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

Year Number of Results
1963 6
1964 10
1965 10
1966 7
1967 14
1968 12
1969 20
1970 16
1971 17
1972 18
1973 11
1974 11
1975 12
1976 13
1977 20
1978 16
1979 15
1980 30
1981 14
1982 22
1983 31
1984 16
1985 12
1986 22
1987 24
1988 57
1989 71
1990 50
1991 52
1992 53
1993 93
1994 68
1995 86
1996 98
1997 92
1998 93
1999 110
2000 108
2001 139
2002 118
2003 101
2004 119
2005 153
2006 141
2007 137
2008 131
2009 122
2010 152
2011 160
2012 166
2013 201
2014 171
2015 175
2016 171
2017 203
2018 243
2019 209
2020 212
2021 226
2022 176
2023 158
2024 37

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4,884 results

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Page 1
Global prevalence of Duchenne and Becker muscular dystrophy: a systematic review and meta-analysis.
Salari N, Fatahi B, Valipour E, Kazeminia M, Fatahian R, Kiaei A, Shohaimi S, Mohammadi M. Salari N, et al. J Orthop Surg Res. 2022 Feb 15;17(1):96. doi: 10.1186/s13018-022-02996-8. J Orthop Surg Res. 2022. PMID: 35168641 Free PMC article. Review.
BACKGROUND: A variety of mutations in the largest human gene, dystrophin, cause a spectrum from mild to severe dystrophin-associated muscular dystrophies. Duchenne (DMD) and Becker (BMD) muscular dystrophies are located at the severe end of the spectru …
BACKGROUND: A variety of mutations in the largest human gene, dystrophin, cause a spectrum from mild to severe dystrophin-associated musc …
Congenital Muscular Dystrophy and Congenital Myopathy.
Butterfield RJ. Butterfield RJ. Continuum (Minneap Minn). 2019 Dec;25(6):1640-1661. doi: 10.1212/CON.0000000000000792. Continuum (Minneap Minn). 2019. PMID: 31794464 Review.
PURPOSE OF REVIEW: Congenital muscular dystrophies and congenital myopathies are a heterogeneous group of disorders resulting in hypotonia, muscle weakness, and dystrophic or myopathic features on muscle biopsy. ...This article reviews the clinical and genetic featu …
PURPOSE OF REVIEW: Congenital muscular dystrophies and congenital myopathies are a heterogeneous group of disorders resulting …
Muscular Dystrophies.
Carter JC, Sheehan DW, Prochoroff A, Birnkrant DJ. Carter JC, et al. Clin Chest Med. 2018 Jun;39(2):377-389. doi: 10.1016/j.ccm.2018.01.004. Clin Chest Med. 2018. PMID: 29779596 Review.
Muscular dystrophies represent a complex, varied, and important subset of neuromuscular disorders likely to require the care of a pulmonologist. ...The authors present an overview of the muscular dystrophies, including their basic features, common clin …
Muscular dystrophies represent a complex, varied, and important subset of neuromuscular disorders likely to require the care o …
Duchenne and Becker muscular dystrophies.
Flanigan KM. Flanigan KM. Neurol Clin. 2014 Aug;32(3):671-88, viii. doi: 10.1016/j.ncl.2014.05.002. Neurol Clin. 2014. PMID: 25037084 Review.
The dystrophinopathies Duchenne and Becker muscular dystrophies (DMD and BMD) represent the most common inherited disorders of muscle. ...
The dystrophinopathies Duchenne and Becker muscular dystrophies (DMD and BMD) represent the most common inherited disorders of …
Muscular dystrophies.
Mercuri E, Bönnemann CG, Muntoni F. Mercuri E, et al. Lancet. 2019 Nov 30;394(10213):2025-2038. doi: 10.1016/S0140-6736(19)32910-1. Lancet. 2019. PMID: 31789220 Review.
Muscular dystrophies are primary diseases of muscle due to mutations in more than 40 genes, which result in dystrophic changes on muscle biopsy. ...The improved understanding of the pathogenesis of these diseases is being used for the development of novel therapies. …
Muscular dystrophies are primary diseases of muscle due to mutations in more than 40 genes, which result in dystrophic changes …
Skeletal muscle in health and disease.
Morgan J, Partridge T. Morgan J, et al. Dis Model Mech. 2020 Feb 6;13(2):dmm042192. doi: 10.1242/dmm.042192. Dis Model Mech. 2020. PMID: 32066552 Free PMC article. Review.
They are formed by fusion of muscle precursor cells, and grow into elongating myofibres by the addition of further precursor cells, called satellite cells, which are also responsible for regeneration following injury. Skeletal muscle regeneration occurs in most muscular …
They are formed by fusion of muscle precursor cells, and grow into elongating myofibres by the addition of further precursor cells, called s …
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 p …
The muscular dystrophies are inherited myogenic disorders characterised by progressive muscle wasting and weakness of variable …
Dystrophinopathies.
Brandsema JF, Darras BT. Brandsema JF, et al. Semin Neurol. 2015 Aug;35(4):369-84. doi: 10.1055/s-0035-1558982. Epub 2015 Oct 6. Semin Neurol. 2015. PMID: 26502761 Review.
The dystrophinopathies fall along a spectrum of muscular dystrophy phenotypes, with variable involvement of skeletal and cardiac muscle. ...Management of the dystrophinopathies is focused primarily on supportive care, although steroid therapy has changed the natural …
The dystrophinopathies fall along a spectrum of muscular dystrophy phenotypes, with variable involvement of skeletal and cardi …
Childhood muscular dystrophies.
Younger DS. Younger DS. Handb Clin Neurol. 2023;195:461-496. doi: 10.1016/B978-0-323-98818-6.00024-8. Handb Clin Neurol. 2023. PMID: 37562882 Review.
Infancy- and childhood-onset muscular dystrophies are associated with a characteristic distribution and progression of motor dysfunction. The underlying causes of progressive childhood muscular dystrophies are heterogeneous involving diverse genetic pa …
Infancy- and childhood-onset muscular dystrophies are associated with a characteristic distribution and progression of motor d …
Muscular dystrophy.
Janas J. Janas J. Nurse Pract Forum. 1996 Dec;7(4):167-73. Nurse Pract Forum. 1996. PMID: 9043296 Review.
Muscular dystrophy can be a devastating diagnosis for children and their families. Understanding the potential course, prognosis, and genetic implications for the child and his/her family is dependent on the diagnosis of the specific type of dystrophy. This a …
Muscular dystrophy can be a devastating diagnosis for children and their families. Understanding the potential course, prognos …
4,884 results