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S E Baranzini

Showing results (1-10 of 22) with videos related to

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Muscle & Nerve|October 28, 1997
Four new polymorphisms in the human dystrophin gene from an Argentinian populationS E Baranzini, U Lenk, I Szijan, et al.
Journal of Neuroimmunology|February 13, 2001
Multiple sclerosis: genomic rewardsJ R Oksenberg, S E Baranzini, L F Barcellos, et al.
American Journal of Medical Genetics|June 13, 1997
Patient with an Xp21 contiguous gene deletion syndrome in association with agenesis of the corpus callosumS E Baranzini, G del Rey, N Nigro, et al.
Clinical Genetics|January 23, 1999
Carrier detection in Duchenne and Becker muscular dystrophy Argentine familiesS E Baranzini, F Giliberto, V Dalamon, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 22, 2000
Transcriptional analysis of multiple sclerosis brain lesions reveals a complex pattern of cytokine expressionS E Baranzini, C Elfstrom, S Y Chang, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 21, 1999
B cell repertoire diversity and clonal expansion in multiple sclerosis brain lesionsS E Baranzini, M C Jeong, C Butunoi, et al.
Neurology|March 13, 2002
Analysis of antibody gene rearrangement, usage, and specificity in chronic focal encephalitisS E Baranzini, K Laxer, R Saketkhoo, et al.
Neuroscience|September 19, 2012
Transcriptional expression patterns triggered by chemically distinct neuroprotective moleculesD J Pappas, P A Gabatto, D Oksenberg, et al.
Neurological Research|July 17, 1998
Deletion patterns in Argentine patients with Duchenne and Becker muscular dystrophyS E Baranzini, F Giliberto, M Herrera, et al.
Thyroid : Official Journal of the American Thyroid Association|February 1, 1997
A new point mutation (M313T) in the thyroid hormone receptor beta gene in a patient with resistance to thyroid hormoneM di Fulvio, A E Chiesa, S E Baranzini, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Muscle & Nerve|October 28, 1997
Four new polymorphisms in the human dystrophin gene from an Argentinian populationS E Baranzini, U Lenk, I Szijan, et al.
Journal of Neuroimmunology|February 13, 2001
Multiple sclerosis: genomic rewardsJ R Oksenberg, S E Baranzini, L F Barcellos, et al.
American Journal of Medical Genetics|June 13, 1997
Patient with an Xp21 contiguous gene deletion syndrome in association with agenesis of the corpus callosumS E Baranzini, G del Rey, N Nigro, et al.
Clinical Genetics|January 23, 1999
Carrier detection in Duchenne and Becker muscular dystrophy Argentine familiesS E Baranzini, F Giliberto, V Dalamon, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 22, 2000
Transcriptional analysis of multiple sclerosis brain lesions reveals a complex pattern of cytokine expressionS E Baranzini, C Elfstrom, S Y Chang, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 21, 1999
B cell repertoire diversity and clonal expansion in multiple sclerosis brain lesionsS E Baranzini, M C Jeong, C Butunoi, et al.
Neurology|March 13, 2002
Analysis of antibody gene rearrangement, usage, and specificity in chronic focal encephalitisS E Baranzini, K Laxer, R Saketkhoo, et al.
Neuroscience|September 19, 2012
Transcriptional expression patterns triggered by chemically distinct neuroprotective moleculesD J Pappas, P A Gabatto, D Oksenberg, et al.
Neurological Research|July 17, 1998
Deletion patterns in Argentine patients with Duchenne and Becker muscular dystrophyS E Baranzini, F Giliberto, M Herrera, et al.
Thyroid : Official Journal of the American Thyroid Association|February 1, 1997
A new point mutation (M313T) in the thyroid hormone receptor beta gene in a patient with resistance to thyroid hormoneM di Fulvio, A E Chiesa, S E Baranzini, et al.
Pageof 3