Alfonsina Lopez-Ballester
Madrid, MD 28029, Spain
Last Updated: 09/26/2026
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Found 14 publications
Characterization of RAN Translation and Antisense Transcription in Primary Cell Cultures of Patients with Myotonic Dystrophy Type 1.
Journal: Journal of clinical medicine
Published: October 30, 2021
The Biomarker Potential of miRNAs in Myotonic Dystrophy Type I.
Journal: Journal of clinical medicine
Published: October 21, 2020
The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1.
Journal: Genes
Published: May 27, 2020
Three-dimensional imaging in myotonic dystrophy type 1: Linking molecular alterations with disease phenotype.
Journal: Neurology. Genetics
Published: February 21, 2020
Correction to: Manifesting heterozygotes in McArdle disease: a myth or a reality-role of statins.
Journal: Journal of inherited metabolic disease
Published: July 22, 2018
Missense mutations have unexpected consequences: The McArdle disease paradigm.
Journal: Human mutation
Published: May 03, 2018
A novel mutation in the valosin-containing-protein gene found in a Spanish family.
Journal: Journal of the neurological sciences
Published: April 27, 2018
Manifesting heterozygotes in McArdle disease: a myth or a reality-role of statins.
Journal: Journal of inherited metabolic disease
Published: January 31, 2018
Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 update.
Journal: BMC genomics
Published: November 17, 2017
Myotilinopathy unmasked by statin treatment: A case report.
Journal: Muscle & nerve
Published: March 07, 2017
Last Updated: 09/26/2026