Search Results - "Gallo, Olivier"

Molecular Study of the Fukutin-Related Protein ( FKRP ) Gene in Patients from Southern Italy with Duchenne/Becker-like Phenotype by Qualtieri, Antonio, De Benedittis, Selene, Cerantonio, Annamaria, Citrigno, Luigi, Di Palma, Gemma, Gallo, Olivier, Cavalcanti, Francesca, Spadafora, Patrizia

“…Pathogenic variants localized in the gene coding for the Fukutin-Related Protein (FKRP) are responsible for Limb-Girdle Muscular Dystrophy type 9 (LGMDR9),…”
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MR imaging index for differentiation of progressive supranuclear palsy from Parkinson disease and the Parkinson variant of multiple system atrophy by Quattrone, Aldo, Nicoletti, Giuseppe, Messina, Demetrio, Fera, Francesco, Condino, Francesca, Pugliese, Pierfrancesco, Lanza, Pierluigi, Barone, Paolo, Morgante, Letterio, Zappia, Mario, Aguglia, Umberto, Gallo, Olivier

“…To prospectively assess sensitivity and specificity of magnetic resonance (MR) imaging measurements of midbrain, pons, middle cerebellar peduncles (MCPs), and…”
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A Novel Homozygous Variant in DYSF Gene Is Associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B by Spadafora, Patrizia, Qualtieri, Antonio, Cavalcanti, Francesca, Di Palma, Gemma, Gallo, Olivier, De Benedittis, Selene, Cerantonio, Annamaria, Citrigno, Luigi

“…Mutations in the DYSF gene, encoding dysferlin, are responsible for Limb Girdle Muscular Dystrophy type R2/2B (LGMDR2/2B), Miyoshi myopathy (MM), and Distal…”
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Accuracy of magnetic resonance parkinsonism index for differentiation of progressive supranuclear palsy from probable or possible Parkinson disease by Morelli, Maurizio, Arabia, Gennarina, Salsone, Maria, Novellino, Fabiana, Giofrè, Laura, Paletta, Rosina, Messina, Demetrio, Nicoletti, Giuseppe, Condino, Francesca, Gallo, Olivier, Lanza, Pierluigi, Quattrone, Aldo

“…Background: Combined measurements on conventional magnetic resonance imaging (MRI), such as midbrain area/pons area or magnetic resonance parkinsonism index…”
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An magnetic resonance imaging T2-weighted sequence at short echo time to detect putaminal hypointensity in Parkinsonisms by Arabia, Gennarina, Morelli, Maurizio, Paglionico, Sandra, Novellino, Fabiana, Salsone, Maria, Giofrè, Laura, Torchia, Giusi, Nicoletti, Giuseppe, Messina, Demetrio, Condino, Francesca, Lanza, Pierluigi, Gallo, Olivier, Quattrone, Aldo

“…At 1.5 T, T2*‐weighted gradient echo (GE) sequences are more sensitive in revealing mineral deposition in the basal ganglia than standard T2 weighted…”
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Dopaminergic modulation of cognitive interference after pharmacological washout in Parkinson's disease by Fera, Francesco, Nicoletti, Giuseppe, Cerasa, Antonio, Romeo, Nelide, Gallo, Olivier, Gioia, Maria C, Arabia, Gennarina, Pugliese, Pierfrancesco, Zappia, Mario, Quattrone, Aldo

“…Abstract The dopaminergic modulation of prefrontal function in Parkinson's disease (PD) has been consistently demonstrated. There is evidence that the effects…”
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Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies by Citrigno, Luigi, Qualtieri, Antonio, Cerantonio, Annamaria, De Benedittis, Selene, Gallo, Olivier, Di Palma, Gemma, Spadafora, Patrizia, Cavalcanti, Francesca

“…Mitochondrial DNA (mtDNA) is a 16,569 base pairs, double-stranded, circular molecule that contains 37 genes coding for 13 subunits of the respiratory chain…”
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A new CYS1678TYR mutation responsible of LGMD2B identified in a family from Southern Italy by Spadafora, Patrizia, Qualtieri, Antonio, Cavalcanti, Francesca, Lanza, Pierluigi, Gallo, Olivier, Di Palma, Gemma, Citrigno, Luigi

