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1. Bonifati, V; De Michele, G; Lucking, CB; Durr, A; Fabrizio, E; Ambrosio, G; Vanacore, N; De Mari, M; Marconi, R; Capus, L; Breteler, MMB; Gasser, T; Oostra, B; Wood, N; Agid, Y; Filla, A; Meco, G; Brice, A
   The parkin gene and its phenotype
   NEUROLOGICAL SCIENCES
   
   V. Bonifati et al., "The parkin gene and its phenotype", NEUROL SCI, 22(1), 2001, pp. 51-52
2. Vanacore, N; Bonifati, V; Fabbrini, G; Colosimo, C; De Michele, G; Marconi, R; Nicholl, D; Locuratolo, N; Talarico, G; Romano, S; Stocchi, F; Bonuccelli, U; De Mari, M; Vieregge, P; Meco, G
   Epidemiology of multiple system atrophy
   NEUROLOGICAL SCIENCES
   
   N. Vanacore et al., "Epidemiology of multiple system atrophy", NEUROL SCI, 22(1), 2001, pp. 97-99
3. Vanacore, N; Bonifati, V; Colosimo, C; Fabbrini, G; De Michele, G; Marconi, R; Nicholl, D; Locuratolo, N; Romano, S; Talarico, G; Stocchi, F; Bonuccelli, U; Lamberti, P; Vieregge, P; Meco, G
   Epidemiology of progressive supranuclear palsy
   NEUROLOGICAL SCIENCES
   
   N. Vanacore et al., "Epidemiology of progressive supranuclear palsy", NEUROL SCI, 22(1), 2001, pp. 101-103
4. Gasparini, M; Bonifati, V; Fabrizio, E; Fabbrini, G; Brusa, L; Lenzi, GL; Meco, G
   Frontal lobe dysfunction in essential tremor - A preliminary study
   JOURNAL OF NEUROLOGY
   
   M. Gasparini et al., "Frontal lobe dysfunction in essential tremor - A preliminary study", J NEUROL, 248(5), 2001, pp. 399-402
5. Lucking, CB; Bonifati, V; Periquet, M; Vanacore, N; Brice, A; Meco, G
   Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations
   NEUROLOGY
   
   C.B. Lucking et al., "Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations", NEUROLOGY, 57(5), 2001, pp. 924-927
6. Casali, C; Bonifati, V; Santorelli, FM; Casari, G; Fortini, D; Patrignani, A; Fabbrini, G; Carrozzo, R; D'Amati, G; Locuratolo, N; Vanacore, N; Damiano, M; Pierallini, A; Pierelli, F; Amabile, GA; Meco, G
   Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a sephardic Jewish family
   NEUROLOGY
   
   C. Casali et al., "Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a sephardic Jewish family", NEUROLOGY, 56(6), 2001, pp. 802-805
7. Bonifati, V; Lucking, CB; Fabrizio, E; Periquet, M; Meco, G; Brice, A
   Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism
   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
   
   V. Bonifati et al., "Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism", J NE NE PSY, 71(4), 2001, pp. 531-534
8. Periquet, M; Lucking, CB; Vaughan, JR; Bonifati, V; Durr, A; De Michele, G; Horstink, MW; Farrer, M; Illarioshkin, SN; Pollak, P; Borg, M; Brefel-Courbon, C; Denefle, P; Meco, G; Gasser, T; Breteler, MMB; Wood, NW; Agid, Y; Brice, A
   Origin of the mutations in the parkin gene in europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects
   AMERICAN JOURNAL OF HUMAN GENETICS
   
   M. Periquet et al., "Origin of the mutations in the parkin gene in europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects", AM J HU GEN, 68(3), 2001, pp. 617-626
9. Colosimo, C; Vanacore, N; Bonifati, V; Fabbrini, G; Rum, A; De Michele, G; De Mari, M; Bonuccelli, U; Nicholl, DJ; Meco, G
   Clinical diagnosis of multiple system atrophy: level of agreement between Quinn's criteria and the consensus conference guidelines
   ACTA NEUROLOGICA SCANDINAVICA
   
   C. Colosimo et al., "Clinical diagnosis of multiple system atrophy: level of agreement between Quinn's criteria and the consensus conference guidelines", ACT NEUR SC, 103(4), 2001, pp. 261-264
10. Fabbrini, G; Barbanti, P; Bonifati, V; Colosimo, C; Gasparini, M; Vanacore, N; Meco, G
    Donepezil in the treatment of progressive supranuclear palsy
    ACTA NEUROLOGICA SCANDINAVICA
    
