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Andrew G Engel

Showing results (11-20 of 129) with videos related to

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Current Neurology and Neuroscience Reports|October 15, 2011
Congenital myasthenic syndromes in 2012Andrew G Engel
Annals of Neurology|January 26, 2005
Mutations in ZASP define a novel form of muscular dystrophy in humansDuygu Selcen, Andrew G Engel
Annals of Neurology|December 19, 2003
Myofibrillar myopathy caused by novel dominant negative alpha B-crystallin mutationsDuygu Selcen, Andrew G Engel
Neuromuscular Disorders : NMD|January 15, 2004
Congenital myasthenic syndromes:gene mutationsKinji Ohno, Andrew G Engel
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Splicing abnormalities in congenital myasthenic syndromesKinji Ohno, Andrew G Engel
Human Genetics|September 13, 2005
Gene symbol: CHRNE. Disease: Endplate acetylcholine receptor deficiencyK Ohno, Andrew G Engel
Neurology|April 28, 2004
Mutations in myotilin cause myofibrillar myopathyDuygu Selcen, Andrew G Engel
Advances in Neurology|March 23, 2002
Congenital myasthenic syndromesAndrew G Engel, Kinji Ohno
Human Genetics|September 13, 2005
Gene symbol: CHRNE. Disease: Endplate acetylcholine receptor deficiencyK Ohno, Andrew G Engel
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 27, 2003
Congenital myasthenic syndromesKinji Ohno, Andrew G Engel
Pageof 13

Showing results (11-20 of 129) with videos related to

Sort By:
Pageof 13
Current Neurology and Neuroscience Reports|October 15, 2011
Congenital myasthenic syndromes in 2012Andrew G Engel
Annals of Neurology|January 26, 2005
Mutations in ZASP define a novel form of muscular dystrophy in humansDuygu Selcen, Andrew G Engel
Annals of Neurology|December 19, 2003
Myofibrillar myopathy caused by novel dominant negative alpha B-crystallin mutationsDuygu Selcen, Andrew G Engel
Neuromuscular Disorders : NMD|January 15, 2004
Congenital myasthenic syndromes:gene mutationsKinji Ohno, Andrew G Engel
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Splicing abnormalities in congenital myasthenic syndromesKinji Ohno, Andrew G Engel
Human Genetics|September 13, 2005
Gene symbol: CHRNE. Disease: Endplate acetylcholine receptor deficiencyK Ohno, Andrew G Engel
Neurology|April 28, 2004
Mutations in myotilin cause myofibrillar myopathyDuygu Selcen, Andrew G Engel
Advances in Neurology|March 23, 2002
Congenital myasthenic syndromesAndrew G Engel, Kinji Ohno
Human Genetics|September 13, 2005
Gene symbol: CHRNE. Disease: Endplate acetylcholine receptor deficiencyK Ohno, Andrew G Engel
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 27, 2003
Congenital myasthenic syndromesKinji Ohno, Andrew G Engel
Pageof 13