Lista de obras - Merih Berberoğlu - Dominio Público Uruguay

A Neonatal Form of Isolated ACTH Deficiency Frequently Associated with Tpit Gene Mutations

article

A novel TWIST1 gene mutation in a patient with Saethre-Chotzen syndrome.

artículo científico publicado en 2017

A novel heterozygous mutation in steroidogenic factor-1 in pubertal virilization of a 46,XY female adolescent

artículo científico publicado en 2013

Acute reversible cardiomyopathy and heart failure in a child with acute adrenal crisis.

artículo científico publicado en 2016

Adherence to growth hormone therapy: results of a multicenter study

artículo científico publicado en 2014

Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA-Genotyping Results-Original Article ⬇️

artículo científico publicado el 3 de noviembre de 2010

Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V2811 mutation in patients with premature pubarche

artículo científico publicado en 2011

Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey

artículo científico publicado en 2018

Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell

artículo científico publicado en 2011

Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy

scientific article published on 14 May 2016

Congenital early onset isolated adrenocorticotropin deficiency associated with a TPIT gene mutation

artículo científico publicado en 2004

Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents

artículo científico publicado en 2011

Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey

artículo científico publicado en 2015

Diagnostic characteristics and metabolic risk factors of cases with polycystic ovary syndrome during adolescence.

artículo científico publicado en 2014

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

artículo científico publicado el 1 de noviembre de 2010

Does long-term use of valproate cause weight gain in prepubertal epileptic children?

artículo científico publicado en 2002

Effects of zinc supplementation on somatomedin-C level, in beta thalassemia

artículo científico publicado el 1 de octubre de 1992

Effects on bone mineral density of gonadotropin releasing hormone analogs used in the treatment of central precocious puberty

artículo científico publicado en 2003

Evaluation of Efficacy of Long-term Growth Hormone Therapy in Patients with Hypochondroplasia

artículo científico publicado en 2018

Evaluation of Renal Function in Obese Children and Adolescents Using Serum Cystatin C Levels, Estimated Glomerular Filtration Rate Formulae and Proteinuria: Which is most Useful?

article

Evaluation of glucose homeostasis in transfusion-dependent thalassemic patients

artículo científico publicado en 2008

Evaluation of hypercoagulability in obese children with thrombin generation test and microparticle release: effect of metabolic parameters

scientific article published on 17 May 2011

Exaggerated TSH responses to TRH in patients with goiter and 'normal' basal TSH levels

scientific article published on 16 November 2005

Experience with long-term glucocorticoid treatment in congenital adrenal hyperplasia: growth pattern compared with genetic height potential

artículo científico publicado en 2006

Factors contributing to sex assignment and reassignment decisions in Turkish children with 46,XY disorders of sex development

artículo científico publicado en 2007

Functional ovarian hyperandrogenism and polycystic ovary syndrome in prepubertal girls with obesity and/or premature pubarche

artículo científico publicado en 2007

Gastric carcinoid tumor in a 14-year old girl

artículo científico publicado en 2014

Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in Turkey

scientific article published on 01 August 2008

Importance of thyroglobulin levels for diagnosis and monitoring of follicular thyroid carcinoma in an adolescent with severe iodine deficiency

artículo científico publicado en 2006

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 exc

artículo científico publicado en 2006

Is adrenocorticotropic hormone deficiency really rare in patients with idiopathic growth hormone deficiency and normal thyroid function tests?

scientific article published on 02 November 2010

Isolated central diabetes insipidus in a newborn with congenital toxoplasmosis.

artículo científico publicado en 2006

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

artículo científico publicado en 2004

Long-term follow-up of a pseudohypoparathyroidism type 1A patient with missense mutation (Pro115Ser) in exon 5 ⬇️

artículo científico publicado el 7 de mayo de 2010

Management of central diabetes insipidus with oral desmopressin in a premature neonate

artículo científico publicado en 2004

Melanocortin-4 receptor polymorphisms in Turkish pediatric obese patients

artículo científico publicado en 2010

Mutations of the 5alpha-steroid reductase type 2 gene in six Turkish patients from unrelated families and a large pedigree of an isolated Turkish village.

artículo científico publicado en 2002

Neonatal diabetes with hyperchylomicronemia

artículo científico publicado en 2002

No seasonality of birth in children with type 1 diabetes mellitus in Ankara, Turkey

artículo científico publicado en 2002

Persistently raised thyroid stimulating hormone in adequately treated congenital hypothyroidism on long-term follow-up

artículo científico publicado en 2008

Rare childhood tumors in a Turkish pediatric oncology center

artículo científico publicado en 2013

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

artículo científico publicado en 2017

Refinement of the critical genomic region for hypoglycaemia in the Chromosome 9p deletion syndrome

scientific article published on 08 October 2019

Relationship between functional promoter polymorphism in the XBP1 gene (-116C/G) and obesity

scientific article published on 07 October 2008

Relationship between plasma leptin, insulin and tumor necrosis factor alpha in obese children

artículo científico publicado en 2005

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).

artículo científico publicado en 2005

Risk factors for non-alcoholic fatty liver disease in obese children.