    G. Fabbrini et al., "Donepezil in the treatment of progressive supranuclear palsy", ACT NEUR SC, 103(2), 2001, pp. 123-125
11. Meco, G; Vanacore, N; Locuratolo, N; Bonifati, V; Vella, C; Giovani, A; Tubani, L; Baratta, L; Mastrocola, C
    Heart rate variability in Parkinson's disease patients treated with tolcapone
    PARKINSONISM & RELATED DISORDERS
    
    G. Meco et al., "Heart rate variability in Parkinson's disease patients treated with tolcapone", PARKINS R D, 6(4), 2000, pp. 223-227
12. Lucking, CB; Durr, A; Bonifati, V; Vaughan, J; De Michele, G; Gasser, T; Harhangi, BS; Meco, G; Denefle, P; Wood, NW; Agid, Y; Brice, A
    Association between early-onset Parkinson's disease and mutations in the parkin gene
    NEW ENGLAND JOURNAL OF MEDICINE
    
    C.B. Lucking et al., "Association between early-onset Parkinson's disease and mutations in the parkin gene", N ENG J MED, 342(21), 2000, pp. 1560-1567
13. Vanacore, N; Bonifati, V; Fabbrini, G; Colosimo, C; Marconi, R; Nicholl, D; Bonuccelli, U; Stocchi, F; Lamberti, P; Volpe, G; De Michele, G; Iavarone, I; Bennett, P; Vieregge, P; Meco, G
    Smoking habits in multiple system atrophy and progressive supranuclear palsy
    NEUROLOGY
    
    N. Vanacore et al., "Smoking habits in multiple system atrophy and progressive supranuclear palsy", NEUROLOGY, 54(1), 2000, pp. 114-119
14. Abbas, N; Lucking, CB; Ricard, S; Durr, A; Bonifati, V; De Michele, G; Bouley, S; Vaughan, JR; Gasser, T; Marconi, R; Broussolle, E; Brefel-Courbon, C; Harhangi, BS; Oostra, AB; Fabrizio, E; Bohme, GA; Pradier, L; Wood, NW; Filla, A; Meco, G; Denefle, P; Agid, Y; Brice, A
    A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe
    HUMAN MOLECULAR GENETICS
    
    N. Abbas et al., "A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe", HUM MOL GEN, 8(4), 1999, pp. 567-574
15. Bonifati, V; Joosse, M; Nicholl, DJ; Vanacore, N; Bennett, P; Rizzu, P; Fabbrini, G; Marconi, R; Colosimo, C; Locuratolo, N; Stocchi, F; Bonuccelli, U; De Mari, M; Wenning, G; Vieregge, P; Oostra, B; Meco, G; Heutink, P
    The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronicvariant of the disease-associated H1 haplotype in Italian cases
    NEUROSCIENCE LETTERS
    
    V. Bonifati et al., "The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronicvariant of the disease-associated H1 haplotype in Italian cases", NEUROSCI L, 274(1), 1999, pp. 61-65
16. Harhangi, BS; Farrer, MJ; Lincoln, S; Bonifati, V; Meco, G; De Michele, G; Brice, A; Durr, A; Martinez, M; Gasser, T; Bereznai, B; Vaughan, JR; Wood, NW; Hardy, J; Oostra, BA; Breteler, MMB
    The lle93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease
    NEUROSCIENCE LETTERS
    
    B.S. Harhangi et al., "The lle93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease", NEUROSCI L, 270(1), 1999, pp. 1-4
17. Bonifati, V; Meco, G
    New, selective catechol-O-methyltransferase inhibitors as therapeutic agents in Parkinson's disease
    PHARMACOLOGY & THERAPEUTICS
    
    V. Bonifati e G. Meco, "New, selective catechol-O-methyltransferase inhibitors as therapeutic agents in Parkinson's disease", PHARM THERA, 81(1), 1999, pp. 1-36
18. Nicholl, DJ; Bennett, P; Hiller, L; Bonifati, V; Vanacore, N; Fabbrini, G; Marconi, R; Colosimo, C; Lamberti, P; Stocchi, F; Bonuccelli, U; Vieregge, P; Ramsden, DB; Meco, G; Williams, AC
    A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders
    NEUROLOGY
    
