- ►nih.gov C Lautier, S Goldwurm, A Dürr, B Giovannone, … - The American Journal of Human Genetics, 2008 - Elsevier The genetic basis for association of the PARK11 region of chromosome 2 with
familial Parkinson disease (PD) is unknown. This study examined the GIGYF2
(Grb10-Interacting GYF Protein-2) (TNRC15) gene, which contains the PARK11 ... Cited by 26 - Related articles - BL Direct - All 5 versions
SA Schneider, KP Bhatia, J Hardy, BS … - Mov Disord, 2009 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 3 - Related articles - All 2 versions
E Lohmann, S Thobois, S Lesage, E Broussolle, … - Neurology, 2009 - AAN Enterprises E. Lohmann, MD S. Thobois, MD, PhD S. Lesage, PhD E. Broussolle, MD, PhD S.
Tezenas du Montcel, MD, PhD M.-J. Ribeiro, PhD P. Remy, MD, PhD A. Pelissolo, MD
B. Dubois, MD L. Mallet, MD P. Pollak, MD, PhD Y. Agid, MD, PhD A. Brice, ... Cited by 3 - Related articles - All 3 versions
MG Macedo, D Verbaan, Y Fang, SM van Rooden … - Movement disorders: official journal of the Movement …, 2009 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
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ISL Foundation, I Rome - Human Mutation - interscience.wiley.com Heterozygous rare variants in the PINK1 gene, as well as in other genes causing
autosomal recessive parkinsonism, have been reported both in patients and
healthy controls. Their pathogenic significance is uncertain, but they have ... Related articles
MIN BRIEF - albanese.biz 1 IRCCS CSS-Mendel Institute, Rome, Italy; 2 Dept. of Experimental Medicine and
Pathology, La Sapienza University, Rome, Italy; 3 Inst. of Neurology, Catholic
University, Rome, Italy; 4 Dept. of Neurology and 5 Unit of Molecular ... Related articles - View as HTML
[CITATION] Genetic analysis of Parkin in early onset Parkinson's disease (PD): Novel intron 9 g> a …
YR Wu, CH Wu - American Journal of Medical Genetics Part B: …, 2009 - Wiley Subscription Services, Inc., A Wiley Company … Related articles
J Eerola-Rautio - oa.doria.fi ACADEMIC DISSERTATION To be publicly discussed with the permission of the
Medical Faculty of the University of Helsinki in lecture hall 2, Helsinki
University Central Hospital, Meilahti, Haartmaninkatu 4, on December 19, ... Related articles - View as HTML
- ►leidenuniv.nl [PDF] D Verbaan, 2009 - openaccess.leidenuniv.nl Page 1. 139 8 Martine Visser 1 , Stephanie M. van Rooden 1 , Dagmar Verbaan 1 ,
Johan Marinus 1 , Anne M. Stiggelbout 2 *, Jacobus J. van Hilten 1 * ... Related articles - View as HTML - All 4 versions
N Brüggemann, M Mitterer, AJ Lanthaler, A … - Parkinsonism and Related Disorders, 2009 - Elsevier The role of single heterozygous mutations in the putatively recessive Parkin
gene in Parkinson disease (PD) is a vividly debated issue, partly caused by the
largely unknown frequency of these mutations in healthy individuals. We ... Related articles - All 11 versions
