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Brenda Banwell

Showing results (71-80 of 250) with videos related to

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Neuromuscular Disorders : NMD|February 24, 2009
Becker muscular dystrophy caused by an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin geneBerivan Baskin, Brenda Banwell, Reem Al Khater, et al.
Neurology|August 31, 2016
Consensus definitions for pediatric MS and other demyelinating disorders in childhoodMarc Tardieu, Brenda Banwell, Jerry S Wolinsky, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Magnetic resonance imaging of a unique mutation in a family with Pelizaeus-Merzbacher diseaseElka Miller, Elysa Widjaja, Daniel Nilsson, et al.
Neuropsychological Rehabilitation|September 19, 2017
A feasibility study of working memory training for individuals with paediatric-onset multiple sclerosisChristine Till, Bravina Kuni, Elisea De Somma, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|April 27, 2013
2010 McDonald criteria in a pediatric cohort: is positivity at onset associated with a more aggressive multiple sclerosis course?Sandra Bigi, Ruth A Marrie, Leonard Verhey, et al.
Multiple Sclerosis and Related Disorders|April 17, 2015
Editors' welcomeBrenda Banwell Md, Gavin Giovannoni Md, Christopher Hawkes Md, et al.
Journal of Child Neurology|May 11, 2011
Solitary tumefactive demyelinating lesions in childrenMarie-Paule Morin, Yves Patenaude, Anna B Sinsky, et al.
Pediatric Neurology|June 25, 2024
Solitary Tumefactive Demyelinating Lesions in Children: Clinical and Magnetic Resonance Imaging Features, Pathologic Characteristics, and OutcomesSarah Frankl, Angela Viaene, Arastoo Vossough, et al.
Journal of Magnetic Resonance Imaging : JMRI|October 12, 2013
Cerebral arterial and venous blood flow in adolescent multiple sclerosis patients and age-matched controls using phase contrast MRIChristopher K Macgowan, Katherine Y Chan, Suzanne Laughlin, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
Mosaic microdeletion of 17p11.2-p12 and duplication of 17q22-q24 in a girl with Smith-Magenis phenotype and peripheral neuropathyElaine Suk-Ying Goh, Brenda Banwell, Dimitri James Stavropoulos, et al.
Pageof 25

Showing results (71-80 of 250) with videos related to

Sort By:
Pageof 25
Neuromuscular Disorders : NMD|February 24, 2009
Becker muscular dystrophy caused by an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin geneBerivan Baskin, Brenda Banwell, Reem Al Khater, et al.
Neurology|August 31, 2016
Consensus definitions for pediatric MS and other demyelinating disorders in childhoodMarc Tardieu, Brenda Banwell, Jerry S Wolinsky, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Magnetic resonance imaging of a unique mutation in a family with Pelizaeus-Merzbacher diseaseElka Miller, Elysa Widjaja, Daniel Nilsson, et al.
Neuropsychological Rehabilitation|September 19, 2017
A feasibility study of working memory training for individuals with paediatric-onset multiple sclerosisChristine Till, Bravina Kuni, Elisea De Somma, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|April 27, 2013
2010 McDonald criteria in a pediatric cohort: is positivity at onset associated with a more aggressive multiple sclerosis course?Sandra Bigi, Ruth A Marrie, Leonard Verhey, et al.
Multiple Sclerosis and Related Disorders|April 17, 2015
Editors' welcomeBrenda Banwell Md, Gavin Giovannoni Md, Christopher Hawkes Md, et al.
Journal of Child Neurology|May 11, 2011
Solitary tumefactive demyelinating lesions in childrenMarie-Paule Morin, Yves Patenaude, Anna B Sinsky, et al.
Pediatric Neurology|June 25, 2024
Solitary Tumefactive Demyelinating Lesions in Children: Clinical and Magnetic Resonance Imaging Features, Pathologic Characteristics, and OutcomesSarah Frankl, Angela Viaene, Arastoo Vossough, et al.
Journal of Magnetic Resonance Imaging : JMRI|October 12, 2013
Cerebral arterial and venous blood flow in adolescent multiple sclerosis patients and age-matched controls using phase contrast MRIChristopher K Macgowan, Katherine Y Chan, Suzanne Laughlin, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
Mosaic microdeletion of 17p11.2-p12 and duplication of 17q22-q24 in a girl with Smith-Magenis phenotype and peripheral neuropathyElaine Suk-Ying Goh, Brenda Banwell, Dimitri James Stavropoulos, et al.
Pageof 25