Laura Martí-Sánchez

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 4

Top Topics

Smoking Cessation

Deep Brain Stimulation

Top Venues

Movement disorders clinical practice

Science translational medicine

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

Publications

Laia Nou-Fontanet, Laura Martí-Sánchez, Loreto Martorell, Jesús Casas, Juan Dario Ortigoza-Escobar
Atypical Mowat-Wilson Syndrome: Dystonia, Choreoathetosis and Cognitive Features. Movement disorders clinical practice (2024)
Laia Nou-Fontanet, Laura Martí-Sánchez, Loreto Martorell, Jesús Casas, Juan Dario Ortigoza-Escobar
Atypical Mowat-Wilson Syndrome: Dystonia, Choreoathetosis and Cognitive Features. Movement disorders clinical practice 11 (7) (2024)
Laia Nou-Fontanet, Laura Martí-Sánchez, Loreto Martorell, Jesús Casas, Juan Dario Ortigoza-Escobar
Atypical Mowat-Wilson Syndrome: Dystonia, Choreoathetosis and Cognitive Features. Movement disorders clinical practice 11 (7) (2024)
Sara Picó, Alberto Parras, María Santos-Galindo, Julia Pose-Utrilla, Margarita Castro, Enrique Fraga, Ivó H Hernández, Ainara Elorza, Héctor Anta, Nan Wang, Laura Martí-Sánchez, Eulàlia Belloc, Paula Garcia-Esparcia, Juan José Garrido, Isidro Ferrer, Daniel Macías-García, Pablo Mir, Rafael Artuch, Belén Pérez, Félix Hernández, Pilar Navarro, José Luis López-Sendon Moreno, Teresa Iglesias, X William Yang, Raúl Méndez, José J Lucas
CPEB alteration and aberrant transcriptome-polyadenylation lead to a treatable SLC19A3 deficiency in Huntington's disease. Science translational medicine 13 (613) (2021)