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Items: 1 to 50 of 133

1.

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]

2.

Low DHEAS Concentration in a Girl Presenting with Short Stature and Premature Pubarche: A Novel PAPSS2 Gene Mutation.

Eltan M, Yavas Abali Z, Arslan Ates E, Kirkgoz T, Kaygusuz SB, Türkyılmaz A, Bereket A, Turan S, Guran T.

Horm Res Paediatr. 2019 Aug 28:1-7. doi: 10.1159/000502114. [Epub ahead of print]

PMID:
31461705
3.

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
4.

Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross-sectional study.

Hatun S, Mutlu GY, Cinaz P, Turan S, Ekberzade A, Bereket A, Erbas MY, Akcay T, Onal H, Bolu S, Arslanoglu I, Doger E, Yilmaz AA, Ucakturk A, Karabulut GS, Tuhan HÜ, Demir K, Erdeve SS, Aycan Z, Nalbantoğlu Ö, Kara C, Gungor N.

Diabet Med. 2019 May 17. doi: 10.1111/dme.14038. [Epub ahead of print]

PMID:
31099079
5.

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
6.

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
7.

Editorial: Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey

Bereket A.

J Clin Res Pediatr Endocrinol. 2019 Feb 20;11(1):1-3. doi: 10.4274/jcrpe.galenos.2019.2019.0001. No abstract available.

8.

Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature.

Abali ZY, Yesil G, Kirkgoz T, Kaygusuz SB, Eltan M, Turan S, Bereket A, Guran T.

Hormones (Athens). 2019 Jun;18(2):229-236. doi: 10.1007/s42000-019-00096-7. Epub 2019 Feb 12. Review.

PMID:
30747411
9.

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.

10.

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.

11.

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.

12.

Acquired modification of sphingosine-1-phosphate lyase activity is not related to adrenal insufficiency.

Sunter G, Enver EO, Akbarzade A, Turan S, Vatansever P, Gunal DI, Haklar G, Bereket A, Agan K, Guran T.

BMC Neurol. 2018 Apr 23;18(1):48. doi: 10.1186/s12883-018-1049-9.

13.

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
14.

A Critical Appraisal of the Effect of Gonadotropin-Releasing Hormon Analog Treatment on Adult Height of Girls with Central Precocious Puberty.

Bereket A.

J Clin Res Pediatr Endocrinol. 2017 Dec 30;9(Suppl 2):33-48. doi: 10.4274/jcrpe.2017.S004. Epub 2017 Dec 27. Review.

15.

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
16.

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.

17.

Evaluation and Treatment Results of Ovarian Cysts in Childhood and Adolescence: A Multicenter, Retrospective Study of 100 Patients.

Aydin BK, Saka N, Bas F, Yilmaz Y, Haliloglu B, Guran T, Turan S, Bereket A, Yesiltepe Mutlu G, Cizmecioglu F, Hatun S, Bezen D, Tutunculer F, Cebeci N, Isguven P, Memioglu N, Ercan O, Poyrazoglu S, Bundak R, Darendeliler F.

J Pediatr Adolesc Gynecol. 2017 Aug;30(4):449-455. doi: 10.1016/j.jpag.2017.01.011. Epub 2017 Feb 3.

PMID:
28167139
18.

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
20.

Evaluation of therapeutics management patterns and glycemic control of pediatric type 1 diabetes mellitus patients in Turkey: A nationwide cross-sectional study.

Hatun Ş, Demirbilek H, Darcan Ş, Yüksel A, Binay C, Şimşek DG, Kara C, Çetinkaya E, Ünüvar T, Uçaktürk A, Tütüncüler F, Cesur Y, Bundak R, Sağlam H, Şimşek E, Bereket A; Turkish Pediatric Diabetes Research Group.

Diabetes Res Clin Pract. 2016 Sep;119:32-40. doi: 10.1016/j.diabres.2016.04.059. Epub 2016 Jun 27.

PMID:
27423071
21.

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.

22.

