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Quoted phrase not found in phrase index: "Late-onset proximal muscle weakness"
Page 1
Sporadic Late-Onset Nemaline Myopathy: Current Landscape.
Nicolau S, Milone M. Nicolau S, et al. Curr Neurol Neurosci Rep. 2023 Nov;23(11):777-784. doi: 10.1007/s11910-023-01311-0. Epub 2023 Oct 19. Curr Neurol Neurosci Rep. 2023. PMID: 37856049 Review.
PURPOSE OF REVIEW: Sporadic late-onset nemaline myopathy (SLONM) is a rare adult-onset, acquired, muscle disease that can be associated with monoclonal gammopathy or HIV infection. ...RECENT FINDINGS: SLONM usually manifests with subacutely progressive pro …
PURPOSE OF REVIEW: Sporadic late-onset nemaline myopathy (SLONM) is a rare adult-onset, acquired, muscle disease that c …
Distal muscular dystrophies.
Udd B. Udd B. Handb Clin Neurol. 2011;101:239-62. doi: 10.1016/B978-0-08-045031-5.00016-5. Handb Clin Neurol. 2011. PMID: 21496636 Review.
Distal muscular dystrophies are a group of inherited primary muscle disorders showing progressive weakness and atrophy preferentially in the hands, forearm, lower legs, or feet. ...Distal phenotypes first have to be differentiated from neurogenic disorders. The axon …
Distal muscular dystrophies are a group of inherited primary muscle disorders showing progressive weakness and atrophy prefere …
Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases.
Schnitzler LJ, Schreckenbach T, Nadaj-Pakleza A, Stenzel W, Rushing EJ, Van Damme P, Ferbert A, Petri S, Hartmann C, Bornemann A, Meisel A, Petersen JA, Tousseyn T, Thal DR, Reimann J, De Jonghe P, Martin JJ, Van den Bergh PY, Schulz JB, Weis J, Claeys KG. Schnitzler LJ, et al. Orphanet J Rare Dis. 2017 May 11;12(1):86. doi: 10.1186/s13023-017-0640-2. Orphanet J Rare Dis. 2017. PMID: 28490364 Free PMC article. Review.
BACKGROUND: Sporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset muscle disorder, characterized by the presence of nemaline rods in muscle fibers. ...RESULTS: SLONM patients had a mean age at onset of 52 years. The predomin …
BACKGROUND: Sporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset muscle disorder, characte …
Practical Recommendations for Diagnosis and Management of Respiratory Muscle Weakness in Late-Onset Pompe Disease.
Boentert M, Prigent H, Várdi K, Jones HN, Mellies U, Simonds AK, Wenninger S, Barrot Cortés E, Confalonieri M. Boentert M, et al. Int J Mol Sci. 2016 Oct 17;17(10):1735. doi: 10.3390/ijms17101735. Int J Mol Sci. 2016. PMID: 27763517 Free PMC article. Review.
Progressive respiratory muscle weakness is a major cause of morbidity and mortality in late-onset Pompe disease even if enzyme replacement therapy has been established. ...Based on the authors' own experience in over 200 patients, this article conveys …
Progressive respiratory muscle weakness is a major cause of morbidity and mortality in late-onset Pompe disease …
Motor neuropathies and lower motor neuron syndromes.
Verschueren A. Verschueren A. Rev Neurol (Paris). 2017 May;173(5):320-325. doi: 10.1016/j.neurol.2017.03.018. Epub 2017 Apr 20. Rev Neurol (Paris). 2017. PMID: 28434507 Review.
The term LMNS is more generally used, rather than motor neuronopathy, although both entities are clinically similar. Common features are muscle weakness (distal or proximal) with atrophy and hyporeflexia, but no sensory involvement. ...The main hereditary LMN …
The term LMNS is more generally used, rather than motor neuronopathy, although both entities are clinically similar. Common features are …
Emerging and established biomarkers of oculopharyngeal muscular dystrophy.
Smith IC, Chakraborty S, Bourque PR, Sampaio ML, Melkus G, Lochmüller H, Woulfe J, Parks RJ, Brais B, Warman-Chardon J. Smith IC, et al. Neuromuscul Disord. 2023 Nov;33(11):824-834. doi: 10.1016/j.nmd.2023.09.010. Epub 2023 Oct 6. Neuromuscul Disord. 2023. PMID: 37926637 Review.
Oculopharyngeal muscular dystrophy (OPMD) is a rare, primarily autosomal dominant, late onset muscular dystrophy commonly presenting with ptosis, dysphagia, and subsequent weakness of proximal muscles. ...Accordingly, there is a pressing need for more …
Oculopharyngeal muscular dystrophy (OPMD) is a rare, primarily autosomal dominant, late onset muscular dystrophy commonly pres …
Late-onset mitochondrial myopathy.
Johnston W, Karpati G, Carpenter S, Arnold D, Shoubridge EA. Johnston W, et al. Ann Neurol. 1995 Jan;37(1):16-23. doi: 10.1002/ana.410370106. Ann Neurol. 1995. PMID: 7818252
Here we report on a group of 9 older patients (> 69 years old) with late-onset skeletal myopathy characterized by focal accumulations of deleted mitochondrial DNAs (mtDNAs) and altered muscle energy status, suggestive of a primary mitochondrial disease. .. …
Here we report on a group of 9 older patients (> 69 years old) with late-onset skeletal myopathy characterized by focal acc …
Diagnosis of Pompe disease: muscle biopsy vs blood-based assays.
Vissing J, Lukacs Z, Straub V. Vissing J, et al. JAMA Neurol. 2013 Jul;70(7):923-7. doi: 10.1001/2013.jamaneurol.486. JAMA Neurol. 2013. PMID: 23649721 Review.
This review evaluates some of the methods used in the diagnosis and differential diagnosis of late-onset Pompe disease. Muscle biopsy is commonly used as an early diagnostic tool in the evaluation of muscle disease. ...Serum creatine kinase level can b …
This review evaluates some of the methods used in the diagnosis and differential diagnosis of late-onset Pompe disease. Mus …
LAMA2-related muscular dystrophy mimicking multiple sclerosis.
Koshorek J, de Macena Sobreira N, Saidha S. Koshorek J, et al. BMJ Case Rep. 2022 Jul 22;15(7):e249061. doi: 10.1136/bcr-2022-249061. BMJ Case Rep. 2022. PMID: 35868801
Laminin-alpha2-related muscular dystrophy (LAMA2-MD) is a genetic condition due to reduced LAMA2, a protein found throughout the nervous system. Late-onset LAMA2-MD may present with proximal muscle weakness, joint contractures, neuropathy, epile …
Laminin-alpha2-related muscular dystrophy (LAMA2-MD) is a genetic condition due to reduced LAMA2, a protein found throughout the nervous sys …
Brachial plexopathy after breast cancer: A persistent late effect of radiotherapy.
Harris SR. Harris SR. PM R. 2024 Jan;16(1):85-91. doi: 10.1002/pmrj.13007. Epub 2023 Jul 31. PM R. 2024. PMID: 37272709 Review.
Radiation-induced brachial plexopathy (RIBP) is an iatrogenic, progressively disabling, and often very late effect of adjuvant radiotherapy most commonly seen in breast cancer survivors but also in those treated for lymphoma, lung, and head and neck cancers. In late-ons …
Radiation-induced brachial plexopathy (RIBP) is an iatrogenic, progressively disabling, and often very late effect of adjuvant radiotherapy …
91 results