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1. Absence of polysialylated NCAM is an unfavorable prognostic phenotype for advanced stage neuroblastoma

6. A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

16. VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy

22. CADASIL and CARASIL

30. Muscle injuries: biology and treatment

32. Monoclonal antibodies selective for α-synuclein oligomers/protofibrils recognize brain pathology in Lewy body disorders and α-synuclein transgenic mice with the disease-causing A30P mutation

44. Mutations in the V‐ATPase Assembly Factor VMA21 Cause a Congenital Disorder of Glycosylation With Autophagic Liver Disease

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