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@ARTICLE{Lapp:280051,
author = {Lapp, Hanna Sophie and Günther, René},
title = {{SOD}1-{ALS} mimicking an inflammatory neuropathy: a case
report.},
journal = {Amyotrophic lateral sclerosis $\&$ frontotemporal
degeneration},
volume = {26},
number = {5-6},
issn = {2167-8421},
address = {Abingdon},
publisher = {Taylor Francis Group},
reportid = {DZNE-2025-00888},
pages = {591 - 594},
year = {2025},
abstract = {We present the case of a 36-year-old patient with a rapidly
progressing SOD1-ALS, who was initially diagnosed as
inflammatory acute motor axonal neuropathy due to
contrast-enhancement of the lumbar spinal cord and a pure
secondary motor neuron phenotype. Since the initiation of
tofersen, disease progression and neurofilament levels
impressively declined.},
keywords = {Humans / Adult / Amyotrophic Lateral Sclerosis: genetics /
Amyotrophic Lateral Sclerosis: diagnosis / Diagnosis,
Differential / Male / Superoxide Dismutase-1: genetics /
Disease Progression / ALS (Other) / Amyotrophic lateral
sclerosis (Other) / MRI (Other) / SOD1 mutation (Other) /
contrast enhancement (Other) / Superoxide Dismutase-1 (NLM
Chemicals) / SOD1 protein, human (NLM Chemicals)},
cin = {AG Falkenburger},
ddc = {610},
cid = {I:(DE-2719)1710012},
pnm = {353 - Clinical and Health Care Research (POF4-353)},
pid = {G:(DE-HGF)POF4-353},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40219902},
doi = {10.1080/21678421.2025.2488296},
url = {https://pub.dzne.de/record/280051},
}