Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1975 1
1976 1
1985 1
1986 1
1989 1
1990 1
1992 1
1994 1
1995 4
1996 1
1997 2
1998 1
1999 1
2001 1
2004 4
2005 3
2006 1
2007 1
2008 2
2009 1
2011 1
2012 1
2013 1
2014 2
2015 3
2016 1
2017 2
2018 4
2019 2
2020 3
2021 1
2022 2
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

49 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Myoclonus, familial, 1"
Page 1
A comprehensive narrative review of epilepsy with eyelid myoclonia.
Smith KM, Wirrell EC, Andrade DM, Choi H, Trenité DK, Knupp KG, Nordli DR Jr, Riva A, Stern JM, Striano P, Thiele EA, Zawar I. Smith KM, et al. Epilepsy Res. 2023 Jul;193:107147. doi: 10.1016/j.eplepsyres.2023.107147. Epub 2023 Apr 26. Epilepsy Res. 2023. PMID: 37121024 Free article. Review.
Epilepsy with eyelid myoclonia (EEM) is a generalized epilepsy syndrome with childhood-onset and 2:1 female predominance that consists of: 1. eyelid myoclonia with or without absence seizures, 2. eye closure induced seizures or EEG paroxysms, 3. clinical or E …
Epilepsy with eyelid myoclonia (EEM) is a generalized epilepsy syndrome with childhood-onset and 2:1 female predominance that consist …
Carbamazepine-, Oxcarbazepine-, Eslicarbazepine-Associated Movement Disorder: A Literature Review.
Rissardo JP, Caprara ALF. Rissardo JP, et al. Clin Neuropharmacol. 2020 May/Jun;43(3):66-80. doi: 10.1097/WNF.0000000000000387. Clin Neuropharmacol. 2020. PMID: 32384309 Review.
BACKGROUND: Carbamazepine (CBZ), oxcarbazepine (OXC), and eslicarbazepine (ESL) acetate belong to the dibenzazepine family. In this context, the aim of this literature review is to evaluate the clinical epidemiological profile, pathological mechanisms, and managemen …
BACKGROUND: Carbamazepine (CBZ), oxcarbazepine (OXC), and eslicarbazepine (ESL) acetate belong to the dibenzazepine family. In this c …
Tardive tremor.
Stacy M, Jankovic J. Stacy M, et al. Mov Disord. 1992;7(1):53-7. doi: 10.1002/mds.870070110. Mov Disord. 1992. PMID: 1348352
The tremor was accompanied by other tardive movement disorders, including akathisia, chorea, dystonia, myoclonus, and stereotypy. There was no family history or other explanation for tremor in these patients. ...
The tremor was accompanied by other tardive movement disorders, including akathisia, chorea, dystonia, myoclonus, and stereotypy. The …
Topiramate-Associated Movement Disorder: Case Series and Literature Review.
Rissardo JP, Caprara ALF. Rissardo JP, et al. Clin Neuropharmacol. 2020 Jul/Aug;43(4):116-120. doi: 10.1097/WNF.0000000000000395. Clin Neuropharmacol. 2020. PMID: 32541330 Review.
The mean time of onset and recovery of the MD were 1.37 1.10 and 1.02 0.77 months, respectively. The mean TPM dose was 87.5 47.87 mg. ...CONCLUSIONS: To the authors' knowledge, there are 6 cases of myoclonus, 5 RLS, 2 dystonia, 1 dyskinesia, and …
The mean time of onset and recovery of the MD were 1.37 1.10 and 1.02 0.77 months, respectively. The mean TPM dose was …
Lafora disease: a case report.
Zeka N, Zogaj L, Gerguri A, Bejiqi R, Ratkoceri R, Maloku A, Mustafa A, Shahini L, Maxharaj J. Zeka N, et al. J Med Case Rep. 2022 Oct 3;16(1):360. doi: 10.1186/s13256-022-03537-x. J Med Case Rep. 2022. PMID: 36192771 Free PMC article.
