Abstract | PURPOSE OF REVIEW: RECENT FINDINGS: SUMMARY: SLONM-MGUS is now considered as a treatable disease. Antiplasma cell dyscrasia therapy is a promising therapeutic option. Meanwhile, the pathomechanic link between muscle degeneration and monoclonal gammopathy remains unclear and further investigations are warranted.
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Authors | Akinori Uruha, Olivier Benveniste |
Journal | Current opinion in neurology
(Curr Opin Neurol)
Vol. 30
Issue 5
Pg. 457-463
(10 2017)
ISSN: 1473-6551 [Electronic] England |
PMID | 28678037
(Publication Type: Journal Article, Meta-Analysis, Review)
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Topics |
- Humans
- Monoclonal Gammopathy of Undetermined Significance
(pathology, physiopathology, therapy)
- Muscle, Skeletal
(pathology)
- Myopathies, Nemaline
(pathology, physiopathology, therapy)
- Stem Cell Transplantation
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