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

Year Number of Results
1945 1
1947 4
1948 4
1949 2
1950 4
1951 12
1952 5
1953 5
1954 10
1955 7
1956 1
1957 9
1958 3
1959 3
1960 8
1961 12
1962 4
1963 8
1964 8
1965 4
1966 1
1967 1
1969 1
1970 1
1971 2
1973 5
1974 3
1975 6
1976 19
1977 44
1978 45
1979 38
1980 45
1981 47
1982 39
1983 39
1984 35
1985 59
1986 67
1987 53
1988 49
1989 69
1990 76
1991 112
1992 103
1993 130
1994 94
1995 117
1996 111
1997 111
1998 116
1999 145
2000 145
2001 139
2002 150
2003 136
2004 128
2005 168
2006 173
2007 172
2008 158
2009 201
2010 187
2011 245
2012 229
2013 237
2014 214
2015 210
2016 222
2017 215
2018 235
2019 265
2020 279
2021 303
2022 240
2023 267
2024 245
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2026 155

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6,851 results

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Page 1
Epilepsy with myoclonic-atonic seizures: an update on genetic causes, nosological limits, and treatment strategies.
Guerrini R, Scheffer I, Balestrini S. Guerrini R, et al. Lancet Neurol. 2025 Apr;24(4):348-360. doi: 10.1016/S1474-4422(25)00032-8. Lancet Neurol. 2025. PMID: 40120618 Review.
Epilepsy with myoclonic-atonic seizures is a childhood-onset epilepsy syndrome characterised by a range of seizure types, including myoclonic-atonic, atonic, myoclonic, absence, and generalised tonic-clonic …
Epilepsy with myoclonic-atonic seizures is a childhood-onset epilepsy syndrome characterised by a …
Epilepsy with myoclonic-atonic seizures, also known as Doose syndrome: Modification of the diagnostic criteria.
Oguni H. Oguni H. Eur J Paediatr Neurol. 2022 Jan;36:37-50. doi: 10.1016/j.ejpn.2021.11.009. Epub 2021 Dec 1. Eur J Paediatr Neurol. 2022. PMID: 34883415 Review.
The aim of this review is to propose the updated diagnostic criteria of epilepsy with myoclonic-atonic seizures (EMAS), which is a recent subject of genetic studies. ...At present, the most updated ILAE diagnostic manual of EMAS includes: (1) no …
The aim of this review is to propose the updated diagnostic criteria of epilepsy with myoclonic-atonic seizur …
International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions.
Specchio N, Wirrell EC, Scheffer IE, Nabbout R, Riney K, Samia P, Guerreiro M, Gwer S, Zuberi SM, Wilmshurst JM, Yozawitz E, Pressler R, Hirsch E, Wiebe S, Cross HJ, Perucca E, Moshé SL, Tinuper P, Auvin S. Specchio N, et al. Epilepsia. 2022 Jun;63(6):1398-1442. doi: 10.1111/epi.17241. Epub 2022 May 3. Epilepsia. 2022. PMID: 35503717 Free article.
Based on the 2017 Classification of Seizures and Epilepsies, some syndrome names have been updated using terms directly describing the seizure semiology. Epilepsy syndromes beginning in childhood have been divided into three categories: (1) self-limited focal …
Based on the 2017 Classification of Seizures and Epilepsies, some syndrome names have been updated using terms directly descri …
Childhood epilepsy.
Menon RN, Helen Cross J. Menon RN, et al. Lancet. 2025 Aug 9;406(10503):636-649. doi: 10.1016/S0140-6736(25)00773-1. Epub 2025 Jul 17. Lancet. 2025. PMID: 40684779 Review.
Epilepsies that present during childhood pose unique challenges and include developmental and epileptic encephalopathies, specific distinctive constellations, and epilepsies with seizure subtypes, such as epileptic spasms, myoclonic-atonic seizures …
Epilepsies that present during childhood pose unique challenges and include developmental and epileptic encephalopathies, specific di …
POLR3B is associated with a developmental and epileptic encephalopathy with myoclonic-atonic seizures and ataxia.
Symonds JD, Park KL, Mignot C, Macleod S, Armstrong M, Ashrafian H, Bernard G, Brown K, Brunklaus A, Callaghan M, Classen G, Cohen JS, Cutcutache I, de Sainte Agathe JM, Dyment D, Elliot KS, Isapof A, Joss S, Keren B, Marble M, McTague A, Osmond M, Page M, Planes M, Platzer K, Redon S, Reese J, Saenz M, Smith-Hicks C, Stobo D, Stockhaus C, Vuillaume ML, Wolf NI, Wakeling EL, Yoon G, Knight JC, Zuberi SM. Symonds JD, et al. Epilepsia. 2024 Nov;65(11):3303-3323. doi: 10.1111/epi.18115. Epub 2024 Sep 30. Epilepsia. 2024. PMID: 39348199
