ARIDON, Paolo
ARIDON, Paolo
Biomedicina, Neuroscienze e Diagnostica avanzata
A Brief Overview on BDNF-Trk Pathway in the Nervous System: A Potential Biomarker or Possible Target in Treatment of Multiple Sclerosis?
2022-07-12 Schiro G.; Iacono S.; Ragonese P.; Aridon P.; Salemi G.; Balistreri C.R.
A case control study to evaluate the relationship between cigarette smoking or coffee consumption and multiple sclerosis
2007-01-01 SALEMI G; CASTIGLIA G; RAGONESE P; BATTAGLIERI F; CUSIMANO V; ARIDON P; SAVETTIERI G
A CASE-CONTROL STUDY ON THE ASSOCIATION BETWEEN DIABETES AND PD
2007-01-01 D'AMELIO M; P RAGONESE; G CALLARI; B PALMERI; N DI BENEDETTO; P ARIDON; V TERRUSO; G SALEMI; G SAVETTIERI
A Door-to-Door population based survey on cognitive performance In Bagheria, Sicily.
2008-01-01 Ragonese P; Aridon P; D'amelio M; Mazzola M; Terruso V; Salemi G; Savettieri G
A population-based survey of cognitive performance in a Sicilian elderly community.
2011-01-01 Ragonese, P; Aridon, P; D'Amelio, M; Aiello, F; Mazzola, MA; Realmuto, S; Salemi, G; Savettieri, G
A population-based survey on cognitive performance in Sicily. Cognitive impairment is modified by fertile life characteristics.
2009-01-01 Ragonese, P; Aridon, P; D’Amelio, M; Mazzola, MA; Salemi, G; Savettieri, G
A SPG4 GENE MUTATION CAUSES AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA IN AN ITALIAN FAMILY
2006-01-01 P ARIDON; P RAGONESE; M DE FUSCO; D LO COCO; G SALEMI; G CASARI; SAVETTIERI G
A TRAPPC6B splicing variant associates to restless legs syndrome
2016-01-01 Aridon, P.; De Fusco, M.; Winkelmann, J.; Zucconi, M.; Arnao, V.; Ferini-Strambi, L.; Casari, G.
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population
2003-01-01 Liguori, M.; Sawcer, S.; Setakis, E.; Compston, A.; Giordano, M.; D'Alfonso, S.; Mellai, M.; Malferrari, G.; Trojano, M.; Livrea, P.; De Robertis, F.; Massacesi, L.; Repice, A.; Ballerini, C.; Biagioli, T.; Bomprezzi, R.; Cannoni, S.; Ristori, G.; Salvetti, M.; Grimaldi, L.; Biunno, I.; Comi, G.; Leone, M.; Ferro, I.; Naldi, P.; Milanese, C.; Gellera, C.; Loredana, L.; Savettieri, G.; Salemi, G.; Aridon, P.; Caputo, D.; Guerini, F.; Ferrante, P.; Momigliano-Richiardi, P.
Accuracy of death certificates for motor neuron disease and multiple sclerosis in the province of Palermo in southern Italy
2002-01-01 Ragonese, P.; Salemi, G.; Aridon, P.; Conte, S.; Cuccia, G.; Lupo, I.; Savettieri, G.
Acute onset parkinsonism during leukoencephalopathy and CMV infection
2012-01-01 Mazzola , MA; Arnao,V; Aridon,P; D'Amelio,M; Ragonese,P; Savettieri,G.
Alpha2-I279N human nicotinic acetylcholine receptor, linked to a form of nocturnal epilepsy, presents higher sensitivity to agonists.
2006-01-01 DI RESTA C; TAIANA M; ARIDON P; CASARI G; BECCHETTI A
AN UNESPECTED ASSOCIATION BETWEEN INTRACRANIAL HYPOTENSION AND SPLIT CORD MALFORMATION
2007-01-01 CALLARI G; D'AMELIO M; BENCIVINNI F; ARIDON P; GRASSO G; RAGONESE P; SAVETTIERI G
An unexpected association between intracranial hypotension and split cord malformation
2007-01-01 CALLARI G; D'AMELIO M; BENCIVINNI F; ARIDON P; GRASSO G; RAGONESE P; SAVETTIERI G
AN UNUSUAL ASSOCIATION OF MYASTHENIA GRAVIS (MG) AND PANCREATIC NEUROENDOCRINE TUMOR (PNET): A CASE REPORT
2014-01-01 RIOLO, M; ALESSI, S; CINTURINO, A; D’AMELIO, M; RAGONESE, P; ARIDON, P; SAVETTIERI G.
Answer to: The possible risk of cancer in multiple sclerosis patients: A controversial issue.
2011-01-01 Ragonese P, Aridon P, Salemi G, D’Amelio M, Savettieri G
Aspetti clinici e genetici della RLS familiare
2005-01-01 ARIDON P
Association between multiple sclerosis, cancer risk, and immunosuppressant treatment: A cohort study
2017-01-01 Ragonese, Paolo*; Aridon, Paolo; Vazzoler, Giulia; Mazzola, Maria Antonietta; Lo Re, Vincenzina; Lo Re, Marianna; Realmuto, Sabrina; Alessi, Simona; D'Amelio, Marco; Savettieri, Giovanni; Salemi, Giuseppe
ATP1A2 mutations in 11 families with familial hemiplegic migraine.
2005-01-01 RIANT F; DE FUSCO M; ARIDON P; DUCROS A; PLOTON C; MARCHELLI F; MACIAZEK J; BOUSSER MG; CASARI G; TOURNIER-LASSERVE E
Autosomal dominant hereditary spastic paraplegia: report of a large italian family with R581X spastin mutation.
2007-01-01 ARIDON P; RAGONESE P; DE FUSCO M; LO COCO D; SALEMI G; CASARI G; SAVETTIERI G