Linking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson's diseaseBONIFATI, Vincenzo; OOSTRA, Ben A; HEUTINK, Peter et al.Journal of molecular medicine (Berlin. Print). 2004, Vol 82, Num 3, pp 163-174, issn 0946-2716, 12 p.Article

Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindredBREEDVELD, Guido J; FABBRINI, Giovanni; OOSTRA, Ben A et al.Neurogenetics (Oxford. Print). 2010, Vol 11, Num 4, pp 417-423, issn 1364-6745, 7 p.Article

Psychopathological features of obsessive-compulsive disorder in an Italian family with Gilles de la Tourette syndrome not linked to the SLITRK1 genePASQUINI, Massimo; FABBRINI, Giovanni; BERARDELLI, Isabella et al.Psychiatry research (Print). 2008, Vol 161, Num 1, pp 109-111, issn 0165-1781, 3 p.Article

Homozygous PINK1 C-terminus mutation causing early-onset parkinsonismROHE, Christan F; MONTAGNA, Pasquale; BREEDVELD, Guido et al.Annals of neurology. 2004, Vol 56, Num 3, pp 427-431, issn 0364-5134, 5 p.Article

PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathologyTSZ HANG WONG; WANG ZHENG CHIU; LAMMERS, Gert-Jan et al.Brain. 2014, Vol 137, pp 1361-1373, issn 0006-8950, 13 p., 5Article

The LRRK2 R1441 C Mutation is More Frequent Than G2019S in Parkinson's Disease Patients from Southern ItalyCRISCUOLO, Chiara; DE ROSA, Anna; DE MICHELE, Giuseppe et al.Movement disorders. 2011, Vol 26, Num 9, pp 1733-1736, issn 0885-3185, 4 p.Article

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's diseaseDI FONZO, Alessio; TASSORELLI, Cristina; MARCONI, Roberto et al.European journal of human genetics. 2006, Vol 14, Num 3, pp 322-331, issn 1018-4813, 10 p.Article

Striatal dopamine transporter binding in Parkinson's disease associated with the LRRK2 Gly2019Ser mutationISAIAS, Ioannis U; BENTI, Riccardo; GOLDWURM, Stefano et al.Movement disorders. 2006, Vol 21, Num 8, pp 1144-1147, issn 0885-3185, 4 p.Article

Does parkin play a role in the peripheral nervous system? A family reportABBRUZZESE, Giovanni; PIGULLO, Simona; AJMAR, Franco et al.Movement disorders. 2004, Vol 19, Num 8, pp 978-981, issn 0885-3185, 4 p.Article

Exclusion of the Nurr1 gene in autosomal recessive Parkinson's diseaseRAWAL, Nina; PERIQUET, Magali; DÜRR, Alexandra et al.Journal of neurology. 2002, Vol 249, Num 8, pp 1127-1129, issn 0340-5354, 3 p.Article

Biological effects of the PINK1 c.1366C>T mutation : implications in Parkinson disease pathogenesisGRÜNEWALD, Anne; BREEDVELD, Guido J; LESAGE, Suzanne et al.Neurogenetics (Oxford. Print). 2007, Vol 8, Num 2, pp 103-109, issn 1364-6745, 7 p.Article

A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in TaiwanDI FONZO, Alessio; WU-CHOU, Yah-Huei; BREEDVELD, Guido J et al.Neurogenetics (Oxford. Print). 2006, Vol 7, Num 3, pp 133-138, issn 1364-6745, 6 p.Article

Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern BrazilCHIEN, Hsin F; ROHE, Christan F; COSTA, Maria D. L et al.Neurogenetics (Oxford. Print). 2006, Vol 7, Num 1, pp 13-19, issn 1364-6745, 7 p.Article

Evidence for novel loci for late-onset Parkinson's disease in a genetic isolate from the netherlandsBERTOLI-AVELLA, Aida M; DEKKER, Marieke C. J; BONIFATI, Vincenzo et al.Human genetics. 2006, Vol 119, Num 1-2, pp 51-60, issn 0340-6717, 10 p.Article

How much phenotypic variation can be attributed to parkin genotype?LOHMANN, Ebba; PERIQUET, Magali; VERPILLAT, Patrice et al.Annals of neurology. 2003, Vol 54, Num 2, pp 176-185, issn 0364-5134, 10 p.Article

Origin of the mutations in the parkin gene in Europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effectsPERIQUET, Magali; LÜCKING, Christoph B; BORG, Michel et al.American journal of human genetics. 2001, Vol 68, Num 3, pp 617-626, issn 0002-9297Article

PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsionsVAN VLIET, Rianne; BREEDVELD, Guido; OOSTRA, Ben et al.Neurology. 2012, Vol 79, Num 8, pp 777-784, issn 0028-3878, 8 p.Article

Pallidopyramidal Disease: A Misnomer?HORSTINK, Martin W. I. M; DEKKER, Marieke C; MONTAGNA, Pasquale et al.Movement disorders. 2010, Vol 25, Num 9, pp 1109-1115, issn 0885-3185, 7 p.Article

The LRRK2 Argl628Pro variant is a risk factor for Parkinson's disease in the Chinese populationLU, Chin-Song; WU-CHOU, Yah-Huei; OOSTRA, Ben A et al.Neurogenetics (Oxford. Print). 2008, Vol 9, Num 4, pp 271-276, issn 1364-6745, 6 p.Article

Glutathione S-transferase polymorphisms and onset age in α-synuclein A53T mutant Parkinson's diseaseGOLBE, Lawrence I; DI IORIO, Giuseppe; STENROOS, E. Scot et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2007, Vol 144, Num 2, pp 254-258, issn 1552-4841, 5 p.Article

Neuropathology of Parkinson's disease associated with the LRRK2 Ile1371val mutationGIORDANA, Maria Teresa; D'AGOSTINO, Carla; ALBANI, Giovanni et al.Movement disorders. 2007, Vol 22, Num 2, pp 275-278, issn 0885-3185, 4 p.Article

DJ-1 colocalizes with tau inclusions: A link between parkinsonism and dementiaRIZZU, Patrizia; HINKLE, David A; TROJANOWSKI, John Q et al.Annals of neurology. 2004, Vol 55, Num 1, pp 113-118, issn 0364-5134, 6 p.Article

Familial influence on parkinsonism in a rural area of Turkey (Kizilcaboluk-Denizli) : A community-based case-control studyDUZCAN, Fusun; ZENCIR, Mehmet; OZDEMIR, Fatma et al.Movement disorders. 2003, Vol 18, Num 7, pp 799-804, issn 0885-3185, 6 p.Article

The DJ-1^L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexesMACEDO, Maria G; ANAR, Burcu; BRONNER, Iraad F et al.Human molecular genetics (Print). 2003, Vol 12, Num 21, pp 2807-2816, issn 0964-6906, 10 p.Article

Complex relationship between Parkin mutations and Parkinson diseaseWEST, Andrew; PERIQUET, Magali; MARAGANORE, Demetrius et al.American journal of medical genetics. 2002, Vol 114, Num 5, pp 584-591, issn 0148-7299Article