246 related articles for article (PubMed ID: 33916893)
1. Neurological Disorders Associated with WWOX Germline Mutations-A Comprehensive Overview.
Banne E; Abudiab B; Abu-Swai S; Repudi SR; Steinberg DJ; Shatleh D; Alshammery S; Lisowski L; Gold W; Carlen PL; Aqeilan RI
Cells; 2021 Apr; 10(4):. PubMed ID: 33916893
[TBL] [Abstract][Full Text] [Related]
2. Neonatal neuronal WWOX gene therapy rescues Wwox null phenotypes.
Repudi S; Kustanovich I; Abu-Swai S; Stern S; Aqeilan RI
EMBO Mol Med; 2021 Dec; 13(12):e14599. PubMed ID: 34747138
[TBL] [Abstract][Full Text] [Related]
3. The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature.
Piard J; Hawkes L; Milh M; Villard L; Borgatti R; Romaniello R; Fradin M; Capri Y; Héron D; Nougues MC; Nava C; Arsene OT; Shears D; Taylor J; Pagnamenta A; Taylor JC; Sogawa Y; Johnson D; Firth H; Vasudevan P; Jones G; Nguyen-Morel MA; Busa T; Roubertie A; van den Born M; Brischoux-Boucher E; Koenig M; Mignot C; ; Kini U; Philippe C
Genet Med; 2019 Jun; 21(6):1308-1318. PubMed ID: 30356099
[TBL] [Abstract][Full Text] [Related]
4. WWOX Loss of Function in Neurodevelopmental and Neurodegenerative Disorders.
Aldaz CM; Hussain T
Int J Mol Sci; 2020 Nov; 21(23):. PubMed ID: 33255508
[TBL] [Abstract][Full Text] [Related]
5. Recently defined epileptic encephalopathy related to WWOX gene mutation: six patients and new mutations.
Havali C; Ekici A; Dorum S; Görükmez Ö; Topak A
Neurol Res; 2021 Sep; 43(9):744-750. PubMed ID: 34034642
[No Abstract] [Full Text] [Related]
6. Epilepsy in patients with WWOX-related epileptic encephalopathy (WOREE) syndrome.
Al Baradie R; Mir A; Alsaif A; Ali M; Al Ghamdi F; Bashir S; Howsawi Y
Epileptic Disord; 2022 Aug; 24(4):697-712. PubMed ID: 35792847
[TBL] [Abstract][Full Text] [Related]
7. WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk.
Oliver KL; Trivisano M; Mandelstam SA; De Dominicis A; Francis DI; Green TE; Muir AM; Chowdhary A; Hertzberg C; Goldhahn K; Metreau J; Prager C; Pinner J; Cardamone M; Myers KA; Leventer RJ; Lesca G; Bahlo M; Hildebrand MS; Mefford HC; Kaindl AM; Specchio N; Scheffer IE
Epilepsia; 2023 May; 64(5):1351-1367. PubMed ID: 36779245
[TBL] [Abstract][Full Text] [Related]
8. Novel compound heterozygous mutations in the WWOX gene cause early infantile epileptic encephalopathy.
Yang C; Zhang Y; Song Z; Yi Z; Li F
Int J Dev Neurosci; 2019 Dec; 79():45-48. PubMed ID: 31669195
[TBL] [Abstract][Full Text] [Related]
9. Neuronal deletion of Wwox, associated with WOREE syndrome, causes epilepsy and myelin defects.
Repudi S; Steinberg DJ; Elazar N; Breton VL; Aquilino MS; Saleem A; Abu-Swai S; Vainshtein A; Eshed-Eisenbach Y; Vijayaragavan B; Behar O; Hanna JJ; Peles E; Carlen PL; Aqeilan RI
Brain; 2021 Nov; 144(10):3061-3077. PubMed ID: 33914858
[TBL] [Abstract][Full Text] [Related]
10. WWOX-associated encephalopathies: identification of the phenotypic spectrum and the resulting genotype-phenotype correlation.
Serin HM; Simsek E; Isik E; Gokben S
Neurol Sci; 2018 Nov; 39(11):1977-1980. PubMed ID: 30094525
[TBL] [Abstract][Full Text] [Related]
11. WWOX P47T partial loss-of-function mutation induces epilepsy, progressive neuroinflammation, and cerebellar degeneration in mice phenocopying human SCAR12.
