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Vincenzo Bonifati

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Tianna Zhao; Ping-Pin Zheng; Renate K Hukema; Johan M Kros; Ben A Oostra; Lies-Anne Severijnen; Marcel van der Weiden; Rob Willemsen; Vincenzo Bonifati
FBXO7 Immunoreactivity in α-Synuclein-Containing Inclusions in Parkinson Disease and Multiple System Atrophy.
Alfredo Berardelli; D Berg; B R Bloem; Vincenzo Bonifati; D Brooks; D J Burn; Carlo Colosimo; A Fanciulli; J Ferreira; Thomas Gasser; F Grandas; Petr Kanovsky; V Kostic; J Kulisevsky; W Oertel; W Poewe; J-P Reese; M Relja; Evzen Ruzicka; A Schrag; K Seppi; P Taba; Angelo Antonini; G K Wenning; M Vidailhet
EFNS/MDS-ES recommendations for the diagnosis of Parkinson's disease.
Ekaterina Yonova-Doing; Masharip Atadzhanov; Guido J Breedveld; Paul Kelly; Sheila T S Musonda; Ben A Oostra; Marialuisa Quadri; Nyambura Shawa; Erik J Simons; Vincenzo Bonifati
Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease.

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2013: Tianna Zhao; Ping-Pin Zheng; Renate K Hukema; Johan M Kros; Ben A Oostra; Lies-Anne Severijnen; Marcel van der Weiden; Rob Willemsen; Vincenzo Bonifati
FBXO7 Immunoreactivity in α-Synuclein-Containing Inclusions in Parkinson Disease and Multiple System Atrophy.
Journal of neuropathology and experimental neurology 2013;72(6):482-8.
2013: Alfredo Berardelli; D Berg; B R Bloem; Vincenzo Bonifati; D Brooks; D J Burn; Carlo Colosimo; A Fanciulli; J Ferreira; Thomas Gasser; F Grandas; Petr Kanovsky; V Kostic; J Kulisevsky; W Oertel; W Poewe; J-P Reese; M Relja; Evzen Ruzicka; A Schrag; K Seppi; P Taba; Angelo Antonini; G K Wenning; M Vidailhet
EFNS/MDS-ES recommendations for the diagnosis of Parkinson's disease.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2013;20(1):16-34.
2012: Ekaterina Yonova-Doing; Masharip Atadzhanov; Guido J Breedveld; Paul Kelly; Sheila T S Musonda; Ben A Oostra; Marialuisa Quadri; Nyambura Shawa; Erik J Simons; Vincenzo Bonifati
Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease.
Parkinsonism & related disorders 2012;18(5):567-71.
2012: Marialuisa Quadri; Fabrizio Rasi; Antioco Sanna; Lies-Anne Severijnen; Bart P C van de Warrenburg; Rob Willemsen; Tianna Zhao; Carla Battisti; Guido J Breedveld; Giovanni Cossu; Cathérine Delnooz; Lara Di Toro Mammarella; Antonio Federico; Peng Lu; Andrea Mignarri; Lucia Monti; Ben A Oostra; Francesca Punzo; Vincenzo Bonifati
Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease.
American journal of human genetics 2012;90(3):467-77.
2012: Tianna Zhao; Herma Zondervan-van der Linde; Ben A Oostra; Lies-Anne Severijnen; Rob Willemsen; Vincenzo Bonifati
Dopaminergic neuronal loss and dopamine-dependent locomotor defects in Fbxo7-deficient zebrafish.
PloS one 2012;7(11):e48911.
2011: Peter Elfferich; Sylvia A Eshuis; Ad Hovestadt; Klaus L Leenders; Saskia A J Lesnik-Oberstein; Leonardo Lopiano; JA Maat-Kievit; Jan-Pieter M Stroy; Cristina Tassorelli; Bart P C van de Warrenburg; Klaartje van Engelen; Wilson F Abdo; Vincenzo Bonifati; Agnita J W Boon; Dennis Dooijes; John C van Swieten; Marja C Verleun-Mooijman; Corien C Verschuuren-Bemelmans; Jan C M Zijlmans; Rick van Minkelen
Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations.
Neurogenetics 2011;12(4):263-71.
2011: Marialuisa Quadri; Valeria Saddi; Erik J Simons; Anna Ticca; Giovanni Cossu; Maurizio Melis; Daniela Murgia; Ben A Oostra; Vincenzo Bonifati
Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson's disease in Sardinia.
Neurogenetics 2011;12(3):203-9.
2011: Chiara Criscuolo; Vincenzo Bonifati; Guido J Breedveld; Anna De Rosa; Alessandro Filla; Anna Guacci; Ben A Oostra; Silvio Peluso; Erik J Simons; Giampiero Volpe; Giuseppe De Michele
The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from southern Italy.
Movement disorders : official journal of the Movement Disorder Society 2011;26(9):1733-6.
2011: Hsin Fen Chien; Vincenzo Bonifati; Egberto R Barbosa
ATP13A2-related neurodegeneration (PARK9) without evidence of brain iron accumulation.
Movement disorders : official journal of the Movement Disorder Society 2011;26(7):1364-5.
2011: Lucio Santoro; Guido J Breedveld; Fiore Manganelli; Rosa Iodice; Chiara Pisciotta; Maria Nolano; Francesca Punzo; Mario Quarantelli; Sabina Pappatà; Alessio Di Fonzo; Ben A Oostra; Vincenzo Bonifati
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability.
Neurogenetics 2011;12(1):33-9.
2011: Tianna Zhao; Esther de Graaff; Guido J Breedveld; Agnese Loda; Lies-Anne Severijnen; Cokkie H Wouters; Frans W Verheijen; Marieke C J Dekker; Pasquale Montagna; Rob Willemsen; Ben A Oostra; Vincenzo Bonifati
Loss of nuclear activity of the FBXO7 protein in patients with parkinsonian-pyramidal syndrome (PARK15).
PloS one 2011;6(2):e16983.
2010: Laura Silveira-Moriyama; Renato Pupi Munhoz; Margarete de J Carvalho; Salmo Raskin; Ekaterina Rogaeva; Patricia de C Aguiar; Rodrigo A Bressan; Andre C Felicio; Orlando G P Barsottini; Luiz Augusto F Andrade; Hsin F Chien; Vincenzo Bonifati; Egberto R Barbosa; Helio A Teive; Andrew J Lees
Olfactory heterogeneity in LRRK2 related Parkinsonism.
Movement disorders : official journal of the Movement Disorder Society 2010;25(16):2879-83.
2010: Guido J Breedveld; Giovanni Fabbrini; Ben A Oostra; Alfredo Berardelli; Vincenzo Bonifati
Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindred.
Neurogenetics 2010;11(4):417-23.
