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D H Geschwind

Neurology

Showing results (1-10 of 9) with videos related to

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Neurology|March 1, 1995
Sneddon's syndrome is a thrombotic vasculopathy: neuropathologic and neuroradiologic evidenceD H Geschwind, M FitzPatrick, P S Mischel, et al.
Neurology|October 10, 2001
SCA8 repeat expansions in ataxia: a controversial associationM J Sobrido, J A Cholfin, S Perlman, et al.
Neurology|April 1, 1995
Alien hand syndrome: interhemispheric motor disconnection due to a lesion in the midbody of the corpus callosumD H Geschwind, M Iacoboni, M S Mega, et al.
Neurology|December 31, 1997
Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlationsD H Geschwind, S Perlman, K P Figueroa, et al.
Neurology|October 27, 1997
Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxiaD H Geschwind, S Perlman, W W Grody, et al.
Neurology|March 12, 2003
Possible association of the tau H1/H1 genotype with primary progressive aphasiaM-J Sobrido, A Abu-Khalil, S Weintraub, et al.
Neurology|December 15, 2004
Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)J R M Oliveira, E Spiteri, M J Sobrido, et al.
Neurology|May 30, 2008
Biochemical markers in persons with preclinical familial Alzheimer diseaseJ M Ringman, S G Younkin, D Pratico, et al.
Neurology|December 24, 2010
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriersN Finch, M M Carrasquillo, M Baker, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Neurology|March 1, 1995
Sneddon's syndrome is a thrombotic vasculopathy: neuropathologic and neuroradiologic evidenceD H Geschwind, M FitzPatrick, P S Mischel, et al.
Neurology|October 10, 2001
SCA8 repeat expansions in ataxia: a controversial associationM J Sobrido, J A Cholfin, S Perlman, et al.
Neurology|April 1, 1995
Alien hand syndrome: interhemispheric motor disconnection due to a lesion in the midbody of the corpus callosumD H Geschwind, M Iacoboni, M S Mega, et al.
Neurology|December 31, 1997
Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlationsD H Geschwind, S Perlman, K P Figueroa, et al.
Neurology|October 27, 1997
Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxiaD H Geschwind, S Perlman, W W Grody, et al.
Neurology|March 12, 2003
Possible association of the tau H1/H1 genotype with primary progressive aphasiaM-J Sobrido, A Abu-Khalil, S Weintraub, et al.
Neurology|December 15, 2004
Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)J R M Oliveira, E Spiteri, M J Sobrido, et al.
Neurology|May 30, 2008
Biochemical markers in persons with preclinical familial Alzheimer diseaseJ M Ringman, S G Younkin, D Pratico, et al.
Neurology|December 24, 2010
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriersN Finch, M M Carrasquillo, M Baker, et al.
Pageof 1