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Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-α Mutations

The journal of clinical endocrinology and metabolism, 2016-08, Vol.101 (8), p.2945-2954

2016

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Prader-Willi syndrome and growth hormone deficiency

Journal of clinical research in pediatric endocrinology, 2014-01, Vol.6 (2), p.62-67

2014

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What has national screening program changed in cases with congenital hypothyroidism?

Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2014-06, Vol.24 (3), p.255-260

2014

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Hyperinsulinemic hypoglycemia: experience in a series of 17 cases

Journal of clinical research in pediatric endocrinology, 2013-09, Vol.5 (3), p.150-155

2013

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A case of Langerhans cell histiocytosis with thyroid involvement

Journal of Pediatric Endocrinology and Metabolism, 2011-12, Vol.24 (11-12), p.1059-1061

2011

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Diabetic euglycemic ketoacidosis in newly diagnosed type 1 diabetes mellitus during Ramadan fasting

Journal of pediatric endocrinology & metabolism : JPEM, 2015-03, Vol.28 (3-4), p.333

2015

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Seizure due to somatostatin analog discontinuation in a case diagnosed as congenital hyperinsulinism novel mutation

Journal of Pediatric Endocrinology and Metabolism, 2012, Vol.25 (5), p.553-555

2012

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Adherence to growth hormone therapy: results of a multicenter study

Endocrine practice, 2014-01, Vol.20 (1), p.46-51

2014

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Bone mineral density and bone metabolic markers' status in children with neurofibromatosis type 1

Journal of pediatric endocrinology & metabolism : JPEM, 2017-02, Vol.30 (2), p.175

2017

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Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing

Journal of pediatric endocrinology & metabolism : JPEM, 2016-04, Vol.29 (4), p.487

2016

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Long-term follow-up of Cushing's disease:a case report

Journal of clinical research in pediatric endocrinology, 2013-09, Vol.5 (3), p.202-205

2013

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Diseases accompanying congenital hypothyroidism

Journal of pediatric endocrinology & metabolism : JPEM, 2014-05, Vol.27 (5-6), p.485

2014

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Effects of L-thyroxine treatment on heart functions in infants with congenital hypothyroidism

Journal of pediatric endocrinology & metabolism : JPEM, 2017-05, Vol.30 (5), p.557

2017

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Iatrogenic Cushing syndrome due to nasal steroid drops

European journal of pediatrics, 2012-04, Vol.171 (4), p.735-736

2012

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Investigation of autoimmune diseases accompanying Hashimoto's thyroiditis in children and adolescents and evaluation of cardiac signs

Journal of pediatric endocrinology & metabolism : JPEM, 2015-07, Vol.28 (7-8), p.767

2015

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Effects of GnRH analogue treatment on anterior pituitary hormones in children with central precocious puberty

Journal of pediatric endocrinology & metabolism : JPEM, 2015-09, Vol.28 (9-10), p.1145

2015

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Acute renal failure due to severe hypercalcemia and nephrocalcinosis treated with two doses of pamidronate in an infant with Williams-Beuren syndrome

Turkish journal of pediatrics, 2018, Vol.60 (2), p.210-215

2018

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Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation

Journal of Pediatric Endocrinology and Metabolism, 2012-12, Vol.25 (11-12), p.1153-1156

2012

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A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect

Journal of pediatric endocrinology & metabolism : JPEM, 2014-03, Vol.27 (3-4), p.383

2014

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Report of the first case of precocious puberty in Rett syndrome

Journal of pediatric endocrinology & metabolism : JPEM, 2013-10, Vol.26 (9-10), p.937-939

2013

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Thiamine-responsive megaloblastic anemia syndrome with atrial standstill: a case report

Journal of pediatric hematology/oncology, 2011-03, Vol.33 (2), p.144-147

2011

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Prevalence of hyperthyrotropinemia in obese children before and after weight loss

Eating and weight disorders, 2013-03, Vol.18 (1), p.87-90

2013

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Thyroid nodules in children and adolescents: a single institution’s experience

Journal of Pediatric Endocrinology and Metabolism, 2012-08, Vol.25 (7), p.633-638

2012

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Effects of Vitamin D Levels on Asthma Control and Severity in Children

Astım allerji immünoloji, 2016-12, Vol.14 (3), p.148-156

2016

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Assessment of the knowledge of diabetes mellitus among school teachers within the scope of the managing diabetes at school program

Journal of clinical research in pediatric endocrinology, 2012-12, Vol.4 (4), p.199-203

2012

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Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-α Mutations

Prader-Willi syndrome and growth hormone deficiency

What has national screening program changed in cases with congenital hypothyroidism?

Hyperinsulinemic hypoglycemia: experience in a series of 17 cases

A case of Langerhans cell histiocytosis with thyroid involvement

Diabetic euglycemic ketoacidosis in newly diagnosed type 1 diabetes mellitus during Ramadan fasting

Seizure due to somatostatin analog discontinuation in a case diagnosed as congenital hyperinsulinism novel mutation

Adherence to growth hormone therapy: results of a multicenter study

Bone mineral density and bone metabolic markers' status in children with neurofibromatosis type 1

Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing

Long-term follow-up of Cushing's disease:a case report

Diseases accompanying congenital hypothyroidism

Effects of L-thyroxine treatment on heart functions in infants with congenital hypothyroidism

Iatrogenic Cushing syndrome due to nasal steroid drops

Investigation of autoimmune diseases accompanying Hashimoto's thyroiditis in children and adolescents and evaluation of cardiac signs

Effects of GnRH analogue treatment on anterior pituitary hormones in children with central precocious puberty

Acute renal failure due to severe hypercalcemia and nephrocalcinosis treated with two doses of pamidronate in an infant with Williams-Beuren syndrome

Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation

A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect

Report of the first case of precocious puberty in Rett syndrome

Thiamine-responsive megaloblastic anemia syndrome with atrial standstill: a case report

Prevalence of hyperthyrotropinemia in obese children before and after weight loss

Thyroid nodules in children and adolescents: a single institution’s experience

Effects of Vitamin D Levels on Asthma Control and Severity in Children

Assessment of the knowledge of diabetes mellitus among school teachers within the scope of the managing diabetes at school program

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