2010: Antonetta M G Sas; Alessio Di Fonzo; Stef L M Bakker; Erik J Simons; Ben A Oostra; Anneke J Maat-Kievit; A J W Boon; Vincenzo Bonifati
Autosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS-5) in a Dutch kindred.
Movement disorders : official journal of the Movement Disorder Society 2010;25(11):1715-22.
2010: Vincenzo Bonifati
Shaking the genome: new studies reveal genetic risk for Parkinson's disease.
Lancet neurology 2010;9(2):136-8.
2009: Owen A Ross; Cleanthe Spanaki; Alida Griffith; Chin-Hsien Lin; Jennifer Kachergus; Kristoffer Haugarvoll; Helen Latsoudis; Andreas Plaitakis; Joaquim Ferreira; Cristina Sampaio; Vincenzo Bonifati; Ruey-Meei Wu; Cyrus Zabetian; Matthew J Farrer
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
Parkinsonism & related disorders 2009;15(6):466-7.
2009: Vincenzo Bonifati
Is GIGYF2 the defective gene at the PARK11 locus?
Current neurology and neuroscience reports 2009;9(3):185-7.
2009: A Di Fonzo; M C J Dekker; Pasquale Montagna; Agostino Baruzzi; E H Yonova; L Correia Guedes; A Szczerbinska; T Zhao; L O M Dubbel-Hulsman; C H Wouters; Esther de Graaff; W J G Oyen; Erik J Simons; Guido J Breedveld; Ben A Oostra; Martin Horstink; Vincenzo Bonifati
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome.
Neurology 2009;72(3):240-5.
2009: Jon Infante; José Berciano; Pascual Sánchez-Juan; Antonio García; Alessio Di Fonzo; Guido Breedveld; Ben Oostra; Vincenzo Bonifati
Pseudo-orthostatic and resting leg tremor in a large Spanish family with homozygous truncating parkin mutation.
Movement disorders : official journal of the Movement Disorder Society 2009;24(1):144-7.
2008: Massimo Pasquini; Giovanni Fabbrini; Isabella Berardelli; Vincenzo Bonifati; Massimo Biondi; Alfredo Berardelli
Psychopathological features of obsessive-compulsive disorder in an Italian family with Gilles de la Tourette syndrome not linked to the SLITRK1 gene.
Psychiatry research 2008;161(1):109-11.
2008: Chin-Song Lu; Yah-Huei Wu Chou; Marina van Doeselaar; Erik J Simons; Hsiu-Chen Chang; Guido J Breedveld; Alessio Di Fonzo; Rou-Shayn Chen; Yi-Hsin Weng; Szu-Chia Lai; Ben A Oostra; Vincenzo Bonifati
The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese population.
Neurogenetics 2008;9(4):271-6.
2008: Laura Silveira-Moriyama; L C Guedes; Ann E Kingsbury; H Ayling; K Shaw; E R Barbosa; Vincenzo Bonifati; Niall Quinn; Patrick M Abou-Sleiman; Nicholas W Wood; A Petrie; Cristina Sampaio; Joaquim Ferreira; J Holton; Tamas Revesz; Andrew J Lees
Hyposmia in G2019S LRRK2-related parkinsonism: clinical and pathologic data.
Neurology 2008;71(13):1021-6.
2008: Daniel G Healy; Mario Falchi; Sean S O'Sullivan; Vincenzo Bonifati; Alexandra Durr; Susan Bressman; Alexis Brice; Jan Aasly; Cyrus Zabetian; Stefano Goldwurm; Joaquim Ferreira; Eduardo Tolosa; Denise M Kay; Christine Klein; David R Williams; Connie Marras; Anthony E Lang; Zbigniew K Wszolek; Jose Berciano; Anthony H V Schapira; Timothy Lynch; Kailash P Bhatia; Thomas Gasser; Andrew J Lees; Nicholas W Wood
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.
Lancet neurology 2008;7(7):583-90.
2008: Vincenzo Bonifati; Y-H Wu-Chou; D Schweiger; A Di Fonzo; C-S Lu; B Oostra
Re: LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8.
Neurology 2008;70(24):2348; author reply 2348-9.
2008: Vincenzo Bonifati
Recent advances in the genetics of dementia with lewy bodies.
Current neurology and neuroscience reports 2008;8(3):187-9.
2008: K Haugarvoll; R Rademakers; Jennifer Kachergus; K Nuytemans; O A Ross; J M Gibson; E-K Tan; C Gaig; E Tolosa; S Goldwurm; M Guidi; Giulio Riboldazzi; L Brown; U Walter; R Benecke; Daniela Berg; T Gasser; J Theuns; P Pals; Patrick cras; P Paul De Deyn; S Engelborghs; B Pickut; Ryan Uitti; T Foroud; W C Nichols; J Hagenah; Christine Klein; Amir Samii; Cyrus Zabetian; Vincenzo Bonifati; Christine Van Broeckhoven; Matthew J Farrer; Zbigniew K Wszolek
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.
Neurology 2008;70(16 Pt 2):1456-60.
2008: Chin-Song Lu; Hsiu-Chen Chang; Yi-Hsin Weng; Rou-Shayn Chen; Vincenzo Bonifati; Yah-Huei Wu Chou
Analysis of the LRRK2 Gly2385Arg variant in primary dystonia and multiple system atrophy in Taiwan.
Parkinsonism & related disorders 2008;14(5):393-6.
2007: Giovanni Fabbrini; Massimo Pasquini; Cinzia Aurilia; Isabella Berardelli; Guido J Breedveld; Ben A Oostra; Vincenzo Bonifati; Alfredo Berardelli
A large Italian family with Gilles de la Tourette syndrome: clinical study and analysis of the SLITRK1 gene.
Movement disorders : official journal of the Movement Disorder Society 2007;22(15):2229-34.
2007: Vincenzo Bonifati
LRRK2 low-penetrance mutations (Gly2019Ser) and risk alleles (Gly2385Arg)-linking familial and sporadic Parkinson's disease.
Neurochemical research 2007;32(10):1700-8.
2007: Vincenzo Bonifati
Common neurodegenerative diseases: dissection by genome-wide association.
Current neurology and neuroscience reports 2007;7(5):425-7.
2007: Christine Klein; Vincenzo Bonifati
Dissecting the complexity of frontotemporal dementia: genotypes, phenotypes, and phenocopies.
Neurology 2007;69(2):129-30.
2007: Joaquim Ferreira; Leonor Correia Guedes; Mário Miguel Rosa; Miguel Coelho; Marina van Doeselaar; Dorothea Schweiger; Alessio Di Fonzo; Ben A Oostra; Cristina Sampaio; Vincenzo Bonifati
High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal.
Movement disorders : official journal of the Movement Disorder Society 2007;22(8):1194-201.
