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V Bonifati

Showing results (71-80 of 78) with videos related to

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Neurology|October 27, 2004
PARK6-linked autosomal recessive early-onset parkinsonism in Asian populationsY Hatano, K Sato, B Elibol, et al.
European Journal of Neurology|January 3, 2013
EFNS/MDS-ES/ENS [corrected] recommendations for the diagnosis of Parkinson's diseaseA Berardelli, G K Wenning, A Antonini, et al.
Human Molecular Genetics|March 11, 1999
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 DiseaseN Abbas, C B Lücking, S Ricard, et al.
Neurology|May 9, 2007
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson diseaseA Di Fonzo, H F Chien, M Socal, et al.
Journal of Medical Genetics|November 8, 2005
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestorS Goldwurm, A Di Fonzo, E J Simons, et al.
Neurology|July 13, 2005
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypesV Bonifati, C F Rohé, G J Breedveld, et al.
Neurology|March 14, 2008
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson diseaseK Haugarvoll, R Rademakers, J M Kachergus, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 10, 2017
Past, present, and future of Parkinson's disease: A special essay on the 200th Anniversary of the Shaking PalsyJ A Obeso, M Stamelou, C G Goetz, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Neurology|October 27, 2004
PARK6-linked autosomal recessive early-onset parkinsonism in Asian populationsY Hatano, K Sato, B Elibol, et al.
European Journal of Neurology|January 3, 2013
EFNS/MDS-ES/ENS [corrected] recommendations for the diagnosis of Parkinson's diseaseA Berardelli, G K Wenning, A Antonini, et al.
Human Molecular Genetics|March 11, 1999
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 DiseaseN Abbas, C B Lücking, S Ricard, et al.
Neurology|May 9, 2007
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson diseaseA Di Fonzo, H F Chien, M Socal, et al.
Journal of Medical Genetics|November 8, 2005
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestorS Goldwurm, A Di Fonzo, E J Simons, et al.
Neurology|July 13, 2005
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypesV Bonifati, C F Rohé, G J Breedveld, et al.
Neurology|March 14, 2008
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson diseaseK Haugarvoll, R Rademakers, J M Kachergus, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 10, 2017
Past, present, and future of Parkinson's disease: A special essay on the 200th Anniversary of the Shaking PalsyJ A Obeso, M Stamelou, C G Goetz, et al.
Pageof 8