artículo científico publicado en 2009

Severe hypercalcemia of an infant due to vitamin D toxicity associated with hypercholesterolemia

artículo científico publicado en 2001

The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels

artículo científico publicado en 2015

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

artículo científico publicado en 2012

The incidence and evolution of thyroid dysfunction during interferon-alpha therapy in children with chronic hepatitis B infection

artículo científico publicado en 2007

The risk of functional ovarian hyperandrogenism and polycystic ovary syndrome in patients with hyperandrogenism

artículo científico publicado en 2003

Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant

artículo científico publicado en 2011

Two Siblings with Isolated GH Deficiency Due to Loss-of-Function Mutation in the GHRHR Gene: Successful Treatment with Growth Hormone Despite Late Admission and Severe Growth Retardation-Case Report ⬇️

artículo científico publicado el 6 de noviembre de 2010

Vitamin D Deficiency in Turkish Mothers and Their Neonates and in Women of Reproductive Age ⬇️

artículo científico publicado el 3 de noviembre de 2009

Lista de obras de Merih Berberoğlu

A Neonatal Form of Isolated ACTH Deficiency Frequently Associated with Tpit Gene Mutations

A novel TWIST1 gene mutation in a patient with Saethre-Chotzen syndrome.

A novel heterozygous mutation in steroidogenic factor-1 in pubertal virilization of a 46,XY female adolescent

Acute reversible cardiomyopathy and heart failure in a child with acute adrenal crisis.

Adherence to growth hormone therapy: results of a multicenter study

Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA-Genotyping Results-Original Article ⬇️

Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V2811 mutation in patients with premature pubarche

Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey

Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell

Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy

Congenital early onset isolated adrenocorticotropin deficiency associated with a TPIT gene mutation

Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents

Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey

Diagnostic characteristics and metabolic risk factors of cases with polycystic ovary syndrome during adolescence.

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

Does long-term use of valproate cause weight gain in prepubertal epileptic children?

Effects of zinc supplementation on somatomedin-C level, in beta thalassemia

Effects on bone mineral density of gonadotropin releasing hormone analogs used in the treatment of central precocious puberty

Evaluation of Efficacy of Long-term Growth Hormone Therapy in Patients with Hypochondroplasia

Evaluation of Renal Function in Obese Children and Adolescents Using Serum Cystatin C Levels, Estimated Glomerular Filtration Rate Formulae and Proteinuria: Which is most Useful?

Evaluation of glucose homeostasis in transfusion-dependent thalassemic patients

Evaluation of hypercoagulability in obese children with thrombin generation test and microparticle release: effect of metabolic parameters

Exaggerated TSH responses to TRH in patients with goiter and 'normal' basal TSH levels

Experience with long-term glucocorticoid treatment in congenital adrenal hyperplasia: growth pattern compared with genetic height potential

Factors contributing to sex assignment and reassignment decisions in Turkish children with 46,XY disorders of sex development

Functional ovarian hyperandrogenism and polycystic ovary syndrome in prepubertal girls with obesity and/or premature pubarche

Gastric carcinoid tumor in a 14-year old girl

Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in Turkey

Importance of thyroglobulin levels for diagnosis and monitoring of follicular thyroid carcinoma in an adolescent with severe iodine deficiency

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 exc

Is adrenocorticotropic hormone deficiency really rare in patients with idiopathic growth hormone deficiency and normal thyroid function tests?

Isolated central diabetes insipidus in a newborn with congenital toxoplasmosis.

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

Long-term follow-up of a pseudohypoparathyroidism type 1A patient with missense mutation (Pro115Ser) in exon 5 ⬇️

Management of central diabetes insipidus with oral desmopressin in a premature neonate

Melanocortin-4 receptor polymorphisms in Turkish pediatric obese patients

Mutations of the 5alpha-steroid reductase type 2 gene in six Turkish patients from unrelated families and a large pedigree of an isolated Turkish village.

Neonatal diabetes with hyperchylomicronemia

No seasonality of birth in children with type 1 diabetes mellitus in Ankara, Turkey

Persistently raised thyroid stimulating hormone in adequately treated congenital hypothyroidism on long-term follow-up

Rare childhood tumors in a Turkish pediatric oncology center

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

Refinement of the critical genomic region for hypoglycaemia in the Chromosome 9p deletion syndrome

Relationship between functional promoter polymorphism in the XBP1 gene (-116C/G) and obesity

Relationship between plasma leptin, insulin and tumor necrosis factor alpha in obese children

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).

Risk factors for non-alcoholic fatty liver disease in obese children.

Severe hypercalcemia of an infant due to vitamin D toxicity associated with hypercholesterolemia

The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels

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

The incidence and evolution of thyroid dysfunction during interferon-alpha therapy in children with chronic hepatitis B infection

The risk of functional ovarian hyperandrogenism and polycystic ovary syndrome in patients with hyperandrogenism

Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant

Two Siblings with Isolated GH Deficiency Due to Loss-of-Function Mutation in the GHRHR Gene: Successful Treatment with Growth Hormone Despite Late Admission and Severe Growth Retardation-Case Report ⬇️

Vitamin D Deficiency in Turkish Mothers and Their Neonates and in Women of Reproductive Age ⬇️