    D.J. Nicholl et al., "A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders", NEUROLOGY, 53(7), 1999, pp. 1415-1421
19. GASSER T; MULLERMYHSOK B; WSZOLEK ZK; OEHLMANN R; CALNE DB; BONIFATI V; BEREZNAI B; FABRIZIO E; VIEREGGE P; HORSTMANN RD
    A SUSCEPTIBILITY LOCUS FOR PARKINSONS-DISEASE MAPS TO CHROMOSOME 2P13
    Nature genetics
    
    T. Gasser et al., "A SUSCEPTIBILITY LOCUS FOR PARKINSONS-DISEASE MAPS TO CHROMOSOME 2P13", Nature genetics, 18(3), 1998, pp. 262-265
20. VAUGHAN JR; FARRER MJ; WSZOLEK ZK; GASSER T; DURR A; AGID Y; BONIFATI V; DEMICHELE G; VOLPE G; LINCOLN S; BRETELER M; MECO G; BRICE A; MARSDEN CD; HARDY J; WOOD NW
    SEQUENCING OF THE ALPHA-SYNUCLEIN GENE IN A LARGE SERIES OF CASES OF FAMILIAL PARKINSONS-DISEASE FAILS TO REVEAL ANY FURTHER MUTATIONS
    Human molecular genetics
    
    J.R. Vaughan et al., "SEQUENCING OF THE ALPHA-SYNUCLEIN GENE IN A LARGE SERIES OF CASES OF FAMILIAL PARKINSONS-DISEASE FAILS TO REVEAL ANY FURTHER MUTATIONS", Human molecular genetics, 7(4), 1998, pp. 751-753
21. VAUGHAN J; DURR A; TASSIN J; BEREZNAI B; GASSER T; BONIFATI V; DEMICHELE G; FABRIZIO E; VOLPE G; BANDMANN O; JOHNSON WG; GOLBE LI; BRETELER M; MECO G; AGID Y; BRICE A; MARSDEN CD; WOOD NW
    THE ALPHA-SYNUCLEIN ALA53THR MUTATION IS NOT A COMMON-CAUSE OF FAMILIAL PARKINSONS-DISEASE - A STUDY OF 230 EUROPEAN CASES
    Annals of neurology
    
    J. Vaughan et al., "THE ALPHA-SYNUCLEIN ALA53THR MUTATION IS NOT A COMMON-CAUSE OF FAMILIAL PARKINSONS-DISEASE - A STUDY OF 230 EUROPEAN CASES", Annals of neurology, 44(2), 1998, pp. 270-273
22. LUCKING CB; ABBAS N; DURR A; BONIFATI V; BONNET AM; DEBROUCKER T; DEMICHELE G; WOOD NW; AGID Y; BRICE A
    HOMOZYGOUS DELETIONS IN PARKIN GENE IN EUROPEAN AND NORTH-AFRICAN FAMILIES WITH AUTOSOMAL RECESSIVE JUVENILE PARKINSONISM
    Lancet
    
    C.B. Lucking et al., "HOMOZYGOUS DELETIONS IN PARKIN GENE IN EUROPEAN AND NORTH-AFRICAN FAMILIES WITH AUTOSOMAL RECESSIVE JUVENILE PARKINSONISM", Lancet, 352(9137), 1998, pp. 1355-1356
23. BENNETT P; BONIFATI V; BONUCCELLI U; COLOSIMO C; DEMARI M; FABBRINI G; MARCONI R; MECO G; NICHOLL DJ; STOCCHI F; VANACORE N; VIEREGGE P; WILLIAMS AC
    DIRECT GENETIC-EVIDENCE FOR INVOLVEMENT OF TAU IN PROGRESSIVE SUPRANUCLEAR PALSY
    Neurology
    
    P. Bennett et al., "DIRECT GENETIC-EVIDENCE FOR INVOLVEMENT OF TAU IN PROGRESSIVE SUPRANUCLEAR PALSY", Neurology, 51(4), 1998, pp. 982-985
24. MECO G; FABRIZIO E; ALESSANDRI A; VANACORE N; BONIFATI V
    RISPERIDONE IN LEVODOPA-INDUCED DYSKINESIAE
    Journal of Neurology, Neurosurgery and Psychiatry
    
