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Neurology|September 4, 2008

King-denborough syndrome caused by a novel mutation in the ryanodine receptor geneC E D'Arcy, A Bjorksten, E M Yiu, et al.

Annals of Neurology|September 18, 2001

Nemaline myopathy: a clinical study of 143 casesM M Ryan, C Schnell, C D Strickland, 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.

The Journal of Pediatrics|August 4, 1999

The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathyC Bruno, D M Kirby, Y Koga, et al.

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Search research articles

Showing results (31-40 of 34) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 34 results.

Neurology|September 4, 2008

King-denborough syndrome caused by a novel mutation in the ryanodine receptor geneC E D'Arcy, A Bjorksten, E M Yiu, et al.

Annals of Neurology|September 18, 2001

Nemaline myopathy: a clinical study of 143 casesM M Ryan, C Schnell, C D Strickland, 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.

The Journal of Pediatrics|August 4, 1999

The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathyC Bruno, D M Kirby, Y Koga, et al.

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