2007: Alessio Di Fonzo; Hsin F Chien; Mariana Peixoto Socal; Sabrina Giraudo; Cristina Tassorelli; G Iliceto; Giovanni Fabbrini; Roberto Marconi; E Fincati; Giovanni Abbruzzese; P Marini; Ferdinando Squitieri; Martin Horstink; Pasquale Montagna; A Dalla Libera; Fabrizio Stocchi; Stefano Goldwurm; Joaquim Ferreira; Giuseppe Meco; Emilia Martignoni; Leonardo Lopiano; Laura B Jardim; Ben A Oostra; Egberto R Barbosa; Vincenzo Bonifati
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease.
Neurology 2007;68(19):1557-62.
2007: Stefano Goldwurm; Michela Zini; Luigi Mariani; Silvana Tesei; Rosalba Miceli; Francesca Sironi; M Clementi; Vincenzo Bonifati; Gianni Pezzoli
Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease.
Neurology 2007;68(14):1141-3.
2007: Anne Grünewald; Guido J Breedveld; Katja Lohmann-Hedrich; Christan F Rohé; Inke R König; Johann Hagenah; Nicola Vanacore; Giuseppe Meco; Angelo Antonini; Stefano Goldwurm; Suzanne Lesage; Alexandra Dürr; Ferdinand Binkofski; Hartwig R Siebner; Alexander Münchau; Alexis Brice; Ben A Oostra; Christine Klein; Vincenzo Bonifati
Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis.
Neurogenetics 2007;8(2):103-9.
2007: Lawrence I Golbe; Giuseppe Di Iorio; Katerina Markopoulou; Aglaia Athanassiadou; Spiridon Papapetropoulos; Ray L Watts; Jeffery Vance; Vincenzo Bonifati; Tanishia A Williams; John R Spychala; Edward S Stenroos; William G Johnson
Glutathione S-transferase polymorphisms and onset age in alpha-synuclein A53T mutant Parkinson's disease.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(2):254-8.
2007: Giovanni Cossu; Marina van Doeselaar; Marcello Deriu; Maurizio Melis; Andrea Molari; Alessio Di Fonzo; Ben A Oostra; Vincenzo Bonifati
LRRK2 mutations and Parkinson's disease in Sardinia--A Mediterranean genetic isolate.
Parkinsonism & related disorders 2007;13(1):17-21.
2007: Eng-King Tan; Yi Zhao; Lisa Skipper; Michelle G K Tan; Alessio Di Fonzo; Li Sun; Stephanie Fook-Chong; S Tang; Eva Chua; Yih Yuen; Louis Tan ; Ratnagopal Pavanni; Meng-Cheong Wong; Prasanna Kolatkar; C S Lu; Vincenzo Bonifati; Jian-Jun Liu
The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence.
Human genetics 2007;120(6):857-63.
2007: Maria Teresa Giordana; Carla D'Agostino; Giovanni Albani; Alessandro Mauro; Alessio Di Fonzo; Angelo Antonini; Vincenzo Bonifati
Neuropathology of Parkinson's disease associated with the LRRK2 Ile1371Val mutation.
Movement disorders : official journal of the Movement Disorder Society 2007;22(2):275-8.
2007: Vincenzo Bonifati
Genetics of parkinsonism.
Parkinsonism & related disorders 2007;13 Suppl 3():S233-41.
2006: Vincenzo Bonifati
Parkinson's disease: the LRRK2-G2019S mutation: opening a novel era in Parkinson's disease genetics.
European journal of human genetics : EJHG 2006;14(10):1061-2.
2006: Stefano Goldwurm; Michela Zini; Alessio Di Fonzo; Danilo De Gaspari; Chiara Siri; Erik J Simons; Marina van Doeselaar; Silvana Tesei; Angelo Antonini; Margherita Canesi; Anna Zecchinelli; Claudio Mariani; Nicoletta Meucci; Giorgio Sacilotto; Roberto Cilia; Ioannis Isaias; A Bonetti; Francesca Sironi; Sara Ricca; Ben A Oostra; Vincenzo Bonifati; Gianni Pezzoli
LRRK2 G2019S mutation and Parkinson's disease: a clinical, neuropsychological and neuropsychiatric study in a large Italian sample.
Parkinsonism & related disorders 2006;12(7):410-9.
2006: Vincenzo Bonifati
The pleomorphic pathology of inherited Parkinson's disease: lessons from LRRK2.
Current neurology and neuroscience reports 2006;6(5):355-7.
2006: Ioannis Isaias; Riccardo Benti; Stefano Goldwurm; Michela Zini; Roberto Cilia; Paolo Gerundini; Alessio Di Fonzo; Vincenzo Bonifati; Gianni Pezzoli; Angelo Antonini
Striatal dopamine transporter binding in Parkinson's disease associated with the LRRK2 Gly2019Ser mutation.
Movement disorders : official journal of the Movement Disorder Society 2006;21(8):1144-7.
2006: Alessio Di Fonzo; Yah-Huei Wu Chou; Chin-Song Lu; Marina van Doeselaar; Erik J Simons; Christan F Rohé; Hsiu-Chen Chang; Rou-Shayn Chen; Yi-Hsin Weng; Nicola Vanacore; Guido J Breedveld; Ben A Oostra; Vincenzo Bonifati
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan.
Neurogenetics 2006;7(3):133-8.
2006: Manu Sharma; Jakob C Mueller; Alexander Zimprich; Peter Lichtner; Anne Hofer; Petra Leitner; Sylvia Maass; Daniela Berg; Alexandra Dürr; Vincenzo Bonifati; Giuseppe De Michele; B Oostra; Alexis Brice; Nicholas W Wood; Bertram Muller-Myhsok; Thomas Gasser
The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations.
Journal of medical genetics 2006;43(7):557-62.
2006: Aida M Bertoli Avella; Marieke C J Dekker; Yurii Aulchenko; Jeanine J Houwing-Duistermaat; Erik J Simons; Leon Testers; Luba M Pardo; Tessa Rademaker-Havinga; Pieter J L M Snijders; John C van Swieten; Vincenzo Bonifati; Peter Heutink; C.M. Duijn; Ben A Oostra
Evidence for novel loci for late-onset Parkinson's disease in a genetic isolate from the Netherlands.
Human genetics 2006;119(1-2):51-60.
2006: Alessio Di Fonzo; Cristina Tassorelli; Michele De Mari; Hsin F Chien; Joaquim Ferreira; Christan F Rohé; Giulio Riboldazzi; Angelo Antonini; Gianni Albani; Alessandro Mauro; Roberto Marconi; Giovanni Abbruzzese; Leonardo Lopiano; Emiliana Fincati; Marco Guidi; Paolo Marini; Fabrizio Stocchi; Marco Onofrj; Vincenzo Toni; Michele Tinazzi; Giovanni Fabbrini; Paolo Lamberti; Nicola Vanacore; Giuseppe Meco; Petra Leitner; Ryan Uitti; Zbigniew K Wszolek; Thomas Gasser; Erik J Simons; Guido J Breedveld; Stefano Goldwurm; Gianni Pezzoli; Cristina Sampaio; Egberto Barbosa; Emilia Martignoni; Ben A Oostra; Vincenzo Bonifati
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease.
