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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2019 | 1 |
2021 | 1 |
2022 | 1 |
2024 | 0 |
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Daratumumab for treatment-refractory antibody-mediated diseases in neurology.
Eur J Neurol. 2022 Jun;29(6):1847-1854. doi: 10.1111/ene.15266. Epub 2022 Feb 10.
Eur J Neurol. 2022.
PMID: 35098616
METHODS: In this retrospective, single-center case series, seven patients with autoantibody-driven neurological autoimmune diseases (autoimmune encephalitis, n = 5; neurofascin antibody-associated chronic inflammatory demyelinating polyneuropathy associated with sporadic late ons …
METHODS: In this retrospective, single-center case series, seven patients with autoantibody-driven neurological autoimmune diseases (autoimm …
Sporadic late-onset nemaline myopathy: Clinical spectrum, survival, and treatment outcomes.
Naddaf E, Milone M, Kansagra A, Buadi F, Kourelis T.
Naddaf E, et al.
Neurology. 2019 Jul 16;93(3):e298-e305. doi: 10.1212/WNL.0000000000007777. Epub 2019 Jun 5.
Neurology. 2019.
PMID: 31167932
OBJECTIVE: To describe the clinical phenotype, long-term treatment outcome, and overall survival of sporadic late-onset nemaline myopathy (SLONM) with or without a monoclonal protein (MP). ...A total of 7/9 (78%) patients receiving IV immunoglobulin (IVIg), 6/8 …
OBJECTIVE: To describe the clinical phenotype, long-term treatment outcome, and overall survival of sporadic late-onset nemaline m …
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Chemotherapy-based approach is the preferred treatment for sporadic late-onset nemaline myopathy with a monoclonal protein.
Kotchetkov R, Susman D, Bhutani D, Broch K, Dispenzieri A, Buadi FK.
Kotchetkov R, et al.
Int J Cancer. 2021 Jun 1;148(11):2807-2814. doi: 10.1002/ijc.33483. Epub 2021 Feb 12.
Int J Cancer. 2021.
PMID: 33529362
Free article.
Sporadic late-onset nemaline myopathy (SLONM) associated with monoclonal protein (MP) is a rare disease with an aggressive, and often fatal course. ...Neurological improvement in the nonchemotherapy group (N = 25) was observed in 52% of patients: 8% reached m …
Sporadic late-onset nemaline myopathy (SLONM) associated with monoclonal protein (MP) is a rare disease with an aggressive, an …
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