M.J. Sobrido

A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism

Patricia Blanco, Anja P. Einholm, Hafsa Mamsa et al. · Human Molecular Genetics · 2009 · 65 citations · Full text

SCA8 repeat expansions in ataxia: A controversial association

M.J. Sobrido, Jeremy A. Cholfin, Susan Perlman et al. · Neurology · 2001 · 57 citations

Neurodegenerative Diseases, Allelic Variant, Alzheimer's Disease +14

Possible association of the <i>tau</i> H1/H1 genotype with primary progressive aphasia

M.J. Sobrido, Amir Abu‐Khalil, Nancy Johnson et al. · Neurology · 2003 · 44 citations

Automated semantic annotation of rare disease cases: a case study

M. Taboada, Herb Rodriguez, D. Martínez et al. · Database · 2014 · 41 citations · Full text

Analysis of Candidate Genes at the IBGC1 Locus Associated with Idiopathic Basal Ganglia Calcification (“Fahr” Disease’)

João Ricardo Mendes de Oliveira, M.J. Sobrido, Elizabeth Spiteri et al. · Journal of Molecular Neuroscience · 2007 · 27 citations · Full text

Candidate Genes, Neurobiology Of Disease, Ibgc1 Locus Associated +8