Naïma Bouslam
Centre Hospitalier Ibn Sina(MA)Hôpital Ibn Sina-Rabat(MA)
Publications by Year
Research Areas
Neurological diseases and metabolism, Hereditary Neurological Disorders, Genetic Neurodegenerative Diseases, Parkinson's Disease Mechanisms and Treatments, Mitochondrial Function and Pathology
Most-Cited Works
- → Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders(2014)537 cited
- → Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2(2004)518 cited
- → Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum(2007)331 cited
- → Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia(2012)197 cited
- → Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia(2016)114 cited
- → Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p(2003)94 cited
- → Mutation in the Catalytic Domain of Protein Kinase C γ and Extension of the Phenotype Associated With Spinocerebellar Ataxia Type 14(2004)92 cited
- → New mutations in protein kinase Cγ associated with spinocerebellar ataxia type 14(2005)88 cited
- → KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction(2013)82 cited
- → Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)(2005)69 cited