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S A Robb

Showing results (31-40 of 39) with videos related to

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Brain : a Journal of Neurology|April 1, 1990
Acute disseminated encephalomyelitis. MRI findings and the distinction from multiple sclerosisJ Kesselring, D H Miller, S A Robb, et al.
Developmental Medicine and Child Neurology|February 1, 1990
Magnetic resonance imaging of inflammatory and demyelinating white-matter diseases of childhoodD H Miller, S A Robb, I E Ormerod, et al.
Neurology|July 1, 2009
Natural history of Ullrich congenital muscular dystrophyA Nadeau, M Kinali, M Main, et al.
Neuromuscular Disorders : NMD|June 22, 2014
RYR1-related congenital myopathy with fatigable weakness, responding to pyridostigimineM A Illingworth, M Main, M Pitt, et al.
Neuromuscular Disorders : NMD|April 7, 2012
Relative frequency of congenital muscular dystrophy subtypes: analysis of the UK diagnostic service 2001-2008E M Clement, L Feng, R Mein, et al.
Neuromuscular Disorders : NMD|February 12, 2013
Congenital myopathies--clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United KingdomL Maggi, M Scoto, S Cirak, et al.
Neuromuscular Disorders : NMD|October 19, 2010
Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myastheniaP Munot, D Lashley, H Jungbluth, et al.
Journal of Neuroimmunology|August 19, 2008
Congenital myasthenic syndromes in childhood: diagnostic and management challengesM Kinali, D Beeson, M C Pitt, et al.
Neurology|December 29, 2005
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 geneH Jungbluth, H Zhou, L Hartley, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Brain : a Journal of Neurology|April 1, 1990
Acute disseminated encephalomyelitis. MRI findings and the distinction from multiple sclerosisJ Kesselring, D H Miller, S A Robb, et al.
Developmental Medicine and Child Neurology|February 1, 1990
Magnetic resonance imaging of inflammatory and demyelinating white-matter diseases of childhoodD H Miller, S A Robb, I E Ormerod, et al.
Neurology|July 1, 2009
Natural history of Ullrich congenital muscular dystrophyA Nadeau, M Kinali, M Main, et al.
Neuromuscular Disorders : NMD|June 22, 2014
RYR1-related congenital myopathy with fatigable weakness, responding to pyridostigimineM A Illingworth, M Main, M Pitt, et al.
Neuromuscular Disorders : NMD|April 7, 2012
Relative frequency of congenital muscular dystrophy subtypes: analysis of the UK diagnostic service 2001-2008E M Clement, L Feng, R Mein, et al.
Neuromuscular Disorders : NMD|February 12, 2013
Congenital myopathies--clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United KingdomL Maggi, M Scoto, S Cirak, et al.
Neuromuscular Disorders : NMD|October 19, 2010
Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myastheniaP Munot, D Lashley, H Jungbluth, et al.
Journal of Neuroimmunology|August 19, 2008
Congenital myasthenic syndromes in childhood: diagnostic and management challengesM Kinali, D Beeson, M C Pitt, et al.
Neurology|December 29, 2005
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 geneH Jungbluth, H Zhou, L Hartley, et al.
Pageof 4