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

Year Number of Results
1874 1
1947 1
1951 2
1952 1
1953 1
1956 1
1959 1
1962 1
1963 1
1964 1
1967 1
1968 1
1969 3
1971 1
1972 1
1973 5
1975 7
1976 15
1977 7
1978 10
1979 9
1980 17
1981 10
1982 18
1983 19
1984 22
1985 18
1986 25
1987 31
1988 35
1989 29
1990 36
1991 47
1992 50
1993 59
1994 58
1995 66
1996 66
1997 82
1998 76
1999 89
2000 88
2001 105
2002 92
2003 115
2004 136
2005 149
2006 132
2007 168
2008 173
2009 201
2010 219
2011 193
2012 226
2013 230
2014 275
2015 255
2016 207
2017 199
2018 226
2019 275
2020 262
2021 313
2022 311
2023 253
2024 66

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5,170 results

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Page 1
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 important to diagnose due to frequent life …
Emery-Dreifuss Muscular Dystrophy.
Bonne G, Leturcq F, Ben Yaou R. Bonne G, et al. 2004 Sep 29 [updated 2019 Aug 15]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2004 Sep 29 [updated 2019 Aug 15]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301609 Free Books & Documents. Review.
Evaluation of relatives at risk: Molecular genetic testing if the pathogenic variant(s) in the family are known; clinical evaluation, including at least muscular and cardiac assessments if the pathogenic variant(s) in the family are not known. ...At conception, each …
Evaluation of relatives at risk: Molecular genetic testing if the pathogenic variant(s) in the family are known; clinical evaluation, …
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 of the Achilles tendo …
Net39 protects muscle nuclei from mechanical stress during the pathogenesis of Emery-Dreifuss muscular dystrophy.
Zhang Y, Ramirez-Martinez A, Chen K, McAnally JR, Cai C, Durbacz MZ, Chemello F, Wang Z, Xu L, Bassel-Duby R, Liu N, Olson EN. Zhang Y, et al. J Clin Invest. 2023 Jul 3;133(13):e163333. doi: 10.1172/JCI163333. J Clin Invest. 2023. PMID: 37395273 Free PMC article.
Mutations in genes encoding nuclear envelope proteins lead to diseases known as nuclear envelopathies, characterized by skeletal muscle and heart abnormalities, such as Emery-Dreifuss muscular dystrophy (EDMD). The tissue-specific role of the nuclear envelope in the etiolo …
Mutations in genes encoding nuclear envelope proteins lead to diseases known as nuclear envelopathies, characterized by skeletal muscle and …
Emery-Dreifuss muscular dystrophy: focal point nuclear envelope.
Muchir A, Worman HJ. Muchir A, et al. Curr Opin Neurol. 2019 Oct;32(5):728-734. doi: 10.1097/WCO.0000000000000741. Curr Opin Neurol. 2019. PMID: 31460960 Free PMC article. Review.
PURPOSE OF REVIEW: Emery-Dreifuss muscular dystrophy (EDMD) is caused by mutations in EMD encoding emerin and LMNA encoding A-type lamins, proteins of the nuclear envelope. ...
PURPOSE OF REVIEW: Emery-Dreifuss muscular dystrophy (EDMD) is caused by mutations in EMD encoding emerin and LMNA encoding A-type la …
Emery-Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure.
Cannie DE, Syrris P, Protonotarios A, Bakalakos A, Pruny JF, Ditaranto R, Martinez-Veira C, Larrañaga-Moreira JM, Medo K, Bermúdez-Jiménez FJ, Ben Yaou R, Leturcq F, Mezcua AR, Marini-Bettolo C, Cabrera E, Reuter C, Limeres Freire J, Rodríguez-Palomares JF, Mestroni L, Taylor MRG, Parikh VN, Ashley EA, Barriales-Villa R, Jiménez-Jáimez J, Garcia-Pavia P, Charron P, Biagini E, García Pinilla JM, Bourke J, Savvatis K, Wahbi K, Elliott PM. Cannie DE, et al. Eur Heart J. 2023 Dec 21;44(48):5064-5073. doi: 10.1093/eurheartj/ehad561. Eur Heart J. 2023. PMID: 37639473 Free PMC article.
BACKGROUND AND AIMS: Emery-Dreifuss muscular dystrophy (EDMD) is caused by variants in EMD (EDMD1) and LMNA (EDMD2). ...
BACKGROUND AND AIMS: Emery-Dreifuss muscular dystrophy (EDMD) is caused by variants in EMD (EDMD1) and LMNA (EDMD2). ...
Profile of Emery N. Brown.
Viegas J. Viegas J. Proc Natl Acad Sci U S A. 2022 Nov 22;119(47):e2215827119. doi: 10.1073/pnas.2215827119. Epub 2022 Nov 14. Proc Natl Acad Sci U S A. 2022. PMID: 36375058 Free PMC article. No abstract available.
Splenic emergencies.
Emery KH. Emery KH. Radiol Clin North Am. 1997 Jul;35(4):831-43. Radiol Clin North Am. 1997. PMID: 9216627 Review.
Stepping out of your comfort zone.
Emery S. Emery S. Br J Nurs. 2020 Jan 9;29(1):55. doi: 10.12968/bjon.2020.29.1.55. Br J Nurs. 2020. PMID: 31917938
Sophie Emery, Student Children's Nurse at the University of Hertfordshire, reflects on her elective placement in Zambia....
Sophie Emery, Student Children's Nurse at the University of Hertfordshire, reflects on her elective placement in Zambia....
Molecular signatures of Emery-Dreifuss muscular dystrophy.
Wheeler MA, Ellis JA. Wheeler MA, et al. Biochem Soc Trans. 2008 Dec;36(Pt 6):1354-8. doi: 10.1042/BST0361354. Biochem Soc Trans. 2008. PMID: 19021555 Review.
These include dilated cardiomyopathy, limb-girdle muscular dystrophy and X-linked and autosomal dominant EDMD (Emery-Dreifuss muscular dystrophy). The molecular mechanisms underlying these disorders are poorly understood; however, recent work using animal models has identi …
These include dilated cardiomyopathy, limb-girdle muscular dystrophy and X-linked and autosomal dominant EDMD (Emery-Dreifuss muscula …
5,170 results