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K N North

Showing results (41-50 of 48) with videos related to

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Neurology|January 17, 2007
Outcome of noninvasive ventilation in children with neuromuscular diseaseH K Young, A Lowe, D A Fitzgerald, et al.
Neurology|October 10, 2001
Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular studyY He, K J Jones, N Vignier, et al.
Human Molecular Genetics|February 7, 2001
A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathyM A Corbett, C S Robinson, G F Dunglison, et al.
Nature Genetics|March 4, 2000
Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosisJ M Kaplan, S H Kim, K N North, et al.
Neurology|April 12, 2012
Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophyM P Menezes, L B Waddell, F J Evesson, et al.
Neurology|February 26, 2003
Clinical course correlates poorly with muscle pathology in nemaline myopathyM M Ryan, B Ilkovski, C D Strickland, et al.
American Journal of Human Genetics|May 3, 2001
Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin geneB Ilkovski, S T Cooper, K Nowak, et al.
Nature Genetics|October 3, 1999
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathyK J Nowak, D Wattanasirichaigoon, H H Goebel, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Neurology|January 17, 2007
Outcome of noninvasive ventilation in children with neuromuscular diseaseH K Young, A Lowe, D A Fitzgerald, et al.
Neurology|October 10, 2001
Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular studyY He, K J Jones, N Vignier, et al.
Human Molecular Genetics|February 7, 2001
A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathyM A Corbett, C S Robinson, G F Dunglison, et al.
Nature Genetics|March 4, 2000
Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosisJ M Kaplan, S H Kim, K N North, et al.
Neurology|April 12, 2012
Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophyM P Menezes, L B Waddell, F J Evesson, et al.
Neurology|February 26, 2003
Clinical course correlates poorly with muscle pathology in nemaline myopathyM M Ryan, B Ilkovski, C D Strickland, et al.
American Journal of Human Genetics|May 3, 2001
Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin geneB Ilkovski, S T Cooper, K Nowak, et al.
Nature Genetics|October 3, 1999
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathyK J Nowak, D Wattanasirichaigoon, H H Goebel, et al.
Pageof 5