Mark Busby

NeuPSIG guidelines on neuropathic pain assessment

European Federation of Neurological Societies/Peripheral Nerve Society Guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society — First Revision

Glycosylation defects: a new mechanism for muscular dystrophy?

Dystroglycan: important player in skeletal muscle and beyond

Peripheral neuropathy

Late-onset Rasmussen Encephalitis: A literature appraisal

EFNS guideline on diagnosis and management of limb girdle muscular dystrophies

Prevalence of Muscular Dystrophies: A Systematic Literature Review

Muscular dystrophies

Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy

Biological roles of glycans

Defective glycosylation in congenital muscular dystrophies

Respiratory involvement in inherited primary muscle conditions

Utility of somatosensory evoked potentials in chronic acquired demyelinating neuropathy

A Putative Src Homology 3 Domain Binding Motif but Not the C-terminal Dystrophin WW Domain Binding Motif Is Required for Dystroglycan Function in Cellular Polarity in Drosophila

High prevalence and phenotype–genotype correlations of limb girdle muscular dystrophy type 2I in Denmark

Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue

Glycosylation defects in muscular dystrophies

Limb-girdle muscular dystrophy in the Netherlands: Gene defect identified in half the families

Recommendations on diagnostic strategies for chronic inflammatory demyelinating polyradiculoneuropathy

Chronic dysimmune neuropathy

The phenotype of limb-girdle muscular dystrophy type 2I

Hemiatrophy and seizures: a case of adult-onset Rasmussen encephalitis