Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1987 1
1988 1
1989 2
1992 2
1993 1
1997 2
1999 3
2000 3
2001 3
2002 1
2003 2
2004 2
2005 3
2006 3
2007 5
2008 3
2010 1
2011 3
2013 1
2016 1
2022 1
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

44 results

Results by year

Filters applied: . Clear all
Page 1
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. EDMD is also distinctive for its association with defects of the cardiac conduction system that c
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. X-linked EDMD is caused by mutations in EMD, which encodes an integral protein of the nuclear envelope inner membrane called emerin. .
Emery-Dreifuss muscular dystrophy (EDMD) is inherited in an X-linked or autosomal manner. X
Emery-Dreifuss syndrome.
Emery AE. Emery AE. J Med Genet. 1989 Oct;26(10):637-41. doi: 10.1136/jmg.26.10.637. J Med Genet. 1989. PMID: 2685312 Free PMC article. Review.
Emery-Dreifuss muscular dystrophy is characterised by the triad of (1) early contractures of the elbows, Achilles tendons, and postcervical muscles; (2) slowly progressive muscle wasting and weakness with a humeroperoneal distribution in the early stag
Emery-Dreifuss muscular dystrophy is characterised by the triad of (1) early contractures of the elbows, Achille
Emerin.
Tews DS. Tews DS. Int J Biochem Cell Biol. 1999 Sep;31(9):891-4. doi: 10.1016/s1357-2725(99)00040-0. Int J Biochem Cell Biol. 1999. PMID: 10533281 Review.
Emerin encoded by the STA gene is the first nuclear protein linked with a muscular dystrophy. Emerin is a 34 kDa, predominantly hydrophilic protein with a single hydrophobic region supposed to serve as a transmembrane domain. ...During mitosis, emerin is cell-cycle- …
Emerin encoded by the STA gene is the first nuclear protein linked with a muscular dystrophy. Emerin is a 34 kDa, predominantl …
X-linked muscular dystrophy with early contractures and cardiomyopathy (Emery-Dreifuss type).
Emery AE. Emery AE. Clin Genet. 1987 Nov;32(5):360-7. doi: 10.1111/j.1399-0004.1987.tb03302.x. Clin Genet. 1987. PMID: 3319295 Review.
The original Virginia family with X-linked muscular dystrophy with early contractures and cardiomyopathy (Emery-Dreifuss type) has been reinvestigated 25 years later. The findings confirm that a cardiomyopathy, presenting most often as at …
The original Virginia family with X-linked muscular dystrophy with early contractures and cardiomyopathy (Eme
Emery-Dreifuss muscular dystrophy: the most recognizable laminopathy.
Madej-Pilarczyk A, Kochański A. Madej-Pilarczyk A, et al. Folia Neuropathol. 2016;54(1):1-8. doi: 10.5114/fn.2016.58910. Folia Neuropathol. 2016. PMID: 27179216 Free article. Review.
Emery-Dreifuss muscular dystrophy (EDMD), a rare inherited disease, is characterized clinically by humero-peroneal muscle atrophy and weakness, multijoint contractures, spine rigidity and cardiac insufficiency with conduction defects. ...The majority o
Emery-Dreifuss muscular dystrophy (EDMD), a rare inherited disease, is characterized clinically by humero-perone
Emery-Dreifuss muscular dystrophy, laminopathies, and other nuclear envelopathies.
Bonne G, Quijano-Roy S. Bonne G, et al. Handb Clin Neurol. 2013;113:1367-76. doi: 10.1016/B978-0-444-59565-2.00007-1. Handb Clin Neurol. 2013. PMID: 23622360 Free article. Review.
The nuclear envelopathies, more frequently known as laminopathies are a rapidly expanding group of human hereditary diseases caused by mutations of genes that encode proteins of the nuclear envelope. The most frequent and best known form is Emery-Dreifuss muscula
The nuclear envelopathies, more frequently known as laminopathies are a rapidly expanding group of human hereditary diseases caused by mutat …
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 syn
Emery-Dreifuss muscular dystrophy (EDMD) is the third most common X-linked muscular dyst
[Emery-Dreifuss muscular dystrophy].
Kubo S, Tsukahara T, Arahata K. Kubo S, et al. Nihon Rinsho. 1997 Dec;55(12):3186-9. Nihon Rinsho. 1997. PMID: 9436433 Review. Japanese.
Emery-Dreifuss muscular dystrophy (EDMD) is an inherited muscular disorder characterized by the triad of progressive weakness in humero-peroneal muscles, early onset contractures and cardiomyopathy with conduction block that shows a high risk of
Emery-Dreifuss muscular dystrophy (EDMD) is an inherited muscular disorder characterized by the triad of
44 results