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

Year Number of Results
1949 2
1951 1
1953 2
1955 1
1959 1
1960 1
1963 1
1970 1
1971 4
1972 4
1973 4
1974 3
1975 1
1976 2
1977 2
1978 7
1979 8
1980 4
1981 5
1982 7
1983 2
1984 8
1985 5
1986 5
1987 10
1988 7
1989 5
1990 7
1991 5
1992 5
1993 13
1994 3
1995 11
1996 14
1997 15
1998 25
1999 14
2000 20
2001 17
2002 29
2003 35
2004 31
2005 27
2006 24
2007 25
2008 40
2009 30
2010 31
2011 45
2012 51
2013 57
2014 49
2015 48
2016 56
2017 68
2018 74
2019 65
2020 92
2021 68
2022 54
2023 72
2024 24

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1,229 results

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Page 1
Classification of myasthenia gravis and congenital myasthenic syndromes in dogs and cats.
Mignan T, Targett M, Lowrie M. Mignan T, et al. J Vet Intern Med. 2020 Sep;34(5):1707-1717. doi: 10.1111/jvim.15855. Epub 2020 Jul 15. J Vet Intern Med. 2020. PMID: 32668077 Free PMC article. Review.
Myasthenia, a syndrome of impaired neuromuscular transmission, occurs as either an acquired or congenital condition. Myasthenia gravis (MG) is an acquired autoimmune disorder with autoantibodies against the neuromuscular junction (NMJ) of skeletal muscle whereas congeni
Myasthenia, a syndrome of impaired neuromuscular transmission, occurs as either an acquired or congenital condition. Myasthenia gravi …
Myasthenia Gravis and Congenital Myasthenic Syndromes.
Ciafaloni E. Ciafaloni E. Continuum (Minneap Minn). 2019 Dec;25(6):1767-1784. doi: 10.1212/CON.0000000000000800. Continuum (Minneap Minn). 2019. PMID: 31794470 Review.
PURPOSE OF REVIEW: Myasthenia gravis (MG) is an autoimmune neuromuscular disease that causes fluctuating weakness in ocular, bulbar, and limb muscles and can, in 15% of cases, cause myasthenic crisis, a neurologic emergency characterized by respiratory failure. ...Special …
PURPOSE OF REVIEW: Myasthenia gravis (MG) is an autoimmune neuromuscular disease that causes fluctuating weakness in ocular, bulbar, and lim …
Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment.
Engel AG, Shen XM, Selcen D, Sine SM. Engel AG, et al. Lancet Neurol. 2015 Apr;14(4):420-34. doi: 10.1016/S1474-4422(14)70201-7. Lancet Neurol. 2015. PMID: 25792100 Free PMC article. Review.
The congenital myasthenic syndromes (CMS) are a diverse group of genetic disorders caused by abnormal signal transmission at the motor endplate, a special synaptic contact between motor axons and each skeletal muscle fibre. ...
The congenital myasthenic syndromes (CMS) are a diverse group of genetic disorders caused by abnormal signal transmissi …
Congenital myasthenic syndromes.
Finsterer J. Finsterer J. Orphanet J Rare Dis. 2019 Feb 26;14(1):57. doi: 10.1186/s13023-019-1025-5. Orphanet J Rare Dis. 2019. PMID: 30808424 Free PMC article.
OBJECTIVES: Congenital myasthenic syndromes (CMSs) are a genotypically and phenotypically heterogeneous group of neuromuscular disorders, which have in common an impaired neuromuscular transmission. ...
OBJECTIVES: Congenital myasthenic syndromes (CMSs) are a genotypically and phenotypically heterogeneous group of neurom …
Congenital Myasthenic Syndromes.
Shieh PB, Oh SJ. Shieh PB, et al. Neurol Clin. 2018 May;36(2):367-378. doi: 10.1016/j.ncl.2018.01.007. Neurol Clin. 2018. PMID: 29655455 Review.
The congenital myasthenic syndromes (CMS) are a group of rare genetic conditions characterized by abnormal neuromuscular transmission. Typically, these conditions have been the result of a dysfunctional protein that is present in the presynaptic terminal, the …
The congenital myasthenic syndromes (CMS) are a group of rare genetic conditions characterized by abnormal neuromuscula …
Congenital Myasthenic Syndromes.
Iyadurai SJP. Iyadurai SJP. Neurol Clin. 2020 Aug;38(3):541-552. doi: 10.1016/j.ncl.2020.03.004. Neurol Clin. 2020. PMID: 32703467 Review.
Congenital myasthenic syndromes comprise a rare heterogeneous group of diseases that impair neuromuscular transmission and are characterized by muscle fatigability and transient or permanent weakness. Symptoms are often present from birth or early childhood.
Congenital myasthenic syndromes comprise a rare heterogeneous group of diseases that impair neuromuscular transmission
Prevelance in congenital myasthenic syndrome.
Finsterer J. Finsterer J. Eur J Paediatr Neurol. 2020 May;26:5-6. doi: 10.1016/j.ejpn.2020.04.011. Epub 2020 Apr 23. Eur J Paediatr Neurol. 2020. PMID: 32359833 No abstract available.
Congenital myasthenic syndromes.
Eymard B, Hantaï D, Estournet B. Eymard B, et al. Handb Clin Neurol. 2013;113:1469-80. doi: 10.1016/B978-0-444-59565-2.00016-2. Handb Clin Neurol. 2013. PMID: 23622369 Review.
Congenital myasthenic syndromes (CMS) are a heterogeneous group of disorders caused by genetic defects affecting neuromuscular transmission and leading to muscle weakness accentuated by exertion. ...
Congenital myasthenic syndromes (CMS) are a heterogeneous group of disorders caused by genetic defects affecting neurom
Congenital Myasthenic Syndromes in 2018.
Engel AG. Engel AG. Curr Neurol Neurosci Rep. 2018 Jun 12;18(8):46. doi: 10.1007/s11910-018-0852-4. Curr Neurol Neurosci Rep. 2018. PMID: 29892917 Review.
PURPOSE OF REVIEW: Summarize features of the currently recognized congenital myasthenic syndromes (CMS) with emphasis on novel findings identified in the past 6 years. ...
PURPOSE OF REVIEW: Summarize features of the currently recognized congenital myasthenic syndromes (CMS) with emphasis o …
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, …
1,229 results