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Vitamin D Deficiency in Children and Adolescents

Journal of clinical research in pediatric endocrinology, 2012-03, Vol.4 (1), p.25-29

2012

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The evaluation of possible role of endocrine disruptors in central and peripheral precocious puberty

Toxicology mechanisms and methods, 2016-09, Vol.26 (7), p.493-500

2016

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Choroidal Thickness in Childhood Obesity

Ophthalmic surgery, lasers & imaging retina, 2017-01, Vol.48 (1), p.10-17

2017

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Ocular manifestations of Type 1 diabetes mellitus in pediatric population

Indian journal of ophthalmology, 2016-09, Vol.64 (9), p.654-658

2016

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Cyclic pamidronate treatment in Bruck syndrome: Proposal of a new modality of treatment

Pediatrics international, 2008-12, Vol.50 (6), p.836-838

2008

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A case of autoimmune polyendocrine syndrome type 1 with ocular findings and unique AIRE gene defect

Journal of Clinical Ophthalmology and Research, 2016, Vol.4 (1), p.37

2016

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Oxidative stress markers, trace elements, and endocrine disrupting chemicals in children with Hashimoto's thyroiditis

Toxicology mechanisms and methods, 2019-11, Vol.29 (9), p.633-643

2019

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Vitamin D deficiency in children and adolescents

Journal of clinical research in pediatric endocrinology, 2012-03, Vol.4 (1), p.25-29

2012

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Homozygosity for two missense mutations in the leptin receptor gene (P316T;W646C) in a Turkmenian girl with severe early-onset obesity

Journal of Pediatric Endocrinology and Metabolism, 2011-12, Vol.24 (11-12), p.1043-1045

2011

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Reply

Journal of pediatric surgery, 2007-02, Vol.42 (2), p.440-441

Andiran, Nesibe

2007

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Reply

Journal of pediatric surgery, 2007, Vol.42 (2), p.440-441

Andiran, Nesibe

2007

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The effects of type 1 diabetes mellitus on cardiac functions in children: evaluation by conventional and tissue Doppler echocardiography

Journal of Pediatric Endocrinology and Metabolism, 2016-12, Vol.29 (12), p.1389

2016

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TNF-α levels in children with growth hormone deficiency and the effect of long-term growth hormone replacement therapy

Growth hormone & IGF research, 2007-04, Vol.17 (2), p.149-153

2007

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The relationship between serum magnesium levels wıth childhood obesity and insulin resistance: a review of the literature

Journal of Pediatric Endocrinology and Metabolism, 2011-10, Vol.24 (9-10), p.675-678

2011

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Lipoprotein(a) levels in girls with premature adrenarche

Journal of paediatrics and child health, 2008-03, Vol.44 (3), p.138-142

2008

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Assessment of Ventricular Functions by Tissue Doppler Echocardiography in Children with Asthma

Pediatric cardiology, 2013-03, Vol.34 (3), p.553-559

2013

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Primary familial hypomagnesemia syndrome: a new approach in treatment

Journal of Pediatric Endocrinology and Metabolism, 2012-06, Vol.25 (5), p.599-602

2012

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Blastocystis hominis—an emerging and imitating cause of acute abdomen in children

Journal of pediatric surgery, 2006-08, Vol.41 (8), p.1489-1491

2006

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Insulin Edema in Type 1 Diabetes Mellitus: Report of a Case and Brief Review of the Literature

Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2016-08, Vol.26 (4), p.1

2016

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Effects of 25 hydroxy vitamin D levels on the severity and asthma control in school age asthma patients

Archivos argentinos de pediatría, 2017-08, Vol.115 (4), p.336-342

2017

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Pattern of acute poisonings in childhood in Ankara: what has changed in twenty years?

Turkish journal of pediatrics, 2004-04, Vol.46 (2), p.147

2004

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Insulin Edema in Type 1 Diabetes Mellitus: Report of a Case and Brief Review of the Literature

Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2016-08, Vol.26 (4), p.e5077-e5077

2016

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A case of autoimmune polyendocrine syndrome type 1 with ocular findings and unique AIRE gene defect

Journal of clinical ophthalmology and research, 2016-01, Vol.4 (1), p.37-39

2016

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Neurodevelopmental evaluation of very low birth weight infants with transient hypothyroxinemia at corrected age of 18–24 months

Indian pediatrics, 2012-09, Vol.49 (9), p.711-715

2012

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Unilateral Ectrodactyly in a Newborn with Trisomy 18 Syndrome: An Unusual Association

Journal of the College of Physicians and Surgeons--Pakistan, 2015-08, Vol.25 (8), p.619-620

2015

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Vitamin D Deficiency in Children and Adolescents

The evaluation of possible role of endocrine disruptors in central and peripheral precocious puberty

Choroidal Thickness in Childhood Obesity

Ocular manifestations of Type 1 diabetes mellitus in pediatric population

Cyclic pamidronate treatment in Bruck syndrome: Proposal of a new modality of treatment

A case of autoimmune polyendocrine syndrome type 1 with ocular findings and unique AIRE gene defect

Oxidative stress markers, trace elements, and endocrine disrupting chemicals in children with Hashimoto's thyroiditis

Vitamin D deficiency in children and adolescents

Homozygosity for two missense mutations in the leptin receptor gene (P316T;W646C) in a Turkmenian girl with severe early-onset obesity

Reply

Reply

The effects of type 1 diabetes mellitus on cardiac functions in children: evaluation by conventional and tissue Doppler echocardiography

TNF-α levels in children with growth hormone deficiency and the effect of long-term growth hormone replacement therapy

The relationship between serum magnesium levels wıth childhood obesity and insulin resistance: a review of the literature

Lipoprotein(a) levels in girls with premature adrenarche

Assessment of Ventricular Functions by Tissue Doppler Echocardiography in Children with Asthma

Primary familial hypomagnesemia syndrome: a new approach in treatment

Blastocystis hominis—an emerging and imitating cause of acute abdomen in children

Insulin Edema in Type 1 Diabetes Mellitus: Report of a Case and Brief Review of the Literature

Effects of 25 hydroxy vitamin D levels on the severity and asthma control in school age asthma patients

Pattern of acute poisonings in childhood in Ankara: what has changed in twenty years?

Insulin Edema in Type 1 Diabetes Mellitus: Report of a Case and Brief Review of the Literature

A case of autoimmune polyendocrine syndrome type 1 with ocular findings and unique AIRE gene defect

Neurodevelopmental evaluation of very low birth weight infants with transient hypothyroxinemia at corrected age of 18–24 months

Unilateral Ectrodactyly in a Newborn with Trisomy 18 Syndrome: An Unusual Association

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