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American Journal of Human Genetics|February 11, 1999
Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophyM Seri, R Cusano, P Forabosco, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
Epidemiology of multiple system atrophy. ESGAP Consortium. European Study Group on Atypical ParkinsonismsN Vanacore, V Bonifati, G Fabbrini, et al.
Neurology|September 24, 2011
Mild cognitive impairment in drug-naive patients with PD is associated with cerebral hypometabolismSabina Pappatà, G Santangelo, D Aarsland, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2000
Accuracy of clinical diagnostic criteria for Friedreich's ataxiaA Filla, G De Michele, G Coppola, et al.
European Journal of Gastroenterology & Hepatology|June 1, 1996
Epidemiology of cholelithiasis in southern Italy. Part II: Risk factorsG Misciagna, C Leoci, V Guerra, et al.
European Journal of Neurology|April 5, 2013
Insulin-like growth factor-1 predicts cognitive functions at 2-year follow-up in early, drug-naïve Parkinson's diseaseM T Pellecchia, G Santangelo, M Picillo, et al.
European Journal of Neurology|May 23, 2014
Relationship between apathy and cognitive dysfunctions in de novo untreated Parkinson's disease: a prospective longitudinal studyG Santangelo, C Vitale, L Trojano, et al.
Journal of Medical Genetics|January 31, 2006
The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populationsM Sharma, J C Mueller, A Zimprich, et al.
Neurology|April 26, 2006
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic studyC Criscuolo, L Chessa, S Di Giandomenico, et al.
American Journal of Human Genetics|June 23, 1998
Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseJ Tassin, A Dürr, T de Broucker, et al.
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