European journal of human genetics : EJHG 2006;14(3):322-31.
2006: Hsin F Chien; Christan F Rohé; Maria D L Costa; Guido J Breedveld; Ben A Oostra; Egberto R Barbosa; Vincenzo Bonifati
Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern Brazil.
Neurogenetics 2006;7(1):13-9.
2005: Chin-Song Lu; Erik J Simons; Yah-Huei Wu Chou; Alessio Di Fonzo; Hsiu-Chen Chang; Rou-Shayn Chen; Yi-Hsin Weng; Christan F Rohé; Guido J Breedveld; Nobutaka Hattori; Thomas Gasser; Ben A Oostra; Vincenzo Bonifati
The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease.
Parkinsonism & related disorders 2005;11(8):521-2.
2005: Stefano Goldwurm; Alessio Di Fonzo; Erik J Simons; Christan F Rohé; Michela Zini; Margherita Canesi; Silvana Tesei; Anna Zecchinelli; Angelo Antonini; Claudio Mariani; Nicoletta Meucci; Giorgio Sacilotto; Francesca Sironi; Giuliana Salani; J Ferreira; H F Chien; Edito Fabrizio; N Vanacore; A Dalla Libera; Fabrizio Stocchi; Cosimo Diroma; P Lamberti; Cristina Sampaio; Giuseppe Meco; E Barbosa; Aida M Bertoli Avella; Guido J Breedveld; Ben A Oostra; Gianni Pezzoli; Vincenzo Bonifati
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor.
Journal of medical genetics 2005;42(11):e65.
2005: Vincenzo Bonifati
Progress in the genetics of progressive supranuclear palsy: tau gene and beyond.
Current neurology and neuroscience reports 2005;5(6):419-21.
2005: Vincenzo Bonifati; C F Rohé; G J Breedveld; E Fabrizio; M De Mari; C Tassorelli; A Tavella; R Marconi; D J Nicholl; H F Chien; E Fincati; G Abbruzzese; P Marini; A De Gaetano; Martin Horstink; anneke maat-kievit; Cristina Sampaio; Angelo Antonini; Fabrizio Stocchi; P Montagna; V Toni; M Guidi; A Dalla Libera; M Tinazzi; F De Pandis; G Fabbrini; S Goldwurm; A de Klein; E Barbosa; L Lopiano; E Martignoni; P Lamberti; N Vanacore; Giuseppe Meco; B A Oostra
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.
Neurology 2005;65(1):87-95.
2005: Maria Martinez; Alexis Brice; Jenny R Vaughan; Alexander Zimprich; Monique Breteler; Giuseppe Meco; Alessandro Filla; Matthew J Farrer; Christine Bétard; Andrew Singleton; John Hardy; Giuseppe De Michele; Vincenzo Bonifati; Ben A Oostra; Thomas Gasser; Nicholas W Wood; Alexandra Dürr
Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;136B(1):72-4.
2005: Vincenzo Bonifati
Genetics of Parkinson's disease.
Minerva medica 2005;96(3):175-86.
2005: Aida M Bertoli-Avella; José L Giroud-Benitez; Ali Akyol; Egberto Barbosa; Onno Schaap; Herma C van der Linde; Emilia Martignoni; Leonardo Lopiano; Paolo Lamberti; Emiliana Fincati; Angelo Antonini; Fabrizio Stocchi; Pasquale Montagna; Ferdinando Squitieri; Paolo Marini; Giovanni Abbruzzese; Giovanni Fabbrini; Roberto Marconi; Alessio Dalla Libera; Giorgio Trianni; Marco Guidi; Antonio De Gaetano; Gustavo Boff Maegawa; Antonino De Leo; Virgilio Gallai; Giulia de Rosa; Nicola Vanacore; Giuseppe Meco; C.M. Duijn; Ben A Oostra; Peter Heutink; Vincenzo Bonifati
Novel parkin mutations detected in patients with early-onset Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2005;20(4):424-31.
2005: Jürgen Prestel; Manu Sharma; Petra Leitner; Alexander Zimprich; Jenny R Vaughan; Alexandra Dürr; Vincenzo Bonifati; Giuseppe De Michele; Hasmet Hanagasi; Matthew J Farrer; Anne Hofer; Friedrich Asmus; Giampiero Volpe; Giuseppe Meco; Alexis Brice; Nicholas W Wood; Bertram Müller-Myhsok; Thomas Gasser
PARK11 is not linked with Parkinson's disease in European families.
European journal of human genetics : EJHG 2005;13(2):193-7.
2005: Nicola Vanacore; Vincenzo Bonifati; Giovanni Fabbrini; Carlo Colosimo; Giuseppe De Michele; Roberto Marconi; Fabrizio Stocchi; David Nicholl; Ubaldo Bonuccelli; Michele De Mari; Peter Vieregge; Giuseppe Meco
Case-control study of multiple system atrophy.
Movement disorders : official journal of the Movement Disorder Society 2005;20(2):158-63.
2005: William P Gilks; Patrick M Abou-Sleiman; Sonia Gandhi; Shushant Jain; Andrew Singleton; Andrew J Lees; Karen Shaw; Kailash P Bhatia; Vincenzo Bonifati; Niall Quinn; John Lynch; Daniel G Healy; Janice L Holton; Tamas Revesz; Nicholas W Wood
A common LRRK2 mutation in idiopathic Parkinson's disease.
Lancet 2005;365(9457):415-6.
2005: Alessio Di Fonzo; Christan F Rohé; Joaquim Ferreira; Hsin F Chien; Laura Vacca; Fabrizio Stocchi; Leonor Guedes; Edito Fabrizio; Mario Manfredi; Nicola Vanacore; Stefano Goldwurm; Guido J Breedveld; Cristina Sampaio; Giuseppe Meco; Egberto Barbosa; Ben A Oostra; Vincenzo Bonifati
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.
Lancet 2005;365(9457):412-5.
2004: Maria Martinez; Alexis Brice; Jenny R Vaughan; Alexander Zimprich; Monique Breteler; Giuseppe Meco; Alessandro Filla; Matthew J Farrer; Christine Bétard; John Hardy; Giuseppe De Michele; Vincenzo Bonifati; Ben A Oostra; Thomas Gasser; Nicholas W Wood; Alexandra Dürr
Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease.
Journal of medical genetics 2004;41(12):900-7.
