Neuromuscular disorders: molecular and therapeutic insights
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical)
Reference5 articles.
1. Two major histocompatibility complex haplotypes influence susceptibility to sporadic inclusion body myositis: critical evaluation of an association with HLA-DR3;Price;Tissue Antigens,2004
2. Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion body myositis muscle fibers;Fratta;Neurology,2004
3. Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause Laing early-onset distal myopathy (MPD1);Meredith;Am J Hum Genet,2004
4. Carbohydrate mimicry between human ganglioside GM1 and Campylobacter jejuni lipooligosaccharide causes Guillain-Barré syndrome;Yuki;Proc Natl Acad Sci USA,2004
5. Effects of methylprednisolone when added to standard treatment with intravenous immunoglobulin for Guillain-Barré syndrome: randomised trial;van Koningsveld;Lancet,2004
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