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Arthur Burghes

Showing results (1-10 of 6) with videos related to

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Neuromuscular Disorders : NMD|December 29, 2019
244th ENMC international workshop: Newborn screening in spinal muscular atrophy May 10-12, 2019, Hoofdorp, The NetherlandsTamara Dangouloff, Arthur Burghes, Eduardo F Tizzano, et al.
Orphanet Journal of Rare Diseases|March 22, 2013
SMA-EUROPE workshop report: Opportunities and challenges in developing clinical trials for spinal muscular atrophy in EuropeNathalie Kayadjanian, Arthur Burghes, Richard S Finkel, et al.
Human Molecular Genetics|June 10, 2005
Diverse small-molecule modulators of SMN expression found by high-throughput compound screening: early leads towards a therapeutic for spinal muscular atrophyJill Jarecki, Xiaocun Chen, Alexandra Bernardino, et al.
Human Molecular Genetics|September 15, 2024
Pathomechanisms of Monoallelic variants in TTN causing skeletal muscle diseaseJochen Gohlke, Johan Lindqvist, Zaynab Hourani, et al.
Molecular Therapy. Methods & Clinical Development|September 25, 2023
In-depth comparison of Anc80L65 and AAV9 retinal targeting and characterization of cross-reactivity to multiple AAV serotypes in humansMaura K Schwartz, Shibi Likhite, Tatyana A Vetter, et al.
Neuromuscular Disorders : NMD|January 6, 2024
270th ENMC International Workshop: Consensus for SMN2 genetic analysis in SMA patients 10-12 March, 2023, Hoofddorp, the NetherlandsEmanuela Abiusi, Mar Costa-Roger, Enrico Silvio Bertini, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Neuromuscular Disorders : NMD|December 29, 2019
244th ENMC international workshop: Newborn screening in spinal muscular atrophy May 10-12, 2019, Hoofdorp, The NetherlandsTamara Dangouloff, Arthur Burghes, Eduardo F Tizzano, et al.
Orphanet Journal of Rare Diseases|March 22, 2013
SMA-EUROPE workshop report: Opportunities and challenges in developing clinical trials for spinal muscular atrophy in EuropeNathalie Kayadjanian, Arthur Burghes, Richard S Finkel, et al.
Human Molecular Genetics|June 10, 2005
Diverse small-molecule modulators of SMN expression found by high-throughput compound screening: early leads towards a therapeutic for spinal muscular atrophyJill Jarecki, Xiaocun Chen, Alexandra Bernardino, et al.
Human Molecular Genetics|September 15, 2024
Pathomechanisms of Monoallelic variants in TTN causing skeletal muscle diseaseJochen Gohlke, Johan Lindqvist, Zaynab Hourani, et al.
Molecular Therapy. Methods & Clinical Development|September 25, 2023
In-depth comparison of Anc80L65 and AAV9 retinal targeting and characterization of cross-reactivity to multiple AAV serotypes in humansMaura K Schwartz, Shibi Likhite, Tatyana A Vetter, et al.
Neuromuscular Disorders : NMD|January 6, 2024
270th ENMC International Workshop: Consensus for SMN2 genetic analysis in SMA patients 10-12 March, 2023, Hoofddorp, the NetherlandsEmanuela Abiusi, Mar Costa-Roger, Enrico Silvio Bertini, et al.
Pageof 1