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
1946 1
1947 2
1948 2
1950 2
1951 1
1952 2
1953 6
1955 1
1957 4
1958 2
1959 1
1960 2
1961 1
1963 3
1964 5
1965 2
1966 3
1967 3
1968 1
1969 2
1970 1
1971 4
1972 3
1973 4
1974 6
1975 53
1976 53
1977 48
1978 64
1979 50
1980 66
1981 82
1982 87
1983 110
1984 123
1985 118
1986 148
1987 133
1988 150
1989 151
1990 190
1991 232
1992 288
1993 263
1994 284
1995 316
1996 314
1997 373
1998 364
1999 436
2000 482
2001 466
2002 444
2003 513
2004 535
2005 660
2006 711
2007 736
2008 813
2009 875
2010 877
2011 1026
2012 1080
2013 1195
2014 1279
2015 1328
2016 1400
2017 1493
2018 1518
2019 1528
2020 1823
2021 2069
2022 1894
2023 1832
2024 747

Text availability

Article attribute

Article type

Publication date

Search Results

28,138 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Muscular dystrophy, congenital, with or without seizures"
Page 1
Seizure prediction and intervention.
Meisel C, Loddenkemper T. Meisel C, et al. Neuropharmacology. 2020 Aug 1;172:107898. doi: 10.1016/j.neuropharm.2019.107898. Epub 2019 Dec 5. Neuropharmacology. 2020. PMID: 31839204 Review.
Epilepsy treatment is challenging due to a lack of essential diagnostic tools, including methods for reliable seizure detection in the ambulatory setting, to assess seizure risk over time and to monitor treatment efficacy. ...Here, we provide an overview on data- an …
Epilepsy treatment is challenging due to a lack of essential diagnostic tools, including methods for reliable seizure detection in th …
Automated seizure prediction.
Acharya UR, Hagiwara Y, Adeli H. Acharya UR, et al. Epilepsy Behav. 2018 Nov;88:251-261. doi: 10.1016/j.yebeh.2018.09.030. Epub 2018 Oct 11. Epilepsy Behav. 2018. PMID: 30317059 Review.
In recent years, the frontiers of computational epilepsy research have moved to seizure prediction, a more challenging problem. While antiepileptic medication can result in complete seizure freedom in many patients with epilepsy, up to one-third of patients l …
In recent years, the frontiers of computational epilepsy research have moved to seizure prediction, a more challenging problem …
Seizure Detection, Prediction, and Forecasting.
Fu A, Lado FA. Fu A, et al. J Clin Neurophysiol. 2024 Mar 1;41(3):207-213. doi: 10.1097/WNP.0000000000001045. J Clin Neurophysiol. 2024. PMID: 38436388 Review.
Among the many fears associated with seizures, patients with epilepsy are greatly frustrated and distressed over seizure's apparent unpredictable occurrence. ...The pattern in rises and falls of seizure rate that varies over 24 hours, weeks, months, an …
Among the many fears associated with seizures, patients with epilepsy are greatly frustrated and distressed over seizure's …
Poststroke seizure: optimising its management.
Xu MY. Xu MY. Stroke Vasc Neurol. 2018 Dec 9;4(1):48-56. doi: 10.1136/svn-2018-000175. eCollection 2019 Mar. Stroke Vasc Neurol. 2018. PMID: 31105979 Free PMC article. Review.
Seizure after stroke or poststroke seizure (PSS) is a common and very important complication of stroke. It can be divided into early seizure and late seizure, depending on seizure onset time after the stroke. ...
Seizure after stroke or poststroke seizure (PSS) is a common and very important complication of stroke. It can be divided into …
Epilepsy in patients with advanced Fukuyama congenital muscular dystrophy.
Kuwayama R, Suzuki Y, Nishikawa M, Kimizu T, Nakajima K, Ikeda T, Mogami Y, Yanagihara K. Kuwayama R, et al. Brain Dev. 2021 Jan;43(1):106-110. doi: 10.1016/j.braindev.2020.06.017. Epub 2020 Jul 25. Brain Dev. 2021. PMID: 32723526
