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Neuromuscular Disorders : NMD|June 30, 2006
Decrement pattern in Lambert-Eaton myasthenic syndrome is different from myasthenia gravisM Baris Baslo, Feza Deymeer, Piraye Serdaroglu, et al.
Neuromuscular Disorders : NMD|June 30, 2006
Distinct phenotypic features and gender-specific disease manifestations in a Spanish family with desmin L370P mutationManuel Arias, Julio Pardo, Patricia Blanco-Arias, et al.
Neuromuscular Disorders : NMD|May 30, 2006
Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophyJuliane S Müller, Henriett Piko, Benedikt G H Schoser, et al.
Neuromuscular Disorders : NMD|April 17, 2007
GDAP1 mutations in Czech families with early-onset CMTL Baránková, E Vyhnálková, S Züchner, et al.
Neuromuscular Disorders : NMD|October 25, 2008
Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patientMontse Olivé, Alexey Shatunov, Laura Gonzalez, et al.
Neuromuscular Disorders : NMD|March 24, 2009
Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) geneHeinz Jungbluth, Suzanne Lillis, Haiyan Zhou, et al.
Neuromuscular Disorders : NMD|March 24, 2009
Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2HMireille Cossée, Clotilde Lagier-Tourenne, Claire Seguela, et al.
Neuromuscular Disorders : NMD|March 10, 2009
Characterization of the DMD/BMD patient population in Czech Republic and Slovakia using an innovative registry approachPetr Brabec, Petr Vondrácek, Daniel Klimes, et al.
Neuromuscular Disorders : NMD|June 26, 2007
Genotype-phenotype analysis in patients with giant axonal neuropathy (GAN)Olga Koop, Anja Schirmacher, Eva Nelis, et al.
Neuromuscular Disorders : NMD|August 28, 2007
Ataxia-oculomotor apraxia 2 patients show no increased sensitivity to ionizing radiationS A Nahas, A Duquette, K Roddier, et al.
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