Paola S. Denora
Centre National de la Recherche Scientifique(FR)Inserm(FR)École Pratique des Hautes Études(FR)Sorbonne Université(FR)Pitié-Salpêtrière Hospital(FR)Bambino Gesù Children's Hospital(IT)Institut du Cerveau(FR)Istituti di Ricovero e Cura a Carattere Scientifico(IT)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Neurological diseases and metabolism, Genetic Neurodegenerative Diseases, Neurogenetic and Muscular Disorders Research, Genomics and Rare Diseases
Most-Cited Works
- → Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum(2007)331 cited
- → Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration(2007)250 cited
- → Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome(2008)213 cited
- → SPG11 spastic paraplegia(2009)97 cited
- → Cellular distribution and subcellular localization of spatacsin and spastizin, two proteins involved in hereditary spastic paraplegia(2011)83 cited
- → Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions(2016)65 cited