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A Abicht

Showing results (31-40 of 34) 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.
Neuromuscular Disorders : NMD|January 20, 2016
Long-term follow-up in patients with congenital myasthenic syndrome due to RAPSN mutationsD Natera-de Benito, M Bestué, J J Vilchez, 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.
Neuromuscular Disorders : NMD|October 22, 2017
Molecular characterization of congenital myasthenic syndromes in SpainD Natera-de Benito, A Töpf, J J Vilchez, et al.
Pageof 4

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|October 26, 1999
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic originA Abicht, R Stucka, V Karcagi, et al.
Neuromuscular Disorders : NMD|January 20, 2016
Long-term follow-up in patients with congenital myasthenic syndrome due to RAPSN mutationsD Natera-de Benito, M Bestué, J J Vilchez, 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.
Neuromuscular Disorders : NMD|October 22, 2017
Molecular characterization of congenital myasthenic syndromes in SpainD Natera-de Benito, A Töpf, J J Vilchez, et al.
Pageof 4