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Journal of Neurology|October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluationM Sciacco, A Prelle, G P Comi, et al.European Journal of Neurology|May 27, 2010
EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disordersJ-M Burgunder, L Schöls, J Baets, et al.Transplantation Proceedings|March 23, 2010
Role of adenosine on intestinal ischemia-reperfusion injury in rabbitsM O Taha, R Miranda-Ferreira, R S Simões, et al.European Journal of Neurology|January 7, 2010
EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegiasT Gasser, J Finsterer, J Baets, et al.European Journal of Neurology|December 2, 2009
EFNS guidelines on the molecular diagnosis of mitochondrial disordersJ Finsterer, H F Harbo, J Baets, et al.Rare Tumors|April 29, 2015
Giant cells glioblastoma: case report and pathological analysis from this uncommon subtype of gliomaTelmo A B Belsuzarri, João F M Araujo, Aguinaldo P Catanoce, et al.Nature Genetics|June 30, 2001
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondriaJ N Spelbrink, F Y Li, V Tiranti, et al.Journal of Neurology|August 18, 2022
Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohortV Montano, P Lopriore, F Gruosso, et al.Cell Transplantation|October 5, 2007
Autologous transplantation of muscle-derived CD133+ stem cells in Duchenne muscle patientsY Torrente, M Belicchi, C Marchesi, et al.European Journal of Human Genetics : EJHG|October 31, 2002
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosisC Dobson-Stone, A Danek, L Rampoldi, et al.Pageof 18