I. Aran

发表

High Prevalence of Systemic Autoimmune Diseases in Patients with Menière's Disease

J. Lopez-Escamez, A. Soto-Varela, I. Gazquez, 2011, PloS one.

Time course of episodes of definitive vertigo in Meniere's disease.

R. Barona, J. Lopez-Escamez, C. Morera, 2008, Archives of otolaryngology--head & neck surgery.

Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease

T. Requena, A. Gallego-Martinez, J. Lopez-Escamez, 2018, Scientific Reports.

Extended phenotype and clinical subgroups in unilateral Meniere disease: A cross‐sectional study with cluster analysis

J. Lopez-Escamez, A. Soto-Varela, S. Santos-Pérez, 2017, Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery.

Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière’s disease

T. Requena, J. Lopez-Escamez, M. López-Nevot, 2013, European Archives of Oto-Rhino-Laryngology.

Poly(ADP-ribose) polymerase-1 (PARP-1) longer alleles spanning the promoter region may confer protection to bilateral Meniere's disease

J. Lopez-Escamez, M. López-Nevot, A. Soto-Varela, 2009, Acta oto-laryngologica.

MICA-STR A.4 Is Associated With Slower Hearing Loss Progression in Patients With Ménière’s Disease

T. Requena, J. Lopez-Escamez, M. López-Nevot, 2012, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

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

J. Lopez-Escamez, M. López-Nevot, A. Soto-Varela, 2011, BMC Medical Genetics.

nF-κB Underlies inflammation in Meniere’s Disease

T. Requena, A. Gallego-Martinez, J. Lopez-Escamez, 2017 .

Differential Proinflammatory Signature in Vestibular Migraine and Meniere Disease

A. Gallego-Martinez, J. Lopez-Escamez, A. Soto-Varela, 2019, Front. Immunol..

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

A. Gallego-Martinez, J. Lopez-Escamez, A. Soto-Varela, 2021, Biomedicines.

Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease.

A. Gallego-Martinez, J. Lopez-Escamez, A. Soto-Varela, 2020, Ear and hearing.

Rare Variants in the OTOG Gene Are a Frequent Cause of Familial Meniere’s Disease

A. Gallego-Martinez, J. Lopez-Escamez, A. Soto-Varela, 2019 .

Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease

J. Lopez-Escamez, A. Soto-Varela, D. Bächinger, 2021, Hearing Research.

[Superficial siderosis of the central nervous system: report of two new cases].

I. Aran, M. Seijo-Martínez, F. Vázquez, 2004, Revista de neurologia.

HLA-DRB1*1101 Allele May Be Associated With Bilateral Méniére's Disease in Southern European Population

J. Lopez-Escamez, M. López-Nevot, A. Soto-Varela, 2007, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Clinical Subgroups in Bilateral Meniere Disease

J. Lopez-Escamez, A. Soto-Varela, S. Santos-Pérez, 2016, Front. Neurol..

Familial clustering and genetic heterogeneity in Meniere's disease

T. Requena, J. Lopez-Escamez, E. Martín, 2014, Clinical genetics.

Intronic Variants in the NFKB1 Gene May Influence Hearing Forecast in Patients with Unilateral Sensorineural Hearing Loss in Meniere's Disease

M. Martínez-Bueno, T. Requena, J. Lopez-Escamez, 2014, PloS one.

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

P. May, B. Canlon, A. Gallego-Martinez, 2021, EBioMedicine.

Defective α‐tectorin may involve tectorial membrane in familial Meniere disease

A. Gallego-Martinez, J. Lopez-Escamez, A. Soto-Varela, 2022, Clinical and translational medicine.

Ultrarare missense and frameshift variants in the TECTA gene may involve tectorial membrane in familial Meniere disease

A. Gallego-Martinez, J. Lopez-Escamez, A. Soto-Varela, 2022, medRxiv.