Alfonsina Ballester-Lopez

ORCID

Publication Activity (10 Years)

Years Active: 2018-2020
Publications (10 Years): 5

Top Venues

Human mutation

Genes

Neurology. Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Alfonsina Ballester-Lopez, Judit Núñez-Manchón, Emma Koehorst, Ian Linares-Pardo, Miriam Almendrote, Giuseppe Lucente, Nicolau Guanyabens, Marta Lopez-Osias, Adrián Suárez-Mesa, Shaliza Ann Hanick, Jakub Chojnacki, Alejandro Lucia, Guillem Pintos-Morell, Jaume Coll-Cantí, Alicia Martínez-Piñeiro, Alba Ramos-Fransi, Gisela Nogales-Gadea
Three-dimensional imaging in myotonic dystrophy type 1: Linking molecular alterations with disease phenotype. Neurology. Genetics 6 (4) (2020)
Alfonsina Ballester-Lopez, Ian Linares-Pardo, Emma Koehorst, Judit Núñez-Manchón, Guillem Pintos-Morell, Jaume Coll-Cantí, Miriam Almendrote, Giuseppe Lucente, Andrea Arbex, Jonathan Javier Magaña, Nadia M Murillo-Melo, Alejandro Lucia, Darren G Monckton, Sarah A Cumming, Alba Ramos-Fransi, Alicia Martínez-Piñeiro, Gisela Nogales-Gadea
The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1. Genes 11 (7) (2020)
Alfonsina Ballester-Lopez, Emma Koehorst, Ian Linares-Pardo, Judit Núñez-Manchón, Miriam Almendrote, Giuseppe Lucente, Andrea Arbex, Carles Puente, Alejandro Lucia, Darren G Monckton, Sarah A Cumming, Guillem Pintos-Morell, Jaume Coll-Cantí, Alba Ramos-Fransi, Alicia Martínez-Piñeiro, Gisela Nogales-Gadea
Preliminary Findings on CTG Expansion Determination in Different Tissues from Patients with Myotonic Dystrophy Type 1. Genes 11 (11) (2020)
Alfonsina Ballester-Lopez, Emma Koehorst, Miriam Almendrote, Alicia Martínez-Piñeiro, Giuseppe Lucente, Ian Linares-Pardo, Judit Núñez-Manchón, Nicolau Guanyabens, Antoni Cano, Alejandro Lucia, Gayle Overend, Sarah A Cumming, Darren G Monckton, Teresa Casadevall, Irina Isern, Josep Sánchez-Ojanguren, Albert Planas, Agustín Rodriguez-Palmero, Laura Monlleó-Neila, Guillem Pintos-Morell, Alba Ramos-Fransi, Jaume Coll-Cantí, Gisela Nogales-Gadea
A DM1 family with interruptions associated with atypical symptoms and late onset but not with a milder phenotype. Human mutation 41 (2) (2019)
Inés García-Consuegra, Sara Asensio-Peña, Alfonsina Ballester-Lopez, Rosario Francisco-Velilla, Tomás Pinos, Guillem Pintos-Morell, Jaume Coll-Cantí, Adrián González-Quintana, Antoni L Andreu, Joaquín Arenas, Alejandro Lucia, Gisela Nogales-Gadea, Miguel A Martín
Missense mutations have unexpected consequences: The McArdle disease paradigm. Human mutation 39 (10) (2018)

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Publication Activity (10 Years)

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Alfonsina Ballester-Lopez