Joachim Weis
Medizinische Fakultät, RWTH Aachen University
229 papers found
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Bi-allelic variants of FILIP1 cause congenital myopathy, dysmorphism and neurological defects
UploadNonregional small fibre neuropathy in cases of autoimmune autonomic neuropathy
Download from link.springer.comSGPL1 stimulates VPS39 recruitment to the mitochondria in MICU1 deficient cells
Download from doi.orgFirst report from the German COVID-19 autopsy registry
Download from doi.orgOrgan manifestations of COVID-19: what have we learned so far (not only) from autopsies?
Download from link.springer.comTechniques for the standard histological and ultrastructural assessment of nerve biopsies
Download from onlinelibrary.wiley.comGMPPA defects cause a neuromuscular disorder with α-dystroglycan hyperglycosylation
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