2004: Yasuko Hatano; Kenichi Sato; B Elibol; Hiroyo Yoshino; Yasuhiro Yamamura; Vincenzo Bonifati; Hitoshi Shinotoh; Masato Asahina; S Kobayashi; A R Ng; R L Rosales; Sharon Hassin-Baer; Y Shinar; Chin-Song Lu; H C Chang; Yah-Huei Wu Chou; F Belgin Ataç; Tomonori Kobayashi; Tatsushi Toda; Yoshikuni Mizuno; Nobutaka Hattori
PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations.
Neurology 2004;63(8):1482-5.
2004: Christan F Rohé; Pasquale Montagna; Guido J Breedveld; Pietro Cortelli; Ben A Oostra; Vincenzo Bonifati
Homozygous PINK1 C-terminus mutation causing early-onset parkinsonism.
Annals of neurology 2004;56(3):427-31.
2004: Giovanni Abbruzzese; Simona Pigullo; Angelo Schenone; Emilia Bellone; Roberta Marchese; Emilio Di Maria; Luana Benedetti; Paola Ciotti; Lucilla Nobbio; Vincenzo Bonifati; Franco Ajmar; Paola Mandich
Does parkin play a role in the peripheral nervous system? A family report.
Movement disorders : official journal of the Movement Disorder Society 2004;19(8):978-81.
2004: Vincenzo Bonifati; Ben A Oostra; Peter Heutink
Unraveling the pathogenesis of Parkinson's disease--the contribution of monogenic forms.
Cellular and molecular life sciences : CMLS 2004;61(14):1729-50.
2004: Vincenzo Bonifati; Ben A Oostra; Peter Heutink
Linking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson's disease.
Journal of molecular medicine (Berlin, Germany) 2004;82(3):163-74.
2004: Katja Hedrich; Ana Djarmati; Nora Schäfer; Robert Hering; Claudia Wellenbrock; Peter H Weiss; Rüdiger Hilker; Peter Vieregge; Laurie J Ozelius; Peter Heutink; Vincenzo Bonifati; Eberhard Schwinger; Anthony E Lang; J Noth; Susan Bressman; Peter P Pramstaller; Olaf Riess; Christine Klein
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.
Neurology 2004;62(3):389-94.
2004: Patrizia Rizzu; David A Hinkle; Victoria Zhukareva; Vincenzo Bonifati; Lies-Anne Severijnen; Daniel Martinez; Rivka Ravid; Wouter Kamphorst; james eberwine; Virginia M-Y Lee; John Q Trojanowski; Peter Heutink
DJ-1 colocalizes with tau inclusions: a link between parkinsonism and dementia.
Annals of neurology 2004;55(1):113-8.
2003: Pablo Ibáñez; Giuseppe De Michele; Vincenzo Bonifati; Ebba Lohmann; Stéphane Thobois; Pierre Pollak; Yves Agid; Peter Heutink; Alexandra Dürr; Alexis Brice
Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism.
Neurology 2003;61(10):1429-31.
2003: Aida M Bertoli Avella; Jose L Giroud-Benitez; Vincenzo Bonifati; Eduardo Alvarez-Gonzalez; Luis Heredero-Baute; C.M. Duijn; Peter Heutink
Suggestive linkage to chromosome 19 in a large Cuban family with late-onset Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2003;18(11):1240-9.
2003: Maria G Macedo; Burcu Anar; Iraad F Bronner; Milena Cannella; Ferdinando Squitieri; Vincenzo Bonifati; André Hoogeveen; Peter Heutink; Patrizia Rizzu
The DJ-1L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexes.
Human molecular genetics 2003;12(21):2807-16.
2003: Vincenzo Bonifati; Patrizia Rizzu; Ferdinando Squitieri; Elmar Krieger; Nicola Vanacore; John C van Swieten; Alexis Brice; C.M. Duijn; Ben A Oostra; Giuseppe Meco; Peter Heutink
DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2003;24(3):159-60.
2003: Stephen Hague; Ekaterina Rogaeva; Dena Hernandez; Cindy Gulick; Andrew Singleton; Melissa Hanson; Janel Johnson; Roberto Weiser; Marisol Gallardo; Bernard Ravina; Katrina Gwinn-Hardy; Anthony Crawley; Peter St George-Hyslop; Anthony E Lang; Peter Heutink; Vincenzo Bonifati; John Hardy; Andrew Singleton
Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.
Annals of neurology 2003;54(2):271-4.
2003: Ebba Lohmann; Magali Periquet; Vincenzo Bonifati; Nicholas W Wood; Giuseppe De Michele; Anne-Marie Bonnet; Valérie Fraix; Emmanuel Broussolle; Martin Horstink; Marie Vidailhet; Patrice Verpillat; Thomas Gasser; David Nicholl; Hélio A G Teive; Salmo Raskin; Olivier Rascol; Alain Destée; Merle Ruberg; Francesca Gasparini; Giuseppe Meco; Yves Agid; Alexandra Durr; Alexis Brice
How much phenotypic variation can be attributed to parkin genotype?
Annals of neurology 2003;54(2):176-85.
2003: Marieke C J Dekker; Vincenzo Bonifati; C.M. Duijn
Parkinson's disease: piecing together a genetic jigsaw.
Brain : a journal of neurology 2003;126(Pt 8):1722-33.
2003: Fusun Duzcan; Mehmet Zencir; Fatma Ozdemir; G Ozan Cetin; Huseyin Bagci; Peter Heutink; Vincenzo Bonifati; Türker Sahiner
Familial influence on parkinsonism in a rural area of Turkey (Kizilcaboluk-Denizli): a community-based case-control study.
Movement disorders : official journal of the Movement Disorder Society 2003;18(7):799-804.
2003: Marieke C J Dekker; Vincenzo Bonifati; John C van Swieten; Nico Leenders; R J H Galjaard; Pieter J L M Snijders; Martin Horstink; Peter Heutink; Ben A Oostra; C.M. Duijn
Clinical features and neuroimaging of PARK7-linked parkinsonism.
Movement disorders : official journal of the Movement Disorder Society 2003;18(7):751-7.
2003: Vincenzo Bonifati; Patrizia Rizzu; Marijke J van Baren; Onno Schaap; Guido J Breedveld; Elmar Krieger; Marieke C J Dekker; Ferdinando Squitieri; Pablo Ibanez; Marijke Joosse; Jeroen W F van Dongen; Nicola Vanacore; John C van Swieten; Alexis Brice; Giuseppe Meco; C.M. Duijn; Ben A Oostra; Peter Heutink
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.
Science (New York, N.Y.) 2003;299(5604):256-9.
2002: Nicola Vanacore; A Nappo; M Gentile; A Brustolin; Stefania Palange; A Liberati; Simone Di Rezze; G Caldora; M Gasparini; F Benedetti; Vincenzo Bonifati; Francesco Forastiere; A Quercia; Giuseppe Meco
Evaluation of risk of Parkinson's disease in a cohort of licensed pesticide users.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2002;23 Suppl 2():S119-20.
