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Neurobiology of Aging|September 19, 2020
The role of RHOT1 and RHOT2 genetic variation on Parkinson disease risk and onsetMaría Teresa Periñán, Pilar Gómez-Garre, Cornelis Blauwendraat, et al.
Epilepsia|May 3, 2006
MRI volumetry and proton MR spectroscopy of the brain in Lafora diseaseVicente Villanueva, Juan Alvarez-Linera, Pilar Gómez-Garre, et al.
Epilepsia|July 28, 2010
Familial partial epilepsy with variable foci: a new family with suggestion of linkage to chromosome 22q12José Morales-Corraliza, Pilar Gómez-Garre, Raúl Sanz, et al.
Epilepsia|September 29, 2007
Autosomal dominant nocturnal frontal lobe epilepsy with a mutation in the CHRNB2 geneFernando Díaz-Otero, Mar Quesada, José Morales-Corraliza, et al.
Epilepsy Research|December 4, 2003
Characterization of a 6p21 translocation breakpoint in a family with idiopathic generalized epilepsyLaura Sáez-Hernández, Belén Peral, Raúl Sanz, et al.
European Neurology|September 6, 2012
PSMC1 Gene in Parkinson's DiseasePilar Gómez-Garre, Silvia Jesús, Fátima Carrillo, et al.
Parkinsonism & Related Disorders|January 22, 2019
Increased bilirubin levels in Parkinson's diseaseDaniel Macías-García, Carlota Méndez-Del Barrio, Silvia Jesús, et al.
NPJ Parkinson'S Disease|November 13, 2022
Transcriptomic analysis reveals an association of FCGBP with Parkinson's diseasePilar Gómez-Garre, María Teresa Periñán, Silvia Jesús, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 22, 2015
Low serum uric acid levels in progressive supranuclear palsyJuan Manuel Oropesa-Ruiz, Ismael Huertas-Fernández, Silvia Jesús, et al.
Neuroscience Letters|August 21, 2019
A replication study of GWAS-genetic risk variants associated with Parkinson's disease in a Spanish populationCristina Tejera-Parrado, Silvia Jesús, María Teresa Periñán, et al.
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