Diagnosis of Charcot-Marie-Tooth Disease

por Banchs, Isabel, Casasnovas, Carlos, Albertí, Antonia, De Jorge, Laura, Povedano, Mónica, Montero, Jordi, Martínez-Matos, Juan Antonio, Volpini, Victor
Publicado 2009

Allelic and genotypic associations of DRD2 TaqI A polymorphism with heroin dependence in Spanish subjects: a case control study

por Perez de los Cobos, Jose, Baiget, Montserrat, Trujols, Joan, Sinol, Nuria, Volpini, Victor, Banuls, Enrique, Calafell, Francesc, Luquero, Elena, del Rio, Elisabeth, Alvarez, Enric
Publicado 2007

Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia

por Sintas, Cèlia, Carreño, Oriel, Fernàndez-Castillo, Noèlia, Corominas, Roser, Vila-Pueyo, Marta, Toma, Claudio, Cuenca-León, Ester, Barroeta, Isabel, Roig, Carles, Volpini, Víctor, Macaya, Alfons, Cormand, Bru
Publicado 2017

A clinical report of the massive CAG repeat expansion in spinocerebellar ataxia type 2: Severe onset in a Mexican child and review previous cases

por Sánchez-Corona, José, Ramirez-Garcia, Sergio Alberto, Castañeda-Cisneros, Gema, Gutiérrez-Rubio, Susan Andrea, Volpini, Víctor, Sánchez-Garcia, Diana M., García-Ortiz, José Elías, García-Cruz, Diana
Publicado 2020

New spinocerebellar ataxia subtype caused by SAMD9L mutation triggering mitochondrial dysregulation (SCA49)

por Corral-Juan, Marc, Casquero, Pilar, Giraldo-Restrepo, Natalia, Laurie, Steve, Martinez-Piñeiro, Alicia, Mateo-Montero, Raidili Cristina, Ispierto, Lourdes, Vilas, Dolores, Tolosa, Eduardo, Volpini, Victor, Alvarez-Ramo, Ramiro, Sánchez, Ivelisse, Matilla-Dueñas, Antoni
Publicado 2022