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Emery-Dreifuss muscular dystrophy.
Heller SA, Shih R, Kalra R, Kang PB. Heller SA, et al. Muscle Nerve. 2020 Apr;61(4):436-448. doi: 10.1002/mus.26782. Epub 2019 Dec 28. Muscle Nerve. 2020. PMID: 31840275 Free PMC article. Review.
Emery-Dreifuss muscular dystrophy (EDMD) is a rare muscular dystrophy, but is particularly important to diagnose due to frequent life-threatening cardiac complications. ...
Emery-Dreifuss muscular dystrophy (EDMD) is a rare muscular dystrophy, but is particularly importa
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 …
Genetics and muscle pathology in the diagnosis of muscular dystrophies: An update.
Narasimhaiah D, Uppin MS, Ranganath P. Narasimhaiah D, et al. Indian J Pathol Microbiol. 2022 May;65(Supplement):S259-S270. doi: 10.4103/ijpm.ijpm_1074_21. Indian J Pathol Microbiol. 2022. PMID: 35562158 Review.
They have a progressive clinical course and are characterized by muscle fiber degeneration. Congenital muscular dystrophies (CMD) include dystroglycanopathies, merosin-deficient CMD, collagen VI-deficient CMD, SELENON-related rigid spine muscular dystrophy, a …
They have a progressive clinical course and are characterized by muscle fiber degeneration. Congenital muscular dystrophies (CMD) inc …
Update on Muscular Dystrophies with Focus on Novel Treatments and Biomarkers.
Datta N, Ghosh PS. Datta N, et al. Curr Neurol Neurosci Rep. 2020 May 14;20(6):14. doi: 10.1007/s11910-020-01034-6. Curr Neurol Neurosci Rep. 2020. PMID: 32409939 Review.
PURPOSE OF REVIEW: Muscular dystrophies are a heterogeneous group of inherited muscular disorders characterized by progressive muscle weakness and in many cases cardiac and respiratory muscle involvement. ...RECENT FINDINGS: The therapeutic landscape of muscular
PURPOSE OF REVIEW: Muscular dystrophies are a heterogeneous group of inherited muscular disorders characterized by progressive …
Cardiac Involvement in Emery-Dreifuss Muscular Dystrophy and Related Management Strategies.
Wang S, Peng D. Wang S, et al. Int Heart J. 2019 Jan 25;60(1):12-18. doi: 10.1536/ihj.17-604. Epub 2018 Dec 5. Int Heart J. 2019. PMID: 30518714 Free article. Review.
Emery-Dreifuss muscular dystrophy (EDMD) is a group of hereditary muscular dystrophy syndrome caused by deficiency of genes encoding nuclear envelope proteins. Patients having EDMD show the triad of muscle dystrophy, joint contract
Emery-Dreifuss muscular dystrophy (EDMD) is a group of hereditary muscular dystrophy syndrome caus
Emery-Dreifuss muscular dystrophy.
Puckelwartz M, McNally EM. Puckelwartz M, et al. Handb Clin Neurol. 2011;101:155-66. doi: 10.1016/B978-0-08-045031-5.00012-8. Handb Clin Neurol. 2011. PMID: 21496632 Review.
Emery-Dreifuss muscular dystrophy (EDMD) is a progressive muscle-wasting disorder defined by early contractures of the Achilles tendon, spine, and elbows. ...
Emery-Dreifuss muscular dystrophy (EDMD) is a progressive muscle-wasting disorder defined by early contractures
Emery-Dreifuss muscular dystrophy.
Muchir A, Worman HJ. Muchir A, et al. Curr Neurol Neurosci Rep. 2007 Jan;7(1):78-83. doi: 10.1007/s11910-007-0025-3. Curr Neurol Neurosci Rep. 2007. PMID: 17217858 Review.
Emery-Dreifuss muscular dystrophy (EDMD) is inherited in an X-linked or autosomal manner. ...
Emery-Dreifuss muscular dystrophy (EDMD) is inherited in an X-linked or autosomal manner. ...
Emery-Dreifuss muscular dystrophy.
Zacharias AS, Wagener ME, Warren ST, Hopkins LC. Zacharias AS, et al. Semin Neurol. 1999;19(1):67-79. doi: 10.1055/s-2008-1040827. Semin Neurol. 1999. PMID: 10711990 Review.
Emery-Dreifuss muscular dystrophy (EDMD) is the third most common X-linked muscular dystrophy. ...Emerin is localized to the nuclear membrane of skeletal, cardiac, and smooth muscle. The term Emery-Dreifuss syndrome describe
Emery-Dreifuss muscular dystrophy (EDMD) is the third most common X-linked muscular dystrophy. ...
Skeletal and Cardiac Muscle Disorders Caused by Mutations in Genes Encoding Intermediate Filament Proteins.
Maggi L, Mavroidis M, Psarras S, Capetanaki Y, Lattanzi G. Maggi L, et al. Int J Mol Sci. 2021 Apr 20;22(8):4256. doi: 10.3390/ijms22084256. Int J Mol Sci. 2021. PMID: 33923914 Free PMC article. Review.
Diseases include desmin-related myopathy and cardiomyopathy (desminopathy), which can be manifested with dilated, restrictive, hypertrophic, arrhythmogenic, or even left ventricular non-compaction cardiomyopathy, Emery-Dreifuss Muscular Dystrophy (EDMD …
Diseases include desmin-related myopathy and cardiomyopathy (desminopathy), which can be manifested with dilated, restrictive, hypertrophic, …
164 results