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G M Hadjigeorgiou

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British Journal of Neurosurgery|January 29, 2008
The role of 3D-computed tomography angiography (3D-CTA) in investigation of spontaneous subarachnoid haemorrhage: comparison with digital subtraction angiography (DSA) and surgical findingsC Kokkinis, M Vlychou, G M Zavras, et al.
European Journal of Neurology|January 16, 2007
Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variantsG Xiromerisiou, G M Hadjigeorgiou, V Gourbali, et al.
AJNR. American Journal of Neuroradiology|December 17, 2011
Investigation of unmedicated early onset restless legs syndrome by voxel-based morphometry, T2 relaxometry, and functional MR imaging during the night-time hoursP N Margariti, L G Astrakas, S G Tsouli, et al.
Neuromuscular Disorders : NMD|March 4, 1999
A nonsense mutation in the myophosphorylase gene in a Japanese family with McArdle's diseaseC Bruno, L Tamburino, N Kawashima, et al.
Journal of Clinical Pharmacy and Therapeutics|August 21, 2013
A network meta-analysis of randomized controlled trials for comparing the effectiveness and safety profile of treatments with marketing authorization for relapsing multiple sclerosisG M Hadjigeorgiou, C Doxani, M Miligkos, et al.
Neuropediatrics|October 12, 2005
Brain MRI and proton MRS findings in infants and children with respiratory chain defectsA Dinopoulos, K M Cecil, M B Schapiro, et al.
Journal of the Neurological Sciences|August 18, 1999
Molecular characterization of McArdle's disease in two large Finnish familiesC Bruno, M Löfberg, L Tamburino, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) geneG M Hadjigeorgiou, N Kawashima, C Bruno, et al.
Journal of the Neurological Sciences|July 13, 1999
A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathyG M Hadjigeorgiou, S H Kim, K H Fischbeck, et al.
Annals of Neurology|June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 geneA L Andreu, K Tanji, C Bruno, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
British Journal of Neurosurgery|January 29, 2008
The role of 3D-computed tomography angiography (3D-CTA) in investigation of spontaneous subarachnoid haemorrhage: comparison with digital subtraction angiography (DSA) and surgical findingsC Kokkinis, M Vlychou, G M Zavras, et al.
European Journal of Neurology|January 16, 2007
Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variantsG Xiromerisiou, G M Hadjigeorgiou, V Gourbali, et al.
AJNR. American Journal of Neuroradiology|December 17, 2011
Investigation of unmedicated early onset restless legs syndrome by voxel-based morphometry, T2 relaxometry, and functional MR imaging during the night-time hoursP N Margariti, L G Astrakas, S G Tsouli, et al.
Neuromuscular Disorders : NMD|March 4, 1999
A nonsense mutation in the myophosphorylase gene in a Japanese family with McArdle's diseaseC Bruno, L Tamburino, N Kawashima, et al.
Journal of Clinical Pharmacy and Therapeutics|August 21, 2013
A network meta-analysis of randomized controlled trials for comparing the effectiveness and safety profile of treatments with marketing authorization for relapsing multiple sclerosisG M Hadjigeorgiou, C Doxani, M Miligkos, et al.
Neuropediatrics|October 12, 2005
Brain MRI and proton MRS findings in infants and children with respiratory chain defectsA Dinopoulos, K M Cecil, M B Schapiro, et al.
Journal of the Neurological Sciences|August 18, 1999
Molecular characterization of McArdle's disease in two large Finnish familiesC Bruno, M Löfberg, L Tamburino, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) geneG M Hadjigeorgiou, N Kawashima, C Bruno, et al.
Journal of the Neurological Sciences|July 13, 1999
A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathyG M Hadjigeorgiou, S H Kim, K H Fischbeck, et al.
Annals of Neurology|June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 geneA L Andreu, K Tanji, C Bruno, et al.
Pageof 4