Lista de obras - Behzat Ozkan - Dominio Público Uruguay

A novel mutation of AMH in three siblings with persistent Mullerian duct syndrome.

artículo científico publicado en 2015

A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel.

artículo científico publicado en 2016

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

artículo científico publicado en 2016

Anti-cyclic citrullinated peptide antibodies are not frequently observed in children with type 1 diabetes mellitus: a single-center study.

artículo científico publicado en 2016

Assessment of early atherosclerosis and left ventricular dysfunction in children with 21-hydroxylase deficiency.

artículo científico publicado en 2016

Association of Wolfram syndrome with Fallot tetralogy in a girl

artículo científico publicado en 2016

Comparison of Treatment Regimens for the Management of Severe Hypercalcemia due to Vitamin D Intoxication in Children

artículo científico publicado en 2018

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

artículo científico publicado en 2016

Effect of Terminal Patient Care Training on the Nurses' Attitudes Toward Death in an Oncology Hospital in Turkey

artículo científico publicado en 2017

Factors Influencing Serum Vitamin D Concentration in Turkish Children Residing in İzmir: A Single-Center Experience

artículo científico publicado en 2015

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy.

artículo científico publicado en 2015

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

artículo científico publicado en 2015

Higher-Than-Conventional Subcutaneous Regular Insulin Doses in Diabetic Ketoacidosis in Children and Adolescents.

artículo científico publicado en 2016

Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report.

artículo científico publicado en 2017

Intracranial Haemorrhage in a Patient Diagnosed with Idiopathic Thrombocytopaenic Purpura and Diabetic Ketoacidosis.

artículo científico publicado en 2015

Long-term monitoring of Graves’ disease in children and adolescents: a single-center experience

artículo científico publicado en 2019

Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents.

artículo científico publicado en 2017

Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing.

artículo científico publicado en 2015

Neurodevelopmental Outcome of Children with Congenital Hypothyroidism Diagnosed in a National Screening Program in Turkey.

artículo científico publicado en 2017

Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A.

artículo científico publicado en 2015

Results of videothoracoscopic thymectomy in children: an analysis of 40 patients†.

artículo científico publicado en 2015

Stethoscope versus point-of-care ultrasound in the differential diagnosis of dyspnea: a randomized trial.

artículo científico publicado en 2015

The Relationship Between Skinfold Thickness and Leptin, Ghrelin, Adiponectin, and Resistin Levels in Infants of Diabetic Mothers

artículo científico publicado en 2016

The assessment of peripapillary retinal nerve fiber layer and macular ganglion cell layer changes in obese children: a cross-sectional study using optical coherence tomography.

artículo científico publicado en 2016

The relation of anthropometric measurements and insulin resistance in patients with polycystic kidney disease

artículo científico publicado en 2016

Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel Loss-of-Function Mutation

scientific article published on 25 March 2019

Turner syndrome and associated problems in Turkish children: a multicenter study

artículo científico publicado en 2015

Two different patterns of mini-puberty in two 46,XY newborns with 17β-hydroxysteroid dehydrogenase type 3 deficiency

artículo científico publicado en 2015

Lista de obras de Behzat Ozkan

A novel mutation of AMH in three siblings with persistent Mullerian duct syndrome.

A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel.

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

Anti-cyclic citrullinated peptide antibodies are not frequently observed in children with type 1 diabetes mellitus: a single-center study.

Assessment of early atherosclerosis and left ventricular dysfunction in children with 21-hydroxylase deficiency.

Association of Wolfram syndrome with Fallot tetralogy in a girl

Comparison of Treatment Regimens for the Management of Severe Hypercalcemia due to Vitamin D Intoxication in Children

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

Effect of Terminal Patient Care Training on the Nurses' Attitudes Toward Death in an Oncology Hospital in Turkey

Factors Influencing Serum Vitamin D Concentration in Turkish Children Residing in İzmir: A Single-Center Experience

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy.

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

Higher-Than-Conventional Subcutaneous Regular Insulin Doses in Diabetic Ketoacidosis in Children and Adolescents.

Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report.

Intracranial Haemorrhage in a Patient Diagnosed with Idiopathic Thrombocytopaenic Purpura and Diabetic Ketoacidosis.

Long-term monitoring of Graves’ disease in children and adolescents: a single-center experience

Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents.

Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing.

Neurodevelopmental Outcome of Children with Congenital Hypothyroidism Diagnosed in a National Screening Program in Turkey.

Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A.

Results of videothoracoscopic thymectomy in children: an analysis of 40 patients†.

Stethoscope versus point-of-care ultrasound in the differential diagnosis of dyspnea: a randomized trial.

The Relationship Between Skinfold Thickness and Leptin, Ghrelin, Adiponectin, and Resistin Levels in Infants of Diabetic Mothers

The assessment of peripapillary retinal nerve fiber layer and macular ganglion cell layer changes in obese children: a cross-sectional study using optical coherence tomography.

The relation of anthropometric measurements and insulin resistance in patients with polycystic kidney disease

Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel Loss-of-Function Mutation

Turner syndrome and associated problems in Turkish children: a multicenter study

Two different patterns of mini-puberty in two 46,XY newborns with 17β-hydroxysteroid dehydrogenase type 3 deficiency