about
Genetics of vestibular disorders: pathophysiological insightsClinical Subgroups in Bilateral Meniere Disease.Generation of human iPSC line GRX-MCiPS4F-A2 from adult peripheral blood mononuclear cells (PBMCs) with Spanish genetic background.A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease.Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease.Extended phenotype and clinical subgroups in unilateral Meniere disease: A cross-sectional study with cluster analysis.Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease.Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family.Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease.Recommendations on Collecting and Storing Samples for Genetic Studies in Hearing and Tinnitus Research
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description
researcher ORCID ID = 0000-0002-6104-0941
@en
wetenschapper
@nl
name
Lidia Frejo
@ast
Lidia Frejo
@en
Lidia Frejo
@es
Lidia Frejo
@nl
type
label
Lidia Frejo
@ast
Lidia Frejo
@en
Lidia Frejo
@es
Lidia Frejo
@nl
prefLabel
Lidia Frejo
@ast
Lidia Frejo
@en
Lidia Frejo
@es
Lidia Frejo
@nl
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P21
P31
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0000-0002-6104-0941