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Scandinavian Journal of Rehabilitation Medicine. Supplement
|
June 17, 1999
Physiotherapy in muscular dystrophy
A K Kroksmark
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 5, 2001
Muscle strength and motor function in children and adolescents with spinal muscular atrophy II and III
A K Kroksmark, E Beckung, M Tulinius
Neurology
|
August 23, 2006
A mutation in the fast skeletal muscle troponin I gene causes myopathy and distal arthrogryposis
E Kimber, H Tajsharghi, A-K Kroksmark, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 21, 2007
Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I
N Darin, A-K Kroksmark, A-C Ahlander, et al.
European Journal of Neurology
|
February 10, 2017
Benign mitochondrial myopathy with exercise intolerance in a large multigeneration family due to a homoplasmic m.3250T>C mutation in MTTL1
N Darin, C Hedberg-Oldfors, A-K Kroksmark, et al.
Journal of Musculoskeletal & Neuronal Interactions
|
March 1, 2013
Whole body vibration therapy in patients with Duchenne muscular dystrophy--a prospective observational study
A-C Söderpalm, A-K Kroksmark, P Magnusson, et al.
Journal of Musculoskeletal & Neuronal Interactions
|
April 10, 2008
Bone markers and bone mineral density in Duchenne muscular dystrophy
A C Söderpalm, P Magnusson, A C Ahlander, et al.
Neuromuscular Disorders : NMD
|
June 6, 2000
A randomized comparative study of two methods for controlling Tendo Achilles contracture in Duchenne muscular dystrophy
S A Hyde, I FlŁytrup, S Glent, et al.
Neuromuscular Disorders : NMD
|
March 21, 2001
Longitudinal data analysis: an application to construction of a natural history profile of Duchenne muscular dystrophy
S A Hyde, B F Steffensen, I Fløytrup, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Scandinavian Journal of Rehabilitation Medicine. Supplement
|
June 17, 1999
Physiotherapy in muscular dystrophy
A K Kroksmark
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 5, 2001
Muscle strength and motor function in children and adolescents with spinal muscular atrophy II and III
A K Kroksmark, E Beckung, M Tulinius
Neurology
|
August 23, 2006
A mutation in the fast skeletal muscle troponin I gene causes myopathy and distal arthrogryposis
E Kimber, H Tajsharghi, A-K Kroksmark, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 21, 2007
Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I
N Darin, A-K Kroksmark, A-C Ahlander, et al.
European Journal of Neurology
|
February 10, 2017
Benign mitochondrial myopathy with exercise intolerance in a large multigeneration family due to a homoplasmic m.3250T>C mutation in MTTL1
N Darin, C Hedberg-Oldfors, A-K Kroksmark, et al.
Journal of Musculoskeletal & Neuronal Interactions
|
March 1, 2013
Whole body vibration therapy in patients with Duchenne muscular dystrophy--a prospective observational study
A-C Söderpalm, A-K Kroksmark, P Magnusson, et al.
Journal of Musculoskeletal & Neuronal Interactions
|
April 10, 2008
Bone markers and bone mineral density in Duchenne muscular dystrophy
A C Söderpalm, P Magnusson, A C Ahlander, et al.
Neuromuscular Disorders : NMD
|
June 6, 2000
A randomized comparative study of two methods for controlling Tendo Achilles contracture in Duchenne muscular dystrophy
S A Hyde, I FlŁytrup, S Glent, et al.
Neuromuscular Disorders : NMD
|
March 21, 2001
Longitudinal data analysis: an application to construction of a natural history profile of Duchenne muscular dystrophy
S A Hyde, B F Steffensen, I Fløytrup, et al.
Page
of 1