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Try235Phe homozygous mutation of the steroid 5-a reductase type 2 (SRD5A2) gene in a Turkish patient

Annals of Saudi medicine, 2014-05, Vol.34 (3), p.254-256

2014

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Permanent Neonatal Diabetes Mellitus Caused by a Novel Homozygous (T168A) Glucokinase ( GCK ) Mutation: Initial Response to Oral Sulphonylurea Therapy

The Journal of pediatrics, 2008-07, Vol.153 (1), p.122-126

2008

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Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)

Journal of clinical research in pediatric endocrinology, 2017-03, Vol.9 (1), p.80-84

2017

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Remarkable Increase in the Prevalence of Overweight and Obesity Among School Age Children in Antalya, Turkey, Between 2003 and 2015

Journal of clinical research in pediatric endocrinology, 2019-03, Vol.11 (1), p.76-81

2019

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The results of 16 years iodization: Assessment of iodine deficiency among school-age children in Antalya, Turkey

Journal of clinical research in pediatric endocrinology, 2020-09, Vol.12 (3), p.256-260

2020

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Genetics of Obesity

Journal of clinical research in pediatric endocrinology, 2009-01, Vol.1 (1)

Bircan, Iffet

2009

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A combination of nifedipine and octreotide treatment in an hyperinsulinemic hypoglycemic infant

Journal of clinical research in pediatric endocrinology, 2014-01, Vol.6 (2), p.119-121

2014

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Urinary bisphenol a levels in girls with idiopathic central precocious puberty

Journal of clinical research in pediatric endocrinology, 2014-01, Vol.6 (1), p.16-21

2014

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Intrathyroidal ectopic thymic tissue may mimic thyroid cancer: a case report

Journal of Pediatric Endocrinology and Metabolism, 2012-10, Vol.25 (9), p.997-1000

2012

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Leptin and Ghrelin Levels in Children before and after Adenoidectomy or Adenotonsillectomy

Hormone research in paediatrics, 2014-01, Vol.81 (1), p.20-24

2014

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Evaluation of the Response to the First Two Years of Growth Hormone Treatment in Kabuki Make-Up Syndrome

Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (2), p.7

2017

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A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree

Journal of Pediatric Endocrinology and Metabolism, 2013-05, Vol.26 (5), p.551-555

2013

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Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene

Journal of clinical research in pediatric endocrinology, 2016-09, Vol.8 (3), p.360-364

2016

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Novel human pathological mutations. Gene symbol: TPO. Disease: Thyroid peroxidase deficiency

Human genetics, 2010-01, Vol.127 (1), p.120-120

2010

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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

Journal of Pediatric Endocrinology and Metabolism, 2012-10, Vol.25 (9), p.1035-1039

2012

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Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism

European journal of pediatrics, 2013-09, Vol.172 (9), p.1215-1219

2013

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An Infantile Hypophosphatasia Patient with a Homozygous Mutation in the ALPS Gene

Journal of clinical research in pediatric endocrinology, 2015-09, Vol.7 (2)

2015

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Variability in the age at diagnosis of diabetes in two unrelated patients with a homozygous glucokinase gene mutation

Journal of Pediatric Endocrinology and Metabolism, 2012-08, Vol.25 (7), p.805-808

2012

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Severe rhabdomyolysis and acute renal failure in an adolescent with hypothyroidism

Turkish journal of pediatrics, 2011-09, Vol.53 (5), p.586-589

2011

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The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency

The journal of clinical endocrinology and metabolism, 1998-09, Vol.83 (9), p.3346-3349

1998

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Urinary phthalate metabolite concentrations in girls with premature thelarche

Environmental toxicology and pharmacology, 2018-04, Vol.59, p.172-181

2018

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Prevalence and risk factors of obesity in school children in Antalya, Turkey

Saudi medical journal, 2006-07, Vol.27 (7), p.1028

2006

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Bone mineral density and alterations of bone metabolism in children and adolescents with type 1 diabetes mellitus

Journal of Pediatric Endocrinology and Metabolism, 2006-06, Vol.19 (6), p.805

2006

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Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 gene

Journal of clinical research in pediatric endocrinology, 2012-06, Vol.4 (2), p.101-103

2012

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Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey

Journal of clinical research in pediatric endocrinology, 2015-03, Vol.7 (1), p.37-44

2015

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Try235Phe homozygous mutation of the steroid 5-a reductase type 2 (SRD5A2) gene in a Turkish patient

Permanent Neonatal Diabetes Mellitus Caused by a Novel Homozygous (T168A) Glucokinase ( GCK ) Mutation: Initial Response to Oral Sulphonylurea Therapy

Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)

Remarkable Increase in the Prevalence of Overweight and Obesity Among School Age Children in Antalya, Turkey, Between 2003 and 2015

The results of 16 years iodization: Assessment of iodine deficiency among school-age children in Antalya, Turkey

Genetics of Obesity

A combination of nifedipine and octreotide treatment in an hyperinsulinemic hypoglycemic infant

Urinary bisphenol a levels in girls with idiopathic central precocious puberty

Intrathyroidal ectopic thymic tissue may mimic thyroid cancer: a case report

Leptin and Ghrelin Levels in Children before and after Adenoidectomy or Adenotonsillectomy

Evaluation of the Response to the First Two Years of Growth Hormone Treatment in Kabuki Make-Up Syndrome

A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree

Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene

Novel human pathological mutations. Gene symbol: TPO. Disease: Thyroid peroxidase deficiency

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

Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism

An Infantile Hypophosphatasia Patient with a Homozygous Mutation in the ALPS Gene

Variability in the age at diagnosis of diabetes in two unrelated patients with a homozygous glucokinase gene mutation

Severe rhabdomyolysis and acute renal failure in an adolescent with hypothyroidism

The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency

Urinary phthalate metabolite concentrations in girls with premature thelarche

Prevalence and risk factors of obesity in school children in Antalya, Turkey

Bone mineral density and alterations of bone metabolism in children and adolescents with type 1 diabetes mellitus

Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 gene

Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey

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