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Damian Clark

Showing results (21-30 of 27) with videos related to

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Neuromuscular Disorders : NMD|July 27, 2012
Mutations in TPM2 and congenital fibre type disproportionNigel F Clarke, Leigh B Waddell, Lilian T L Sie, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Phenotypic variation of TTC19-deficient mitochondrial complex III deficiency: a case report and literature reviewDylan A Mordaunt, Alexandra Jolley, Shanti Balasubramaniam, et al.
Mitochondrion|August 1, 2016
Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial diseaseManoj P Menezes, Shamima Rahman, Kaustuv Bhattacharya, et al.
Journal of Paediatrics and Child Health|July 4, 2020
Benefits of powered standing wheelchair devices for adolescents with Duchenne muscular dystrophy in the first year of useKlair Bayley, Stephanie Parkinson, Peter Jacoby, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 28, 2012
Epilepsy with cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGHJillian Nicholl, Wendy Waters, Shanna Suwalski, et al.
Neurology|August 21, 2015
SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizuresKatherine B Howell, Jacinta M McMahon, Gemma L Carvill, et al.
Journal of Paediatrics and Child Health|June 5, 2013
High resolution chromosomal microarray in undiagnosed neurological disordersKatherine B Howell, Andrew J Kornberg, A Simon Harvey, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Neuromuscular Disorders : NMD|July 27, 2012
Mutations in TPM2 and congenital fibre type disproportionNigel F Clarke, Leigh B Waddell, Lilian T L Sie, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Phenotypic variation of TTC19-deficient mitochondrial complex III deficiency: a case report and literature reviewDylan A Mordaunt, Alexandra Jolley, Shanti Balasubramaniam, et al.
Mitochondrion|August 1, 2016
Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial diseaseManoj P Menezes, Shamima Rahman, Kaustuv Bhattacharya, et al.
Journal of Paediatrics and Child Health|July 4, 2020
Benefits of powered standing wheelchair devices for adolescents with Duchenne muscular dystrophy in the first year of useKlair Bayley, Stephanie Parkinson, Peter Jacoby, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 28, 2012
Epilepsy with cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGHJillian Nicholl, Wendy Waters, Shanna Suwalski, et al.
Neurology|August 21, 2015
SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizuresKatherine B Howell, Jacinta M McMahon, Gemma L Carvill, et al.
Journal of Paediatrics and Child Health|June 5, 2013
High resolution chromosomal microarray in undiagnosed neurological disordersKatherine B Howell, Andrew J Kornberg, A Simon Harvey, et al.
Pageof 3