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Seminars in Neurology|August 27, 2002
Genetics of primary dystoniaC Klein, X O Breakefield, L J OzeliusEuropean Journal of Neurology|June 28, 2016
Cortical sensorimotor alterations classify clinical phenotype and putative genotype of spasmodic dysphoniaG Battistella, S Fuertinger, L Fleysher, et al.American Journal of Human Genetics|December 5, 1998
Search for a founder mutation in idiopathic focal dystonia from Northern GermanyC Klein, L J Ozelius, J Hagenah, et al.Annals of Neurology|September 28, 1998
Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South TyrolC Klein, P P Pramstaller, C C Castellan, et al.Neurology|August 25, 2004
Increased risk for recurrent major depression in DYT1 dystonia mutation carriersG A Heiman, R Ottman, R J Saunders-Pullman, et al.Annals of Neurology|November 30, 1999
Distribution of the mRNAs encoding torsinA and torsinB in the normal adult human brainS J Augood, D M Martin, L J Ozelius, et al.The American Journal of Pathology|July 5, 2001
A close association of torsinA and alpha-synuclein in Lewy bodies: a fluorescence resonance energy transfer studyN Sharma, J Hewett, L J Ozelius, et al.Cancer Research|December 16, 1998
A single nucleotide polymorphism in the matrix metalloproteinase-1 promoter creates an Ets binding site and augments transcriptionJ L Rutter, T I Mitchell, G Butticè, et al.Genomics|September 1, 1990
A genetic linkage map of chromosome 17J L Haines, L J Ozelius, H McFarlane, et al.Pageof 7