A novel Double RET E768D/L790F mutation associated with a MEN2B-like phenotype

Thyroid

Very Severe Resistance to Thyroid Hormone β in One of Three Affected Members of a Family with a Novel Mutation in the THRB Gene

Thyroid.

Fujisawa H, Gagné J, Dumitrescu AM, Refetoff S

doi: 10.1089/thy.2019.0095.

Thyroid

Macrofollicular variant of follicular thyroid carcinoma: a rare, underappreciated pitfall in the diagnosis of thyroid carcinoma

Thyroid.

Bongiovanni M, Sykiotis GP, La Rosa S, Bisig B, Trimech M, Missiaglia E, Gremaud M, Salvatori-Chappuis V, De Vito C, Sciarra A, Foulkes W, Pusztaszeri MP

doi: 10.1089/thy.2018.0607.

Genetic Aspects of DiabetesPediatric Diabetes

Phenotypic variability in two siblings with monogenic diabetes due to the same ABCC8 gene mutation

Pediatr Diabetes.

Cattoni A, Jackson C, Bain M, Houghton J, Wei C

doi: 10.1111/pedi.

Thyroid

Rapid Improvement of thyroid storm-related hemodynamic collapse by aggressive anti-thyroid therapy including steroid pulse: A case report

Medicine (Baltimore).

Kiriyama H, Amiya E, Hatano M, Hosoya Y, Maki H, Nitta D, Saito A, Shiraishi Y, Minatsuki S, Sato T, Murakami H, Uehara M, Manaka K, Makita N, Watanabe M, Komuro I

doi: 10.1097/

Obesity and Bariatric SurgeryThyroid

Congenital hypothyroidism due to ectopic sublingual thyroid gland in Prader-Willi Syndrome: a case report

Ital J Pediatr.

Bocchini S, Fintini D, Grugni G, Boiani A, Convertino A, Crinò A

doi: 10.1186/s13052-017-0403-7.

Thyroid

Case Report: A Case of Pituitary Adenoma Producing Growth Hormone and Thyroid-Stimulating Hormone Simultaneously

Front Endocrinol (Lausanne)

Sanada J, Tatsumi F, Kamei S, Fushimi Y, Shimoda M, Kohara K, Nakanishi S, Kaku K, Mune T, Kaneto H

doi: 10.3389/fendo.2021.659076

Thyroid

Unusual Presentation of Polyautoimmunity and Renal Tubular Acidosis in an Adolescent With Hashimoto's Thyroiditis and Central Pontine Myelinolysis

Front Endocrinol (Lausanne).

Bruns N, Finkelberg I, Al-Attrach I, Hoyer PF, Büscher R

doi: 10.3389/fendo.2020.548877.Visit the full text of the original publication at www.frontiersin.org

Thyroid

Steroid responsive encephalopathy associated with autoimmune thyroiditis (SREAT) presenting as major depression.

BMC Psychiatry.

Endres D, Perlov E, Stich O, Tebartz van Elst L

doi: 10.1186/s12888-016-0897-3.

Obesity and Bariatric Surgery

A novel MYT1L mutation in a patient with severe early-onset obesity and intellectual disability

Am J Med Genet A.

Loid P, Mäkitie R, Costantini A, Viljakainen H, Pekkinen M, Mäkitie O

doi: 10.1002/ajmg.a.40370.

Related content

Very Severe Resistance to Thyroid Hormone β in One of Three Affected Members of a Family with a Novel Mutation in the THRB Gene

Macrofollicular variant of follicular thyroid carcinoma: a rare, underappreciated pitfall in the diagnosis of thyroid carcinoma

Phenotypic variability in two siblings with monogenic diabetes due to the same ABCC8 gene mutation

Rapid Improvement of thyroid storm-related hemodynamic collapse by aggressive anti-thyroid therapy including steroid pulse: A case report

Congenital hypothyroidism due to ectopic sublingual thyroid gland in Prader-Willi Syndrome: a case report

Case Report: A Case of Pituitary Adenoma Producing Growth Hormone and Thyroid-Stimulating Hormone Simultaneously

Unusual Presentation of Polyautoimmunity and Renal Tubular Acidosis in an Adolescent With Hashimoto's Thyroiditis and Central Pontine Myelinolysis

Steroid responsive encephalopathy associated with autoimmune thyroiditis (SREAT) presenting as major depression.

A novel MYT1L mutation in a patient with severe early-onset obesity and intellectual disability