CNR Institutional Research Information System

GALLO, OLIVIER

GALLO, OLIVIER  

Istituto per la Ricerca e l'Innovazione Biomedica - IRIB - Sede Secondaria Cosenza  

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Titolo Data di pubblicazione Autore(i) File
Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies 1-gen-2024 Citrigno, Luigi; Qualtieri, Antonio; Cerantonio, Annamaria; De Benedittis, Selene; Gallo, Olivier; Di Palma, Gemma; Spadafora, Patrizia; Cavalcanti, Francesca
Molecular Study of the Fukutin-Related Protein (FKRP) Gene in Patients from Southern Italy with Duchenne/Becker-like Phenotype 1-gen-2024 Qualtieri, Antonio; De Benedittis, Selene; Cerantonio, Annamaria; Citrigno, Luigi; Di Palma, Gemma; Gallo, Olivier; Cavalcanti, Francesca; Spadafora, Patrizia
Sex and APOE genotype modulate neuropsychological profile and depression in temporal lobe epilepsy 1-gen-2024 Bruno, Francesco; Spadafora, Patrizia; Veltri, Ida; Cuconati, Mario L.; Condino, Francesca; Cerantonio, Annamaria; De Benedittis, Selene; Greco, Beatrice M.; Di Palma, Gemma; Gallo, Olivier; Citrigno, Luigi; Qualtieri, Antonio; Cundari, Maurizio; Cavalcanti, Francesca
A new mutation detected by NGS in MT-ATP6 gene associated with MELAS and in silico 3D protein analysis 1-gen-2023 Cavalcanti, Francesca; Citrigno, Luigi; Spadafora, Patrizia; DE BENEDITTIS, Selene; Gallo, Olivier; DI PALMA, Gemma; Qualtieri, Antonio
HOMOZYGOUS R596G VARIANT IN TRIM32 GENE RELATED TO LGMD IN A NON-HUTTERITE PATIENT 1-gen-2023 Patrizia Spadafora; Luigi Citrigno; Selene De Benedittis; Antonio Qualtieri; Francesca Cavalcanti; Gemma Di Palma; Olivier Gallo; Nelide Romeo
MALDI-ISD mass spectrometry analysis as a simple and reliable tool to detect post-translational modifications of hemoglobin variants: the case of Hb Raleigh 1-gen-2023 DE BENEDITTIS, Selene; Spadafora, Patrizia; Gaspari, Marco; I, Gabriele Qualtier; Gallo, Olivier; DI PALMA, Gemma; Cavalcanti, Francesca; Citrigno, Luigi; Qualtieri, Antonio
A novel homozygous variant in DYSF gene is associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B 1-gen-2022 Spadafora, Patrizia; Qualtieri, Antonio; Cavalcanti, Francesca; DI PALMA, Gemma; Gallo, Olivier; DE BENEDITTIS, Selene; Cerantonio, Annamaria; Citrigno, Luigi
Italian folk plant-based remedies to heal headache (XIX-XX century) 1-gen-2018 Mazzei, R; De Marco, E V; Gallo, O; Tagarelli, G
From Disease to Holiness: Religious-based health remedies of Italian folk medicine (XIX-XX century) 1-gen-2015 Nelide Romeo; Olivier Gallo; Giuseppe Tagarelli
Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case 1-gen-2014 Mazzei, Rosalucia; Valentini, Sergio; Conforti, FRANCESCA LUISA; Muglia, Maria; Gallo, Olivier; Cerasa, Antonio; Patitucci, Alessandra; Magariello, Angela; Perrotta, Paolo; Lanza, PIER LUIGI
Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case 1-gen-2014 Rosalucia Mazzei; Sergio Valentini; Francesca Luisa Conforti; Maria Muglia; Olivier Gallo; Antonio Cerasa; Alessandra Patitucci; Angela Magariello; Paolo Perrotta; Pier Luigi Lanza
Accuracy of magnetic resonance parkinsonism index for differentiation of progressive supranuclear palsy from probable or possible Parkinson disease. 1-gen-2011 Morelli M; Arabia G; Salsone M; Novellino F; Giofrè L; Paletta R; Messina D; Nicoletti G; Condino F; Gallo O; Lanza P; Quattrone A.
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man 1-gen-2011 La Russa, Antonella; Cittadella, Rita; Andreoli, Virginia; Valentino, Paola; Trecroci, Francesca; Caracciolo, Manuela; Gallo, Olivier; Gambardella, Antonio; Quattrone, Aldo
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man. 1-gen-2011 La Russa, A; Cittadella, R; Andreoli, V; Valentino, P; Trecroci, F; Caracciolo, M; Gallo, O; Gambardella, A; Quattrone, A
An magnetic resonance imaging T2*-weighted sequence at short echo time to detect putaminal hypointensity in Parkinsonisms. 1-gen-2010 Arabia, G; Morelli, M; Paglionico, S; Novellino, F; Salsone, M; Giofrè, L; Torchia, G; Nicoletti, G; Messina, D; Condino, F; Lanza, P; Gallo, O; Quattrone, A
Cognitive deficits in multiple sclerosis patients with cerebellar symptoms. 1-gen-2009 Valentino, P; Cerasa, A; Chiriaco, C; Nisticò, R; Pirritano, D; Gioia, M; Lanza, P; Canino, M; Del Giudice, F; Gallo, O; Condino, F; Torchia, G; Quattrone, A
MR imaging index for differentiation of progressive supranuclear palsy from Parkinson disease and the Parkinson variant of multiple system atrophy. 1-gen-2008 Quattrone, A; Nicoletti, G; Messina, D; Fera, F; Condino, F; Pugliese, P; Lanza, P; Barone, P; Morgante, L; Zappia, M; Aguglia, U; Gallo, O
Dopaminergic modulation of cognitive interference after pharmacological washout in Parkinson's disease 1-gen-2007 Fera, F; Nicoletti, G; Cerasa, A; Romeo, N; Gallo, O; Gioia, Mc; Arabia, G; Pugliese, P; Zappia, M; Quattrone, A
Monoamine oxidase-a genetic variations influence brain activity associated with inhibitory control: new insight into the neural correlates of impulsivity 1-gen-2006 Passamonti, L; Fera, F; Magariello, A; Cerasa, A; Gioia, Mc; Muglia, M; Nicoletti, G; Gallo, O; Provinciali, L; Quattrone, A
MR imaging of middle cerebellar peduncle width: differentiation of multiple system atrophy from Parkinson disease. 1-gen-2006 Nicoletti, G; Fera, F; Condino, F; Auteri, W; Gallo, O; Pugliese, P; Arabia, G; Morgante, L; Barone, P; Zappia, M; Quattrone, A