Herminia Argente‐Escrig
Hospital Universitari i Politècnic La Fe(ES)ERN GUARD-Heart(NL)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Neurogenetic and Muscular Disorders Research, Cardiomyopathy and Myosin Studies, Neuroscience and Neuropharmacology Research, Genetic Neurodegenerative Diseases
Most-Cited Works
- → Distal hereditary motor neuropathies: Mutation spectrum and genotype–phenotype correlation(2020)67 cited
- → Isoform-selective decrease of glycogen synthase kinase-3-beta (GSK-3β) reduces synaptic tau phosphorylation, transcellular spreading, and aggregation(2021)35 cited
- → Early Referral to an ALS Center Reduces Several Months the Diagnostic Delay: A Multicenter-Based Study(2020)26 cited
- → Antibodies against nodo-paranodal proteins are not present in genetic neuropathies(2020)17 cited
- → Clinical spectrum of BICD2 mutations(2020)15 cited
- → A study of the phenotypic variability and disease progression in Laing myopathy through the evaluation of muscle imaging(2020)15 cited
- → Charcot–Marie–Tooth disease due to MORC2 mutations in Spain(2021)12 cited
- → Pediatric inherited peripheral neuropathy: a prospective study at a Spanish referral center(2021)12 cited
- → A novel TRMT5 mutation causes a complex inherited neuropathy syndrome: The role of nerve pathology in defining a demyelinating neuropathy(2022)11 cited
- → A very mild phenotype of Charcot-Marie-Tooth disease type 4H caused by two novel mutations in FGD4(2019)10 cited