Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 26

1.

A rare cause of hypertension in childhood: Answers.

Kucuk N, Yavas Abalı Z, Abalı S, Canpolat N, Yesil G, Turan S, Bereket A, Guran T.

Pediatr Nephrol. 2019 Sep 20. doi: 10.1007/s00467-019-04329-0. [Epub ahead of print] No abstract available.

PMID:
31541304
2.

A rare cause of hypertension in childhood: Questions.

Kucuk N, Yavas Abali Z, Abali S, Canpolat N, Yesil G, Turan S, Bereket A, Guran T.

Pediatr Nephrol. 2019 Sep 20. doi: 10.1007/s00467-019-04326-3. [Epub ahead of print] No abstract available.

PMID:
31541303
3.

Nationwide Hypophosphatemic Rickets Cohort Study

Şıklar Z, Turan S, Bereket A, Baş F, Güran T, Akberzade A, Abacı A, Demir K, Böber E, Özbek MN, Kara C, Poyrazoğlu Ş, Aydın M, Kardelen A, Tarım Ö, Eren E, Hatipoğlu N, Büyükinan M, Akyürek N, Çetinkaya S, Bayramoğlu E, Selver Eklioğlu B, Uçaktürk A, Abalı S, Gökşen D, Kor Y, Ünal E, Esen İ, Yıldırım R, Akın O, Çayır A, Dilek E, Kırel B, Anık A, Çatlı G, Berberoğlu M.

J Clin Res Pediatr Endocrinol. 2019 Sep 13. doi: 10.4274/jcrpe.galenos.2019.2019.0098. [Epub ahead of print]

4.

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
5.

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.

6.

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
7.

CDH3 gene related hypotrichosis and juvenile macular dystrophy - A case with a novel mutation.

Karti O, Abali S, Ayhan Z, Gokmeydan E, Nalcaci S, Yaman A, Saatci AO.

Am J Ophthalmol Case Rep. 2017 Jun 26;7:129-133. doi: 10.1016/j.ajoc.2017.06.007. eCollection 2017 Sep.

8.

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.

9.

Retinal Ganglion Cell Loss in Children With Type 1 Diabetes Mellitus Without Diabetic Retinopathy.

Karti O, Nalbantoglu O, Abali S, Ayhan Z, Tunc S, Kusbeci T, Ozkan B.

Ophthalmic Surg Lasers Imaging Retina. 2017 Jun 1;48(6):473-477. doi: 10.3928/23258160-20170601-05. Erratum in: Ophthalmic Surg Lasers Imaging Retina. 2017 Jul 1;48(7):530.

PMID:
28613353
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.

The assessment of peripapillary retinal nerve fiber layer and macular ganglion cell layer changes in obese children: a cross-sectional study using optical coherence tomography.

Karti O, Nalbantoglu O, Abali S, Tunc S, Ozkan B.

Int Ophthalmol. 2017 Aug;37(4):1031-1038. doi: 10.1007/s10792-016-0371-8. Epub 2016 Oct 7.

PMID:
27718081
12.

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.

13.

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.

14.

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group.

Darendeliler F, Yeşilkaya E, Bereket A, Baş F, Bundak R, Sarı E, Küçükemre Aydın B, Darcan Ş, Dündar B, Büyükinan M, Kara C, Mazıcıoğlu MM, 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, 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.

J Clin Res Pediatr Endocrinol. 2015 Sep;7(3):183-91. doi: 10.4274/jcrpe.2023.

15.

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome.

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.

Am J Med Genet A. 2016 Apr;170A(4):942-8. doi: 10.1002/ajmg.a.37498. Epub 2016 Jan 20.

PMID:
26788866
16.

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
17.

Turner syndrome and associated problems in Turkish children: a multicenter study.

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.

J Clin Res Pediatr Endocrinol. 2015 Mar;7(1):27-36. doi: 10.4274/jcrpe.1771.

18.

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
19.

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.

20.

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
21.

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
22.

Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis.

Kühnen P, Turan S, Fröhler S, Güran T, Abali S, Biebermann H, Bereket A, Grüters A, Chen W, Krude H.

J Clin Endocrinol Metab. 2014 Jan;99(1):E169-76. doi: 10.1210/jc.2013-2619. Epub 2013 Dec 20.

PMID:
24248179
23.

Diabetes care, glycemic control, complications, and concomitant autoimmune diseases in children with type 1 diabetes in Turkey: a multicenter study.

Simsek DG, Aycan Z, Özen S, Cetinkaya S, Kara C, Abalı S, Demir K, Tunç O, Uçaktürk A, Asar G, Baş F, Cetinkaya E, Aydın M, Karagüzel G, Orbak Z, Sıklar Z, Altıncık A, Ökten A, Özkan B, Ocal G, Semiz S, Arslanoğlu İ, Evliyaoğlu O, Bundak R, Darcan Ş.

J Clin Res Pediatr Endocrinol. 2013;5(1):20-6. doi: 10.4274/Jcrpe.893. Epub 2013 Feb 19.

24.

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
25.

Effect of iron supplementation on development of iron deficiency anemia in breastfed infants.

Gokcay G, Ozden T, Karakas Z, Karabayir N, Yildiz I, Abali S, Sahip Y.

J Trop Pediatr. 2012 Dec;58(6):481-5. doi: 10.1093/tropej/fms028. Epub 2012 Jun 28.

PMID:
22752418
26.

Assessment of HIV/AIDS awareness and changes in sexual practices among secondary school students in Nsukka environment.

Okonta JM, Momoh MA, Ekwunife OI, Mbagwu IS, Abali SO.

Trop Doct. 2007 Oct;37(4):269-71.

PMID:
17988512

Supplemental Content

Support Center