Cargando…

Sex differences in comorbidities associated with Sjögren's disease

BACKGROUND: Little is known about the association of comorbidities with sex and age at diagnosis in Sjögren's disease. We tested the hypothesis that sex differences occur in comorbidities in patients with Sjögren's disease. METHODS: Patients with Sjögren's disease were identified from...

Descripción completa

Detalles Bibliográficos
Autores principales:	Bruno, Katelyn A., Morales-Lara, Andrea Carolina, Bittencourt, Edsel B., Siddiqui, Habeeba, Bommarito, Gabriella, Patel, Jenil, Sousou, John M., Salomon, Gary R., Paloka, Rinald, Watford, Shelby T., Hodge, David O., Lieberman, Scott M., Rozen, Todd D., Atwal, Paldeep S., Dorsher, Peter T., Seim, Lynsey A., Fairweather, DeLisa
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9387724/ https://www.ncbi.nlm.nih.gov/pubmed/35991633 http://dx.doi.org/10.3389/fmed.2022.958670

Ejemplares similares

Sex Differences, Genetic and Environmental Influences on Dilated Cardiomyopathy
por: Jain, Angita, et al.
Publicado: (2021)

Sex differences in inflammation, redox biology, mitochondria and autoimmunity
por: Di Florio, Damian N., et al.
Publicado: (2020)

Sex differences in Sjögren’s syndrome: a comprehensive review of immune mechanisms
por: Brandt, Jessica E., et al.
Publicado: (2015)

A sleep modulated Channelopathy: a novel CACNA1A pathogenic variant identified in episodic Ataxia type 2 and a potential link to sleep alleviated migraine
por: Ahuja, Abhimanyu S., et al.
Publicado: (2019)

Multimodality imaging of adrenal gland pathologies: A comprehensive pictorial review
por: Paloka, Rinald, et al.
Publicado: (2022)

Type 1 sialidosis presenting with ataxia, seizures and myoclonus with no visual involvement
por: Mohammad, Ahmed N., et al.
Publicado: (2018)

Palpitations and Asthenia Associated with Venlafaxine in a CYP2D6 Poor Metabolizer and CYP2C19 Intermediate Metabolizer
por: Garcia, Sofia, et al.
Publicado: (2017)

Patient with Marfan Syndrome and a Novel Variant in FBN1 Presenting with Bilateral Popliteal Artery Aneurysm
por: Mohammad, Ahmed, et al.
Publicado: (2018)

A complex case of delayed diagnosis of ornithine transcarbamylase deficiency in an adult patient with multiple comorbidities()
por: Abbott, Jessica, et al.
Publicado: (2022)

Regulating Inflammation in the Heart
por: Fairweather, DeLisa
Publicado: (2007)

Sex Differences in Inflammation During Atherosclerosis
por: Fairweather, DeLisa
Publicado: (2015)

424 Considerations Mid-Translation of a Novel Extracellular Vesicle Product in Myocarditis
por: Beetler, Danielle, et al.
Publicado: (2022)

Holocarboxylase synthetase deficiency pre and post newborn screening
por: Donti, Taraka R., et al.
Publicado: (2016)

Women and Autoimmune Diseases
por: Fairweather, DeLisa, et al.
Publicado: (2004)

BARD1 nonsense variant c.1921C>T in a patient with recurrent breast cancer
por: Gass, Jennifer, et al.
Publicado: (2017)

19-Year Follow-up of A Patient With Severe Glutathione Synthetase Deficiency
por: Atwal, Paldeep S., et al.
Publicado: (2016)

High overlap in patients diagnosed with hypermobile Ehlers-Danlos syndrome or hypermobile spectrum disorders with fibromyalgia and 40 self-reported symptoms and comorbidities
por: Fairweather, DeLisa, et al.
Publicado: (2023)

Tpl2 Ablation Leads to Hypercytokinemia and Excessive Cellular Infiltration to the Lungs During Late Stages of Influenza Infection
por: Latha, Krishna, et al.
Publicado: (2021)

Examination of Molecular Effects of MYLK Deletion in a Patient with Extensive Aortic, Carotid, and Abdominal Dissections That Underlie the Genetic Dysfunction
por: Macklin, Sarah K., et al.
Publicado: (2020)

Sex differences in pulmonary arterial hypertension: role of infection and autoimmunity in the pathogenesis of disease
por: Batton, Kyle A., et al.
Publicado: (2018)

Sex and gender differences in myocarditis and dilated cardiomyopathy: An update
por: Fairweather, DeLisa, et al.
Publicado: (2023)

The infantile neuroaxonal dystrophy rating scale (INAD-RS)
por: Atwal, Paldeep S., et al.
Publicado: (2020)

The Dynamics of SARS-CoV-2 (RT-PCR) Testing
por: Joyce, Nicole, et al.
Publicado: (2021)

Personalized molecular modeling for pinpointing associations of protein dysfunction and variants associated with hereditary cancer syndromes
por: Macklin, Sarah, et al.
Publicado: (2018)

Late Treatment for COVID-19 With Convalescent Plasma
por: Senefeld, Jonathon W., et al.
Publicado: (2022)

Immunoregulatory Effect of Preventive Supplementation of Omega-3 Fatty Acid in a Complex Regional Pain Syndrome Type I Model in Mice
por: Fernandes, Paula Franson, et al.
Publicado: (2022)

Ornithine Transcarbamylase Deficiency: If at First You Do Not Diagnose, Try and Try Again
por: Santos, Christan D., et al.
Publicado: (2017)

Expanded phenotype in a patient with spastic paraplegia 7
por: Gass, Jennifer, et al.
Publicado: (2017)

Novel variants in COL4A4 and COL4A5 are rare causes of FSGS in two unrelated families
por: Hines, Stephanie L., et al.
Publicado: (2018)

Correction: Novel variants in COL4A4 and COL4A5 are rare causes of FSGS in two unrelated families
por: Hines, Stephanie L., et al.
Publicado: (2018)

Whole Exome Sequencing Identifies Atypical Welander Distal Myopathy in Patient
por: Gass, Jennifer, et al.
Publicado: (2017)

A Case-Control Study of Peripartum Cardiomyopathy Using the Rochester Epidemiology Project
por: DOUGLASS, ERIKA J., et al.
Publicado: (2021)

Decrease of IL-1β and TNF in the Spinal Cord Mediates Analgesia Produced by Ankle Joint Mobilization in Complete Freund Adjuvant-Induced Inflammation Mice Model
por: Omura, Carlos Minoru, et al.
Publicado: (2022)

Acupuncture's Effects in Treating the Sequelae of Acute and Chronic Spinal Cord Injuries: A Review of Allopathic and Traditional Chinese Medicine Literature
por: Dorsher, Peter T., et al.
Publicado: (2011)

Neurogenic Bladder
por: Dorsher, Peter T., et al.
Publicado: (2012)

Case report: 5 year follow-up of adult late-onset mitochondrial encephalomyopathy with lactic acid and stroke-like episodes (MELAS)
por: Sunde, Kiri, et al.
Publicado: (2016)

Protein molecular modeling shows residue T599 is critical to wild-type function of POLG and description of a novel variant associated with the SANDO phenotype
por: Richter, John E, et al.
Publicado: (2018)

3341 Sex Differences in Vitamin D and Urinary Stone Disease
por: Di Florio, Damian Nicolas, et al.
Publicado: (2019)

Extracellular vesicles as personalized medicine
por: Beetler, Danielle J., et al.
Publicado: (2023)

Maple syrup urine disease: mechanisms and management
por: Blackburn, Patrick R, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_a035vp23517pq6v598qou9v2t0