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Neurology|January 25, 2008
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonusC La Morgia, A Achilli, L Iommarini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003
Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7V Bonifati, M C J Dekker, N Vanacore, et al.
Neurology|November 29, 2008
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndromeA Di Fonzo, M C J Dekker, P Montagna, et al.
Neurology|June 30, 2012
Environmental risk factors for REM sleep behavior disorder: a multicenter case-control studyR B Postuma, J Y Montplaisir, A Pelletier, 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.
Physical Review Letters|December 13, 2006
Evidence for the production of slow antiprotonic hydrogen in vacuumN Zurlo, M Amoretti, C Amsler, et al.
Physical Review Letters|August 11, 2005
New source of dense, cryogenic positron plasmasL V Jørgensen, M Amoretti, G Bonomi, et al.
Physical Review Letters|August 9, 2003
Positron plasma diagnostics and temperature control for antihydrogen productionM Amoretti, C Amsler, G Bonomi, et al.
Physical Review Letters|February 9, 2005
Spatial distribution of cold antihydrogen formationN Madsen, M Amoretti, C Amsler, et al.
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