Maria Helena Ribeiro

Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP

Rita Guerreiro, Miquel Baquero, Rafael Blesa et al. · Neurobiology of Aging · 2008 · 218 citations · Full text

Portuguese family with the co-occurrence of frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis phenotypes due to progranulin gene mutation

Maria Rosário Almeida, Carmo Macário, Lina Ramos et al. · Neurobiology of Aging · 2016 · 123 citations

Frontotemporal Lobar Degeneration, Developmental Biology, Portuguese Family +8

Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal

José Brás, Coro Paisán‐Ruíz, Rita Guerreiro et al. · Neurobiology of Aging · 2007 · 116 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Parkinson Disease Patients +10

G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort

José Brás, Rita Guerreiro, Maria Helena Ribeiro et al. · Movement Disorders · 2005 · 99 citations · Full text

Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort

Rita Guerreiro, José Brás, Isabel Santana et al. · BMC Neurology · 2006 · 90 citations · Full text