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001     280051
005     20250824001730.0
024 7 _ |a 10.1080/21678421.2025.2488296
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037 _ _ |a DZNE-2025-00888
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Lapp, Hanna Sophie
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245 _ _ |a SOD1-ALS mimicking an inflammatory neuropathy: a case report.
260 _ _ |a Abingdon
|c 2025
|b Taylor Francis Group
336 7 _ |a article
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520 _ _ |a 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.
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650 _ 7 |a ALS
|2 Other
650 _ 7 |a Amyotrophic lateral sclerosis
|2 Other
650 _ 7 |a MRI
|2 Other
650 _ 7 |a SOD1 mutation
|2 Other
650 _ 7 |a contrast enhancement
|2 Other
650 _ 7 |a Superoxide Dismutase-1
|0 EC 1.15.1.1
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650 _ 7 |a SOD1 protein, human
|2 NLM Chemicals
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Adult
|2 MeSH
650 _ 2 |a Amyotrophic Lateral Sclerosis: genetics
|2 MeSH
650 _ 2 |a Amyotrophic Lateral Sclerosis: diagnosis
|2 MeSH
650 _ 2 |a Diagnosis, Differential
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Superoxide Dismutase-1: genetics
|2 MeSH
650 _ 2 |a Disease Progression
|2 MeSH
700 1 _ |a Günther, René
|0 P:(DE-2719)2811849
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|e Last author
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773 _ _ |a 10.1080/21678421.2025.2488296
|g Vol. 26, no. 5-6, p. 591 - 594
|0 PERI:(DE-600)2705061-0
|n 5-6
|p 591 - 594
|t Amyotrophic lateral sclerosis & frontotemporal degeneration
|v 26
|y 2025
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856 4 _ |y OpenAccess
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
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