J LAPORTE - JoVE Visualize

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Neuroscience and Biobehavioral Reviews|June 4, 2017

Elucidating opportunities and pitfalls in the treatment of experimental traumatic brain injury to optimize and facilitate clinical translationPatricia B de la Tremblaye, Darik A O'Neil, Megan J LaPorte, et al.

Annales De Chirurgie|January 1, 1994

[Long-term retrograde cerebral perfusion in surgery of the aortic arch. Apropos of 2 cases]J L de Brux, J B Subayi, J G Bukowski, et al.

Genomics|May 1, 1996

A 900-kb cosmid contig and 10 new transcripts within the candidate region for myotubular myopathy (MTM1)P Kioschis, U C Rogner, E Pick, et al.

Genomics|April 7, 1999

Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNAX Zhang, H Yang, M J Corydon, et al.

Human Molecular Genetics|January 1, 1996

Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb regionL J Hu, J Laporte, W Kress, et al.

Human Mutation|May 2, 2000

MTM1 mutations in X-linked myotubular myopathyJ Laporte, V Biancalana, S M Tanner, et al.

American Journal of Human Genetics|April 11, 2003

Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucomaH Azzedine, A Bolino, T Taïeb, et al.

Experimental Neurology|October 4, 2016

Abbreviated environmental enrichment confers neurobehavioral, cognitive, and histological benefits in brain-injured female ratsHannah L Radabaugh, Lauren J Carlson, Darik A O'Neil, et al.

Neuroscience Letters|December 13, 2017

Albeit nocturnal, rats subjected to traumatic brain injury do not differ in neurobehavioral performance whether tested during the day or nightPeter J Niesman, Jiahui Wei, Megan J LaPorte, et al.

Human Molecular Genetics|September 26, 1997

Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular CenterJ Laporte, C Guiraud-Chaumeil, M C Vincent, et al.

Pageof 13

Showing results (111-120 of 125) with videos related to

Sort By:

Pageof 13

Neuroscience and Biobehavioral Reviews|June 4, 2017

Elucidating opportunities and pitfalls in the treatment of experimental traumatic brain injury to optimize and facilitate clinical translationPatricia B de la Tremblaye, Darik A O'Neil, Megan J LaPorte, et al.

Annales De Chirurgie|January 1, 1994

[Long-term retrograde cerebral perfusion in surgery of the aortic arch. Apropos of 2 cases]J L de Brux, J B Subayi, J G Bukowski, et al.

Genomics|May 1, 1996

A 900-kb cosmid contig and 10 new transcripts within the candidate region for myotubular myopathy (MTM1)P Kioschis, U C Rogner, E Pick, et al.

Genomics|April 7, 1999

Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNAX Zhang, H Yang, M J Corydon, et al.

Human Molecular Genetics|January 1, 1996

Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb regionL J Hu, J Laporte, W Kress, et al.

Human Mutation|May 2, 2000

MTM1 mutations in X-linked myotubular myopathyJ Laporte, V Biancalana, S M Tanner, et al.

American Journal of Human Genetics|April 11, 2003

Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucomaH Azzedine, A Bolino, T Taïeb, et al.

Experimental Neurology|October 4, 2016

Abbreviated environmental enrichment confers neurobehavioral, cognitive, and histological benefits in brain-injured female ratsHannah L Radabaugh, Lauren J Carlson, Darik A O'Neil, et al.

Neuroscience Letters|December 13, 2017

Albeit nocturnal, rats subjected to traumatic brain injury do not differ in neurobehavioral performance whether tested during the day or nightPeter J Niesman, Jiahui Wei, Megan J LaPorte, et al.

Human Molecular Genetics|September 26, 1997

Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular CenterJ Laporte, C Guiraud-Chaumeil, M C Vincent, et al.

Pageof 13