    G. Meco et al., "RISPERIDONE IN LEVODOPA-INDUCED DYSKINESIAE", Journal of Neurology, Neurosurgery and Psychiatry, 64(1), 1998, pp. 135-135
25. FABBRINI G; VANACORE N; BONIFATI V; COLOSIMO C; MECO G
    PRESYMPTOMATIC HYPERTENSION IN PROGRESSIVE SUPRANUCLEAR PALSY
    Archives of neurology
    
    G. Fabbrini et al., "PRESYMPTOMATIC HYPERTENSION IN PROGRESSIVE SUPRANUCLEAR PALSY", Archives of neurology, 55(8), 1998, pp. 1153-1154
26. TASSIN J; DURR A; DEBROUCKER T; ABBAS N; BONIFATI V; DEMICHELE G; BONNET AM; BROUSSOLLE E; POLLAK P; VIDAILHET M; DEMARI M; MARCONI R; MEDJBEUR S; FILLA A; MECO G; AGID Y; BRICE A
    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
    American journal of human genetics
    
    J. Tassin et al., "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", American journal of human genetics, 63(1), 1998, pp. 88-94
27. MECO G; ALESSANDRI A; GIUSTINI P; BONIFATI V
    RISPERIDONE IN LEVODOPA-INDUCED PSYCHOSIS IN ADVANCED PARKINSONS-DISEASE - AN OPEN-LABEL, LONG-TERM STUDY
    Movement disorders
    
    G. Meco et al., "RISPERIDONE IN LEVODOPA-INDUCED PSYCHOSIS IN ADVANCED PARKINSONS-DISEASE - AN OPEN-LABEL, LONG-TERM STUDY", Movement disorders, 12(4), 1997, pp. 610-612
28. GASPARINI M; FABRIZIO E; BONIFATI V; MECO G
    COGNITIVE IMPROVEMENT DURING TOLCAPONE TREATMENT IN PARKINSONS-DISEASE
    Journal of neural transmission
    
    M. Gasparini et al., "COGNITIVE IMPROVEMENT DURING TOLCAPONE TREATMENT IN PARKINSONS-DISEASE", Journal of neural transmission, 104(8-9), 1997, pp. 887-894
29. GASSER T; MULLERMYHSOK B; WSZOLEK ZK; DURR A; VAUGHAN JR; BONIFATI V; MECO G; BEREZNAI B; OEHLMANN R; AGID Y; BRICE A; WOOD N
    GENETIC COMPLEXITY AND PARKINSONS-DISEASE
    Science
    
    T. Gasser et al., "GENETIC COMPLEXITY AND PARKINSONS-DISEASE", Science, 277(5324), 1997, pp. 388-389
30. BONIFATI V
    FAMILIAL PARKINSONS-DISEASE - A CLINICAL GENETIC-ANALYSIS (VOL 22, PG272, 1995)
    Canadian journal of neurological sciences
    
    V. Bonifati, "FAMILIAL PARKINSONS-DISEASE - A CLINICAL GENETIC-ANALYSIS (VOL 22, PG272, 1995)", Canadian journal of neurological sciences, 23(2), 1996, pp. 158-158
31. BONIFATI V
    FAMILIAL PARKINSONS-DISEASE - A CLINICAL GENETIC-ANALYSIS (VOL 23, PG90, 1996)
    Canadian journal of neurological sciences
    
    V. Bonifati, "FAMILIAL PARKINSONS-DISEASE - A CLINICAL GENETIC-ANALYSIS (VOL 23, PG90, 1996)", Canadian journal of neurological sciences, 23(2), 1996, pp. 158-158
32. BONIFATI V
    FAMILIAL PARKINSONS-DISEASE - A CLINICAL GENETIC-ANALYSIS (VOL 22, PG272, 1995)
    Canadian journal of neurological sciences
    
    V. Bonifati, "FAMILIAL PARKINSONS-DISEASE - A CLINICAL GENETIC-ANALYSIS (VOL 22, PG272, 1995)", Canadian journal of neurological sciences, 23(1), 1996, pp. 90-90
33. GASSER T; MULLERMYHSOK B; SUPALA A; ZIMMER E; WIEDITZ G; WSZOLEK ZK; VIEREGGE P; BONIFATI V; OERTEL WH
    THE CYP2D6B ALLELE IS NOT OVERREPRESENTED IN A POPULATION OF GERMAN PATIENTS WITH IDIOPATHIC PARKINSONS-DISEASE
    Journal of Neurology, Neurosurgery and Psychiatry
    
