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Volker Straub

Showing results (81-90 of 374) with videos related to

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Journal of Neuromuscular Diseases|February 13, 2016
Muscle-Derived Proteins as Serum Biomarkers for Monitoring Disease Progression in Three Forms of Muscular DystrophyPeter M Burch, Oksana Pogoryelova, Richard Goldstein, et al.
The International Journal of Health Planning and Management|November 5, 2022
Understanding paediatric data standards challenges through academia-industry partnerships: A conect4children (c4c) qualitative studyAnando Sen, Avril Palmeri, Joanne Lee, et al.
Human Molecular Genetics|September 20, 2011
Abnormal vascular development in zebrafish models for fukutin and FKRP deficiencyAlasdair J Wood, Juliane S Müller, Catherine D Jepson, et al.
Developmental Medicine and Child Neurology|September 21, 2019
Performance of Upper Limb module for Duchenne muscular dystrophyAnna G Mayhew, Giorgia Coratti, Elena Stacy Mazzone, et al.
European Neurology|July 11, 2009
Lower limb radiology of distal myopathy due to the S60F myotilin mutationAlisdair McNeill, Daniel Birchall, Volker Straub, et al.
Clinical Trials (London, England)|October 5, 2020
A survey of the feasibility of developing osteoporosis clinical trials in Duchenne muscular dystrophy: Survey of the opinion of young people with Duchenne muscular dystrophy, families and cliniciansSze Choong Wong, Shuko Joseph, Nadia Capaldi, et al.
European Journal of Human Genetics : EJHG|March 5, 2009
Does delta-sarcoglycan-associated autosomal-dominant cardiomyopathy exist?Ralf Bauer, Judith Hudson, Harald D Müller, et al.
Frontiers in Public Health|March 14, 2017
Outcomes of an International Workshop on Preconception Expanded Carrier Screening: Some Considerations for GovernmentsCaron M Molster, Karla Lister, Selina Metternick-Jones, et al.
Annals of Neurology|February 29, 2008
Dysferlin-deficient muscular dystrophy features amyloidosisSimone Spuler, Miriam Carl, Joanna Zabojszcza, et al.
European Journal of Human Genetics : EJHG|May 23, 2013
S151A δ-sarcoglycan mutation causes a mild phenotype of cardiomyopathy in miceDésirée Rutschow, Ralf Bauer, Caroline Göhringer, et al.
Pageof 38

Showing results (81-90 of 374) with videos related to

Sort By:
Pageof 38
Journal of Neuromuscular Diseases|February 13, 2016
Muscle-Derived Proteins as Serum Biomarkers for Monitoring Disease Progression in Three Forms of Muscular DystrophyPeter M Burch, Oksana Pogoryelova, Richard Goldstein, et al.
The International Journal of Health Planning and Management|November 5, 2022
Understanding paediatric data standards challenges through academia-industry partnerships: A conect4children (c4c) qualitative studyAnando Sen, Avril Palmeri, Joanne Lee, et al.
Human Molecular Genetics|September 20, 2011
Abnormal vascular development in zebrafish models for fukutin and FKRP deficiencyAlasdair J Wood, Juliane S Müller, Catherine D Jepson, et al.
Developmental Medicine and Child Neurology|September 21, 2019
Performance of Upper Limb module for Duchenne muscular dystrophyAnna G Mayhew, Giorgia Coratti, Elena Stacy Mazzone, et al.
European Neurology|July 11, 2009
Lower limb radiology of distal myopathy due to the S60F myotilin mutationAlisdair McNeill, Daniel Birchall, Volker Straub, et al.
Clinical Trials (London, England)|October 5, 2020
A survey of the feasibility of developing osteoporosis clinical trials in Duchenne muscular dystrophy: Survey of the opinion of young people with Duchenne muscular dystrophy, families and cliniciansSze Choong Wong, Shuko Joseph, Nadia Capaldi, et al.
European Journal of Human Genetics : EJHG|March 5, 2009
Does delta-sarcoglycan-associated autosomal-dominant cardiomyopathy exist?Ralf Bauer, Judith Hudson, Harald D Müller, et al.
Frontiers in Public Health|March 14, 2017
Outcomes of an International Workshop on Preconception Expanded Carrier Screening: Some Considerations for GovernmentsCaron M Molster, Karla Lister, Selina Metternick-Jones, et al.
Annals of Neurology|February 29, 2008
Dysferlin-deficient muscular dystrophy features amyloidosisSimone Spuler, Miriam Carl, Joanna Zabojszcza, et al.
European Journal of Human Genetics : EJHG|May 23, 2013
S151A δ-sarcoglycan mutation causes a mild phenotype of cardiomyopathy in miceDésirée Rutschow, Ralf Bauer, Caroline Göhringer, et al.
Pageof 38