Soreya Belarbi

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration

Giovanni Stévanin, Hamid Azzedine, Paola S. Denora et al. · Brain · 2007 · 246 citations

IFN-γ and TNF-α Are Involved During Alzheimer Disease Progression and Correlate with Nitric Oxide Production: A Study in Algerian Patients

Mourad Belkhelfa, Hayet Rafa, Oussama Medjeber et al. · Journal of Interferon & Cytokine Research · 2014 · 122 citations

Nitric Oxide, Immune Regulation, Immunology +31

LRRK2 G2019S mutation in Parkinson’s disease: A neuropsychological and neuropsychiatric study in a large Algerian cohort

Soreya Belarbi, Nassima Hecham, Suzanne Lesage et al. · Parkinsonism & Related Disorders · 2010 · 92 citations

Neurodegenerative Diseases, Psychiatry, Parkinson Disease +8

Is the common <i>LRRK2</i> G2019S mutation related to dyskinesias in North African Parkinson disease?

Suzanne Lesage, Soreya Belarbi, André R. Troiano et al. · Neurology · 2008 · 50 citations

Corticobasal Degeneration, Genetics, Genetic Epidemiology +22

Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa

Suzanne Lesage, Christel Condroyer, Nassima Hecham et al. · Neurology · 2011 · 42 citations · Full text

Genetics, Genetic Epidemiology, Disease Gene Identification +23