Alessandra Tessa

Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

Giovanni Stévanin, Filippo M. Santorelli, Hamid Azzedine et al. · Nature Genetics · 2007 · 331 citations

Biology, Neuroanatomy, Genetics +8

Congenital muscular dystrophies with defective glycosylation of dystroglycan

Eugenio Mercuri, Sonia Messina, Claudio Bruno et al. · Neurology · 2009 · 185 citations

Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene

Gabriele Siciliano, Alessandra Tessa, Stefania Petrini et al. · Neuromuscular Disorders · 2003 · 109 citations

Bipolar Affective Disorder, Ant1 Gene, Genetic Disorder +8

POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes

Roberta Biancheri, Antonio Falace, Alessandra Tessa et al. · Biochemical and Biophysical Research Communications · 2007 · 96 citations

Rare Diseases, Mendelian Disorder, Genetic Disorder +9

The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndrome

Rosalba Carrozzo, Alessandra Tessa, Marta Elisa Vázquez-Memije et al. · Neurology · 2001 · 93 citations

Genetics, Novel Mtdna Mutation, Molecular Biology +17