Results 181 to 190 of about 397,447 (350)

Autoimmune thyroiditis with systemic idiopathic fibrosis in horses [PDF]

open access: diamond, 2020
Sergey Yu. Smolentsev   +6 more
openalex   +1 more source

Thyroid Cancer Risk in Patients With Type 2 Diabetes Taking Glucagon‐Like Peptide 1 Receptor Agonists

open access: yesOTO Open, Volume 10, Issue 1, January-March 2026.
Abstract Objective Glucagon‐like peptide 1 receptor agonists (GLP‐1RA) have shown remarkable results in glycemic control for patients with type 2 diabetes (T2DM). While no association has been made, there is a concern for thyroid cancer (TC) from GLP‐1RA. We aimed to study the 5‐year risk of TC in T2DM patients taking GLP‐1RA.
Bao Y. Sciscent   +5 more
wiley   +1 more source

Classic autoimmune type 1 diabetes mellitus after a case of drug reaction with eosinophilia and systemic symptoms (DRESS). [PDF]

open access: yes, 2018
Chapman, Lance W   +5 more
core   +1 more source

Effects of Autoimmune Thyroiditis on Pregnancy Outcomes: Analysis of the Nationwide Inpatient Sample, 2016–2020

open access: yesReproductive Medicine and Biology, Volume 25, Issue 1, January/December 2026.
ABSTRACT Purpose To assess whether autoimmune thyroiditis is associated with obstetric, perinatal, and fetal complications in a nationally representative population of pregnant women. Methods This retrospective study utilized data from the U.S. Nationwide Inpatient Sample (NIS) and included women aged ≥ 18 years with delivery‐related hospitalizations ...
Chung‐Jen Teng   +2 more
wiley   +1 more source

Hyperthyroid heart disease: Diagnostic and therapeutic aspects [PDF]

open access: yes, 1990
Reinwein, Dankwart   +2 more
core   +1 more source

Co‐Occurrence of Myasthenia Gravis and Facioscapulohumeral Muscular Dystrophy: A Case Series and Review of Literature

open access: yesEuropean Journal of Neurology, Volume 33, Issue 1, January 2026.
ABSTRACT Background Facioscapulohumeral dystrophy (FSHD) and Myasthenia Gravis (MG) are well‐known rare neuromuscular diseases of respectively genetic and acquired origin. Among muscular dystrophies, the co‐occurrence of MG with FSHD is the most common, representing a non‐negligible “double trouble”.
Giulia Tammam   +14 more
wiley   +1 more source

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