Alessandra Tessa
University of North Carolina at Chapel Hill(US)Fondazione Stella Maris(IT)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Mitochondrial Function and Pathology, Genetic Neurodegenerative Diseases, Neurological diseases and metabolism, Neurogenetic and Muscular Disorders Research
Most-Cited Works
- → Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum(2007)331 cited
- → Congenital muscular dystrophies with defective glycosylation of dystroglycan(2009)192 cited
- → Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene(2003)110 cited
- → POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes(2007)96 cited
- → The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndrome(2001)93 cited
- → The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study(2020)84 cited