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

Year Number of Results
1963 3
1964 1
1965 3
1966 1
1967 2
1968 1
1969 2
1970 5
1971 8
1972 7
1973 1
1974 4
1975 4
1976 4
1977 4
1978 1
1979 3
1980 3
1981 1
1982 4
1983 7
1984 2
1985 5
1986 3
1987 5
1988 9
1989 12
1990 5
1991 8
1992 15
1993 33
1994 23
1995 23
1996 21
1997 30
1998 19
1999 19
2000 24
2001 16
2002 25
2003 18
2004 22
2005 24
2006 29
2007 26
2008 29
2009 25
2010 27
2011 28
2012 33
2013 34
2014 26
2015 25
2016 35
2017 28
2018 31
2019 34
2020 29
2021 36
2022 27
2023 17
2024 2

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902 results

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Page 1
Myotonic dystrophy.
Thornton CA. Thornton CA. Neurol Clin. 2014 Aug;32(3):705-19, viii. doi: 10.1016/j.ncl.2014.04.011. Epub 2014 Jun 6. Neurol Clin. 2014. PMID: 25037086 Free PMC article. Review.
Myotonic dystrophy (dystrophia myotonica, DM) is one of the most common lethal monogenic disorders in populations of European descent. ...Both disorders have autosomal dominant inheritance and multisystem features, including myotonic myopathy, cataract, and c
Myotonic dystrophy (dystrophia myotonica, DM) is one of the most common lethal monogenic disorders in populations of European
Myotonic Dystrophy.
Hamel JI. Hamel JI. Continuum (Minneap Minn). 2022 Dec 1;28(6):1715-1734. doi: 10.1212/CON.0000000000001184. Continuum (Minneap Minn). 2022. PMID: 36537977 Review.
PURPOSE OF REVIEW: Myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2) are genetic disorders affecting skeletal and smooth muscle, heart, brain, eyes, and other organs. ...RECENT FINDINGS: Studies of the multisystem involvement of my
PURPOSE OF REVIEW: Myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2) are genetic disorders aff …
Myotonic dystrophy type 2: the 2020 update.
Meola G. Meola G. Acta Myol. 2020 Dec 1;39(4):222-234. doi: 10.36185/2532-1900-026. eCollection 2020 Dec. Acta Myol. 2020. PMID: 33458578 Free PMC article. Review.
For the enormous understanding of the molecular pathogenesis of myotonic dystrophy type 1 and myotonic dystrophy type 2, these diseases are now called "spliceopathies" and are mediated by a primary disorder of RNA rather than proteins. ...Gene therapy …
For the enormous understanding of the molecular pathogenesis of myotonic dystrophy type 1 and myotonic dystrophy
The myotonic dystrophy type 1 drug development pipeline: 2022 edition.
Pascual-Gilabert M, Artero R, López-Castel A. Pascual-Gilabert M, et al. Drug Discov Today. 2023 Mar;28(3):103489. doi: 10.1016/j.drudis.2023.103489. Epub 2023 Jan 9. Drug Discov Today. 2023. PMID: 36634841 Free article. Review.
The beginning of the 20th decade has witnessed an increase in drug development programs for myotonic dystrophy type 1 (DM1). We have collected nearly 20 candidate drugs with accomplished preclinical and clinical phases, updating our previous drug development pipelin …
The beginning of the 20th decade has witnessed an increase in drug development programs for myotonic dystrophy type 1 (DM1). W …
Metabolic Alterations in Myotonic Dystrophy Type 1 and Their Correlation with Lipin.
Mateus T, Martins F, Nunes A, Herdeiro MT, Rebelo S. Mateus T, et al. Int J Environ Res Public Health. 2021 Feb 12;18(4):1794. doi: 10.3390/ijerph18041794. Int J Environ Res Public Health. 2021. PMID: 33673200 Free PMC article. Review.
