Ariadna Padró-Miquel

10PUBLICATIONS
42CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Molecular targetsEpigenetics (incl. genome methylation and epigenomics)Haematology
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Publications (10)

|Dec 01, 2025
SYNE1 Deficiency Manifesting Primarily With Motor Neuron Disease.

Henriette V F Senghor, Raúl Domínguez Rubio, Carla Marco

|Sep 09, 2025
Personalised genomic strategies improve diagnostic yield in inherited retinal dystrophies: a stepwise, patient-centred approach.

Anna Esteve-Garcia, Ariadna Padró-Miquel, Jaume Català-Mora

|Feb 24, 2024
Intermediate Repeat Expansion in the ATXN2 Gene as a Risk Factor in the ALS and FTD Spanish Population.

Daniel Borrego-Hernández, Juan Francisco Vázquez-Costa, Raúl Domínguez-Rubio

|Mar 29, 2023
Improving Hereditary Hemorrhagic Telangiectasia Molecular Diagnosis: A Referral Center Experience.

Cinthia Aguilera, Ariadna Padró-Miquel, Anna Esteve-Garcia

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