It is inherited by autosomal recessive pattern presenting as a progressive myoclonus epilepsy and neurologic deterioration beginning in adolescence. ...When admitted to the hospital, blood tests and imaging examinations were planned. The blood tests were unremarkable. Ther …
It is inherited by autosomal recessive pattern presenting as a progressive myoclonus epilepsy and neurologic deterioration beginning …
Movement disorders associated with neuronal antibodies: a data-driven approach.
Sturchio A, Dwivedi AK, Gastaldi M, Grimberg MB, Businaro P, Duque KR, Vizcarra JA, Abdelghany E, Balint B, Marsili L, Espay AJ. Sturchio A, et al. J Neurol. 2022 Jul;269(7):3511-3521. doi: 10.1007/s00415-021-10934-7. Epub 2022 Jan 13. J Neurol. 2022. PMID: 35024921 Free PMC article.
We used random forests for variable selection and recursive partitioning and regression trees for the creation of a data-driven decision algorithm, integrated with expert's clinical feedback. RESULTS: Three hundred and seventy-seven studies met eligibility criteria, …
We used random forests for variable selection and recursive partitioning and regression trees for the creation of a data-driven decis …
Parasomnias and Sleep-Related Movement Disorders in Older Adults.
Iranzo A. Iranzo A. Sleep Med Clin. 2018 Mar;13(1):51-61. doi: 10.1016/j.jsmc.2017.09.005. Epub 2017 Nov 15. Sleep Med Clin. 2018. PMID: 29412983 Review.
Parasomnias and sleep-related movement disorders are important problems in older adults. Sleep paralysis is rare, but may occur in families. In a minority of patients with disorders of arousal, the episodes persist until the age of 70. ...
Parasomnias and sleep-related movement disorders are important problems in older adults. Sleep paralysis is rare, but may occur in famili …
Myoclonus epilepsy and ragged-red fibres (MERRF). 1. A clinical, pathological, biochemical, magnetic resonance spectrographic and positron emission tomographic study.
Berkovic SF, Carpenter S, Evans A, Karpati G, Shoubridge EA, Andermann F, Meyer E, Tyler JL, Diksic M, Arnold D, et al. Berkovic SF, et al. Brain. 1989 Oct;112 ( Pt 5):1231-60. doi: 10.1093/brain/112.5.1231. Brain. 1989. PMID: 2508988 Review.
Thirteen patients, including 6 from one family, with the syndrome of myoclonus epilepsy and ragged-red fibres (MERRF) were studied. There was considerable heterogeneity in the age of onset, severity and associated clinical features. Postmortem studies in 3 pa …
Thirteen patients, including 6 from one family, with the syndrome of myoclonus epilepsy and ragged-red fibres (MERRF) were stu …
Absence seizures and variants.
Lockman LA. Lockman LA. Neurol Clin. 1985 Feb;3(1):19-29. Neurol Clin. 1985. PMID: 3921816 Review.
Proper diagnosis requires careful historical elucidation of the actual seizure events, family history of seizures, and of other neurologic abnormalities. ...
Proper diagnosis requires careful historical elucidation of the actual seizure events, family history of seizures, and of other neuro …
Debate: Does genetic information in humans help us treat patients? PRO--genetic information in humans helps us treat patients. CON--genetic information does not help at all.
Delgado-Escueta AV, Bourgeois BF. Delgado-Escueta AV, et al. Epilepsia. 2008 Dec;49 Suppl 9:13-24. doi: 10.1111/j.1528-1167.2008.01922.x. Epilepsia. 2008. PMID: 19087113 Free article. Review.
Genotyping ensures accurate diagnosis, helps treatment and genetic counseling, psychological and social help for patients and families, and directs families to organizations devoted to finding cures for specific epilepsy diseases. ...Since not all individuals with g …
Genotyping ensures accurate diagnosis, helps treatment and genetic counseling, psychological and social help for patients and families …
49 results