PATRICIA
PÉREZ CARPENA
DOCENTE INVITADA
Centro de Investigación Biomédica en Red sobre Enfermedades Raras
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Centro de Investigación Biomédica en Red sobre Enfermedades Raras (8)
2024
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A Systematic Review on Heritability of Sudden Sensorineural Hearing Loss
Laryngoscope
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A Systematic Review on the Genetic Contribution to Tinnitus
JARO - Journal of the Association for Research in Otolaryngology, Vol. 25, Núm. 1, pp. 13-33
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Cognitive Screening and Hearing Assessment in Patients With Chronic Tinnitus
Clinical and Experimental Otorhinolaryngology, Vol. 17, Núm. 1, pp. 15-25
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Cytokine profiling and transcriptomics in mononuclear cells define immune variants in Meniere Disease
Genes and Immunity, Vol. 25, Núm. 2, pp. 124-131
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Phenotypic spectrum of tinnitus patients bearing rare ANK2 gene variants
European Archives of Oto-Rhino-Laryngology
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Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease
Genes, Vol. 15, Núm. 1
2022
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Balance Disorders Including Ménière’s Disease
Comprehensive Pharmacology (Elsevier), pp. 770-782
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Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus
npj Genomic Medicine, Vol. 7, Núm. 1