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Showing results (171-180 of 175) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7qL Notelet, F Chapon, S Khoury, et al.
Neurology|January 10, 2001
Clinical and spectroscopic improvement in HIV-associated cognitive impairmentB Stankoff, A Tourbah, S Suarez, et al.
Journal Francais D'Ophtalmologie|March 17, 2007
[Functional amblyopia: a functional MRI evaluation of the visual cortex response after treatment]T H Nguyen, J L Stiévenart, J F Le Gargasson, et al.
Annals of the New York Academy of Sciences|November 5, 1997
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaA Joutel, C Corpechot, A Ducros, et al.
Nature|October 24, 1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementiaA Joutel, C Corpechot, A Ducros, et al.
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Showing results (171-180 of 175) with videos related to

Sort By:
Pageof 18
You have reached the last page of results.This site can display upto 175 results.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7qL Notelet, F Chapon, S Khoury, et al.
Neurology|January 10, 2001
Clinical and spectroscopic improvement in HIV-associated cognitive impairmentB Stankoff, A Tourbah, S Suarez, et al.
Journal Francais D'Ophtalmologie|March 17, 2007
[Functional amblyopia: a functional MRI evaluation of the visual cortex response after treatment]T H Nguyen, J L Stiévenart, J F Le Gargasson, et al.
Annals of the New York Academy of Sciences|November 5, 1997
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaA Joutel, C Corpechot, A Ducros, et al.
Nature|October 24, 1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementiaA Joutel, C Corpechot, A Ducros, et al.
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