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A E Harding

Showing results (171-180 of 241) with videos related to

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American Journal of Human Genetics|December 1, 1991
Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseasesJ Collinge, M Poulter, M B Davis, et al.
Lancet (London, England)|October 14, 1989
Plasma exchange and immunosuppression in the stiff man syndromeA E Harding, P D Thompson, R S Kocen, et al.
Genomics|February 1, 1989
Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markersH R Middleton-Price, A E Harding, J Berciano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1989
Tyrosine hydroxylase and levodopa responsive dystoniaN A Fletcher, I J Holt, A E Harding, et al.
Lancet (London, England)|March 11, 1989
Molecular genetics of amyloid neuropathy in EuropeI J Holt, A E Harding, L Middleton, et al.
Brain : a Journal of Neurology|June 1, 1995
The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic studyS R Hammans, M G Sweeney, M G Hanna, et al.
Brain : a Journal of Neurology|April 1, 1995
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutationP Riordan-Eva, M D Sanders, G G Govan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1982
X-linked recessive bulbospinal neuronopathy: a report of ten casesA E Harding, P K Thomas, M Baraitser, et al.
Journal of the Neurological Sciences|June 1, 1995
Antibodies to human optic nerve in Leber's hereditary optic neuropathyP R Smith, J M Cooper, G G Govan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1995
Loss of heterozygosity for DNA polymorphisms mapping to chromosomes 10 and 17 and prognosis in patients with gliomasC E Jones, M B Davis, J L Darling, et al.
Pageof 25

Showing results (171-180 of 241) with videos related to

Sort By:
Pageof 25
American Journal of Human Genetics|December 1, 1991
Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseasesJ Collinge, M Poulter, M B Davis, et al.
Lancet (London, England)|October 14, 1989
Plasma exchange and immunosuppression in the stiff man syndromeA E Harding, P D Thompson, R S Kocen, et al.
Genomics|February 1, 1989
Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markersH R Middleton-Price, A E Harding, J Berciano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1989
Tyrosine hydroxylase and levodopa responsive dystoniaN A Fletcher, I J Holt, A E Harding, et al.
Lancet (London, England)|March 11, 1989
Molecular genetics of amyloid neuropathy in EuropeI J Holt, A E Harding, L Middleton, et al.
Brain : a Journal of Neurology|June 1, 1995
The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic studyS R Hammans, M G Sweeney, M G Hanna, et al.
Brain : a Journal of Neurology|April 1, 1995
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutationP Riordan-Eva, M D Sanders, G G Govan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1982
X-linked recessive bulbospinal neuronopathy: a report of ten casesA E Harding, P K Thomas, M Baraitser, et al.
Journal of the Neurological Sciences|June 1, 1995
Antibodies to human optic nerve in Leber's hereditary optic neuropathyP R Smith, J M Cooper, G G Govan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1995
Loss of heterozygosity for DNA polymorphisms mapping to chromosomes 10 and 17 and prognosis in patients with gliomasC E Jones, M B Davis, J L Darling, et al.
Pageof 25