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
23.

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.

24.

Effect of Maternal Factors and Fetomaternal Glucose Homeostasis on Birth Weight and Postnatal Growth.

Özbörü Aşkan Ö, Bozaykut A, Sezer RG, Güran T, Bereket A.

J Clin Res Pediatr Endocrinol. 2015 Sep;7(3):168-74. doi: 10.4274/jcrpe.1914.

25.

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
26.

Endocrinologic Consequences of Pediatric Posterior Fossa Tumours.

Bereket A.

J Clin Res Pediatr Endocrinol. 2015 Dec;7(4):253-9. doi: 10.4274/jcrpe.2135. Review.

27.

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.

28.

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
29.

Normative Data of Thyroid Volume-Ultrasonographic Evaluation of 422 Subjects Aged 0-55 Years.

Aydıner Ö, Karakoç Aydıner E, Akpınar İ, Turan S, Bereket A.

J Clin Res Pediatr Endocrinol. 2015 Jun;7(2):98-101. doi: 10.4274/jcrpe.1818.

30.

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.

31.

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.

32.

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.

33.

Hypothalamic obesity in children: pathophysiology to clinical management.

Haliloglu B, Bereket A.

J Pediatr Endocrinol Metab. 2015 May;28(5-6):503-13. doi: 10.1515/jpem-2014-0512. Review.

PMID:
25781673
34.

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.

35.

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
36.

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.

37.

The frequency and the effects of 21-hydroxylase gene defects in congenital adrenal hyperplasia patients.

Kirac D, Guney AI, Akcay T, Guran T, Ulucan K, Turan S, Ergec D, Koc G, Eren F, Kaspar EC, Bereket A.

Ann Hum Genet. 2014 Nov;78(6):399-409. doi: 10.1111/ahg.12083. Epub 2014 Sep 17.

38.

Reference values for serum dehydroepiandrosterone-sulphate in healthy children and adolescents with emphasis on the age of adrenarche and pubarche.

Guran T, Firat I, Yildiz F, Kaplan Bulut I, Dogru M, Bereket A.

Clin Endocrinol (Oxf). 2015 May;82(5):712-8. doi: 10.1111/cen.12612. Epub 2014 Oct 21.

PMID:
25208296
39.

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
40.

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
41.

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.

42.

AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity.

Akcay T, Fernandez-Cancio M, Turan S, Güran T, Audi L, Bereket A.

Andrology. 2014 Jul;2(4):572-8. doi: 10.1111/j.2047-2927.2014.00215.x. Epub 2014 Apr 16.

43.

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
44.

Does common channel length affect surgical choice in female congenital adrenal hyperplasia patients?

Tugtepe H, Thomas DT, Turan S, Cizmecioglu F, Hatun S, Bereket A, Dagli ET.

J Pediatr Urol. 2014 Oct;10(5):948-54. doi: 10.1016/j.jpurol.2014.02.012. Epub 2014 Mar 21.

PMID:
24703836
45.

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
46.

Maternal thyroid dysfunction and neonatal thyroid problems.

Ozdemir H, Akman I, Coskun S, Demirel U, Turan S, Bereket A, Bilgen H, Ozek E.

Int J Endocrinol. 2013;2013:987843. doi: 10.1155/2013/987843. Epub 2013 Apr 30.

47.

Does transient hypothyroxinemia influence metabolic bone disease of prematurity?

Demirel U, Özek E, Bereket A, Demirel B, Topuzoğlu A, Akman İ.

J Matern Fetal Neonatal Med. 2013 Dec;26(18):1844-9. doi: 10.3109/14767058.2013.804051. Epub 2013 Jul 26.

PMID:
23672243
48.

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
49.

Insulin analogues in children with Type 1 diabetes: a 52-week randomized clinical trial.

Thalange N, Bereket A, Larsen J, Hiort LC, Peterkova V.

Diabet Med. 2013 Feb;30(2):216-25. doi: 10.1111/dme.12041.

50.

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

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