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Showing results (61-70 of 65) with videos related to

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Neurology|September 4, 2008
Distinct muscle imaging patterns in myofibrillar myopathiesD Fischer, R A Kley, K Strach, et al.
Acta Neuropathologica Communications|February 5, 2016
New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analysesA Maerkens, M Olivé, A Schreiner, et al.
Journal of Medical Genetics|April 3, 2004
FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patientsM C Walter, J A Petersen, R Stucka, et al.
Journal of Proteomics|May 4, 2013
Differential proteomic analysis of abnormal intramyoplasmic aggregates in desminopathyA Maerkens, R A Kley, M Olivé, et al.
Annals of Neurology|August 12, 2000
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C geneG Bonne, E Mercuri, A Muchir, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
Neurology|September 4, 2008
Distinct muscle imaging patterns in myofibrillar myopathiesD Fischer, R A Kley, K Strach, et al.
Acta Neuropathologica Communications|February 5, 2016
New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analysesA Maerkens, M Olivé, A Schreiner, et al.
Journal of Medical Genetics|April 3, 2004
FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patientsM C Walter, J A Petersen, R Stucka, et al.
Journal of Proteomics|May 4, 2013
Differential proteomic analysis of abnormal intramyoplasmic aggregates in desminopathyA Maerkens, R A Kley, M Olivé, et al.
Annals of Neurology|August 12, 2000
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C geneG Bonne, E Mercuri, A Muchir, et al.
Pageof 7