Fondazione Pierfranco e Luisa Mariani

Recent papers from Fondazione Pierfranco e Luisa Mariani

1. Sex and gender difference in cognitive and behavioral studies in developmental age: An introductionJournal of Neuroscience Research · 2021
2. Mucuna pruriens for Parkinson's disease: Low-cost preparation method, laboratory measures and pharmacokinetics profileJournal of the Neurological Sciences · 2016
3. From the model of El Sistema in Venezuela to current applications: learning and integration through collective music educationAnnals of the New York Academy of Sciences · 2012
4. Idebenone Treatment In Leber's Hereditary Optic NeuropathyBrain · 2011
5. Idebenone treatment in Leber's hereditary optic neuropathy2011
6. Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromesBrain · 2010
7. Sym1, the yeast ortholog of the MPV17 human disease protein, is a stress-induced bioenergetic and morphogenetic mitochondrial modulatorHuman Molecular Genetics · 2009
8. Paroxysmal non-kinesigenic dyskinesia is caused by mutations of the MR-1 mitochondrial targeting sequenceHuman Molecular Genetics · 2009
9. Influence of basal ganglia on upper limb locomotor synergies. Evidence from deep brain stimulation and L-DOPA treatment in Parkinson's diseaseBrain · 2008
10. Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout miceHuman Molecular Genetics · 2008
11. Train, train, train! No pain, just gainBrain · 2008
12. Nonsense mutation in pseudouridylate synthase 1 (PUS1) in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia (MLASA)Journal of Medical Genetics · 2006
13. ETHE1 mutations are specific to ethylmalonic encephalopathyJournal of Medical Genetics · 2005
14. Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase- ABrain · 2005