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Journal of Medical Genetics
|
January 13, 2016
The importance of genetic diagnosis for Duchenne muscular dystrophy
Annemieke Aartsma-Rus, Ieke B Ginjaar, Kate Bushby
Lancet (London, England)
|
December 1, 2009
Interventions for muscular dystrophy: molecular medicines entering the clinic
Kate Bushby, Hanns Lochmüller, Stephen Lynn, et al.
European Journal of Human Genetics : EJHG
|
July 7, 2016
Challenges raised by cross-border testing of rare diseases in the European union
Pia Pohjola, Victoria Hedley, Kate Bushby, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 13, 2006
Survey of behaviour problems in children with neuromuscular diseases
Joanne Darke, Kate Bushby, Ann Le Couteur, et al.
Brain : a Journal of Neurology
|
May 15, 2008
Developmental defects in a zebrafish model for muscular dystrophies associated with the loss of fukutin-related protein (FKRP)
Paul Thornhill, David Bassett, Hanns Lochmüller, et al.
European Journal of Medical Genetics
|
January 15, 2017
How the EUCERD Joint Action supported initiatives on Rare Diseases
Stephen Lynn, Victoria Hedley, Antonio Atalaia, et al.
Muscle & Nerve
|
April 27, 2013
Magnetic resonance imaging in Duchenne muscular dystrophy: longitudinal assessment of natural history over 18 months
Kieren G Hollingsworth, Penny Garrood, Michelle Eagle, et al.
Archives of Disease in Childhood
|
September 5, 2014
Improving recognition of Duchenne muscular dystrophy: a retrospective case note review
Henriette J A van Ruiten, Volker Straub, Kate Bushby, et al.
European Journal of Heart Failure
|
February 24, 2009
Contrasting effects of steroids and angiotensin-converting-enzyme inhibitors in a mouse model of dystrophin-deficient cardiomyopathy
Ralf Bauer, Volker Straub, Alison Blain, et al.
Archives of Disease in Childhood
|
July 5, 2015
Short stature and pubertal delay in Duchenne muscular dystrophy
Claire L Wood, Volker Straub, Michela Guglieri, et al.
Page
of 16
Search research articles
Search
Showing results (11-20 of 151) with videos related to
Sort By:
Page
of 16
Journal of Medical Genetics
|
January 13, 2016
The importance of genetic diagnosis for Duchenne muscular dystrophy
Annemieke Aartsma-Rus, Ieke B Ginjaar, Kate Bushby
Lancet (London, England)
|
December 1, 2009
Interventions for muscular dystrophy: molecular medicines entering the clinic
Kate Bushby, Hanns Lochmüller, Stephen Lynn, et al.
European Journal of Human Genetics : EJHG
|
July 7, 2016
Challenges raised by cross-border testing of rare diseases in the European union
Pia Pohjola, Victoria Hedley, Kate Bushby, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 13, 2006
Survey of behaviour problems in children with neuromuscular diseases
Joanne Darke, Kate Bushby, Ann Le Couteur, et al.
Brain : a Journal of Neurology
|
May 15, 2008
Developmental defects in a zebrafish model for muscular dystrophies associated with the loss of fukutin-related protein (FKRP)
Paul Thornhill, David Bassett, Hanns Lochmüller, et al.
European Journal of Medical Genetics
|
January 15, 2017
How the EUCERD Joint Action supported initiatives on Rare Diseases
Stephen Lynn, Victoria Hedley, Antonio Atalaia, et al.
Muscle & Nerve
|
April 27, 2013
Magnetic resonance imaging in Duchenne muscular dystrophy: longitudinal assessment of natural history over 18 months
Kieren G Hollingsworth, Penny Garrood, Michelle Eagle, et al.
Archives of Disease in Childhood
|
September 5, 2014
Improving recognition of Duchenne muscular dystrophy: a retrospective case note review
Henriette J A van Ruiten, Volker Straub, Kate Bushby, et al.
European Journal of Heart Failure
|
February 24, 2009
Contrasting effects of steroids and angiotensin-converting-enzyme inhibitors in a mouse model of dystrophin-deficient cardiomyopathy
Ralf Bauer, Volker Straub, Alison Blain, et al.
Archives of Disease in Childhood
|
July 5, 2015
Short stature and pubertal delay in Duchenne muscular dystrophy
Claire L Wood, Volker Straub, Michela Guglieri, et al.
Page
of 16