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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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G M Hadjigeorgiou

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Journal of Medical Genetics|February 10, 2006

Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibriumC Paisán-Ruíz, E W Evans, S Jain, et al.

Neurology|October 22, 1998

Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndromeA Papadimitriou, G P Comi, G M Hadjigeorgiou, et al.

Neuro-Degenerative Diseases|December 29, 2006

Association of tau haplotype-tagging polymorphisms with Parkinson's disease in diverse ethnic Parkinson's disease cohortsH C Fung, G Xiromerisiou, J R Gibbs, et al.

Renal Failure|October 25, 2018

The contribution of genetic variants of SLC2A1 gene in T2DM and T2DM-nephropathy: association study and meta-analysisI Stefanidis, M Tziastoudi, E E Tsironi, et al.

European Journal of Neurology|December 10, 2013

Genetic assessment of familial and early-onset Parkinson's disease in a Greek populationM Bozi, D Papadimitriou, R Antonellou, et al.

Annals of Neurology|June 14, 2000

Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutationsI Nishino, A Spinazzola, A Papadimitriou, et al.

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Search research articles

Showing results (31-40 of 36) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 36 results.

Journal of Medical Genetics|February 10, 2006

Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibriumC Paisán-Ruíz, E W Evans, S Jain, et al.

Neurology|October 22, 1998

Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndromeA Papadimitriou, G P Comi, G M Hadjigeorgiou, et al.

Neuro-Degenerative Diseases|December 29, 2006

Association of tau haplotype-tagging polymorphisms with Parkinson's disease in diverse ethnic Parkinson's disease cohortsH C Fung, G Xiromerisiou, J R Gibbs, et al.

Renal Failure|October 25, 2018

The contribution of genetic variants of SLC2A1 gene in T2DM and T2DM-nephropathy: association study and meta-analysisI Stefanidis, M Tziastoudi, E E Tsironi, et al.

European Journal of Neurology|December 10, 2013

Genetic assessment of familial and early-onset Parkinson's disease in a Greek populationM Bozi, D Papadimitriou, R Antonellou, et al.

Annals of Neurology|June 14, 2000

Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutationsI Nishino, A Spinazzola, A Papadimitriou, et al.

Pageof 4