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

Year Number of Results
1909 1
1910 2
1912 2
1914 1
1915 1
1917 1
1918 1
1923 4
1924 2
1925 2
1932 1
1935 1
1944 1
1945 2
1946 16
1947 12
1948 17
1949 18
1950 14
1951 23
1952 34
1953 18
1954 33
1955 37
1956 28
1957 35
1958 31
1959 26
1960 27
1961 44
1962 48
1963 33
1964 80
1965 36
1966 45
1967 42
1968 59
1969 56
1970 33
1971 50
1972 49
1973 43
1974 51
1975 57
1976 45
1977 47
1978 58
1979 50
1980 49
1981 33
1982 59
1983 47
1984 45
1985 40
1986 44
1987 35
1988 47
1989 47
1990 46
1991 41
1992 48
1993 60
1994 55
1995 58
1996 66
1997 63
1998 59
1999 62
2000 48
2001 52
2002 37
2003 35
2004 42
2005 38
2006 50
2007 52
2008 60
2009 48
2010 49
2011 55
2012 74
2013 91
2014 65
2015 84
2016 70
2017 83
2018 88
2019 85
2020 115
2021 101
2022 80
2023 79
2024 90
2025 84
2026 40

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3,942 results

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Page 1
[Myotonia].
Kuhn E. Kuhn E. Dtsch Med Wochenschr. 1976 Sep 10;101(37):1362-4. doi: 10.1055/s-0028-1104274. Dtsch Med Wochenschr. 1976. PMID: 782813 Review. German. No abstract available.
Muscle Channelopathies.
Trivedi JR. Trivedi JR. Continuum (Minneap Minn). 2022 Dec 1;28(6):1778-1799. doi: 10.1212/CON.0000000000001183. Continuum (Minneap Minn). 2022. PMID: 36537980 Review.
PURPOSE OF REVIEW: This article describes the clinical features, diagnosis, pathophysiology, and management of nondystrophic myotonia and periodic paralysis. RECENT FINDINGS: An increasing awareness exists about the genotype-phenotype overlap in skeletal muscle channelopat …
PURPOSE OF REVIEW: This article describes the clinical features, diagnosis, pathophysiology, and management of nondystrophic myotonia …
Muscle channelopathies.
Statland J, Phillips L, Trivedi JR. Statland J, et al. Neurol Clin. 2014 Aug;32(3):801-15, x. doi: 10.1016/j.ncl.2014.04.002. Epub 2014 May 9. Neurol Clin. 2014. PMID: 25037091 Review.
This article summarizes the clinical manifestations, diagnostic studies, pathophysiology, and treatment options in nondystrophic myotonia, congenital myasthenic syndrome, and periodic paralyses....
This article summarizes the clinical manifestations, diagnostic studies, pathophysiology, and treatment options in nondystrophic myotonia …
Myotonia.
Barchi RL. Barchi RL. Neurol Clin. 1988 Aug;6(3):473-84. Neurol Clin. 1988. PMID: 3065595 Review.
The clinical and electrophysiologic features of myotonia can be seen in a number of human diseases as well as in several well-studied animal models. ...A number of drugs that modify sodium channel activation kinetics can be used to effectively control the symptoms of my …
The clinical and electrophysiologic features of myotonia can be seen in a number of human diseases as well as in several well-studied …
Myotonia fluctuans.
Ricker K, Lehmann-Horn F, Moxley RT 3rd. Ricker K, et al. Arch Neurol. 1990 Mar;47(3):268-72. doi: 10.1001/archneur.1990.00530030034012. Arch Neurol. 1990. PMID: 2310311
The myotonia fluctuated to an unusual degree. It did not worsen with cold but increased markedly with potassium loading. ...Analysis of the contraction force of the flexor digitorum muscle showed a unique type of myotonia, namely, exercise-induced delayed-onset m …
The myotonia fluctuated to an unusual degree. It did not worsen with cold but increased markedly with potassium loading. ...Analysis …
Inherited myotonias.
Suetterlin K, Mӓnnikkӧ R, Jayaseelan DL. Suetterlin K, et al. Handb Clin Neurol. 2024;203:25-38. doi: 10.1016/B978-0-323-90820-7.00008-2. Handb Clin Neurol. 2024. PMID: 39174252
The dystrophic myotonias are caused by genes that alter splicing leading to more systemic effects with myotonia being one of a number of systemic symptoms. This chapter therefore focuses on the key aspects of the NDMs. ...The pathogenicity of different variants can be dete …
The dystrophic myotonias are caused by genes that alter splicing leading to more systemic effects with myotonia being one of a number …
Grip myotonia.
Yanagita Y, Shikino K, Ikusaka M. Yanagita Y, et al. BMJ Case Rep. 2021 May 6;14(5):e240779. doi: 10.1136/bcr-2020-240779. BMJ Case Rep. 2021. PMID: 33958356 Free PMC article. No abstract available.
Treatment of myotonia.
[No authors listed] [No authors listed] Lancet. 1987 May 30;1(8544):1242-4. Lancet. 1987. PMID: 2884374 No abstract available.
Drug treatment for myotonia.
Trip J, Drost G, van Engelen BG, Faber CG. Trip J, et al. Cochrane Database Syst Rev. 2006 Jan 25;2006(1):CD004762. doi: 10.1002/14651858.CD004762.pub2. Cochrane Database Syst Rev. 2006. Update in: Cochrane Database Syst Rev. 2025 Apr 08;4:CD004762. doi: 10.1002/14651858.CD004762.pub3. PMID: 16437496 Free PMC article. Updated.
The primary outcome measure was:reduced clinical myotonia using two categories: (1) no residual myotonia or improvement of myotonia or (2) No change or worsening of myotonia. Secondary outcome measures were:(1) clinical relaxation time; (2) electromyog …
The primary outcome measure was:reduced clinical myotonia using two categories: (1) no residual myotonia or improvement of …
Anaesthesia and myotonia.
Russell SH, Hirsch NP. Russell SH, et al. Br J Anaesth. 1994 Feb;72(2):210-6. doi: 10.1093/bja/72.2.210. Br J Anaesth. 1994. PMID: 8110575 Free article. Review. No abstract available.
3,942 results