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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 gene
Berivan Baskin, Brenda Banwell, Reem Al Khater, et al.
Neurology
|
August 31, 2016
Consensus definitions for pediatric MS and other demyelinating disorders in childhood
Marc 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 disease
Elka 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 sclerosis
Christine 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' welcome
Brenda Banwell Md, Gavin Giovannoni Md, Christopher Hawkes Md, et al.
Journal of Child Neurology
|
May 11, 2011
Solitary tumefactive demyelinating lesions in children
Marie-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 Outcomes
Sarah 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 MRI
Christopher 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 neuropathy
Elaine Suk-Ying Goh, Brenda Banwell, Dimitri James Stavropoulos, et al.
Page
of 25
Search research articles
Search
Showing results (71-80 of 250) with videos related to
Sort By:
Page
of 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 gene
Berivan Baskin, Brenda Banwell, Reem Al Khater, et al.
Neurology
|
August 31, 2016
Consensus definitions for pediatric MS and other demyelinating disorders in childhood
Marc 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 disease
Elka 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 sclerosis
Christine 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' welcome
Brenda Banwell Md, Gavin Giovannoni Md, Christopher Hawkes Md, et al.
Journal of Child Neurology
|
May 11, 2011
Solitary tumefactive demyelinating lesions in children
Marie-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 Outcomes
Sarah 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 MRI
Christopher 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 neuropathy
Elaine Suk-Ying Goh, Brenda Banwell, Dimitri James Stavropoulos, et al.
Page
of 25