2002: Enza Maria Valente; Francesco Brancati; Viviana Caputo; E A Graham; Mary B Davis; Alessandro Ferraris; Monique Breteler; Thomas Gasser; Vincenzo Bonifati; Anna Rita Bentivoglio; Giuseppe De Michele; Alexandra Dürr; Pietro Cortelli; Alessandro Filla; Giuseppe Meco; Ben A Oostra; Alexis Brice; Alberto Albanese; Bruno Dallapiccola; Nicholas W Wood
PARK6 is a common cause of familial parkinsonism.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2002;23 Suppl 2():S117-8.
2002: Vincenzo Bonifati; Marieke C J Dekker; Nicola Vanacore; Giovanni Fabbrini; Ferdinando Squitieri; Roberto Marconi; Angelo Antonini; P Brustenghi; A Dalla Libera; Michele De Mari; Fabrizio Stocchi; P Montagna; V Gallai; Patrizia Rizzu; John C van Swieten; Ben A Oostra; C.M. Duijn; Giuseppe Meco; Peter Heutink
Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2002;23 Suppl 2():S59-60.
2002: Angelo Antonini; Rosa Maria Moresco; Clara Gobbo; Roberta de Notaris; Andrea Panzacchi; Paolo Barone; Vincenzo Bonifati; Gianni Pezzoli; Ferruccio Fazio
Striatal dopaminergic denervation in early and late onset Parkinson's disease assessed by PET and the tracer [11C]FECIT: preliminary findings in one patient with autosomal recessive parkinsonism (Park2).
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2002;23 Suppl 2():S51-2.
2002: Nina Rawal; Magali Periquet; Alexandra Dürr; Giuseppe De Michele; Vincenzo Bonifati; Hélio A G Teive; Salmo Raskin; Joao Guimaraes; Yves Agid; Alexis Brice
Exclusion of the Nurr1 gene in autosomal recessive Parkinson's disease.
Journal of neurology 2002;249(8):1127-9.
2002: Andrew West; Magali Periquet; Sarah J Lincoln; Christoph B Lücking; David Nicholl; Vincenzo Bonifati; Nina Rawal; Thomas Gasser; Ebba Lohmann; Jean-François Deleuze; Demetrius M Maraganore; Allan Levey; Nicholas W Wood; Alexandra Dürr; John Hardy; Alexis Brice; Matthew J Farrer
Complex relationship between Parkin mutations and Parkinson disease.
American journal of medical genetics 2002;114(5):584-91.
2002: Vincenzo Bonifati
Deciphering Parkinson's disease--PARK8.
Lancet neurology 2002;1(2):83.
2002: Vincenzo Bonifati; Guido J Breedveld; Ferdinando Squitieri; Nicola Vanacore; Pierluigi Brustenghi; Biswadjiet S Harhangi; Pasquale Montagna; Milena Cannella; Giovanni Fabbrini; Patrizia Rizzu; C.M. Duijn; Ben A Oostra; Giuseppe Meco; Peter Heutink
Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset.
Annals of neurology 2002;51(2):253-6.
2002: Enza Maria Valente; Francesco Brancati; Alessandro Ferraris; Elizabeth A Graham; Mary B Davis; Monique Breteler; Thomas Gasser; Vincenzo Bonifati; Anna Rita Bentivoglio; Giuseppe De Michele; Alexandra Dürr; Pietro Cortelli; Dietmar Wassilowsky; Biswadjiet S Harhangi; Nina Rawal; Viviana Caputo; Alessandro Filla; Giuseppe Meco; Ben A Oostra; Alexis Brice; Alberto Albanese; Bruno Dallapiccola; Nicholas W Wood
PARK6-linked parkinsonism occurs in several European families.
Annals of neurology 2002;51(1):14-8.
2001: Vincenzo Bonifati; Christoph B Lücking; Edito Fabrizio; Magali Periquet; Giuseppe Meco; Alexis Brice
Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism.
Journal of neurology, neurosurgery, and psychiatry 2001;71(4):531-4.
2001: Christoph B Lücking; Vincenzo Bonifati; Magali Periquet; Nicola Vanacore; Alexis Brice; Giuseppe Meco
Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations.
Neurology 2001;57(5):924-7.
2001: C.M. Duijn; Marieke C J Dekker; Vincenzo Bonifati; R J H Galjaard; Jeanine J Houwing-Duistermaat; Pieter J L M Snijders; Leon Testers; Guido J Breedveld; Martin Horstink; Lodewijk A Sandkuijl; John C van Swieten; Ben A Oostra; Peter Heutink
Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.
American journal of human genetics 2001;69(3):629-34.
2001: M Gasparini; Vincenzo Bonifati; Edito Fabrizio; Giovanni Fabbrini; Livia Brusa; Gian Luigi Lenzi; Giuseppe Meco
Frontal lobe dysfunction in essential tremor: a preliminary study.
Journal of neurology 2001;248(5):399-402.
2001: Carlo Colosimo; Nicola Vanacore; Vincenzo Bonifati; Giovanni Fabbrini; A Rum; Giuseppe De Michele; Michele De Mari; Ubaldo Bonuccelli; David Nicholl; Giuseppe Meco
Clinical diagnosis of multiple system atrophy: level of agreement between Quinn's criteria and the consensus conference guidelines.
Acta neurologica Scandinavica 2001;103(4):261-4.
2001: Carlo Casali; Vincenzo Bonifati; Filippo M Santorelli; Giorgio Casari; Daniela Fortini; A Patrignani; Giovanni Fabbrini; Rosalba Carrozzo; G D'Amati; Nicoletta Locuratolo; Nicola Vanacore; Maria Damiano; Alberto Pierallini; Francesco Pierelli; Giuseppe Amabile; Giuseppe Meco
Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family.
Neurology 2001;56(6):802-5.
2001: Magali Periquet; C Lücking; J Vaughan; Vincenzo Bonifati; Alexandra Dürr; Giuseppe De Michele; Martin Horstink; Matthew J Farrer; Sergei N Illarioshkin; Pierre Pollak; M Borg; C Brefel-Courbon; Patrice DENEFLE; Giuseppe Meco; Thomas Gasser; Monique Breteler; Nicholas W Wood; Yves Agid; Alexis Brice
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 2001;68(3):617-26.
2001: Nicola Vanacore; Vincenzo Bonifati; Giovanni Fabbrini; Carlo Colosimo; Giuseppe De Michele; Roberto Marconi; David Nicholl; Nicoletta Locuratolo; G Talarico; Silvia Romano; Fabrizio Stocchi; Ubaldo Bonuccelli; Michele De Mari; Peter Vieregge; Giuseppe Meco
Epidemiology of multiple system atrophy. ESGAP Consortium. European Study Group on Atypical Parkinsonisms.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2001;22(1):97-9.
