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T T Warner

Showing results (31-40 of 41) with videos related to

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Human Mutation|January 29, 2003
Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) geneC Proukakis, M Auer-Grumbach, K Wagner, et al.
Annals of Neurology|April 1, 1995
A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European familiesT T Warner, L D Williams, R W Walker, et al.
Brain : a Journal of Neurology|June 1, 1993
Linkage analysis in British and French families with idiopathic torsion dystoniaT T Warner, N A Fletcher, M B Davis, et al.
Brain : a Journal of Neurology|January 5, 1999
The role of DYT1 in primary torsion dystonia in EuropeE M Valente, T T Warner, P R Jarman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1993
Linkage analysis with chromosome 9 markers in hereditary essential tremorD Conway, P G Bain, T T Warner, et al.
Clinical Genetics|May 23, 2009
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotypeB N Smith, S Bevan, C Vance, et al.
Journal of Medical Genetics|January 7, 2005
A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14P A Wilkinson, M A Simpson, L Bastaki, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 16, 2015
A panel of nine cerebrospinal fluid biomarkers may identify patients with atypical parkinsonian syndromesN K Magdalinou, R W Paterson, J M Schott, et al.
Parkinsonism & Related Disorders|February 19, 2017
Identification of candidate cerebrospinal fluid biomarkers in parkinsonism using quantitative proteomicsN K Magdalinou, A J Noyce, R Pinto, et al.
Annals of Neurology|October 1, 1996
Exclusion of the DYT1 locus in familial torticollisS B Bressman, T T Warner, L Almasy, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Human Mutation|January 29, 2003
Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) geneC Proukakis, M Auer-Grumbach, K Wagner, et al.
Annals of Neurology|April 1, 1995
A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European familiesT T Warner, L D Williams, R W Walker, et al.
Brain : a Journal of Neurology|June 1, 1993
Linkage analysis in British and French families with idiopathic torsion dystoniaT T Warner, N A Fletcher, M B Davis, et al.
Brain : a Journal of Neurology|January 5, 1999
The role of DYT1 in primary torsion dystonia in EuropeE M Valente, T T Warner, P R Jarman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1993
Linkage analysis with chromosome 9 markers in hereditary essential tremorD Conway, P G Bain, T T Warner, et al.
Clinical Genetics|May 23, 2009
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotypeB N Smith, S Bevan, C Vance, et al.
Journal of Medical Genetics|January 7, 2005
A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14P A Wilkinson, M A Simpson, L Bastaki, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 16, 2015
A panel of nine cerebrospinal fluid biomarkers may identify patients with atypical parkinsonian syndromesN K Magdalinou, R W Paterson, J M Schott, et al.
Parkinsonism & Related Disorders|February 19, 2017
Identification of candidate cerebrospinal fluid biomarkers in parkinsonism using quantitative proteomicsN K Magdalinou, A J Noyce, R Pinto, et al.
Annals of Neurology|October 1, 1996
Exclusion of the DYT1 locus in familial torticollisS B Bressman, T T Warner, L Almasy, et al.
Pageof 5