Publications by authors named "Iffet Bircan"

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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, İffet Bircan

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, İffet Bircan

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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Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty.
Semra Çetinkaya, Şükran Poyrazoğlu, Firdevs Baş, Oya Ercan, Metin Yıldız, İffet Bircan

J Pediatr Endocrinol Metab· January 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, İffet Bircan

J Clin Res Pediatr Endocrinol· March 2017

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Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene.
Banu Güzel Nur, Gamze Çelmeli, Esra Manguoğlu, Erdoğan Soyucen, İffet Bircan

J Clin Res Pediatr Endocrinol· September 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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Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey.
Şükran Poyrazoğlu, Teoman Akçay, İlknur Arslanoğlu, Mehmet Emre Atabek, Zeynep Atay, İffet Bircan

J Clin Res Pediatr Endocrinol· March 2015

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Leptin and ghrelin levels in children before and after adenoidectomy or adenotonsillectomy.
Zeynep Selen Karalok, Mehmet Akdag, Murat Turhan, Gulbahar Uzun, Sebahat Ozdem, Iffet Bircan

Horm Res Paediatr· January 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, Iffet Bircan

J Clin Res Pediatr Endocrinol· January 2015

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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, Iffet Bircan

J Clin Res Pediatr Endocrinol· November 2014

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Evaluating the patients with thalassemia major for long-term endocrinological complications after bone marrow transplantation.
Bilge Aldemir-Kocabaş, Gülsün Tezcan-Karasu, Iffet Bircan, Oğuz Bircan, Anıl Aktaş-Samur

Pediatr Hematol Oncol· October 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, İffet Bircan

J Pediatr Endocrinol Metab· January 2014

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Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism.
Zafer Cetin, Mesut Parlak, Ozden Altiok Clark, Gungor Karaguzel, Guven Luleci, Iffet Bircan

Eur J Pediatr· September 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, Iffet Bircan

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, Iffet Bircan

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, Bircan Iffet

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, Iffet Bircan

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, Iffet Bircan

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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Severe rhabdomyolysis and acute renal failure in an adolescent with hypothyroidism.
Elif Comak, Mustafa Koyun, Bahar Kiliçarslan-Akkaya, Iffet Bircan, Sema Akman

Turk J Pediatr· February 2012

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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, Iffet Bircan

Endocrine· February 2010

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Novel human pathological mutations. Gene symbol: TPO. Disease: Thyroid peroxidase deficiency.
Ozgul Alper, Doga Turkkahraman, Iffet Bircan, Guven Luleci

Hum Genet· January 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, Iffet Bircan

J Pediatr Endocrinol Metab· September 2009

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