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

Year Number of Results
1983 1
1986 1
1990 2
1992 1
1993 2
1997 4
1998 1
1999 1
2000 2
2001 6
2002 2
2003 3
2004 4
2005 5
2006 5
2007 2
2008 3
2009 1
2010 5
2011 4
2012 4
2013 9
2014 1
2015 3
2017 3
2018 3
2019 2
2020 3
2021 1
2022 3
2023 2
2024 0

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83 results

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Page 1
The muscular dystrophies.
Emery AE. Emery AE. Lancet. 2002 Feb 23;359(9307):687-95. doi: 10.1016/S0140-6736(02)07815-7. Lancet. 2002. PMID: 11879882 Review.
The muscular dystrophies are inherited myogenic disorders characterised by progressive muscle wasting and weakness of variable distribution and severity. They can be subdivided into several groups, including congenital forms, in accordance with the distribution of predomin …
The muscular dystrophies are inherited myogenic disorders characterised by progressive muscle wasting and weakness of variable distri …
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. ...
Oculopharyngeal muscular dystrophy (OPMD) is a rare, primarily autosomal dominant, late onset muscular dystro
Distal myopathies.
Pénisson-Besnier I. Pénisson-Besnier I. Rev Neurol (Paris). 2013 Aug-Sep;169(8-9):534-45. doi: 10.1016/j.neurol.2012.09.021. Epub 2013 Sep 3. Rev Neurol (Paris). 2013. PMID: 24008050 Review.
Oculopharyngeal Muscular Dystrophy Ptosis, Mueller's Muscle Involvement, and a Review of Management Over 34 Years.
Jordan DR, Klapper SR, Farmer J. Jordan DR, et al. Ophthalmic Plast Reconstr Surg. 2022 Nov-Dec 01;38(6):535-542. doi: 10.1097/IOP.0000000000002118. Epub 2022 Jan 13. Ophthalmic Plast Reconstr Surg. 2022. PMID: 35030153 Review.
PURPOSE: To review the management of the ptosis associated with oculopharyngeal muscular dystrophy (OPMD) from one author's experience over 34 years, demonstrate Mueller's muscle involvement in this disease, and how this impacts the preferred choice of surger …
PURPOSE: To review the management of the ptosis associated with oculopharyngeal muscular dystrophy (OPMD) from one auth …
Oculopharyngeal muscular dystrophy.
Brais B. Brais B. Handb Clin Neurol. 2011;101:181-92. doi: 10.1016/B978-0-08-045031-5.00014-1. Handb Clin Neurol. 2011. PMID: 21496634 Review. No abstract available.
The muscular dystrophies.
Wicklund MP. Wicklund MP. Continuum (Minneap Minn). 2013 Dec;19(6 Muscle Disease):1535-70. doi: 10.1212/01.CON.0000440659.41675.8b. Continuum (Minneap Minn). 2013. PMID: 24305447 Free PMC article. Review.
RECENT FINDINGS: Some important recent advancements include (1) a much greater understanding of the pathogenetic pathways underlying facioscapulohumeral muscular dystrophy and myotonic dystrophy type 1; (2) the publication of diagnostic and treatment guidelin …
RECENT FINDINGS: Some important recent advancements include (1) a much greater understanding of the pathogenetic pathways underlying faciosc …
Neuro-ophthalmic genetics.
Kerrison JB, Maumenee IH. Kerrison JB, et al. Curr Opin Ophthalmol. 1997 Dec;8(6):35-40. doi: 10.1097/00055735-199712000-00006. Curr Opin Ophthalmol. 1997. PMID: 10176101 Review.
These include disorders of the optic nerve, such as Leber's hereditary optic neuropathy and Kjer-type optic atrophy, and disorders of ocular motility, such as congenital nystagmus, autosomal dominant progressive external ophthalmoplegia, and oculopharyngeal muscular
These include disorders of the optic nerve, such as Leber's hereditary optic neuropathy and Kjer-type optic atrophy, and disorders of ocular …
Oculopharyngeal muscular dystrophy.
Brais B, Rouleau GA, Bouchard JP, Fardeau M, Tomé FM. Brais B, et al. Semin Neurol. 1999;19(1):59-66. doi: 10.1055/s-2008-1040826. Semin Neurol. 1999. PMID: 10711989 Review.
Autosomal dominant oculopharyngeal muscular dystrophy (OPMD) is an adult-onset disease with worldwide distribution. ...
Autosomal dominant oculopharyngeal muscular dystrophy (OPMD) is an adult-onset disease with worldwide distribution. ...
Oropharyngeal dysphagia and oculopharyngeal muscular dystrophy.
Duranceau AC, Beauchamp G, Jamieson GG, Barbeau A. Duranceau AC, et al. Surg Clin North Am. 1983 Aug;63(4):825-32. doi: 10.1016/s0039-6109(16)43083-5. Surg Clin North Am. 1983. PMID: 6351296 Review.
Oculopharyngeal muscular dystrophy is an autosomal dominant transmitted condition seen mainly in French Canada. ...
Oculopharyngeal muscular dystrophy is an autosomal dominant transmitted condition seen mainly in French Canada. ...
Oculopharyngeal muscular dystrophy: Clinical and neurophysiological features.
Luigetti M, Lo Monaco M, Mirabella M, Primiano G, Lucchini M, Monforte M, Servidei S. Luigetti M, et al. Clin Neurophysiol. 2015 Dec;126(12):2406-8. doi: 10.1016/j.clinph.2015.03.005. Epub 2015 Mar 20. Clin Neurophysiol. 2015. PMID: 25842253 Review. No abstract available.
83 results