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Showing results (21-30 of 25) with videos related to

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Neurology|October 26, 1999
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic originA Abicht, R Stucka, V Karcagi, et al.
Journal of Neuromuscular Diseases|April 25, 2025
Liver function in X-linked myotubular myopathy and autosomal dominant centronuclear myopathy: Data of the unite-CNM studyS Colombo, B S Cowling, L Eyler, et al.
Autophagy|November 14, 2017
The Vici syndrome protein EPG5 regulates intracellular nucleic acid trafficking linking autophagy to innate and adaptive immunityE Piano Mortari, V Folgiero, V Marcellini, et al.
Neuromuscular Disorders : NMD|December 28, 2005
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosisM von der Hagen, J Schallner, A M Kaindl, et al.
Neurology|August 1, 2007
Location and type of mutation in the LIS1 gene do not predict phenotypic severityG Uyanik, D J Morris-Rosendahl, J Stiegler, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Neurology|October 26, 1999
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic originA Abicht, R Stucka, V Karcagi, et al.
Journal of Neuromuscular Diseases|April 25, 2025
Liver function in X-linked myotubular myopathy and autosomal dominant centronuclear myopathy: Data of the unite-CNM studyS Colombo, B S Cowling, L Eyler, et al.
Autophagy|November 14, 2017
The Vici syndrome protein EPG5 regulates intracellular nucleic acid trafficking linking autophagy to innate and adaptive immunityE Piano Mortari, V Folgiero, V Marcellini, et al.
Neuromuscular Disorders : NMD|December 28, 2005
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosisM von der Hagen, J Schallner, A M Kaindl, et al.
Neurology|August 1, 2007
Location and type of mutation in the LIS1 gene do not predict phenotypic severityG Uyanik, D J Morris-Rosendahl, J Stiegler, et al.
Pageof 3