Olga Carmona

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

Sandy Hsu, Renee Sears, Roberta R. Lemos et al. · Neurogenetics · 2013 · 147 citations · Full text

Life Sciences, Genetics, Neurology +10

A randomized clinical trial of oral versus intravenous methylprednisolone for relapse of MS

Cristina Ramo‐Tello, Laia Grau‐López, Mar Tintoré et al. · Multiple Sclerosis Journal · 2013 · 75 citations

Pharmacy, Neurology, Pharmacotherapy +15

Economic burden of multiple sclerosis in a population with low physical disability

José Manuel García‐Domínguez, Jorge Mauriño, María Luisa Martínez‐Ginés et al. · BMC Public Health · 2019 · 59 citations · Full text

Pharmacy, Neurology, Cost-effectiveness Analysis +14

Regression to the mean in multiple sclerosis

Sergio Martínez‐Yélamos, Antonio Martı́nez-Yélamos, G Martín Ozaeta et al. · Multiple Sclerosis Journal · 2006 · 54 citations

Life Sciences, Neurology, Clinical Epidemiology +7

Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient

Montse Olivé, Laura González, Olga Carmona et al. · Neuromuscular Disorders · 2008 · 53 citations

Life Sciences, Genetics, Molecular Genetics +7