-0500.

PMID:
26197461

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