Publications by authors named "Akcurin Sema"

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The Results of 16 Years of Iodization: Assessment of Iodine Deficiency Among School-age Children in Antalya, Turkey.
Gamze Çelmeli, Yusuf Çürek, İkbal Özen Küçükçetin, Zümrüt Arslan Gülten, Sebahat Özdem, Sema Akçurin

J Clin Res Pediatr Endocrinol· September 2020

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Remarkable Increase in the Prevalence of Overweight and Obesity Among School Age Children in Antalya, Turkey, Between 2003 and 2015.
Gamze Çelmeli, Yusuf Çürek, Zümrüt Arslan Gülten, Mehmet Yardımsever, Mustafa Koyun, Sema Akçurin

J Clin Res Pediatr Endocrinol· February 2019

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Urinary phthalate metabolite concentrations in girls with premature thelarche.
Erdem Durmaz, Pinar Erkekoglu, Ali Asci, Sema Akçurin, İffet Bircan

Environ Toxicol Pharmacol· April 2018

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Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A).
Gamze Çelmeli, Doğa Türkkahraman, Yusuf Çürek, Jayne Houghton, Sema Akçurin

J Clin Res Pediatr Endocrinol· March 2017

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A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans.
Sema Akçurin, Doğa Türkkahraman, Woo Young Kim, Erdem Durmaz, Jae Gook Shin

J Clin Res Pediatr Endocrinol· June 2016

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Try235Phe homozygous mutation of the steroid 5-a reductase type 2 (SRD5A2) gene in a Turkish patient.
Mesut Parlak, Erdem Durmaz, Semin Gursoy, Iffet Bircan, Sema Akcurin

Ann Saudi Med· June 2015

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A combination of nifedipine and octreotide treatment in an hyperinsulinemic hypoglycemic infant.
Erdem Durmaz, Sarah E Flanagan, Mesut Parlak, Sian Ellard, Sema Akcurin

J Clin Res Pediatr Endocrinol· January 2015

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Mitochondrial ATPase subunit 6 and cytochrome B gene variations in obese Turkish children.
Durkadın Demir, Doğa Türkkahraman, Anıl Aktaş Samur, Güven Lüleci, Sema Akçurin

J Clin Res Pediatr Endocrinol· December 2014

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Urinary bisphenol a levels in girls with idiopathic central precocious puberty.
Erdem Durmaz, Ali Aşçı, Pınar Erkekoğlu, Sema Akçurin, Belma Koçer Gümüşel

J Clin Res Pediatr Endocrinol· November 2014

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Clinical expression of familial Williams-Beuren syndrome in a Turkish family.
Mesut Parlak, Banu Güzel Nur, Ercan Mıhçı, Erdem Durmaz, Sibel Berker Karaüzüm, Sema Akcurin

J Pediatr Endocrinol Metab· January 2014

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CTLA-4 (+49A/G) polymorphism and type-1 diabetes in Turkish children.
Fatih Çelmeli, Doğa Türkkahraman, Deniz Özel, Sema Akçurin, Olcay Yegin

J Clin Res Pediatr Endocrinol· October 2013

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A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree.
Erdem Durmaz, Doga Turkkahraman, Afig Berdeli, Merve Atan, Gulay Karaguzel, Sema Akcurin

J Pediatr Endocrinol Metab· August 2013

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Intrathyroidal ectopic thymic tissue may mimic thyroid cancer: a case report.
Erdem Durmaz, Ebru Barsal, Mesut Parlak, Inanc Gurer, Gungor Karaguzel, Sema Akcurin

J Pediatr Endocrinol Metab· April 2013

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A novel splice site mutation of the beta subunit gene of epithelial sodium channel (ENaC) in one Turkish patient with a systemic form of pseudohypoaldosteronism Type 1.
Cagla Serpil Dogan, Durmaz Erdem, Parlak Mesut, Akan Merve, Akcurin Sema

J Pediatr Endocrinol Metab· April 2013

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Novel and de novo PHEX mutations in patients with hypophosphatemic rickets.
Erdem Durmaz, Minjing Zou, Roua A Al-Rijjal, Essa Y Baitei, Sumaya Hammami, Sema Akçurin

Bone· January 2013

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Variability in the age at diagnosis of diabetes in two unrelated patients with a homozygous glucokinase gene mutation.
Erdem Durmaz, Sarah Flanagan, Afig Berdeli, Serap Semiz, Sema Akcurin

J Pediatr Endocrinol Metab· January 2013

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Clinical and genetic analysis of patients with vitamin D-dependent rickets type 1A.
Erdem Durmaz, Minjing Zou, Roua A Al-Rijjal, Iffet Bircan, Sema Akçurin

Clin Endocrinol (Oxf)· September 2012

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Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 gene.
Ercan Mihci, Doğa Türkkahraman, Sian Ellard, Sema Akçurin, Iffet Bircan

J Clin Res Pediatr Endocrinol· June 2012

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Renal cell carcinoma presented with hypocalcemia in an adolescent.
Bahar Akkaya, Gokben Yildirim-Kupesiz, Gungor Karaguzel, Sema Akcurin, Volkan Hazar

J Pediatr Hematol Oncol· March 2012

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Spontaneous endogenous hypermelatoninemia: a new disease?
Ozgur Duman, Erdem Durmaz, Sema Akcurin, Mustafa Serteser, Senay Haspolat

Horm Res Paediatr· April 2011

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Evaluation of congenital heart diseases and thyroid abnormalities in children with Down syndrome.
Ercan Mıhçı, Gayaz Akçurin, Erdal Eren, Fırat Kardelen, Sema Akçurin

Anadolu Kardiyol Derg· October 2010

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Analysis of TPO gene in Turkish children with iodide organification defect: identification of a novel mutation.
Doga Turkkahraman, Ozgul M Alper, Suray Pehlivanoglu, Funda Aydin, Akin Yildiz, Sema Akcurin

Endocrine· February 2010

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Final diagnosis in children with subclinical hypothyroidism and mutation analysis of the thyroid peroxidase gene (TPO).
Doga Turkkahraman, Ozgul M Alper, Funda Aydin, Akin Yildiz, Suray Pehlivanoglu, Sema Akcurin

J Pediatr Endocrinol Metab· September 2009

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A family with a novel TSH receptor activating germline mutation (p.Ala485Val).
Sema Akcurin, Doga Turkkahraman, Carolyn Tysoe, Sian Ellard, Anne De Leener

Eur J Pediatr· November 2008

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Permanent neonatal diabetes mellitus caused by a novel homozygous (T168A) glucokinase (GCK) mutation: initial response to oral sulphonylurea therapy.
Doga Turkkahraman, Iffet Bircan, Nicholas D Tribble, Sema Akçurin, Sian Ellard

J Pediatr· July 2008

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