2001: Vincenzo Bonifati; Giuseppe De Michele; Christoph B Lücking; Alexandra Dürr; Edito Fabrizio; G Ambrosio; Nicola Vanacore; Michele De Mari; Roberto Marconi; L Capus; Monique Breteler; Thomas Gasser; Ben A Oostra; Nicholas W Wood; Yves Agid; Alessandro Filla; Giuseppe Meco; Alexis Brice
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2001;22(1):51-2.
2001: Nicola Vanacore; Vincenzo Bonifati; Carlo Colosimo; Giovanni Fabbrini; Giuseppe De Michele; Roberto Marconi; David Nicholl; Nicoletta Locuratolo; Silvia Romano; G Talarico; Fabrizio Stocchi; Ubaldo Bonuccelli; P Lamberti; Peter Vieregge; Giuseppe Meco
Epidemiology of progressive supranuclear palsy. ESGAP Consortium. European Study Group on Atypical Parkinsonisms.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2001;22(1):101-3.
2001: Giovanni Fabbrini; Piero Barbanti; Vincenzo Bonifati; Carlo Colosimo; M Gasparini; Nicola Vanacore; Giuseppe Meco
Donepezil in the treatment of progressive supranuclear palsy.
Acta neurologica Scandinavica 2001;103(2):123-5.
2001: Vincenzo Bonifati
Monogenic Parkinsonisms and the genetics of Parkinson's disease.
Functional neurology 2001;16(1):35-44.
2000: Christoph B Lücking; Alexandra Dürr; Vincenzo Bonifati; J Vaughan; Giuseppe De Michele; Thomas Gasser; Biswadjiet S Harhangi; Giuseppe Meco; Patrice DENEFLE; Nicholas W Wood; Yves Agid; Alexis Brice
Association between early-onset Parkinson's disease and mutations in the parkin gene.
The New England journal of medicine 2000;342(21):1560-7.
2000: Nicola Vanacore; Vincenzo Bonifati; Giovanni Fabbrini; Carlo Colosimo; Roberto Marconi; David Nicholl; Ubaldo Bonuccelli; Fabrizio Stocchi; P Lamberti; Giampiero Volpe; Giuseppe De Michele; IVANO IAVARONE; P Bennett; Peter Vieregge; Giuseppe Meco
Smoking habits in multiple system atrophy and progressive supranuclear palsy. European Study Group on Atypical Parkinsonisms.
Neurology 2000;54(1):114-9.
1999: David Nicholl; P Bennett; L Hiller; Vincenzo Bonifati; Nicola Vanacore; Giovanni Fabbrini; Roberto Marconi; Carlo Colosimo; P Lamberti; Fabrizio Stocchi; Ubaldo Bonuccelli; Peter Vieregge; D B Ramsden; Giuseppe Meco; AC Williams
A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders. European Study Group on Atypical Parkinsonism.
Neurology 1999;53(7):1415-21.
1999: Vincenzo Bonifati; Marijke Joosse; David Nicholl; Nicola Vanacore; P Bennett; Patrizia Rizzu; Giovanni Fabbrini; Roberto Marconi; Carlo Colosimo; Nicoletta Locuratolo; Fabrizio Stocchi; Ubaldo Bonuccelli; Michele De Mari; G Wenning; Peter Vieregge; Ben A Oostra; Giuseppe Meco; Peter Heutink
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian cases.
Neuroscience letters 1999;274(1):61-5.
1999: Biswadjiet S Harhangi; Matthew J Farrer; Sarah J Lincoln; Vincenzo Bonifati; Giuseppe Meco; Giuseppe De Michele; Alexis Brice; Alexandra Dürr; M Martinez; Thomas Gasser; Benjamin Bereznai; Jenny R Vaughan; Nicholas W Wood; John Hardy; Ben A Oostra; Monique Breteler
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease.
Neuroscience letters 1999;270(1):1-4.
1999: Nacer Abbas; Christoph B Lücking; Sylvain Ricard; Alexandra Dürr; Vincenzo Bonifati; Giuseppe De Michele; S Bouley; Jenny R Vaughan; Thomas Gasser; Roberto Marconi; Emmanuel Broussolle; C Brefel-Courbon; Biswadjiet S Harhangi; Ben A Oostra; Edito Fabrizio; G A Böhme; Laurent Pradier; Nicholas W Wood; Alessandro Filla; Giuseppe Meco; Patrice DENEFLE; Yves Agid; Alexis Brice
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Human molecular genetics 1999;8(4):567-74.
1999: Vincenzo Bonifati; Giuseppe Meco
New, selective catechol-O-methyltransferase inhibitors as therapeutic agents in Parkinson's disease.
Pharmacology & therapeutics 1999;81(1):1-36.
1998: Christoph B Lücking; Nacer Abbas; Alexandra Dürr; Vincenzo Bonifati; Anne-Marie Bonnet; T de Broucker; G De Michele; Nicholas W Wood; Yves Agid; Alexis Brice
Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group.
Lancet 1998;352(9137):1355-6.
1998: P Bennett; Vincenzo Bonifati; Ubaldo Bonuccelli; Carlo Colosimo; Michele De Mari; Giovanni Fabbrini; Roberto Marconi; Giuseppe Meco; David Nicholl; Fabrizio Stocchi; Nicola Vanacore; Peter Vieregge; AC Williams
Direct genetic evidence for involvement of tau in progressive supranuclear palsy. European Study Group on Atypical Parkinsonism Consortium.
Neurology 1998;51(4):982-5.
1998: Giovanni Fabbrini; Nicola Vanacore; Vincenzo Bonifati; Carlo Colosimo; Giuseppe Meco
Presymptomatic hypertension in progressive supranuclear palsy. Study Group on Atypical Parkinsonisms.
Archives of neurology 1998;55(8):1153-5.
1998: J Vaughan; Alexandra Durr; JP Tassin; Benjamin Bereznai; Thomas Gasser; Vincenzo Bonifati; Giuseppe De Michele; Edito Fabrizio; Giampiero Volpe; O Bandmann; William G Johnson; Lawrence I Golbe; Monique Breteler; Giuseppe Meco; Yves Agid; Alexis Brice; CD Marsden; Nicholas W Wood
The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease.
Annals of neurology 1998;44(2):270-3.
1998: JP Tassin; Alexandra Dürr; T de Broucker; Nacer Abbas; Vincenzo Bonifati; Giuseppe De Michele; Anne-Marie Bonnet; Emmanuel Broussolle; Pierre Pollak; Marie Vidailhet; Michele De Mari; Roberto Marconi; S Medjbeur; Alessandro Filla; Giuseppe Meco; Yves Agid; Alexis Brice
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 Disease.
American journal of human genetics 1998;63(1):88-94.
