Results 61 to 70 of about 5,291,425 (217)

Molecular Mechanisms in Autoimmune Thyroid Disease

open access: yes, 2023
The most common cause of acquired thyroid dysfunction is autoimmune thyroid disease, which is an organ-specific autoimmune disease with two presentation phenotypes: hyperthyroidism (Graves-Basedow disease) and hypothyroidism (Hashimoto’s ...
Hernando Vargas-Uricoechea
core   +1 more source

Intersection of systemic lupus erythematosus and autoimmune thyroid disease: Shared pathophysiology, epidemiology, diagnosis, and management

open access: yesRheumatology &Autoimmunity, EarlyView.
A proposed mechanistic framework of systemic lupus erythematosus (SLE) and autoimmune thyroid disease (AITD) pathogenesis. In Stage 1, genetically susceptible individuals harbor risk variants within major histocompatibility complex (HLA) and non‐HLA loci that impair central and peripheral immune tolerance mechanisms within the thymic and peripheral ...
Elisa Elisa   +3 more
wiley   +1 more source

Enhancing Tea Agrifood System Resilience Amid Geopolitical Tensions: A Resource Nexus‐Based System Dynamics Analysis

open access: yesSustainable Development, EarlyView.
ABSTRACT Geopolitical conflicts are increasingly threatening global food security, economic stability, and peace, impacting Tanzania's tea agrifood system. This study develops a quantitative Resource Nexus‐based system dynamics simulation model assessing the feedbacks and interdependencies among key environmental and socioeconomic resources shaping ...
Ally Mkumbukiy   +3 more
wiley   +1 more source

Sue Hashimoto sits on the bumper of a car at Poston incarceration camp

open access: yes, 1942
Photograph of Sue Hashimoto sitting on the front bumper of an automobile at Poston Incarceration Camp. The barrack buildings can be seen in the background. From Hashimoto Poston Photograph Album, page 13.Suyeko Sue Hashimoto (nee Yagura) was born in 1921

core  

A Case of Probable Creutzfeldt-Jakob Disease with Coexistence of the Features of Hashimoto Encephalopathy [PDF]

open access: yes, 2004
Hashimoto encephalopathy shares common clinical features with Creutzfeldt-Jakob disease and must be regarded as a differential diagnosis because of its good prognosis. We report a case of Hashimoto encephalopathy, which had not been recognized before the
신혜원   +3 more
core  

Treatment Patterns and Pathways of Systemic Drug Therapy in Patients With Plaque, Erythrodermic, and Generalized Pustular Psoriasis: A Retrospective Cohort Study in Japan

open access: yesThe Journal of Dermatology, EarlyView.
ABSTRACT Systemic psoriasis treatment options have rapidly expanded in Japan, including the approval of tyrosine kinase 2 and interleukin‐36 receptor inhibitors in 2022. However, contemporary real‐world treatment patterns across plaque, erythrodermic, and generalized pustular psoriasis remain incompletely characterized.
Yayoi Tada   +9 more
wiley   +1 more source

Melkersson-Rosenthal syndrome in a patient with Hashimoto disease [PDF]

open access: yes, 2014
Introduction: Melkersson-Rosenthal syndrome (MRS) is a rare neurologic disease of unknown etiology. It is characterized by a triad of symptoms: relapsing peripheral facial paralysis; orofacial edema and fissured tongue.
Frąckowiak, L.   +3 more
core  

Multicenter Clinical Comparison Between Anti‐NXP2 and Anti‐TIF1‐γ Antibody‐Positive Myositis, and Analysis of the Clinical Significance of Anti‐NXP2 Antibody Titers in Idiopathic Inflammatory Myopathies

open access: yesThe Journal of Dermatology, EarlyView.
ABSTRACT We aimed to measure anti‐nuclear matrix protein 2 antibody (anti‐NXP2) titers in patients with anti‐NXP2‐positive idiopathic inflammatory myopathies, investigate whether these titers are associated with clinical manifestations, malignancy risk, and treatment response, and compare the clinical and serological features between anti‐NXP2‐positive
Satoshi Kamiya   +15 more
wiley   +1 more source

Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY. [PDF]

open access: yes, 2010
The unparalleled collection of clinical data and biomaterials within the EHDN's REGISTRY can expedite the search for disease modifiers (genetic and environmental) of age at onset and disease progression that could be harnessed for the development of ...
Handley, Olivia J   +59 more
core   +1 more source

Diagnostic Utility of Full‐Length BP180 and Native BP180‐α6β4 Integrin Complex ELISAs in Serologically Inconclusive Mucous Membrane Pemphigoid

open access: yesThe Journal of Dermatology, EarlyView.
ABSTRACT Mucous membrane pemphigoid (MMP) is a chronic autoimmune subepithelial blistering disorder of mucosal surfaces that can cause irreversible scarring, blindness, or dysphagia. Early diagnosis is challenging because histopathology is nonspecific and conventional BP180 NC16A ELISAs have limited sensitivity.
Yukiko Ishizuka   +10 more
wiley   +1 more source

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