BACKGROUND: Recent advances in respiratory management have improved survival for patients with Fukuyama congenital muscular dystrophy (FCMD), characterized by congenital muscular dystrophy and brain malformation. ...In some patients, EEGs …
BACKGROUND: Recent advances in respiratory management have improved survival for patients with Fukuyama congenital muscular …
Chance and risk in epilepsy.
Baud MO, Proix T, Rao VR, Schindler K. Baud MO, et al. Curr Opin Neurol. 2020 Apr;33(2):163-172. doi: 10.1097/WCO.0000000000000798. Curr Opin Neurol. 2020. PMID: 32049738 Review.
This temporal structure of epilepsy has theoretical implications and argues against the conception of seizures as completely random events. The practical significance of cycles in epilepsy is highlighted by their predictive value in computational models for seizu …
This temporal structure of epilepsy has theoretical implications and argues against the conception of seizures as completely random e …
Global muscular dystrophy research: A 25-year bibliometric perspective.
Ram S. Ram S. Neurol India. 2017 Sep-Oct;65(5):993-1000. doi: 10.4103/neuroindia.NI_1241_16. Neurol India. 2017. PMID: 28879884 Free article. Review.
The prevalence of muscular dystrophy has been observed globally and is becoming a critical area of study for better health services. ...This literature-based study was conducted using the documents retrieved from the Science Citation Index using the keywords: …
The prevalence of muscular dystrophy has been observed globally and is becoming a critical area of study for better hea …
Trouble at the junction: When myopathy and myasthenia overlap.
Nicolau S, Kao JC, Liewluck T. Nicolau S, et al. Muscle Nerve. 2019 Dec;60(6):648-657. doi: 10.1002/mus.26676. Epub 2019 Sep 10. Muscle Nerve. 2019. PMID: 31449669 Review.
Inherited causes include myopathies related to mutations in BIN1, DES, DNM2, GMPPB, MTM1, or PLEC and congenital myasthenic syndromes due to mutations in ALG2, ALG14, COL13A1, DOK7, DPAGT1, or GFPT1. Additionally, a decrement due to muscle fiber inexcitability is observ …
Inherited causes include myopathies related to mutations in BIN1, DES, DNM2, GMPPB, MTM1, or PLEC and congenital myasthenic syndromes …
Defining and identifying satellite cell-opathies within muscular dystrophies and myopathies.
Ganassi M, Muntoni F, Zammit PS. Ganassi M, et al. Exp Cell Res. 2022 Feb 1;411(1):112906. doi: 10.1016/j.yexcr.2021.112906. Epub 2021 Nov 3. Exp Cell Res. 2022. PMID: 34740639 Free PMC article.
Muscular dystrophies and congenital myopathies arise from specific genetic mutations causing skeletal muscle weakness that reduces quality of life. ...Here, we explore the effects on satellite cell function of pathogenic mutations in genes (myopathogenes) tha …
Muscular dystrophies and congenital myopathies arise from specific genetic mutations causing skeletal muscle weakness t …
Seizure prediction: methods.
Carney PR, Myers S, Geyer JD. Carney PR, et al. Epilepsy Behav. 2011 Dec;22 Suppl 1(Suppl 1):S94-101. doi: 10.1016/j.yebeh.2011.09.001. Epilepsy Behav. 2011. PMID: 22078526 Free PMC article.
There is great interest in the development of devices that incorporate algorithms capable of detecting early onset of seizures or even predicting them hours before they occur. The lead time provided by these new technologies will allow for new types of interventiona …
There is great interest in the development of devices that incorporate algorithms capable of detecting early onset of seizures or eve …
28,138 results
You have reached the last available page of results. Please see the User Guide for more information.