Showing results (21-30 of 58) with videos related to

Sort By:
Pageof 6
Neurobiology of Disease|February 14, 2021
Mitochondria and calcium defects correlate with axonal dysfunction in GDAP1-related Charcot-Marie-Tooth mouse modelAzahara Civera-Tregón, Laura Domínguez, Paula Martínez-Valero, et al.
Medicina Clinica|February 3, 2007
[COMT Val158Met polymorphism and schizophrenia in a series of Spanish patients]Justo Díez-Martín, Janet Hoenicka, Isabel Martínez, et al.
Neurotoxicity Research|April 24, 2007
Association in alcoholic patients between psychopathic traits and the additive effect of allelic forms of the CNR1 and FAAH endocannabinoid genes, and the 3' region of the DRD2 geneJanet Hoenicka, Guillermo Ponce, Miguel A Jiménez-Arriero, et al.
Autism Research : Official Journal of the International Society for Autism Research|March 22, 2021
PLXNA2 and LRRC40 as candidate genes in autism spectrum disorderJordi Pijuan, Juan Darío Ortigoza-Escobar, Juan Ortiz, et al.
Research Square|January 13, 2025
Abnormal redox balance at membrane contact sites causes axonopathy in GDAP1-related Charcot-Marie-Tooth diseaseLara Cantarero, Mònica Roldán, María Rodríguez-Sanz, et al.
Scientific Reports|May 11, 2021
Regulatory rare variants of the dopaminergic gene ANKK1 as potential risk factors for Parkinson's diseaseEstela Pérez-Santamarina, Pedro García-Ruiz, Dolores Martínez-Rubio, et al.
Archives of Neurology|September 15, 2005
A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsyRaquel Ros, Stéphane Thobois, Nathalie Streichenberger, et al.
Frontiers in Molecular Biosciences|May 28, 2021
Decoding Neuromuscular Disorders Using Phenotypic Clusters Obtained From Co-Occurrence NetworksElena Díaz-Santiago, M Gonzalo Claros, Raquel Yahyaoui, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Steele-Richardson-Olszewski syndrome in a patient with a single C212Y mutation in the parkin proteinBlas Morales, Armando Martínez, Isabel Gonzalo, et al.
Archives of Neurology|June 12, 2002
Molecular findings in familial Parkinson disease in SpainJanet Hoenicka, Lídice Vidal, Blas Morales, et al.
Pageof 6