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Italian folk plant-based remedies to heal headache (XIX-XX century) by Mazzei, Rosalucia, De Marco, Elvira V., Gallo, Olivier, Tagarelli, Giuseppe

“…Headache has been recognized since antiquity. From the late nineteenth to the early to mid-twentieth century, Italian folk remedies to treat headache were…”
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From Disease to Holiness: Religious-based health remedies of Italian folk medicine (XIX-XX century) by Romeo, Nelide, Gallo, Olivier, Tagarelli, Giuseppe

“…The relationship between spirituality, religion and medicine has been recognized since antiquity. Despite large differences in their history, society, economy…”
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Genomic analysis identify a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease by Cerantonio, Annamaria, De Benedittis, Selene, Muglia, Maria, Spadafora, Patrizia, Cavalcanti, Francesca, Lanza, Pierluigi, Gallo, Olivier, Di Palma, Gemma, Romeo, Nelide, Bagalà, Angelo, Mazzei, Rosalucia, Propato, Flavia, Consoli, Domenico, Cerasa, Antonio, Qualtieri, Antonio, Citrigno, Luigi

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MR imaging of middle cerebellar peduncle width: differentiation of multiple system atrophy from Parkinson disease by Nicoletti, Giuseppe, Fera, Francesco, Condino, Francesca, Auteri, William, Gallo, Olivier, Pugliese, Pierfrancesco, Arabia, Gennarina, Morgante, Letterio, Barone, Paolo, Zappia, Mario, Quattrone, Aldo

“…To prospectively assess if middle cerebellar peduncle (MCP) atrophy, evaluated at magnetic resonance (MR) imaging, can help differentiate multiple system…”
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Monoamine Oxidase-A Genetic Variations Influence Brain Activity Associated with Inhibitory Control: New Insight into the Neural Correlates of Impulsivity by Passamonti, Luca, Fera, Francesco, Magariello, Angela, Cerasa, Antonio, Gioia, Maria Cecilia, Muglia, Maria, Nicoletti, Giuseppe, Gallo, Olivier, Provinciali, Leandro, Quattrone, Aldo

“…Previous evidence has shown that genetic variations in the serotonergic system contribute to individual differences in personality traits germane to impulse…”
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Leber’s hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man by La Russa, Antonella, Cittadella, Rita, Andreoli, Virginia, Valentino, Paola, Trecroci, Francesca, Caracciolo, Manuela, Gallo, Olivier, Gambardella, Antonio, Quattrone, Aldo

“…A 35-year-old young man displayed Leber’s optic neuropathy (LHON) due to T14484C and multiple sclerosis (MS) phenotype that was dominated by symptoms and signs…”
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Comparison of different MR venography techniques for detecting transverse sinus stenosis in idiopathic intracranial hypertension by FERA, Francesco, BONO, Francesco, MESSINA, Demetrio, GALLO, Olivier, LANZA, Pier Luigi, AUTERI, William, NICOLETTI, Giuseppe, SANTORO, Giuseppe, QUATTRONE, Aldo

“…Cerebral venous outflow abnormalities, as transverse sinuses (TSs) stenosis,may underlie a picture of idiopathic intracranial hypertension (IIH). To identify…”
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Clinical, genetic and magnetic resonance findings in an Italian patient affected by l-2-hydroxyglutaric aciduria by Mazzei, Rosalucia, Ungaro, Carmine, Garreffa, Girolamo, Conforti, Francesca Luisa, Mollo, Antonella, Sprovieri, Teresa, Servillo, Pasquale, Blasi, Vincenzo, Gallo, Olivier, Cerasa, Antonio, Lanza, Pier Luigi, Quattrone, Aldo

“…l -2-Hydroxyglutaric aciduria ( l -2-HGA) is a neurometabolic disease characterized by the presence of elevated levels of 2-hydroxyglutaric acid in the plasma,…”
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