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Volker Straub

Showing results (101-110 of 374) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|June 17, 2009
New aspects on patients affected by dysferlin deficient muscular dystrophyLars Klinge, Ahmed Aboumousa, Michelle Eagle, et al.
Archives of Neurology|September 14, 2011
Muscle magnetic resonance imaging in congenital myopathies due to ryanodine receptor type 1 gene mutationsAndrea Klein, Heinz Jungbluth, Emma Clement, et al.
Human Molecular Genetics|March 17, 2009
Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophyYen-Hui Chiu, Mark A Hornsey, Lars Klinge, et al.
Neuromuscular Disorders : NMD|November 27, 2004
Albumin targeting of damaged muscle fibres in the mdx mouse can be monitored by MRIHelge Amthor, Thomas Egelhof, Iain McKinnell, et al.
Neuromuscular Disorders : NMD|January 17, 2025
Association between age at loss of ambulation and cardiac function in adults with Duchenne muscular dystrophyMarianela Schiava, John P Bourke, Jordi Díaz-Manera, et al.
Neuromuscular Disorders : NMD|June 19, 2018
A novel compound heterozygous mutation in the POMK gene causing limb-girdle muscular dystrophy-dystroglycanopathy in a sib pairSonja Strang-Karlsson, Katherine Johnson, Ana Töpf, et al.
European Journal of Heart Failure|April 12, 2013
Subepicardial dysfunction leads to global left ventricular systolic impairment in patients with limb girdle muscular dystrophy 2IKieren G Hollingsworth, Tracey A Willis, Matthew G D Bates, et al.
Neuromuscular Disorders : NMD|July 16, 2018
A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvementLidia Gonzalez-Quereda, Eduard Gallardo, Ana Töpf, et al.
Neuromuscular Disorders : NMD|April 23, 2015
Phenotypic variability of TRPV4 related neuropathiesTeresinha Evangelista, Boglarka Bansagi, Angela Pyle, et al.
European Journal of Endocrinology|October 28, 2020
Pubertal induction in adolescents with DMD is associated with high satisfaction, gonadotropin release and increased muscle contractile surface areaClaire L Wood, Kieren G Hollingsworth, Eric Hughes, et al.
Pageof 38

Showing results (101-110 of 374) with videos related to

Sort By:
Pageof 38
Journal of Neurology, Neurosurgery, and Psychiatry|June 17, 2009
New aspects on patients affected by dysferlin deficient muscular dystrophyLars Klinge, Ahmed Aboumousa, Michelle Eagle, et al.
Archives of Neurology|September 14, 2011
Muscle magnetic resonance imaging in congenital myopathies due to ryanodine receptor type 1 gene mutationsAndrea Klein, Heinz Jungbluth, Emma Clement, et al.
Human Molecular Genetics|March 17, 2009
Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophyYen-Hui Chiu, Mark A Hornsey, Lars Klinge, et al.
Neuromuscular Disorders : NMD|November 27, 2004
Albumin targeting of damaged muscle fibres in the mdx mouse can be monitored by MRIHelge Amthor, Thomas Egelhof, Iain McKinnell, et al.
Neuromuscular Disorders : NMD|January 17, 2025
Association between age at loss of ambulation and cardiac function in adults with Duchenne muscular dystrophyMarianela Schiava, John P Bourke, Jordi Díaz-Manera, et al.
Neuromuscular Disorders : NMD|June 19, 2018
A novel compound heterozygous mutation in the POMK gene causing limb-girdle muscular dystrophy-dystroglycanopathy in a sib pairSonja Strang-Karlsson, Katherine Johnson, Ana Töpf, et al.
European Journal of Heart Failure|April 12, 2013
Subepicardial dysfunction leads to global left ventricular systolic impairment in patients with limb girdle muscular dystrophy 2IKieren G Hollingsworth, Tracey A Willis, Matthew G D Bates, et al.
Neuromuscular Disorders : NMD|July 16, 2018
A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvementLidia Gonzalez-Quereda, Eduard Gallardo, Ana Töpf, et al.
Neuromuscular Disorders : NMD|April 23, 2015
Phenotypic variability of TRPV4 related neuropathiesTeresinha Evangelista, Boglarka Bansagi, Angela Pyle, et al.
European Journal of Endocrinology|October 28, 2020
Pubertal induction in adolescents with DMD is associated with high satisfaction, gonadotropin release and increased muscle contractile surface areaClaire L Wood, Kieren G Hollingsworth, Eric Hughes, et al.
Pageof 38