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T Darras

Showing results (111-120 of 303) with videos related to

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Human Mutation|June 30, 2000
Identification of a novel truncating mutation (S171X) in the Emerin gene in five members of a Caucasian American family with Emery-Dreifuss muscular dystrophyC C Menache, C A Brown, J H Donnelly, et al.
Neurology|August 5, 2009
Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutationI A Anselm, K J Sweadner, S Gollamudi, et al.
Neuromuscular Disorders : NMD|October 17, 2003
Paediatric mononeuritis multiplex: a report of three cases and review of the literatureMonique M Ryan, Ann Tilton, Umberto De Girolami, et al.
Muscle & Nerve|November 13, 2013
Minimal training is required to reliably perform quantitative ultrasound of muscleCraig M Zaidman, Jim S Wu, Sarah Wilder, et al.
Journal of Child Neurology|January 19, 2006
Association of Duchenne muscular dystrophy with autism spectrum disorderJoyce Y Wu, Karl C K Kuban, Elizabeth Allred, et al.
Muscle & Nerve|August 1, 2009
Pediatric monomelic amyotrophy: evidence for poliomyelitis in vulnerable populationsHugh J McMillan, Basil T Darras, Peter B Kang, et al.
BMC Genetics|November 17, 2001
Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencingR R Bennett, J den Dunnen, K F O'Brien, et al.
Muscle & Nerve|March 31, 2004
Multifocal slowing of nerve conduction in metachromatic leukodystrophyCarol L Cameron, Peter B Kang, Ted M Burns, et al.
American Journal of Human Genetics|November 1, 1988
Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutationsB T Darras, P Blattner, J F Harper, et al.
Revue Medicale De Bruxelles|April 1, 1988
[Computerized tomography-guided thoracic puncture in the diagnosis of pulmonary nodular lesions. Apropos of 5 year's experience]P Gilbert, J P Quarré, P Cornut, et al.
Pageof 31

Showing results (111-120 of 303) with videos related to

Sort By:
Pageof 31
Human Mutation|June 30, 2000
Identification of a novel truncating mutation (S171X) in the Emerin gene in five members of a Caucasian American family with Emery-Dreifuss muscular dystrophyC C Menache, C A Brown, J H Donnelly, et al.
Neurology|August 5, 2009
Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutationI A Anselm, K J Sweadner, S Gollamudi, et al.
Neuromuscular Disorders : NMD|October 17, 2003
Paediatric mononeuritis multiplex: a report of three cases and review of the literatureMonique M Ryan, Ann Tilton, Umberto De Girolami, et al.
Muscle & Nerve|November 13, 2013
Minimal training is required to reliably perform quantitative ultrasound of muscleCraig M Zaidman, Jim S Wu, Sarah Wilder, et al.
Journal of Child Neurology|January 19, 2006
Association of Duchenne muscular dystrophy with autism spectrum disorderJoyce Y Wu, Karl C K Kuban, Elizabeth Allred, et al.
Muscle & Nerve|August 1, 2009
Pediatric monomelic amyotrophy: evidence for poliomyelitis in vulnerable populationsHugh J McMillan, Basil T Darras, Peter B Kang, et al.
BMC Genetics|November 17, 2001
Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencingR R Bennett, J den Dunnen, K F O'Brien, et al.
Muscle & Nerve|March 31, 2004
Multifocal slowing of nerve conduction in metachromatic leukodystrophyCarol L Cameron, Peter B Kang, Ted M Burns, et al.
American Journal of Human Genetics|November 1, 1988
Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutationsB T Darras, P Blattner, J F Harper, et al.
Revue Medicale De Bruxelles|April 1, 1988
[Computerized tomography-guided thoracic puncture in the diagnosis of pulmonary nodular lesions. Apropos of 5 year's experience]P Gilbert, J P Quarré, P Cornut, et al.
Pageof 31