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A E Harding

Showing results (121-130 of 241) with videos related to

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Clinical Neuropathology|July 1, 1995
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)--confirmation by cerebral biopsy in 2 casesG A Lammie, J Rakshi, M N Rossor, et al.
Archives of Neurology|February 1, 1992
The neuropsychological features of mitochondrial myopathies and encephalomyopathiesL D Kartsounis, D D Troung, J A Morgan-Hughes, et al.
American Journal of Human Genetics|January 1, 1990
Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17H R Middleton-Price, A E Harding, C Monteiro, et al.
Journal of Neurology|October 1, 1995
Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77)M M Reilly, D Adams, M B Davis, et al.
Lancet (London, England)|September 10, 1994
Mutation analysis in patients with possible but apparently sporadic Huntington's diseaseM B Davis, D Bateman, N P Quinn, et al.
Journal of Neurology|May 1, 1995
Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosisR M Chalmers, N Robertson, H Kellar-Wood, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1985
Neuroleptic malignant syndrome associated with metoclopramideM B Robinson, R P Kennett, A E Harding, et al.
Annals of Neurology|July 1, 1994
Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosisH Kellar-Wood, N Robertson, G G Govan, et al.
Annals of Neurology|July 1, 1990
Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: a magnetic stimulation studyD Claus, H M Waddy, A E Harding, et al.
Journal of Medical Genetics|March 1, 1993
Age at onset in Huntington's disease and methylation at D4S95W Reik, E R Maher, P J Morrison, et al.
Pageof 25

Showing results (121-130 of 241) with videos related to

Sort By:
Pageof 25
Clinical Neuropathology|July 1, 1995
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)--confirmation by cerebral biopsy in 2 casesG A Lammie, J Rakshi, M N Rossor, et al.
Archives of Neurology|February 1, 1992
The neuropsychological features of mitochondrial myopathies and encephalomyopathiesL D Kartsounis, D D Troung, J A Morgan-Hughes, et al.
American Journal of Human Genetics|January 1, 1990
Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17H R Middleton-Price, A E Harding, C Monteiro, et al.
Journal of Neurology|October 1, 1995
Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77)M M Reilly, D Adams, M B Davis, et al.
Lancet (London, England)|September 10, 1994
Mutation analysis in patients with possible but apparently sporadic Huntington's diseaseM B Davis, D Bateman, N P Quinn, et al.
Journal of Neurology|May 1, 1995
Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosisR M Chalmers, N Robertson, H Kellar-Wood, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1985
Neuroleptic malignant syndrome associated with metoclopramideM B Robinson, R P Kennett, A E Harding, et al.
Annals of Neurology|July 1, 1994
Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosisH Kellar-Wood, N Robertson, G G Govan, et al.
Annals of Neurology|July 1, 1990
Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: a magnetic stimulation studyD Claus, H M Waddy, A E Harding, et al.
Journal of Medical Genetics|March 1, 1993
Age at onset in Huntington's disease and methylation at D4S95W Reik, E R Maher, P J Morrison, et al.
Pageof 25