Bonifati V - Search Results

1

Familial influence on parkinsonism in a rural area of Turkey (Kizilcaboluk-Denizli): a community-based case-control study.

Duzcan F, Zencir M, Ozdemir F, Cetin GO, Bagci H, Heutink P, Bonifati V, Sahiner T. Duzcan F, et al. Among authors: bonifati v. Mov Disord. 2003 Jul;18(7):799-804. doi: 10.1002/mds.10440. Mov Disord. 2003. PMID: 12815659

2

Clinical features and neuroimaging of PARK7-linked parkinsonism.

Dekker M, Bonifati V, van Swieten J, Leenders N, Galjaard RJ, Snijders P, Horstink M, Heutink P, Oostra B, van Duijn C. Dekker M, et al. Among authors: bonifati v. Mov Disord. 2003 Jul;18(7):751-7. doi: 10.1002/mds.10422. Mov Disord. 2003. PMID: 12815653

3

Suggestive linkage to chromosome 19 in a large Cuban family with late-onset Parkinson's disease.

Bertoli-Avella AM, Giroud-Benitez JL, Bonifati V, Alvarez-Gonzalez E, Heredero-Baute L, van Duijn CM, Heutink P. Bertoli-Avella AM, et al. Among authors: bonifati v. Mov Disord. 2003 Nov;18(11):1240-9. doi: 10.1002/mds.10534. Mov Disord. 2003. PMID: 14639663

4

Case-control study of multiple system atrophy.

Vanacore N, Bonifati V, Fabbrini G, Colosimo C, De Michele G, Marconi R, Stocchi F, Nicholl D, Bonuccelli U, De Mari M, Vieregge P, Meco G; ESGAP Consortium. Vanacore N, et al. Among authors: bonifati v. Mov Disord. 2005 Feb;20(2):158-63. doi: 10.1002/mds.20303. Mov Disord. 2005. PMID: 15382209

5

Novel parkin mutations detected in patients with early-onset Parkinson's disease.

Bertoli-Avella AM, Giroud-Benitez JL, Akyol A, Barbosa E, Schaap O, van der Linde HC, Martignoni E, Lopiano L, Lamberti P, Fincati E, Antonini A, Stocchi F, Montagna P, Squitieri F, Marini P, Abbruzzese G, Fabbrini G, Marconi R, Dalla Libera A, Trianni G, Guidi M, De Gaetano A, Boff Maegawa G, De Leo A, Gallai V, de Rosa G, Vanacore N, Meco G, van Duijn CM, Oostra BA, Heutink P, Bonifati V; Italian Parkinson Genetics Network, MD. Bertoli-Avella AM, et al. Among authors: bonifati v. Mov Disord. 2005 Apr;20(4):424-431. doi: 10.1002/mds.20343. Mov Disord. 2005. PMID: 15584030

6

High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal.

Ferreira JJ, Guedes LC, Rosa MM, Coelho M, van Doeselaar M, Schweiger D, Di Fonzo A, Oostra BA, Sampaio C, Bonifati V. Ferreira JJ, et al. Among authors: bonifati v. Mov Disord. 2007 Jun 15;22(8):1194-201. doi: 10.1002/mds.21525. Mov Disord. 2007. PMID: 17469194

7

Pseudo-orthostatic and resting leg tremor in a large Spanish family with homozygous truncating parkin mutation.

Infante J, Berciano J, Sánchez-Juan P, García A, Di Fonzo A, Breedveld G, Oostra B, Bonifati V. Infante J, et al. Among authors: bonifati v. Mov Disord. 2009 Jan 15;24(1):144-7. doi: 10.1002/mds.22349. Mov Disord. 2009. PMID: 18951541 No abstract available.

8

Autosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS-5) in a Dutch kindred.

Sas AM, Di Fonzo A, Bakker SL, Simons EJ, Oostra BA, Maat-Kievit AJ, Boon AJ, Bonifati V. Sas AM, et al. Among authors: bonifati v. Mov Disord. 2010 Aug 15;25(11):1715-22. doi: 10.1002/mds.23248. Mov Disord. 2010. PMID: 20645405

9

Olfactory heterogeneity in LRRK2 related Parkinsonism.

Silveira-Moriyama L, Munhoz RP, de J Carvalho M, Raskin S, Rogaeva E, de C Aguiar P, Bressan RA, Felicio AC, Barsottini OG, Andrade LA, Chien HF, Bonifati V, Barbosa ER, Teive HA, Lees AJ. Silveira-Moriyama L, et al. Among authors: bonifati v. Mov Disord. 2010 Dec 15;25(16):2879-83. doi: 10.1002/mds.23325. Mov Disord. 2010. PMID: 20818658

10

The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from southern Italy.

Criscuolo C, De Rosa A, Guacci A, Simons EJ, Breedveld GJ, Peluso S, Volpe G, Filla A, Oostra BA, Bonifati V, De Michele G. Criscuolo C, et al. Among authors: bonifati v. Mov Disord. 2011 Aug 1;26(9):1733-6. doi: 10.1002/mds.23735. Epub 2011 Apr 29. Mov Disord. 2011. PMID: 21538529

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