Výsledky vyhledávání - "Diseases::Otorhinolaryngologic Diseases::Ear Diseases::Labyrinth Diseases::Endolymphatic Hydrops::Meniere Disease [Medical Subject Headings]"

DNA Methylation Signature in Mononuclear Cells and Proinflammatory Cytokines May Define Molecular Subtypes in Sporadic Meniere Disease

Autor: Alvaro Gallego-Martinez, Jose A. Lopez-Escamez, Alba Escalera-Balsera, Andrés Soto-Varela, Marisa Flook, Ismael Aran, Juan Manuel Espinosa-Sanchez

Publikováno v: Biomedicines
Volume 9
Issue 11
Biomedicines, Vol 9, Iss 1530, p 1530 (2021)
Digibug. Repositorio Institucional de la Universidad de Granada
Consorcio Madroño

Meniere Disease (MD) is a multifactorial disorder of the inner ear characterized by vertigo attacks associated with sensorineural hearing loss and tinnitus with a significant heritability. Although MD has been associated with several genes, no epigen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fd1b609d1cff4cef353bcb91928f5ba

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Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study

Autor: Patricia Perez-Carpena, Patrick May, Joseph Sollini, Juan Manuel Espinosa-Sanchez, Alvaro Gallego-Martinez, Barbara Canlon, Sana Amanat, Jose A. Lopez-Escamez, Angel Batuecas-Caletrio, Andrés Soto-Varela, Christopher R. Cederroth, Ismael Aran

Publikováno v: EBioMedicine
Digibug: Repositorio Institucional de la Universidad de Granada
Universidad de Granada (UGR)
EBioMedicine, Vol 66, Iss, Pp 103309-(2021)
Digibug. Repositorio Institucional de la Universidad de Granada
instname

Background: tinnitus is a heterogeneous condition associated with audiological and/or mental disorders. Chronic, severe tinnitus is reported in 1% of the population and it shows a relevant heritability, according to twins, adoptees and familial aggre

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https://pubmed.ncbi.nlm.nih.gov/33813136

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A Systematic Review on the Association of Acquired Human Cytomegalovirus Infection with Hearing Loss

Autor: Martinez-Gomez, Estrella, Perez-Carpena, Patricia, Flook, Marisa, Lopez-Escamez, José A.

Congenital cytomegalovirus (CMV) infection induces a clinical syndrome usually associated with hearing loss. However, the effect of acquired CVM infection in adults and children has not been clearly defined. The objective of this review is to critica

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2636::4e9a57de4dc4664aeea06b37f0e484ba
https://hdl.handle.net/10668/3529

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New Insights into Pathophysiology of Vestibular Migraine

Autor: Juan Manuel Espinosa-Sanchez, Jose Antonio Lopez-Escamez

Publikováno v: Frontiers in Neurology, Vol 6 (2015)
Frontiers in Neurology

Journal Article; Review; Vestibular migraine (VM) is a common disorder in which genetic, epigenetic, and environmental factors probably contribute to its development. The pathophysiology of VM is unknown; nevertheless in the last few years, several s

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Accompanying Symptoms Overlap during Attacks in Menière’s Disease and Vestibular Migraine

Autor: Alexandre Bisdorff, Thomas Lempert, Julien Jacobs, Michael von Brevern, Julia Dlugaiczyk, Roberto Teggi, Jose A. Lopez-Escamez

Publikováno v: Frontiers in Neurology

Meniere’s disease and vestibular migraine are the most common causes of spontaneous recurrent vertigo. The current diagnostic criteria for the two disorders are mainly based on patients’ symptoms and no biological marker is available. When applyi

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Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease

Autor: Marta E. Alarcón-Riquelme, Jesus Benitez, Sonia Cabrera, Andrés Soto-Varela, Juan Manuel Espinosa-Sanchez, Eduardo Martin-Sanz, Nicolas Perez, Gabriel Trinidad, Jose A. Lopez-Escamez, Jesus Fraile, Sofía Santos-Pérez, Manuel Martínez-Bueno, Paz Pérez, Teresa Requena, Elena Sánchez, Angel Batuecas, Ismael Aran

Publikováno v: PLoS ONE, Vol 9, Iss 11, p e112171 (2014)
PLoS ONE
Dadun. Depósito Académico Digital de la Universidad de Navarra
instname
Zaguán. Repositorio Digital de la Universidad de Zaragoza

Journal Article; Research Support, Non-U.S. Gov't; Meniere's disease is an episodic vestibular syndrome associated with sensorineural hearing loss (SNHL) and tinnitus. Patients with MD have an elevated prevalence of several autoimmune diseases (rheum

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d67d4446cb022a5f50e5eb5b88219357
https://hdl.handle.net/10668/2060

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Functional Variants in NOS1 and NOS2A Are Not Associated with Progressive Hearing Loss in Ménière's Disease in a European Caucasian Population

Autor: Gazquez, Irene, Lopez-Escamez, Jose A., Moreno, Antonia, Campbell, Colleen A., Meyer, Nicole C., Carey, John P., Minor, Lloyd B., Gantz, Bruce J., Hansen, Marlan R., Della Santina, Charles C., Aran, Ismael, Soto-Varela, Andres, Santos, Sofia, Batuecas, Angel, Perez-Garrigues, Herminio, Lopez-Nevot, Alicia, Smith, Richard J.H., Lopez-Nevot, Miguel A.

This is a copy of an article published in the DNA and Cell Biology © 2011 [copyright Mary Ann Liebert, Inc.]; DNA and Cell Biology is available online at: http://online.liebertpub.com. Hearing loss in Meniere's disease (MD) is associated with loss o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2636::082b784fedbe8285cf097d8b1602381d
https://hdl.handle.net/10668/408

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High prevalence of systemic autoimmune diseases in patients with Menière's disease

Autor: Irene Gazquez, Sofia Santos, Angel Batuecas, Ismael Aran, Herminio Pérez-Garrigues, Carlos Gonzalez-Oller, Lourdes Acosta, Jose A. Lopez-Escamez, Gabriel Trinidad, Andrés Soto-Varela

Publikováno v: PLoS ONE, Vol 6, Iss 10, p e26759 (2011)
PLoS ONE

BackgroundAutoimmunity appears to be associated with the pathophysiology of Meniere's disease (MD), an inner ear disorder characterized by episodes of vertigo associated with hearing loss and tinnitus. However, the prevalence of autoimmune diseases (

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::391eb6add1cb994803b7d3e338dddf16
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22053211/?tool=EBI

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Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: a case-control study

Autor: Irene Gazquez, Antonia Ruiz Moreno, Andrés Soto-Varela, Sofia Santos, Carlos Gonzalez-Oller, Águeda Ibañez, Ismael Aran, Miguel A. López-Nevot, Jose A. Lopez-Escamez, Herminio Pérez-Garrigues, Pablo Saenz-Lopez

Publikováno v: BMC Medical Genetics
BMC Medical Genetics, Vol 12, Iss 1, p 2 (2011)

This study was supported by a research project FIS PI07/0035. JALE was partially supported by ISCIII research grant INT09/229. The 3130 XL Genetics Analyzer was funded by grant IF06/37291 from Ministry of Science. BACKGROUND: Autoimmune diseases with

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https://pubmed.ncbi.nlm.nih.gov/21208440

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