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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 Dystrophy
Peter 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 study
Anando Sen, Avril Palmeri, Joanne Lee, et al.
Human Molecular Genetics
|
September 20, 2011
Abnormal vascular development in zebrafish models for fukutin and FKRP deficiency
Alasdair 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 dystrophy
Anna 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 mutation
Alisdair 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 clinicians
Sze 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 Governments
Caron M Molster, Karla Lister, Selina Metternick-Jones, et al.
Annals of Neurology
|
February 29, 2008
Dysferlin-deficient muscular dystrophy features amyloidosis
Simone 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 mice
Désirée Rutschow, Ralf Bauer, Caroline Göhringer, et al.
Page
of 38
Search research articles
Search
Showing results (81-90 of 374) with videos related to
Sort By:
Page
of 38
Journal of Neuromuscular Diseases
|
February 13, 2016
Muscle-Derived Proteins as Serum Biomarkers for Monitoring Disease Progression in Three Forms of Muscular Dystrophy
Peter 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 study
Anando Sen, Avril Palmeri, Joanne Lee, et al.
Human Molecular Genetics
|
September 20, 2011
Abnormal vascular development in zebrafish models for fukutin and FKRP deficiency
Alasdair 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 dystrophy
Anna 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 mutation
Alisdair 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 clinicians
Sze 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 Governments
Caron M Molster, Karla Lister, Selina Metternick-Jones, et al.
Annals of Neurology
|
February 29, 2008
Dysferlin-deficient muscular dystrophy features amyloidosis
Simone 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 mice
Désirée Rutschow, Ralf Bauer, Caroline Göhringer, et al.
Page
of 38