ESPE Abstracts

ESPE Abstracts

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57th Annual ESPE (ESPE 2018)

Athens, Greece
27 Sept 2018 - 29 Sept 2018

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ESPE 2018 57th European Society for Paediatric Endocrinology Annual Meeting 27-29 September 2018 Athens, Greece

Poster Presentations

Thyroid P2

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Thyroid P1
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Thyroid P3

hrp0089p2-p376 | Thyroid P2

Long Term Monitoring of Graves Disease in Children and Adolescents: Single Center Experience

hrp0089p2-p377 | Thyroid P2

Effects of Thyroid Autoimmunity on Non-Alcoholic Fatty Liver Disease in Euthyroid Girls with Hashimoto’s Thyroiditis

hrp0089p2-p378 | Thyroid P2

The Prevalence of Clinically Significant Anti-TPO Positivity in Children with HLA-Conferred Susceptibility to Type 1 Diabetes

hrp0089p2-p379 | Thyroid P2

Encephalopathy Associated with Autoimmune Thyroid Disease: A Case Report

hrp0089p2-p380 | Thyroid P2

Celiac Disease Screening Should be Routinely Offered in Pediatric Population with Autoimmune Thyroid Disease

hrp0089p2-p381 | Thyroid P2

Autoimmune Thyroiditis in Klippel-Feil Syndrome with Arnold Chiari and Syringomyelia

hrp0089p2-p382 | Thyroid P2

Neonatal Monitoring of Newborns Born from Mothers with Graves’ Disease: Results of a Retrospective Monocentric Study

hrp0089p2-p383 | Thyroid P2

A Successful Switch Experience from High-dose PTU to MMI on Day 4 of Graves’ Thyroid Storm in a 14-Year-Old Girl

hrp0089p2-p384 | Thyroid P2

Graves’s Disease During Pregnancy: The Impact on the Fetus and the Newborn

hrp0089p2-p385 | Thyroid P2

Thyroid Hormone Receptor β (THRB) Mutation: Two New Cases of Heterozygous Mutation with Significant Family History

hrp0089p2-p386 | Thyroid P2

Triac Treatment Response to Thyroid Hormone Resistantance

hrp0089p2-p387 | Thyroid P2

Phenotype and Genotype of Four Patients with Thyroid Hormone Resistance Syndrome due to Mutations in the THRB Gene

hrp0089p2-p388 | Thyroid P2

Clinical Course in a Girl with Two hTPO Mutations – Homozygous c.1268G>A (p.Gly393Arg) and Heterozygous c.208C>G (p.Ala70Pro): 27 Years of Follow Up

hrp0089p2-p389 | Thyroid P2

A Neurological Disease Mimicking Central Hypothyroidism: MCT8 Deficiency

hrp0089p2-p390 | Thyroid P2

Multinodular Goiter in Childhood: Look for DICER1 Mutation

hrp0089p2-p391 | Thyroid P2

Application of Elastography in Assesment of Different Benign Thyroid Lesions in Children and Adolescents

hrp0089p2-p392 | Thyroid P2

Clinical Characteristics and Predictive Factors for the Detection of Thyroid Cancer in Children with Thyroid Nodules

hrp0089p2-p393 | Thyroid P2

Thyroid Nodules in Prader-Willi Syndrome

hrp0089p2-p394 | Thyroid P2

Early Medullary Thyroid Carcinoma (MTC) in an Infant with Multiple Endocrine Neoplasia Type 2B (MEN2B, RETS Mutation codon 891)

hrp0089p2-p395 | Thyroid P2

Serum Level of Biotin Rather than the Daily Dose is the Main Determinant of the Interference on Thyroid Function Assays in Patients with Biotinidase Deficiency

hrp0089p2-p396 | Thyroid P2

Thyroid Function Tests and Affecting Factors in Twins and Triplets

hrp0089p2-p397 | Thyroid P2

Hypothyroidism in a Child During Treatment with Nivolumab for a Glioblastoma

hrp0089p2-p398 | Thyroid P2

Diagnosis and Clinical Course of Amiodarone Induced Hyperthyroidism in Three Adolescent Patients

hrp0089p2-p399 | Thyroid P2

Allogenic Bone Marrow Transplantation in Children: Effect on Thyroid Function

hrp0089p2-p400 | Thyroid P2

Follow-up in Children with Non-obese and Non-autoimmune Subclinical Hypothyroidism

hrp0089p2-p401 | Thyroid P2

Clinical Management of Childhood Hyperthyroidism: A Longitudinal Study at a Single Center

hrp0089p2-p402 | Thyroid P2

Association of Thyroid Stimulating Hormone and Free Thyroxine with Cardiometabolic Risk Factors in Euthyroid Korean children and Adolescents Aged 10–18 Years: The Korean National Health and Nutrition Examination Survey 2015

hrp0089p2-p403 | Thyroid P2

Asymptomatic Hyperthyrotropinaemia in Children, Does it Correlate to true Thyroid Gland Dysfunction?

hrp0089p2-p404 | Thyroid P2

Hearing Loss Among Patients with Congenital Hypothyroidism

hrp0089p2-p405 | Thyroid P2

Predictors of Permanent Congenital Hypothyroidism in Children

hrp0089p2-p406 | Thyroid P2

Absence of Uptake on Scintigraphy Does Not Always Correlate with Athyreosis: Re-evaluation of Patients Diagnosed with Athyreosis Over a 10 Year Period in the Republic of Ireland

hrp0089p2-p407 | Thyroid P2

Bannayan-Riley-Ruvalcaba Syndrome with PTEN Mutation in a Patient Affected by Congenital Hypothyroidism due to TPO Gene Alteration

hrp0089p2-p408 | Thyroid P2

The Congenital Hypothyroidism Screening Programme in a Sigle Italian Centre: a 5-Years Retrospective Study

hrp0089p2-p409 | Thyroid P2

Do Insulin Like Growth Factors also Influence Growth in Children with Congenital Hypothyroidism: A Cohort Analysis

hrp0089p2-p410 | Thyroid P2

Study of Hearing Function in Children with Congenital Hypothyroidism Attending Alexandria University Children’s Hospital

hrp0089p2-p411 | Thyroid P2

Awareness of the Risks of Acquired Iodine Deficiency in Strict Vegan Diets

hrp0089p2-p412 | Thyroid P2

Thyroid Function in the Korean Obese Children and Adolescents: Korea National Health and Nutrition Examination Survey 2013 to 2015

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