Brunella Bagattini

Via Paradisa 2, PI
Pisa, 56124, Italy

Last Updated: 09/26/2026

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Found 12 publications

Effects of iodine supplementation on thyroid function in children with mild congenital hypothyroidism and non-autoimmune subclinical hypothyroidism.

Effects of iodine supplementation on thyroid function in children with mild congenital hypothyroidism and non-autoimmune subclinical hypothyroidism.

Journal: Journal of endocrinological investigation

Published: April 03, 2025

Clinical Course of Congenital Hypothyroidism With Gland In Situ and Necessity of L-Thyroxine Therapy After Re-evaluation.

Clinical Course of Congenital Hypothyroidism With Gland In Situ and Necessity of L-Thyroxine Therapy After Re-evaluation.

Journal: The Journal of clinical endocrinology and metabolism

Published: April 17, 2024

Thyroid autoimmunity in different phenotypes of polycystic ovary syndrome: a single-center experience.

Thyroid autoimmunity in different phenotypes of polycystic ovary syndrome: a single-center experience.

Journal: Journal of endocrinological investigation

Published: December 11, 2023

Late-onset dyshormonogenic goitrous hypothyroidism due to a homozygous mutation of the SLC26A7 gene: a case report.

Late-onset dyshormonogenic goitrous hypothyroidism due to a homozygous mutation of the SLC26A7 gene: a case report.

Journal: Italian journal of pediatrics

Published: August 08, 2023

Thyroid Function Rather Than Thyroid Antibodies Affects Pregnancy and Perinatal Outcomes: Results of a Prospective Study.

Thyroid Function Rather Than Thyroid Antibodies Affects Pregnancy and Perinatal Outcomes: Results of a Prospective Study.

Journal: The Journal of clinical endocrinology and metabolism

Published: May 06, 2022

Effect of aging on clinical features and metabolic complications of women with polycystic ovary syndrome.

Effect of aging on clinical features and metabolic complications of women with polycystic ovary syndrome.

Journal: Journal of endocrinological investigation

Published: March 24, 2021

Gene expression profile in functioning and non-functioning nodules of autonomous multinodular goiter from an area of iodine deficiency: unexpected common characteristics between the two entities.

Gene expression profile in functioning and non-functioning nodules of autonomous multinodular goiter from an area of iodine deficiency: unexpected common characteristics between the two entities.

Journal: Journal of endocrinological investigation

Published: February 09, 2021

The Role of Nuclear Medicine in the Clinical Management of Benign Thyroid Disorders, Part 2: Nodular Goiter, Hypothyroidism, and Subacute Thyroiditis.

The Role of Nuclear Medicine in the Clinical Management of Benign Thyroid Disorders, Part 2: Nodular Goiter, Hypothyroidism, and Subacute Thyroiditis.

Journal: Journal of nuclear medicine : official publication, Society of Nuclear Medicine

Published: October 19, 2020

Papillary thyroid cancer in a patient with congenital goitrous hypothyroidism due to a novel deletion in NIS gene.

Papillary thyroid cancer in a patient with congenital goitrous hypothyroidism due to a novel deletion in NIS gene.

Journal: Endocrine

Published: July 07, 2015

The different requirement of L-T4 therapy in congenital athyreosis compared with adult-acquired hypothyroidism suggests a persisting thyroid hormone resistance at the hypothalamic-pituitary level.

The different requirement of L-T4 therapy in congenital athyreosis compared with adult-acquired hypothyroidism suggests a persisting thyroid hormone resistance at the hypothalamic-pituitary level.

Journal: European journal of endocrinology

Published: October 12, 2014

Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism.

Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism.

Journal: Journal of endocrinological investigation

Published: July 10, 2013

Congenital hypothyroidism caused by a novel homozygous mutation in the thyroglobulin gene.

Congenital hypothyroidism caused by a novel homozygous mutation in the thyroglobulin gene.

Journal: European journal of pediatrics

Published: December 13, 2012

Showing 1-12 of 12

Last Updated: 09/26/2026