These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
173 related articles for article (PubMed ID: 35795805)
1. Presenting Patterns of Genetically Determined Developmental Encephalopathies With Epilepsy and Movement Disorders: A Single Tertiary Center Retrospective Cohort Study. Mastrangelo M; Galosi S; Cesario S; Renzi A; Campea L; Leuzzi V Front Neurol; 2022; 13():855134. PubMed ID: 35795805 [TBL] [Abstract][Full Text] [Related]
2. Genetic Neonatal-Onset Epilepsies and Developmental/Epileptic Encephalopathies with Movement Disorders: A Systematic Review. Spagnoli C; Fusco C; Percesepe A; Leuzzi V; Pisani F Int J Mol Sci; 2021 Apr; 22(8):. PubMed ID: 33919646 [TBL] [Abstract][Full Text] [Related]
3. Rett Syndrome Spectrum in Monogenic Developmental-Epileptic Encephalopathies and Epilepsies: A Review. Spagnoli C; Fusco C; Pisani F Genes (Basel); 2021 Jul; 12(8):. PubMed ID: 34440332 [TBL] [Abstract][Full Text] [Related]
4. Pediatric-Onset Epilepsy and Developmental Epileptic Encephalopathies Followed by Early-Onset Parkinsonism. Spagnoli C; Fusco C; Pisani F Int J Mol Sci; 2023 Feb; 24(4):. PubMed ID: 36835207 [TBL] [Abstract][Full Text] [Related]
6. GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders. Ohba C; Shiina M; Tohyama J; Haginoya K; Lerman-Sagie T; Okamoto N; Blumkin L; Lev D; Mukaida S; Nozaki F; Uematsu M; Onuma A; Kodera H; Nakashima M; Tsurusaki Y; Miyake N; Tanaka F; Kato M; Ogata K; Saitsu H; Matsumoto N Epilepsia; 2015 Jun; 56(6):841-8. PubMed ID: 25864721 [TBL] [Abstract][Full Text] [Related]
7. Developmental and epileptic encephalopathies: what we do and do not know. Specchio N; Curatolo P Brain; 2021 Feb; 144(1):32-43. PubMed ID: 33279965 [TBL] [Abstract][Full Text] [Related]
8. Association between kinetic semiology of psychogenic nonepileptic spells and seizure type in dual disorder. Wei D; Garlinghouse M; Li W; Swingle N; Samson KK; Taraschenko O Epilepsy Behav; 2021 Jan; 114(Pt A):107597. PubMed ID: 33246895 [TBL] [Abstract][Full Text] [Related]
9. The therapeutic implication of a novel SCN2A mutation associated early-onset epileptic encephalopathy with Rett-like features. Liang JS; Lin LJ; Yang MT; Wang JS; Lu JF Brain Dev; 2017 Nov; 39(10):877-881. PubMed ID: 28709814 [TBL] [Abstract][Full Text] [Related]
11. Electroclinical Features of Early-Onset Epileptic Encephalopathies in Congenital Disorders of Glycosylation (CDGs). Fiumara A; Barone R; Del Campo G; Striano P; Jaeken J JIMD Rep; 2016; 27():93-9. PubMed ID: 26453362 [TBL] [Abstract][Full Text] [Related]
12. High prevalence of genetic alterations in early-onset epileptic encephalopathies associated with infantile movement disorders. Kobayashi Y; Tohyama J; Kato M; Akasaka N; Magara S; Kawashima H; Ohashi T; Shiraishi H; Nakashima M; Saitsu H; Matsumoto N Brain Dev; 2016 Mar; 38(3):285-92. PubMed ID: 26482601 [TBL] [Abstract][Full Text] [Related]
13. [Clinical characteristics and gene analysis of GRIN2B gene related neurological developmental disorders in children]. Tian XJ; Wang XH; Ding CH; Fang F; Dai LF; Deng J; Wang HM Zhonghua Er Ke Za Zhi; 2022 Mar; 60(3):232-236. PubMed ID: 35240744 [No Abstract] [Full Text] [Related]
14. [Clinical usefulness of serial EEG examinations in the diagnostic of hereditary epileptic encephalopathies case of severe epileptic encephalopathy type 2]. Terczyńska I; Mierzewska H; Szczepanik E; Antczak-Marach D Przegl Lek; 2010; 67(9):757-61. PubMed ID: 21387820 [TBL] [Abstract][Full Text] [Related]
15. Developmental and epileptic encephalopathies: Is prognosis related to different epileptic network dysfunctions? Lin JJ; Meletti S; Vaudano AE; Lin KL Epilepsy Behav; 2022 Jun; 131(Pt B):107654. PubMed ID: 33349540 [TBL] [Abstract][Full Text] [Related]
16. [Phenomenology and psychiatric origins of psychogenic non-epileptic seizures]. Ristić AJ; Petrović I; Vojvodić N; Janković S; Sokić D Srp Arh Celok Lek; 2004; 132(1-2):22-7. PubMed ID: 15227961 [TBL] [Abstract][Full Text] [Related]
17. Dystonia as a prominent presenting feature in developmental and epileptic encephalopathies: A case series. Dzinovic I; Škorvánek M; Necpál J; Boesch S; Švantnerová J; Wagner M; Havránková P; Pavelekova P; Haň V; Janzarik WG; Berweck S; Diebold I; Kuster A; Jech R; Winkelmann J; Zech M Parkinsonism Relat Disord; 2021 Sep; 90():73-78. PubMed ID: 34399161 [TBL] [Abstract][Full Text] [Related]
18. Epileptic patients with de novo STXBP1 mutations: Key clinical features based on 24 cases. Di Meglio C; Lesca G; Villeneuve N; Lacoste C; Abidi A; Cacciagli P; Altuzarra C; Roubertie A; Afenjar A; Renaldo-Robin F; Isidor B; Gautier A; Husson M; Cances C; Metreau J; Laroche C; Chouchane M; Ville D; Marignier S; Rougeot C; Lebrun M; de Saint Martin A; Perez A; Riquet A; Badens C; Missirian C; Philip N; Chabrol B; Villard L; Milh M Epilepsia; 2015 Dec; 56(12):1931-40. PubMed ID: 26514728 [TBL] [Abstract][Full Text] [Related]