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K B Boylan

Showing results (1-10 of 12) with videos related to

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Annals of Neurology|September 1, 1992
Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritanceK B Boylan, D R Cornblath
Neurology|September 1, 1990
Progressive dystonia following resuscitation from cardiac arrestK B Boylan, J H Chin, S J DeArmond
American Journal of Human Genetics|May 1, 1987
DNA length polymorphism located 5' to the human myelin basic protein geneK B Boylan, N Takahashi, M Diamond, et al.
Annals of Neurology|March 1, 1992
Congenital hypomyelination neuropathy with arthrogryposis multiplex congenitaK B Boylan, D M Ferriero, C M Greco, et al.
Neurology|November 1, 1993
Conjugal amyotrophic lateral sclerosis: report of a young married coupleD R Cornblath, L T Kurland, K B Boylan, et al.
Genomics|January 1, 1990
Repetitive DNA (TGGA)n 5' to the human myelin basic protein gene: a new form of oligonucleotide repetitive sequence showing length polymorphismK B Boylan, T M Ayres, B Popko, et al.
Annals of Neurology|September 1, 1995
Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophinA Ljunggren, D Duggan, E McNally, et al.
Annals of Neurology|March 1, 1990
DNA length polymorphism 5' to the myelin basic protein gene is associated with multiple sclerosisK B Boylan, N Takahashi, D W Paty, et al.
Neurology|April 1, 1995
Autosomal dominant distal spinal muscular atrophy in four generationsK B Boylan, D R Cornblath, J D Glass, et al.
Genomics|December 10, 1995
Characterization of cDNA and genomic DNA encoding SERCA1, the Ca(2+)-ATPase of human fast-twitch skeletal muscle sarcoplasmic reticulum, and its elimination as a candidate gene for Brody diseaseY Zhang, J Fujii, M S Phillips, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Annals of Neurology|September 1, 1992
Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritanceK B Boylan, D R Cornblath
Neurology|September 1, 1990
Progressive dystonia following resuscitation from cardiac arrestK B Boylan, J H Chin, S J DeArmond
American Journal of Human Genetics|May 1, 1987
DNA length polymorphism located 5' to the human myelin basic protein geneK B Boylan, N Takahashi, M Diamond, et al.
Annals of Neurology|March 1, 1992
Congenital hypomyelination neuropathy with arthrogryposis multiplex congenitaK B Boylan, D M Ferriero, C M Greco, et al.
Neurology|November 1, 1993
Conjugal amyotrophic lateral sclerosis: report of a young married coupleD R Cornblath, L T Kurland, K B Boylan, et al.
Genomics|January 1, 1990
Repetitive DNA (TGGA)n 5' to the human myelin basic protein gene: a new form of oligonucleotide repetitive sequence showing length polymorphismK B Boylan, T M Ayres, B Popko, et al.
Annals of Neurology|September 1, 1995
Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophinA Ljunggren, D Duggan, E McNally, et al.
Annals of Neurology|March 1, 1990
DNA length polymorphism 5' to the myelin basic protein gene is associated with multiple sclerosisK B Boylan, N Takahashi, D W Paty, et al.
Neurology|April 1, 1995
Autosomal dominant distal spinal muscular atrophy in four generationsK B Boylan, D R Cornblath, J D Glass, et al.
Genomics|December 10, 1995
Characterization of cDNA and genomic DNA encoding SERCA1, the Ca(2+)-ATPase of human fast-twitch skeletal muscle sarcoplasmic reticulum, and its elimination as a candidate gene for Brody diseaseY Zhang, J Fujii, M S Phillips, et al.
Pageof 2