Lidia Gonzalez-Quereda

10PUBLICATIONS
42CO-AUTHORS
Predictive and prognostic markersCell and nuclear divisionNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Epidemiological modelling
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Publications (10)

|Jun 26, 2026
Exploring Dystrophin Expression and Mutations in the DMD and Dystrophin-Glycoprotein Complex Genes as Prognostic Factors in Leiomyosarcomas.

|Jul 22, 2025
Repeat Expansions in PLIN4 Cause Autosomal Dominant Vacuolar Myopathy With Sarcolemmal Features.

Laura Llansó, Igor Stevanovski, Germán Morís

|Jun 18, 2025
Adult-onset distal myopathy with predominant hand involvement as a rare phenotype of plectinopathy.

Laura Llansó, David Reyes-Leiva, Alba Segarra-Casas

|Jan 01, 2025
A founder variant in the RYR1 gene is associated with hyperCKemia, myalgia and muscle cramps.

Alba Segarra-Casas, Pablo Iruzubieta, Solange Kapetanovic

|Jul 28, 2022
Dystrophinopathy Phenotypes and Modifying Factors in DMD Exon 45-55 Deletion.

Javier Poyatos-García, Pilar Martí, Alessandro Liquori

|Feb 11, 2021
Special Issue "Genetic Advances in Neuromuscular Disorders: From Gene Identification to Gene Therapy".

Virginia Arechavala-Gomeza, Lidia Gonzalez-Quereda

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Frequent Collaborators

3 joint publications

Alba Segarra-Casas

2 joint publications

Pia Gallano

2 joint publications

Pau Riera

2 joint publications

Juliana Salazar