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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
1989 1
1990 1
1992 2
1993 2
1995 1
1999 1
2000 1
2001 1
2009 1
2011 2
2014 1
2016 1
2017 1
2018 1
2019 6
2020 1
2023 1
2024 0

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24 results

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Page 1
[Idiopathic inflammatory myopathies. A review].
Acosta I, Matamala JM, Jara P, Pino F, Gallardo A, Verdugo R. Acosta I, et al. Rev Med Chil. 2019 Mar;147(3):342-355. doi: 10.4067/S0034-98872019000300342. Rev Med Chil. 2019. PMID: 31344172 Free article. Review. Spanish.
Clinically, they are characterized by proximal muscle weakness, elevation of muscle enzymes, myopathic changes on electromyography and an abnormal muscle biopsy. ...
Clinically, they are characterized by proximal muscle weakness, elevation of muscle enzymes, myopathic changes on electromyography …
Myofibrillar myopathies.
Selcen D. Selcen D. Neuromuscul Disord. 2011 Mar;21(3):161-71. doi: 10.1016/j.nmd.2010.12.007. Epub 2011 Jan 20. Neuromuscul Disord. 2011. PMID: 21256014 Free PMC article. Review.
Cardiomyopathy and peripheral neuropathy are frequent associated features. EMG of the affected muscles reveals myopathic motor unit potentials and abnormal irritability often with myotonic discharges. ...
Cardiomyopathy and peripheral neuropathy are frequent associated features. EMG of the affected muscles reveals myopathic motor …
Inflammatory myopathies.
Kingston WJ, Moxley RT 3rd. Kingston WJ, et al. Neurol Clin. 1988 Aug;6(3):545-61. Neurol Clin. 1988. PMID: 3065600 Review.
Additional criteria for diagnosis include elevated serum muscle enzymes, myopathic features on EMG, and muscle biopsy abnormalities, including muscle fiber necrosis, degeneration, and inflammatory infiltrates. Inclusion body myositis is distinctive in that di …
Additional criteria for diagnosis include elevated serum muscle enzymes, myopathic features on EMG, and muscle biopsy abnor …
Autoimmune muscle disease.
Mammen A. Mammen A. Handb Clin Neurol. 2016;133:467-84. doi: 10.1016/B978-0-444-63432-0.00025-6. Handb Clin Neurol. 2016. PMID: 27112692 Review.
Patients with polymyositis (PM), dermatomyositis (DM), and immune-mediated necrotizing myopathy (IMNM) present with the subacute onset of symmetric proximal muscle weakness, elevated muscle enzymes, myopathic findings on electromyography, and autoantibodies. DM pati …
Patients with polymyositis (PM), dermatomyositis (DM), and immune-mediated necrotizing myopathy (IMNM) present with the subacute onset of sy …
Normal and abnormal spontaneous activity.
Rubin DI. Rubin DI. Handb Clin Neurol. 2019;160:257-279. doi: 10.1016/B978-0-444-64032-1.00017-5. Handb Clin Neurol. 2019. PMID: 31277853 Review.
Assessment of spontaneous waveforms recorded in a resting muscle during needle electromyography is important to determine the type of underlying neuromuscular disorder, temporal course of a disease, and severity and prognosis. ...Some waveforms may be recording in patients …
Assessment of spontaneous waveforms recorded in a resting muscle during needle electromyography is important to determine the type of …
Clinical electrophysiology of muscle diseases and episodic muscle disorders.
Fournier E, Tabti N. Fournier E, et al. Handb Clin Neurol. 2019;161:269-280. doi: 10.1016/B978-0-444-64142-7.00053-9. Handb Clin Neurol. 2019. PMID: 31307605 Review.
Answer to the first question mainly requires needle electromyography (EMG) of 4-6 muscles. Recordings may include extraction and measurements of motor unit potentials (MUPs). Reduced MUP spike duration indicates a lack of active muscle fibers within the motor units, …
Answer to the first question mainly requires needle electromyography (EMG) of 4-6 muscles. Recordings may include extraction a …
Electrophysiological evaluation of the neuromuscular junction: a brief review.
Kouyoumdjian JA, Estephan EP. Kouyoumdjian JA, et al. Arq Neuropsiquiatr. 2023 Dec;81(12):1040-1052. doi: 10.1055/s-0043-1777749. Epub 2023 Dec 29. Arq Neuropsiquiatr. 2023. PMID: 38157872 Free PMC article. Review.
Low amplitude compound muscle action potential typically presents in presynaptic disorders, increasing by more than 100% after a 10-second effort in the Lambert-Eaton myasthenic syndrome and less in botulism. Needle electromyography may show myopathic motor unit act …
Low amplitude compound muscle action potential typically presents in presynaptic disorders, increasing by more than 100% after a 10-second e …
Electromyography in congenital nemaline myopathy.
Wallgren-Pettersson C, Sainio K, Salmi T. Wallgren-Pettersson C, et al. Muscle Nerve. 1989 Jul;12(7):587-93. doi: 10.1002/mus.880120710. Muscle Nerve. 1989. PMID: 2674705 Review.
To clarify the discrepancies between earlier reports of electromyography (EMG) in congenital nemaline myopathy (CNM), conventional electromyography was done on 13 patients with CNM, and results were compared with those of 18 earlier EMG examinat …
To clarify the discrepancies between earlier reports of electromyography (EMG) in congenital nemaline myopathy (CNM), c …
Inclusion body myositis.
Chou SM. Chou SM. Baillieres Clin Neurol. 1993 Nov;2(3):557-77. Baillieres Clin Neurol. 1993. PMID: 8156143 Review.
It is generally refractory to treatment with corticosteroids or other immunosuppressants. Muscle biopsy and electromyography may suggest a neurogenic process mixed with myopathic features. ...Until this is clarified, the possibility that the filaments represent eith …
It is generally refractory to treatment with corticosteroids or other immunosuppressants. Muscle biopsy and electromyography may sugg …
Diagnosis and classification of granulomatous myositis.
Prieto-González S, Grau JM. Prieto-González S, et al. Autoimmun Rev. 2014 Apr-May;13(4-5):372-4. doi: 10.1016/j.autrev.2014.01.017. Epub 2014 Jan 12. Autoimmun Rev. 2014. PMID: 24424169 Review.
The term granulomatous myositis is applied to a myopathic syndrome associated with non-specific epithelioid granulomas in striated muscle. ...Although the clinical profile together with electromyography (EMG) studies may be useful, definite diagnosis requires …
The term granulomatous myositis is applied to a myopathic syndrome associated with non-specific epithelioid granulomas in striated mu …
24 results