295 related articles for article (PubMed ID: 30898514)
1. New insights in phenomenology and treatment of epilepsy in CDKL5 encephalopathy.
Melikishvili G; Epitashvili N; Tabatadze N; Chikvinidze G; Dulac O; Bienvenu T; Gataullina S
Epilepsy Behav; 2019 May; 94():308-311. PubMed ID: 30898514
[TBL] [Abstract][Full Text] [Related]
2. Aged heterozygous Cdkl5 mutant mice exhibit spontaneous epileptic spasms.
Mulcahey PJ; Tang S; Takano H; White A; Davila Portillo DR; Kane OM; Marsh ED; Zhou Z; Coulter DA
Exp Neurol; 2020 Oct; 332():113388. PubMed ID: 32585155
[TBL] [Abstract][Full Text] [Related]
3. First report of Tunisian patients with CDKL5-related encephalopathy.
Charfi Triki C; Zouari Mallouli S; Ben Jdila M; Ben Said M; Kamoun Feki F; Weckhuysen S; Masmoudi S; Fakhfakh F
Epilepsia Open; 2024 Jun; 9(3):906-917. PubMed ID: 37701975
[TBL] [Abstract][Full Text] [Related]
4. Novel CDKL5 mutations were found in patients in China: retrospective investigation in cases of CDKL5-related disorders.
Yan Y; He D; Wu J; Hou R; Sun K; Li L
Ital J Pediatr; 2020 Feb; 46(1):27. PubMed ID: 32111237
[TBL] [Abstract][Full Text] [Related]
5. Reflex Seizures in a Patient with CDKL5 Deficiency Disorder.
Peikes T; Hartley JN; Mhanni AA; Greenberg CR; Appendino JP
Can J Neurol Sci; 2019 Jul; 46(4):482-485. PubMed ID: 31030687
[No Abstract] [Full Text] [Related]
6. CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development.
Demarest ST; Olson HE; Moss A; Pestana-Knight E; Zhang X; Parikh S; Swanson LC; Riley KD; Bazin GA; Angione K; Niestroj LM; Lal D; Juarez-Colunga E; Benke TA
Epilepsia; 2019 Aug; 60(8):1733-1742. PubMed ID: 31313283
[TBL] [Abstract][Full Text] [Related]
7. Clinical manifestations and epilepsy treatment in Japanese patients with pathogenic CDKL5 variants.
Kobayashi Y; Tohyama J; Takahashi Y; Goto T; Haginoya K; Inoue T; Kubota M; Fujita H; Honda R; Ito M; Kishimoto K; Nakamura K; Sakai Y; Takanashi JI; Tanaka M; Tanda K; Tominaga K; Yoshioka S; Kato M; Nakashima M; Saitsu H; Matsumoto N
Brain Dev; 2021 Apr; 43(4):505-514. PubMed ID: 33436160
[TBL] [Abstract][Full Text] [Related]
8. CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of life.
Melani F; Mei D; Pisano T; Savasta S; Franzoni E; Ferrari AR; Marini C; Guerrini R
Dev Med Child Neurol; 2011 Apr; 53(4):354-60. PubMed ID: 21309761
[TBL] [Abstract][Full Text] [Related]
9. [Early-onset epileptic encephalopathy caused by CDKL5 mutation].
Hjalmgrim H; Hansen LK; Ousager LB; Møller RS
Ugeskr Laeger; 2014 Dec; 176(25A):. PubMed ID: 25497626
[TBL] [Abstract][Full Text] [Related]
10. Epileptic spasms in clusters without hypsarrhythmia in infancy and childhood: A single age-dependent type of epilepsy or well-defined epileptic syndrome?
Caraballo RH; Gallo A; Reyes G; Flores G; Martín E; Intriago L; Ballesta D
Epilepsy Res; 2024 May; 202():107354. PubMed ID: 38518433
[TBL] [Abstract][Full Text] [Related]
11. Clinical features of early myoclonic encephalopathy caused by a CDKL5 mutation.
Takeda K; Miyamoto Y; Yamamoto H; Ishii A; Hirose S; Yamamoto H
Brain Dev; 2020 Jan; 42(1):73-76. PubMed ID: 31492455
[TBL] [Abstract][Full Text] [Related]
12. Seizure variables and their relationship to genotype and functional abilities in the CDKL5 disorder.
Fehr S; Wong K; Chin R; Williams S; de Klerk N; Forbes D; Krishnaraj R; Christodoulou J; Downs J; Leonard H
Neurology; 2016 Nov; 87(21):2206-2213. PubMed ID: 27770071
[TBL] [Abstract][Full Text] [Related]
13. Epileptic spasms without hypsarrhythmia in infancy and childhood: tonic spasms as a seizure type.
Marchi LR; Seraphim EA; Corso JT; Naves PV; Carvalho KC; Ramirez MD; Ferrari-Marinho T; Guaranha MS; Yacubian EM
Epileptic Disord; 2015 Jun; 17(2):188-93. PubMed ID: 25895540
[TBL] [Abstract][Full Text] [Related]
14. Coexisting seizures in patients with infantile spasms confirmed by long-term video-electroencephalography monitoring.
Kim H; Lee JH; Ryu HW; Lim BC; Chae JH; Choi J; Kim KJ; Hwang YS; Hwang H
Epilepsy Res; 2012 Aug; 101(1-2):70-5. PubMed ID: 22459640
[TBL] [Abstract][Full Text] [Related]
15. Status of epileptic spasms: A study of 21 children.
Caraballo R; Semprino M; Fasulo L; Reyes G; Chacón S; Gallo A; Buompadre C
Epilepsy Behav; 2022 Jan; 126():108451. PubMed ID: 34864379
[TBL] [Abstract][Full Text] [Related]
16. [Analysis of gene mutation of early onset epileptic spasm with unknown reason].
Yang X; Pan G; Li WH; Zhang LM; Wu BB; Wang HJ; Zhang P; Zhou SZ
Zhonghua Er Ke Za Zhi; 2017 Nov; 55(11):813-817. PubMed ID: 29141310
[No Abstract] [Full Text] [Related]
17. Key clinical features to identify girls with CDKL5 mutations.
Bahi-Buisson N; Nectoux J; Rosas-Vargas H; Milh M; Boddaert N; Girard B; Cances C; Ville D; Afenjar A; Rio M; Héron D; N'guyen Morel MA; Arzimanoglou A; Philippe C; Jonveaux P; Chelly J; Bienvenu T
Brain; 2008 Oct; 131(Pt 10):2647-61. PubMed ID: 18790821
[TBL] [Abstract][Full Text] [Related]
18. [Treatment of West syndrome].
Cvitanović-Sojat L; Gjergja R; Sabol Z; Hajnzić TF; Sojat T
Acta Med Croatica; 2005; 59(1):19-29. PubMed ID: 15813352
[TBL] [Abstract][Full Text] [Related]
19. X-linked cellular mosaicism underlies age-dependent occurrence of seizure-like events in mouse models of CDKL5 deficiency disorder.
Terzic B; Cui Y; Edmondson AC; Tang S; Sarmiento N; Zaitseva D; Marsh ED; Coulter DA; Zhou Z
Neurobiol Dis; 2021 Jan; 148():105176. PubMed ID: 33197557
[TBL] [Abstract][Full Text] [Related]
20. A novel mutation in STXBP1 gene in a child with epileptic encephalopathy and an atypical electroclinical pattern.
Romaniello R; Zucca C; Tenderini E; Arrigoni F; Ragona F; Zorzi G; Bassi MT; Borgatti R
J Child Neurol; 2014 Feb; 29(2):249-53. PubMed ID: 24170257
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]