Hussain T; Sanchez K; Crayton J; Saha D; Jeter C; Lu Y; Abba M; Seo R; Noebels JL; Fonken L; Aldaz CM
Prog Neurobiol; 2023 Apr; 223():102425. PubMed ID: 36828035
[TBL] [Abstract][Full Text] [Related]
12. West syndrome, developmental and epileptic encephalopathy, and severe CNS disorder associated with WWOX mutations.
Shaukat Q; Hertecant J; El-Hattab AW; Ali BR; Suleiman J
Epileptic Disord; 2018 Oct; 20(5):401-412. PubMed ID: 30361190
[TBL] [Abstract][Full Text] [Related]
13. Novel WWOX deleterious variants cause early infantile epileptic encephalopathy, severe developmental delay and dysmorphism among Yemenite Jews.
Weisz-Hubshman M; Meirson H; Michaelson-Cohen R; Beeri R; Tzur S; Bormans C; Modai S; Shomron N; Shilon Y; Banne E; Orenstein N; Konen O; Marek-Yagel D; Veber A; Shalva N; Imagawa E; Matsumoto N; Lev D; Lerman Sagie T; Raas-Rothschild A; Ben-Zeev B; Basel-Salmon L; Behar DM; Heimer G
Eur J Paediatr Neurol; 2019 May; 23(3):418-426. PubMed ID: 30853297
[TBL] [Abstract][Full Text] [Related]
14. A novel missense variant in the SDR domain of the WWOX gene leads to complete loss of WWOX protein with early-onset epileptic encephalopathy and severe developmental delay.
Johannsen J; Kortüm F; Rosenberger G; Bokelmann K; Schirmer MA; Denecke J; Santer R
Neurogenetics; 2018 Aug; 19(3):151-156. PubMed ID: 29808465
[TBL] [Abstract][Full Text] [Related]
15. Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy.
Chong SC; Cao Y; Fung ELW; Kleppe S; Gripp KW; Hertecant J; El-Hattab AW; Suleiman J; Clark G; von Allmen G; Rodziyevska O; Lewis RA; Rosenfeld JA; Dong J; ; Wang X; Miller MJ; Bi W; Liu P; Scaglia F
Am J Med Genet A; 2023 Mar; 191(3):776-785. PubMed ID: 36537114
[TBL] [Abstract][Full Text] [Related]
16. The
Kośla K; Kałuzińska Ż; Bednarek AK
Exp Biol Med (Maywood); 2020 Jul; 245(13):1122-1129. PubMed ID: 32389029
[TBL] [Abstract][Full Text] [Related]
17. Early onset epileptic encephalopathy caused by novel compound heterozygous mutation of WWOX gene.
Su T; Yan Y; Xu S; Zhang K; Xu S
Int J Dev Neurosci; 2020 Apr; 80(2):157-161. PubMed ID: 32037574
[TBL] [Abstract][Full Text] [Related]
18. Identification of compound heterozygous deletion of the WWOX gene in WOREE syndrome.
Dong XS; Wen XJ; Zhang S; Wang DG; Xiong Y; Li ZM
BMC Med Genomics; 2023 Nov; 16(1):291. PubMed ID: 37974179
[TBL] [Abstract][Full Text] [Related]
19. Practical clues for diagnosing WWOX encephalopathy.
Tarta-Arsene O; Barca D; Craiu D; Iliescu C
Epileptic Disord; 2017 Sep; 19(3):357-361. PubMed ID: 28721938
[TBL] [Abstract][Full Text] [Related]
20. WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation.
Mignot C; Lambert L; Pasquier L; Bienvenu T; Delahaye-Duriez A; Keren B; Lefranc J; Saunier A; Allou L; Roth V; Valduga M; Moustaïne A; Auvin S; Barrey C; Chantot-Bastaraud S; Lebrun N; Moutard ML; Nougues MC; Vermersch AI; Héron B; Pipiras E; Héron D; Olivier-Faivre L; Guéant JL; Jonveaux P; Philippe C
J Med Genet; 2015 Jan; 52(1):61-70. PubMed ID: 25411445
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
