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High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients

Journal of endocrinological investigation, 2024, Vol.47 (9), p.2213-2224

2024

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Genotype–phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey

Journal of endocrinological investigation, 2019-04, Vol.42 (4), p.453-470

2019

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Nutritional status and body composition in children with inflammatory bowel disease: a prospective, controlled, and longitudinal study

European journal of clinical nutrition, 2020-08, Vol.74 (8), p.1173-1180

2020

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Cytokines as a common components of two different disorders: metabolic syndrome and hemophagocytic lymphohystiositosis

Experimental and clinical endocrinology & diabetes, 2009-02, Vol.117 (2), p.57-59

2009

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1321 The Management of Central Diabetes Insipidus in Neonatal Intensive Care Unit: Experience of Eight Cases

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A376-A377

2012

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Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum

Journal of bone and mineral research, 2016-08, Vol.31 (8), p.1577-1585

2016

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Identification of Frequency and Distribution of the Nine Most Frequent Mutations among Patients with 21-Hydroxylase Deficiency in Turkey

Journal of Pediatric Endocrinology and Metabolism, 2008-08, Vol.21 (8), p.781-788

2008

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Disorders of Sexual Development: An Overview of 18 Years Experience in the Pediatric Endocrinology Department of Ankara University

Journal of Pediatric Endocrinology and Metabolism, 2010-11, Vol.23 (11), p.1123-1132

2010

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A novel mutation in the calcium sensing receptor gene in a neonate with severe hyperparathyroidism

Genetic counseling, 2014-01, Vol.25 (3), p.331

2014

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"Maternal/Neonatal" iodine status in patients with prolonged physiological jaundice

Experimental and clinical endocrinology & diabetes, 2009-07, Vol.117 (7), p.312-315

2009

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Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in children

Journal of Pediatric Endocrinology and Metabolism, 2006-05, Vol.19 (5), p.741

2006

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Gender dysphoria and gender change in an adolescent with 45,X/46,XY mixed gonadal dysgenesis

Experimental and clinical endocrinology & diabetes, 2009-06, Vol.117 (6), p.301-304

2009

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Latent autoimmune diabetes mellitus in children (LADC) with autoimmune thyroiditis and Celiac disease

Journal of Pediatric Endocrinology and Metabolism, 2004-11, Vol.17 (11), p.1565

2004

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Hajdu-Cheney syndrome with growth hormone deficiency and neuropathy

Journal of Pediatric Endocrinology and Metabolism, 2000-07, Vol.13 (7), p.951

2000

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Clinical characteristics of 46,XX males with congenital adrenal hyperplasia

Yearbook of Paediatric Endocrinology, 2021-09

2021

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Multiple dose IVIG treatment in neonatal immune hemolytic jaundice

Journal of tropical pediatrics (1980), 2001-02, Vol.47 (1), p.50-53

2001

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Response to growth hormone with respect to pubertal status on increased dose in idiopathic growth hormone deficiency: an analysis of Turkish children in the KIGS database (Pfizer International Growth Study)

Journal of Pediatric Endocrinology and Metabolism, 2005-01, Vol.18 (10), p.949

2005

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An Infantile Cushing Syndrome Due to Misuse of Topical Steroid

Pediatric dermatology, 2004-09, Vol.21 (5), p.561-563

2004

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Zinc Deficiency: a Contributing Factor of Short Stature in Growth Hormone Deficient Children

Journal of tropical pediatrics (1980), 2003-06, Vol.49 (3), p.187-188

2003

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Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

Yearbook of Paediatric Endocrinology, 2018-09

2018

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Pica and Intoxication in Childhood

Clinical pediatrics, 2000-10, Vol.39 (10), p.624-625

2000

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Diurnal variation of height in children

Pediatrics international, 2005-12, Vol.47 (6), p.645-648

2005

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Characterization of GH-1 Mutations in Children with Isolated Growth Hormone Deficiency in the Turkish Population

Journal of Pediatric Endocrinology and Metabolism, 2009-10, Vol.22 (10), p.937-946

2009

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Antioxidant superoxide dismutase activity in obese children

Biological trace element research, 2004-06, Vol.98 (3), p.219-228

2004

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Incidence of iodine deficiency in patients presenting with goitre--discrepancy between clinical and ultrasonographic evaluation of the thyroid: comparison of patients with and without autoimmune thyroiditis--clinical, hormonal and urinary iodine excretion studies

Journal of Pediatric Endocrinology and Metabolism, 2006-01, Vol.19 (1), p.39

2006

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High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients

Genotype–phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey

Nutritional status and body composition in children with inflammatory bowel disease: a prospective, controlled, and longitudinal study

Cytokines as a common components of two different disorders: metabolic syndrome and hemophagocytic lymphohystiositosis

1321 The Management of Central Diabetes Insipidus in Neonatal Intensive Care Unit: Experience of Eight Cases

Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum

Identification of Frequency and Distribution of the Nine Most Frequent Mutations among Patients with 21-Hydroxylase Deficiency in Turkey

Disorders of Sexual Development: An Overview of 18 Years Experience in the Pediatric Endocrinology Department of Ankara University

A novel mutation in the calcium sensing receptor gene in a neonate with severe hyperparathyroidism

"Maternal/Neonatal" iodine status in patients with prolonged physiological jaundice

Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in children

Gender dysphoria and gender change in an adolescent with 45,X/46,XY mixed gonadal dysgenesis

Latent autoimmune diabetes mellitus in children (LADC) with autoimmune thyroiditis and Celiac disease

Hajdu-Cheney syndrome with growth hormone deficiency and neuropathy

Clinical characteristics of 46,XX males with congenital adrenal hyperplasia

Multiple dose IVIG treatment in neonatal immune hemolytic jaundice

Response to growth hormone with respect to pubertal status on increased dose in idiopathic growth hormone deficiency: an analysis of Turkish children in the KIGS database (Pfizer International Growth Study)

An Infantile Cushing Syndrome Due to Misuse of Topical Steroid

Zinc Deficiency: a Contributing Factor of Short Stature in Growth Hormone Deficient Children

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

Pica and Intoxication in Childhood

Diurnal variation of height in children

Characterization of GH-1 Mutations in Children with Isolated Growth Hormone Deficiency in the Turkish Population

Antioxidant superoxide dismutase activity in obese children

Incidence of iodine deficiency in patients presenting with goitre--discrepancy between clinical and ultrasonographic evaluation of the thyroid: comparison of patients with and without autoimmune thyroiditis--clinical, hormonal and urinary iodine excretion studies

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