Joachim Weis
Medizinische Fakultät, RWTH Aachen University
228 papers found
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A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis
Download from academic.oup.comBi-allelic truncating mutations in VWA1 cause neuromyopathy
Download from academic.oup.comMolecular pathophysiology of human MICU1‐deficiency
Download from onlinelibrary.wiley.comLoss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuoles
Download from academic.oup.comAn integrative correlation of myopathology, phenotype and genotype in late onset Pompe disease
Download from api.wiley.comAnti–pan-neurofascin IgG3 as a marker of fulminant autoimmune neuropathy
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