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About 598 results

ALLMedicine™ Myoclonic Epilepsy Center

Research & Reviews  102 results

Different circuitry dysfunction in drug-naive patients with juvenile myoclonic epilepsy...
https://doi.org/10.1016/j.yebeh.2021.108443
Epilepsy & Behavior : E&B; Canafoglia L, Viganò I et. al.

Nov 28th, 2021 - Juvenile myoclonic epilepsy (JME) and juvenile absence epilepsy (JAE) are generalized epileptic syndromes presenting in the same age range. To explore whether uneven network dysfunctions may underlie the two different phenotypes, we examined drug-...

Topiramate for juvenile myoclonic epilepsy.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612308
The Cochrane Database of Systematic Reviews; Liu J, Tai YJ et. al.

Nov 25th, 2021 - Topiramate is a newer broad-spectrum antiepileptic drug (AED). Some studies have shown the benefits of topiramate in the treatment of juvenile myoclonic epilepsy (JME). However, there are no current systematic reviews to determine the efficacy and...

A systematic review of resting-state and task-based fmri in juvenile myoclonic epilepsy.
https://doi.org/10.1007/s11682-021-00595-5 10.1093/brain/awh136 10.1016/j.neuroimage.2011.04.070 10.1177/155005941004100109 10.1126/science.1736359%JScience 10.1002/mrm.1910250220 10.1016/j.ddmod.2008.07.005 10.1098/rstb.2005.1634 10.1093/brain/awg249 10.1016/j.neuroimage.2009.01.055 10.1046/j.1528-1157.44.s.2.2.x 10.1111/j.1528-1167.2005.00311.x 10.1016/j.eplepsyres.2013.07.003 10.1212/WNL.0b013e3181f11c06 10.1016/s0301-0082(97)00091-9 10.1038/nn.2390 10.1016/s0920-1211(98)00053-9 10.1684/epd.2019.1072 10.1152/jn.00626.2002 10.1016/j.neunet.2009.04.003 10.1016/j.cub.2007.12.014 10.3389/fncel.2019.00433 10.1007/s12311-008-0074-4 10.1016/j.nec.2010.11.001 10.1073/pnas.0504935102 10.1523/JNEUROSCI.4692-12.2013 10.1089/brain.2014.0304 10.1177/1073858415595004 10.1111/j.1528-1167.2011.03117.x 10.1111/epi.12580 10.14581/jer.17013 10.1097/00001756-200508010-00004 10.1016/j.nicl.2017.11.001 10.1111/ane.13138 10.1111/j.1528-1167.2012.03544.x 10.1016/s1053-8119(03)00097-1 10.1111/j.1600-0404.2005.00511.x 10.1111/j.1600-0404.2005.00511.x 10.1016/j.yebeh.2012.06.035 10.1586/14737175.5.6.753 10.1073/pnas.1831638100%JProceedingsoftheNationalAcademyofSciences 10.1038/22547 10.1152/jn.00166.2006 10.1073/pnas.0700668104%JProceedingsoftheNationalAcademyofSciences 10.1016/s0006-8993(00)02351-9 10.1523/jneurosci.2731-14.2015 10.1016/s1525-5050(02)00029-x 10.1073/pnas.87.24.9868 10.1111/j.1528-1157.1994.tb02432.x 10.1111/j.1528-1167.2009.02127.x 10.1371/journal.pone.0179629 10.1016/j.neuroimage.2003.08.034 10.1002/(sici)1097-0193(1996)4:3<174::Aid-hbm3>3.0.Co;2-0 10.1212/01.wnl.0000437303.36064.f8 10.1016/j.yebeh.2012.11.042 10.1212/01.WNL.0000086903.69738.DC%JNeurology 10.1038/484024a 10.1038/502428a 10.1073/pnas.0800005105 10.1212/wnl.47.5.1203 10.1038/nn.2449 10.1073/pnas.91.11.5033 10.1212/WNL.0b013e3181c55d02 10.1002/hbm.20022 10.1111/epi.12350 10.1016/j.nicl.2018.11.014 10.1111/j.1528-1167.2010.02884.x 10.1371/journal.pone.0068910 10.1016/j.seizure.2016.09.005 10.1016/j.neuroimage.2003.12.030 10.1016/j.eplepsyres.2011.07.007
Brain Imaging and Behavior; Sanjari Moghaddam H, Sanjari Moghaddam A et. al.

Nov 18th, 2021 - Functional neuroimaging modalities have enhanced our understanding of juvenile myoclonic epilepsy (JME) underlying neural mechanisms. Due to its non-invasive, sensitive and analytical nature, functional magnetic resonance imaging (fMRI) provides v...

Treatment outcomes in drug resistant juvenile myoclonic epilepsy: Valproate resistance ...
https://doi.org/10.1016/j.seizure.2021.08.019
Seizure Baheti N, Rathore C et. al.

Sep 9th, 2021 - To determine treatment responses to various antiseizure medicines (ASMs) in patients with drug resistant juvenile myoclonic epilepsy (DRJME) METHODS: We reviewed records of all JME patients attending epilepsy clinics at 5 centers during a 5-year p...

Clinical and molecular characterization of Unverricht-Lundborg disease among Egyptian p...
https://doi.org/10.1016/j.eplepsyres.2021.106746
Epilepsy Research; Hosny H, El Tamawy M et. al.

Sep 3rd, 2021 - Unverricht-Lundborg disease (ULD) is a common type of progressive myoclonic epilepsy (PME). It is caused mostly by biallelic dodecamer repeat expansions in the promoter region of CSTB gene. Despite highly prevalent in the Mediterranean countries, ...

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