1998: Jenny R Vaughan; Matthew J Farrer; Zbigniew K Wszolek; Thomas Gasser; Alexandra Durr; Yves Agid; Vincenzo Bonifati; G DeMichele; Giampiero Volpe; Sarah J Lincoln; Monique Breteler; Giuseppe Meco; Alexis Brice; CD Marsden; John Hardy; Nicholas W Wood
Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD).
Human molecular genetics 1998;7(4):751-3.
1998: Thomas Gasser; Bertram Müller-Myhsok; Zbigniew K Wszolek; R Oehlmann; Donald B Calne; Vincenzo Bonifati; Benjamin Bereznai; Edito Fabrizio; Peter Vieregge; R D Horstmann
A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
Nature genetics 1998;18(3):262-5.
1998: Giuseppe Meco; Edito Fabrizio; Andrea Alessandri; Nicola Vanacore; Vincenzo Bonifati
Risperidone in levodopa induced dyskinesiae.
Journal of neurology, neurosurgery, and psychiatry 1998;64(1):135.
1997: Thomas Gasser; Bertram Müller-Myhsok; Zbigniew K Wszolek; Alexandra Dürr; Jenny R Vaughan; Vincenzo Bonifati; Giuseppe Meco; Benjamin Bereznai; R Oehlmann; Yves Agid; Alexis Brice; Nicholas W Wood
Genetic complexity and Parkinson's disease.
Science (New York, N.Y.) 1997;277(5324):388-9; author reply 389.
1997: Giuseppe Meco; Andrea Alessandri; P Giustini; Vincenzo Bonifati
Risperidone in levodopa-induced psychosis in advanced Parkinson's disease: an open-label, long-term study.
Movement disorders : official journal of the Movement Disorder Society 1997;12(4):610-2.
1997: M Gasparini; Edito Fabrizio; Vincenzo Bonifati; Giuseppe Meco
Cognitive improvement during Tolcapone treatment in Parkinson's disease.
Journal of neural transmission (Vienna, Austria : 1996) 1997;104(8-9):887-94.
1996: Thomas Gasser; Bertram Müller-Myhsok; A Supala; E Zimmer; G Wieditz; Zbigniew K Wszolek; Peter Vieregge; Vincenzo Bonifati; Wolfgang H Oertel
The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease.
Journal of neurology, neurosurgery, and psychiatry 1996;61(5):518-20.
1995: Nicola Vanacore; L Corsi; Edito Fabrizio; Vincenzo Bonifati; Giuseppe Meco
[Relationship between exposure to environmental toxins and motor neuron disease: a case report].
La Medicina del lavoro 1995;86(6):522-33.
1995: Vincenzo Bonifati; Edito Fabrizio; Nicola Vanacore; Michele De Mari; Giuseppe Meco
Familial Parkinson's disease: a clinical genetic analysis.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 1995;22(4):272-9.
1995: Francesca Menniti-Ippolito; Stefania Spila Alegiani; Nicola Vanacore; Vincenzo Bonifati; G Diana; Giuseppe Meco; Roberto Raschetti
Estimate of parkinsonism prevalence through drug prescription histories in the Province of Rome, Italy.
Acta neurologica Scandinavica 1995;92(1):49-54.
1994: Vincenzo Bonifati; Nicola Vanacore; Giuseppe Meco
Anticipation of onset age in familial Parkinson's disease.
Neurology 1994;44(10):1978-9.
1994: Giuseppe Meco; Vincenzo Bonifati; Nicola Vanacore; Edito Fabrizio
Parkinsonism after chronic exposure to the fungicide maneb (manganese ethylene-bis-dithiocarbamate).
Scandinavian journal of work, environment & health 1994;20(4):301-5.
1994: Giuseppe Meco; A Alessandria; Vincenzo Bonifati; P Giustini
Risperidone for hallucinations in levodopa-treated Parkinson's disease patients.
Lancet 1994;343(8909):1370-1.
1994: Vincenzo Bonifati; Edito Fabrizio; Rosalba Cipriani; Nicola Vanacore; Giuseppe Meco
Buspirone in levodopa-induced dyskinesias.
Clinical neuropharmacology 1994;17(1):73-82.
1994: Giuseppe Meco; Nicola Vanacore; Vincenzo Bonifati
The mortality rates for multiple sclerosis in Italy (1969-1987).
Neuroepidemiology 1994;13(4):162-74.
1993: Vincenzo Bonifati; Nicola Vanacore; A Bellatreccia; Giuseppe Meco
Mortality rates for parkinsonism in Italy (1969 to 1987).
Acta neurologica Scandinavica 1993;87(1):9-13.
1992: Rita Formisano; L Pratesi; F T Modarelli; Vincenzo Bonifati; Giuseppe Meco
Rehabilitation and Parkinson's disease.
Scandinavian journal of rehabilitation medicine 1992;24(3):157-60.
1992: L Lestingi; Vincenzo Bonifati; Fabrizio Stocchi; Italo Antonozzi; Giuseppe Meco
TRH test and the continuous dopaminergic stimulation in complicated Parkinson's disease.
European neurology 1992;32(2):65-9.
1992: Nicola Vanacore; Vincenzo Bonifati; A Bellatreccia; F Edito; Giuseppe Meco
Mortality rates for Parkinson's disease and parkinsonism in Italy (1969-1987).
Neuroepidemiology 1992;11(2):65-73.
1991: Giuseppe Meco; L Pratesi; Vincenzo Bonifati
Cardiovascular reflexes and autonomic dysfunction in Parkinson's disease.
Journal of neurology 1991;238(4):195-9.
1991: G Cusimano; C Capriani; Vincenzo Bonifati; Giuseppe Meco
Hypothalamo-pituitary function and dopamine dependence in untreated parkinsonian patients.
Acta neurologica Scandinavica 1991;83(3):145-50.
1991: Giuseppe Meco; Vincenzo Bonifati; L Bedini; A Bellatreccia; Nicola Vanacore; A Franzese
Relations between on-off phenomena and cognitive functions in Parkinson disease.
Italian journal of neurological sciences 1991;12(1):57-62.
1990: Giuseppe Meco; Vincenzo Bonifati; G Cusimano; Edito Fabrizio; Nicola Vanacore
Hallucinations in Parkinson disease: neuropsychological study.
Italian journal of neurological sciences 1990;11(4):373-9.
1988: Giuseppe Meco; C Capriani; V Pasqualoni; Vincenzo Bonifati; Nicola Vanacore
[Use of biological markers in depression in the elderly].
Minerva psichiatrica 1988;29(4):175-8.
1987: M Meco; Vincenzo Bonifati; W L Collier; M T Ramacci; F Amenta
Enzyme histochemistry of monoamine oxidase in the heart of aged rats.
Mechanisms of ageing and development 1987;38(2):145-55.