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Unverricht-Lundborg disease.
Crespel A, Ferlazzo E, Franceschetti S, Genton P, Gouider R, Kälviäinen R, Korja M, Lehtinen MK, Mervaala E, Simonato M, Vaarmann A. Crespel A, et al. Among authors: gouider r. Epileptic Disord. 2016 Sep 1;18(S2):28-37. doi: 10.1684/epd.2016.0841. Epileptic Disord. 2016. PMID: 27582036 Review.
Variability of the response to immunotherapy among subgroups of patients with multiple sclerosis.
Diouf I, Malpas CB, Sharmin S, Roos I, Horakova D, Havrdova EK, Patti F, Shaygannejad V, Ozakbas S, Izquierdo G, Eichau S, Onofrj M, Lugaresi A, Alroughani R, Prat A, Girard M, Duquette P, Terzi M, Boz C, Grand'Maison F, Hamdy S, Sola P, Ferraro D, Grammond P, Turkoglu R, Buzzard K, Skibina O, Yamout B, Altintas A, Gerlach O, van Pesch V, Blanco Y, Maimone D, Lechner-Scott J, Bergamaschi R, Karabudak R, Iuliano G, McGuigan C, Cartechini E, Barnett M, Hughes S, Sa MJ, Solaro C, Kappos L, Ramo-Tello C, Cristiano E, Hodgkinson S, Spitaleri D, Soysal A, Petersen T, Slee M, Butler E, Granella F, de Gans K, McCombe P, Ampapa R, Van Wijmeersch B, van der Walt A, Butzkueven H, Prevost J, Sinnige LGF, Sanchez-Menoyo JL, Vucic S, Laureys G, Van Hijfte L, Khurana D, Macdonell R, Gouider R, Castillo-Triviño T, Gray O, Aguera-Morales E, Al-Asmi A, Shaw C, Deri N, Al-Harbi T, Fragoso Y, Csepany T, Perez Sempere A, Trevino-Frenk I, Schepel J, Moore F, Kalincik T. Diouf I, et al. Among authors: gouider r. Eur J Neurol. 2023 Apr;30(4):1014-1024. doi: 10.1111/ene.15706. Epub 2023 Feb 16. Eur J Neurol. 2023. PMID: 36692895 Free PMC article.
Long-term evolution of EEG in Unverricht-Lundborg disease.
Gargouri-Berrechid A, Nasri A, Kacem I, Sidhom Y, Abdelkefi I, Hizem Y, Ben Djebrara M, Gouider R. Gargouri-Berrechid A, et al. Among authors: gouider r. Neurophysiol Clin. 2016 Apr;46(2):119-24. doi: 10.1016/j.neucli.2016.03.003. Epub 2016 May 4. Neurophysiol Clin. 2016. PMID: 27157382
Juvenile myoclonic epilepsy phenotype in a family with Unverricht-Lundborg disease.
Berrechid AG, Bendjebara M, Bouteiller D, Nasri A, Peuvion JN, Marie Y, Baulac S, Mrabet S, Ribierre T, Cazeneuve C, Imenkacem, Leguern E, Gouider R. Berrechid AG, et al. Among authors: gouider r. Epileptic Disord. 2019 Aug 1;21(4):359-365. doi: 10.1684/epd.2019.1078. Epileptic Disord. 2019. PMID: 31368437
Major intra-familial variability in Unverricht-Lundborg disease.
Nasri A, Zidi S, Kacem I, Mrabet S, Ben Djebara M, Gargouri A, Leguern E, Gouider R. Nasri A, et al. Among authors: gouider r. Epileptic Disord. 2022 Feb 1;24(1):163-170. doi: 10.1684/epd.2021.1372. Epileptic Disord. 2022. PMID: 34787084
A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset.
Lalioti MD, Scott HS, Genton P, Grid D, Ouazzani R, M'Rabet A, Ibrahim S, Gouider R, Dravet C, Chkili T, Bottani A, Buresi C, Malafosse A, Antonarakis SE. Lalioti MD, et al. Among authors: gouider r. Am J Hum Genet. 1998 Apr;62(4):842-7. doi: 10.1086/301798. Am J Hum Genet. 1998. PMID: 9529356 Free PMC article.
Familial form of typical childhood absence epilepsy in a consanguineous context.
Abouda H, Hizem Y, Gargouri A, Depienne C, Bouteiller D, Riant F, Tournier-Lasserve E, Gourfinkel-An I, LeGuern E, Gouider R. Abouda H, et al. Among authors: gouider r. Epilepsia. 2010 Sep;51(9):1889-93. doi: 10.1111/j.1528-1167.2010.02649.x. Epilepsia. 2010. PMID: 20561025 Free article.
161 results