Twelve of 13 variants were classified as pathogenic or likely pathogenic as per American College of Medical Genetics (ACMG) criteria. Patients presented with generalized myoclonic, myoclonic-atonic, atypical absence, or tonic-clonic seizures between th …
Twelve of 13 variants were classified as pathogenic or likely pathogenic as per American College of Medical Genetics (ACMG) criteria. Patien …
Progressive Myoclonus Epilepsy: A Scoping Review of Diagnostic, Phenotypic and Therapeutic Advances.
Zimmern V, Minassian B. Zimmern V, et al. Genes (Basel). 2024 Jan 27;15(2):171. doi: 10.3390/genes15020171. Genes (Basel). 2024. PMID: 38397161 Free PMC article.
The progressive myoclonus epilepsies (PME) are a diverse group of disorders that feature both myoclonus and seizures that worsen gradually over a variable timeframe. While each of the disorders is individually rare, they collectively make up a non-trivial portion of …
The progressive myoclonus epilepsies (PME) are a diverse group of disorders that feature both myoclonus and seizures that wors …
Cannabidiol in children with treatment-resistant epilepsy with myoclonic-atonic seizures.
Caraballo RH, Reyes Valenzuela G, Fortini S, Espeche A, Gamboni B, Silva W, Semprino M, Fasulo L, Chacón S, Gallo A, Galicchio S, Cachia P. Caraballo RH, et al. Epilepsy Behav. 2023 Jun;143:109245. doi: 10.1016/j.yebeh.2023.109245. Epub 2023 May 12. Epilepsy Behav. 2023. PMID: 37182500
PURPOSE: This multicenter study aimed to evaluate the efficacy and tolerability of add-on cannabidiol (CBD) in treatment-resistant patients with epilepsy with myoclonic-atonic seizures (EMAtS) (n = 22) and Sturge Weber syndrome (SWS) with myo …
PURPOSE: This multicenter study aimed to evaluate the efficacy and tolerability of add-on cannabidiol (CBD) in treatment-resistant patients …
Results of an international Delphi consensus in epilepsy with myoclonic atonic seizures/ Doose syndrome.
Joshi C, Nickels K, Demarest S, Eltze C, Cross JH, Wirrell E. Joshi C, et al. Seizure. 2021 Feb;85:12-18. doi: 10.1016/j.seizure.2020.11.017. Epub 2020 Dec 28. Seizure. 2021. PMID: 33383403 Free article.
OBJECTIVE: To establish a standard framework for early phenotypic diagnosis, investigations, expected findings from investigations, evolution, effective therapies and prognosis in the syndrome of Epilepsy with myoclonic atonic seizures (EMAS) / …
OBJECTIVE: To establish a standard framework for early phenotypic diagnosis, investigations, expected findings from investigations, evolutio …
Epidemiology of Developmental and Epileptic Encephalopathy and of Intellectual Disability and Epilepsy in Children.
Poke G, Stanley J, Scheffer IE, Sadleir LG. Poke G, et al. Neurology. 2023 Mar 28;100(13):e1363-e1375. doi: 10.1212/WNL.0000000000206758. Epub 2022 Dec 29. Neurology. 2023. PMID: 36581463 Free PMC article.
Cumulative incidence for each epilepsy syndrome was calculated. RESULTS: The cohort comprised 235 children (58% male) with developmental impairment and epilepsy, including 152 (65%) with DEE and 83 (35%) with ID+E. ...Cumulative incidence per 100,000 children was as …
Cumulative incidence for each epilepsy syndrome was calculated. RESULTS: The cohort comprised 235 children (58% male) with developmen …
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures.
Tang S, Addis L, Smith A, Topp SD, Pendziwiat M, Mei D, Parker A, Agrawal S, Hughes E, Lascelles K, Williams RE, Fallon P, Robinson R, Cross HJ, Hedderly T, Eltze C, Kerr T, Desurkar A, Hussain N, Kinali M, Bagnasco I, Vassallo G, Whitehouse W, Goyal S, Absoud M; EuroEPINOMICS-RES Consortium; Møller RS, Helbig I, Weber YG, Marini C, Guerrini R, Simpson MA, Pal DK. Tang S, et al. Epilepsia. 2020 May;61(5):995-1007. doi: 10.1111/epi.16508. Epub 2020 May 29. Epilepsia. 2020. PMID: 32469098
OBJECTIVE: We aimed to describe the extent of neurodevelopmental impairments and identify the genetic etiologies in a large cohort of patients with epilepsy with myoclonic atonic seizures (MAE). METHODS: We deeply phenotyped MAE patients for …
OBJECTIVE: We aimed to describe the extent of neurodevelopmental impairments and identify the genetic etiologies in a large cohort of patien …
6,851 results