Myotonic dystrophy type 1 (DM1) is an autosomal dominant hereditary and multisystemic disease, characterized by progressive distal muscle weakness and myotonia. ...
Myotonic dystrophy type 1 (DM1) is an autosomal dominant hereditary and multisystemic disease, characterized by progressive di
Cerebral involvement and related aspects in myotonic dystrophy type 2.
Peric S, Rakocevic-Stojanovic V, Meola G. Peric S, et al. Neuromuscul Disord. 2021 Aug;31(8):681-694. doi: 10.1016/j.nmd.2021.06.002. Epub 2021 Jun 9. Neuromuscul Disord. 2021. PMID: 34244019 Review.
Myotonic dystrophy type 2 (DM2) is an autosomal dominant multisystemic disorder caused by CCTG repeats expansion in the first intron of the CNBP gene. ...
Myotonic dystrophy type 2 (DM2) is an autosomal dominant multisystemic disorder caused by CCTG repeats expansion in the first
Myotonic dystrophy and the heart: A systematic review of evaluation and management.
Lau JK, Sy RW, Corbett A, Kritharides L. Lau JK, et al. Int J Cardiol. 2015 Apr 1;184:600-608. doi: 10.1016/j.ijcard.2015.03.069. Epub 2015 Mar 5. Int J Cardiol. 2015. PMID: 25769007 Review.
Myotonic dystrophy (MD) is a multisystem, autosomal dominant disorder best known for its skeletal muscle manifestations. ...In addition, "myotonic dystrophy" was searched in conjunction with "electrophysiology", "electrocardiogram", "echocardiograph",
Myotonic dystrophy (MD) is a multisystem, autosomal dominant disorder best known for its skeletal muscle manifestations. ...In
Social cognition in type 1 myotonic dystrophy - A mini review.
Leddy S, Cercignani M, Serra L, Bozzali M. Leddy S, et al. Cortex. 2021 Sep;142:389-399. doi: 10.1016/j.cortex.2021.05.004. Epub 2021 May 27. Cortex. 2021. PMID: 34154799 Free article. Review.
Research in social cognitive neuroscience aims to understand the underlying neurobiology of our social behaviours and interactions with others. Myotonic dystrophy type 1 (DM1) is a genetically inherited neuromuscular disorder characterized by mytonia with systemic m …
Research in social cognitive neuroscience aims to understand the underlying neurobiology of our social behaviours and interactions with othe …
Sleep Complaints, Sleep and Breathing Disorders in Myotonic Dystrophy Type 2.
Romigi A, Maestri M, Nicoletta C, Vitrani G, Caccamo M, Siciliano G, Bonanni E, Centonze D, Sanduzzi A. Romigi A, et al. Curr Neurol Neurosci Rep. 2019 Feb 9;19(2):9. doi: 10.1007/s11910-019-0924-0. Curr Neurol Neurosci Rep. 2019. PMID: 30739220 Review.
PURPOSE OF REVIEW: To update the current knowledge concerning sleep complaints and breathing disorders in myotonic dystrophy type 2 (DM2) and to better understand if sleep and breathing symptoms may add a further clinical definition of DM2. ...
PURPOSE OF REVIEW: To update the current knowledge concerning sleep complaints and breathing disorders in myotonic dystrophy t …
Myotonic Dystrophies: A Genetic Overview.
Soltanzadeh P. Soltanzadeh P. Genes (Basel). 2022 Feb 17;13(2):367. doi: 10.3390/genes13020367. Genes (Basel). 2022. PMID: 35205411 Free PMC article. Review.
Myotonic dystrophies (DM) are the most common muscular dystrophies in adults, which can affect other non-skeletal muscle organs such as the heart, brain and gastrointestinal system. There are two genetically distinct types of myotonic dystrophy: myotonic
Myotonic dystrophies (DM) are the most common muscular dystrophies in adults, which can affect other non-skeletal muscle organs such
902 results