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Homeostasis model assessment is more reliable than the fasting glucose/insulin ratio and quantitative insulin sensitivity check index for assessing insulin resistance among obese children and adolescents

Pediatrics (Evanston), 2005-04, Vol.115 (4), p.e500-e503

2005

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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

International journal of human genetics, 2015-01, Vol.60 (1), p.1-9

2015

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Protein oxidation in obesity and insulin resistance

European journal of pediatrics, 2006-11, Vol.165 (11), p.753-756

2006

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Diabetes mellitus type 1: association with Rett syndrome

Pediatrics international, 2005-02, Vol.47 (1), p.90-91

2005

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Rhabdomyosarcoma with coexistent diabetes insipidus and cerebral salt wasting as postoperative complication

Pediatrics international, 2006-02, Vol.48 (1), p.79-81

2006

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Proton Magnetic Resonance Spectroscopy Findings and Clinical Effects of Montelukast Sodium in a Case With Sjögren-Larsson Syndrome

Journal of child neurology, 2006-12, Vol.21 (12), p.1092-1095

2006

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Prevalence of anti-HAV and anti-HEV antibodies in Konya, Turkey

Health policy (Amsterdam), 2004-03, Vol.67 (3), p.265-269

2004

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Turner's Syndrome with Situs Inversus Totalis

Journal of Pediatric Endocrinology and Metabolism, 2008-07, Vol.21 (7), p.621-622

2008

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Different clinical features of amitraz poisoning in children

Human & experimental toxicology, 2002-01, Vol.21 (1), p.13-16

2002

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Effects of 3 years of intravenous pamidronate treatment on bone markers and bone mineral density in a patient with osteoporosis-pseudoglioma syndrome (OPPG)

Journal of Pediatric Endocrinology and Metabolism, 2006-03, Vol.19 (3), p.275

2006

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Plasmapheresis as an adjunct treatment in severe botulism

Intensive care medicine, 2002-06, Vol.28 (6), p.814-814

2002

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Bardet-Biedl syndrome with syndrome X: a patient report

Journal of Pediatric Endocrinology and Metabolism, 2004-06, Vol.17 (6), p.913

2004

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Plasma homocysteine concentrations in adolescents with subclinical hypothyroidism

Journal of Pediatric Endocrinology and Metabolism, 2003-12, Vol.16 (9), p.1245

2003

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Female pseudohermaphroditism due to classical 21-hydroxylase deficiency and insulin resistance in a girl with Turner syndrome

Turkish journal of pediatrics, 2005-04, Vol.47 (2), p.176-179

2005

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Adrenocortical adenoma associated with inadequately treated congenital adrenal hyperplasia

Journal of Pediatric Endocrinology and Metabolism, 2003-12, Vol.16 (9), p.1311

2003

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Growth hormone deficiency, situs inversus, hypertrichosis and brachydactyly

Journal of Pediatric Endocrinology and Metabolism, 2003-06, Vol.16 (5), p.795

2003

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Acanthosis nigricans in association with congenital adrenal hyperplasia: resolution after treatment. Case report

Turkish journal of pediatrics, 2005-04, Vol.47 (2), p.183-187

2005

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Relationship between cord blood levels of IGF-I and ferritin in healthy term neonates

Journal of Pediatric Endocrinology and Metabolism, 2004-05, Vol.17 (5), p.737

2004

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Triple-x syndrome accompanied by congenital adrenal hyperplasia: case report

Turkish journal of pediatrics, 2004-10, Vol.46 (4), p.377-379

2004

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Stevens-Johnson Syndrome-Like Exanthema Secondary to Methotrexate

Turkish journal of haematology, 2002-09, Vol.19 (3), p.427-430

2002

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Association Between Nonalcoholic Fatty Liver Disease and Cardiovascular Risk in Obese Children and Adolescents

Canadian journal of cardiology, 2013-09, Vol.29 (9), p.1118-1125

2013

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A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype

Annales de génétique, 2002-10, Vol.45 (4), p.181-183

2002

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Homeostasis model assessment is more reliable than the fasting glucose/insulin ratio and quantitative insulin sensitivity check index for assessing insulin resistance among obese children and adolescents

The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

Protein oxidation in obesity and insulin resistance

Diabetes mellitus type 1: association with Rett syndrome

Rhabdomyosarcoma with coexistent diabetes insipidus and cerebral salt wasting as postoperative complication

The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

Proton Magnetic Resonance Spectroscopy Findings and Clinical Effects of Montelukast Sodium in a Case With Sjögren-Larsson Syndrome

Prevalence of anti-HAV and anti-HEV antibodies in Konya, Turkey

Erratum: The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

The Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism and Response to Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome: A Multicenter Study

Turner's Syndrome with Situs Inversus Totalis

Different clinical features of amitraz poisoning in children

Effects of 3 years of intravenous pamidronate treatment on bone markers and bone mineral density in a patient with osteoporosis-pseudoglioma syndrome (OPPG)

Plasmapheresis as an adjunct treatment in severe botulism

Bardet-Biedl syndrome with syndrome X: a patient report

Plasma homocysteine concentrations in adolescents with subclinical hypothyroidism

Female pseudohermaphroditism due to classical 21-hydroxylase deficiency and insulin resistance in a girl with Turner syndrome

Adrenocortical adenoma associated with inadequately treated congenital adrenal hyperplasia

Growth hormone deficiency, situs inversus, hypertrichosis and brachydactyly

Acanthosis nigricans in association with congenital adrenal hyperplasia: resolution after treatment. Case report

Relationship between cord blood levels of IGF-I and ferritin in healthy term neonates

Triple-x syndrome accompanied by congenital adrenal hyperplasia: case report

Stevens-Johnson Syndrome-Like Exanthema Secondary to Methotrexate

Association Between Nonalcoholic Fatty Liver Disease and Cardiovascular Risk in Obese Children and Adolescents

A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype

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