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European Journal of Human Genetics : EJHG
|
December 25, 2014
The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases
Marina Mora, Corrado Angelini, Fabrizia Bignami, et al.
Sleep Medicine
|
April 29, 2026
Sleep disorders in children with Cri du Chat syndrome: A questionnaire-based study
Alessandro Ferretti, Giulia Bellone, Anteo Di Napoli, et al.
Biomolecules
|
October 29, 2025
Landscape Analysis of <i>COL6A1</i>, <i>COL6A2</i>, and <i>COL6A3</i> Pathogenic Variants in a Large Italian Cohort Presenting with Collagen VI-Related Myopathies: A Nationwide Report
Fernanda Fortunato, Laura Fiocco, Alice Margutti, et al.
Plos One
|
January 18, 2013
24 month longitudinal data in ambulant boys with Duchenne muscular dystrophy
Elena Stacy Mazzone, Marika Pane, Maria Pia Sormani, et al.
Plos One
|
June 21, 2018
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data
Marika Pane, Giorgia Coratti, Claudia Brogna, et al.
Journal of Neuromuscular Diseases
|
February 16, 2024
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy
Luca Bello, Daniele Sabbatini, Aurora Fusto, et al.
Neurology
|
June 30, 2012
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy
Luca Bello, Luisa Piva, Andrea Barp, et al.
Neuromuscular Disorders : NMD
|
August 8, 2015
Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper Limb test
Marika Pane, Lavinia Fanelli, Elena Stacy Mazzone, et al.
Orphanet Journal of Rare Diseases
|
June 14, 2012
The empowerment of translational research: lessons from laminopathies
Sara Benedetti, Pia Bernasconi, Enrico Bertini, et al.
Annals of Clinical and Translational Neurology
|
April 29, 2020
Genetic modifiers of respiratory function in Duchenne muscular dystrophy
Luca Bello, Grazia D'Angelo, Matteo Villa, et al.
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Search research articles
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Showing results (581-590 of 638) with videos related to
Sort By:
Page
of 64
European Journal of Human Genetics : EJHG
|
December 25, 2014
The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases
Marina Mora, Corrado Angelini, Fabrizia Bignami, et al.
Sleep Medicine
|
April 29, 2026
Sleep disorders in children with Cri du Chat syndrome: A questionnaire-based study
Alessandro Ferretti, Giulia Bellone, Anteo Di Napoli, et al.
Biomolecules
|
October 29, 2025
Landscape Analysis of <i>COL6A1</i>, <i>COL6A2</i>, and <i>COL6A3</i> Pathogenic Variants in a Large Italian Cohort Presenting with Collagen VI-Related Myopathies: A Nationwide Report
Fernanda Fortunato, Laura Fiocco, Alice Margutti, et al.
Plos One
|
January 18, 2013
24 month longitudinal data in ambulant boys with Duchenne muscular dystrophy
Elena Stacy Mazzone, Marika Pane, Maria Pia Sormani, et al.
Plos One
|
June 21, 2018
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data
Marika Pane, Giorgia Coratti, Claudia Brogna, et al.
Journal of Neuromuscular Diseases
|
February 16, 2024
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy
Luca Bello, Daniele Sabbatini, Aurora Fusto, et al.
Neurology
|
June 30, 2012
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy
Luca Bello, Luisa Piva, Andrea Barp, et al.
Neuromuscular Disorders : NMD
|
August 8, 2015
Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper Limb test
Marika Pane, Lavinia Fanelli, Elena Stacy Mazzone, et al.
Orphanet Journal of Rare Diseases
|
June 14, 2012
The empowerment of translational research: lessons from laminopathies
Sara Benedetti, Pia Bernasconi, Enrico Bertini, et al.
Annals of Clinical and Translational Neurology
|
April 29, 2020
Genetic modifiers of respiratory function in Duchenne muscular dystrophy
Luca Bello, Grazia D'Angelo, Matteo Villa, et al.
Page
of 64