    T. Gasser et al., "THE CYP2D6B ALLELE IS NOT OVERREPRESENTED IN A POPULATION OF GERMAN PATIENTS WITH IDIOPATHIC PARKINSONS-DISEASE", Journal of Neurology, Neurosurgery and Psychiatry, 61(5), 1996, pp. 518-520
34. MECO G; BONIFATI V; ALESSANDRI A; BRUSA L
    RISPERIDONE IN HUNTINGTONS-DISEASE
    Human psychopharmacology
    
    G. Meco et al., "RISPERIDONE IN HUNTINGTONS-DISEASE", Human psychopharmacology, 10(4), 1995, pp. 353-354
35. BONIFATI V; FABRIZIO E; VANACORE N; DEMARI M; MECO G
    FAMILIAL PARKINSONS-DISEASE - A CLINICAL GENETIC-ANALYSIS
    Canadian journal of neurological sciences
    
    V. Bonifati et al., "FAMILIAL PARKINSONS-DISEASE - A CLINICAL GENETIC-ANALYSIS", Canadian journal of neurological sciences, 22(4), 1995, pp. 272-279
36. MENNITIIPPOLITO F; SPILAALEGIANI S; VANACORE N; BONIFATI V; DIANI G; MECO G; RASCHETTI R
    ESTIMATE OF PARKINSONISM PREVALENCE THROUGH DRUG PRESCRIPTION HISTORIES IN THE PROVINCE OF ROME, ITALY
    Acta neurologica Scandinavica
    
    F. Mennitiippolito et al., "ESTIMATE OF PARKINSONISM PREVALENCE THROUGH DRUG PRESCRIPTION HISTORIES IN THE PROVINCE OF ROME, ITALY", Acta neurologica Scandinavica, 92(1), 1995, pp. 49-54
37. MECO G; BONIFATI V; FABRIZIO E; VANACORE N
    WORSENING OF PARKINSONISM WITH FLUVOXAMINE - 2 CASES
    Human psychopharmacology
    
    G. Meco et al., "WORSENING OF PARKINSONISM WITH FLUVOXAMINE - 2 CASES", Human psychopharmacology, 9(6), 1994, pp. 439-441
38. BONIFATI V; FABRIZIO E; CIPRIANI R; VANACORE N; MECO G
    BUSPIRONE IN LEVODOPA-INDUCED DYSKINESIAS
    Clinical neuropharmacology
    
    V. Bonifati et al., "BUSPIRONE IN LEVODOPA-INDUCED DYSKINESIAS", Clinical neuropharmacology, 17(1), 1994, pp. 73-82
39. MECO G; BONIFATI V; VANACORE N; FABRIZIO E
    PARKINSONISM AFTER CHRONIC EXPOSURE TO THE FUNGICIDE MANEB (MANGANESEETHYLENE-BIS-DITHIOCARBAMATE)
    Scandinavian journal of work, environment & health
    
    G. Meco et al., "PARKINSONISM AFTER CHRONIC EXPOSURE TO THE FUNGICIDE MANEB (MANGANESEETHYLENE-BIS-DITHIOCARBAMATE)", Scandinavian journal of work, environment & health, 20(4), 1994, pp. 301-305
40. MECO G; VANACORE N; BONIFATI V
    THE MORTALITY-RATES FOR MULTIPLE-SCLEROSIS IN ITALY (1969-1987)
    Neuroepidemiology
    
    G. Meco et al., "THE MORTALITY-RATES FOR MULTIPLE-SCLEROSIS IN ITALY (1969-1987)", Neuroepidemiology, 13(4), 1994, pp. 162-174
41. MECO G; ALESSANDRIA A; BONIFATI V; GIUSTINI P
    RISPERIDONE FOR HALLUCINATIONS IN LEVODOPA-TREATED PARKINSONS-DISEASEPATIENTS
    Lancet
    
    G. Meco et al., "RISPERIDONE FOR HALLUCINATIONS IN LEVODOPA-TREATED PARKINSONS-DISEASEPATIENTS", Lancet, 343(8909), 1994, pp. 1370-1371
42. BONIFATI V; VANACORE N; MECO G
    ANTICIPATION OF ONSET AGE IN FAMILIAL PARKINSONS-DISEASE
    Neurology
    
    V. Bonifati et al., "ANTICIPATION OF ONSET AGE IN FAMILIAL PARKINSONS-DISEASE", Neurology, 44(10), 1994, pp. 1978-1979