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Quoted phrase not found in phrase index: "Myoclonic epilepsy, juvenile, susceptibility to, 1"
Page 1
Alzheimer Disease and Epilepsy: A Mendelian Randomization Study.
Fang Y, Si X, Wang J, Wang Z, Chen Y, Liu Y, Yan Y, Tian J, Zhang B, Pu J. Fang Y, et al. Neurology. 2023 Jul 25;101(4):e399-e409. doi: 10.1212/WNL.0000000000207423. Epub 2023 May 24. Neurology. 2023. PMID: 37225432 Free PMC article.
Epilepsy phenotypes included all epilepsy, generalized epilepsy, focal epilepsy, childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy, generalized epilepsy with tonic-clonic …
Epilepsy phenotypes included all epilepsy, generalized epilepsy, focal epilepsy, childhood absence epilepsy …
Childhood Absence Epilepsy evolving to Eyelid Myoclonia with Absence Epilepsy.
Galli J, Micheletti S, Malerba L, Fazzi E, Giordano L. Galli J, et al. Seizure. 2018 Oct;61:1-3. doi: 10.1016/j.seizure.2018.07.009. Epub 2018 Jul 18. Seizure. 2018. PMID: 30029089 Free article.
PURPOSE: Children with Childhood Absence Epilepsy (CAE) may develop generalized tonic-clonic seizure or juvenile myoclonic epilepsy. ...These results support the hypothesis that these two epileptic conditions are dynamic processes evolving into one ano …
PURPOSE: Children with Childhood Absence Epilepsy (CAE) may develop generalized tonic-clonic seizure or juvenile myoclonic …
Genetics of myoclonic and myoclonus epilepsies.
Minassian BA, Sainz J, Delgado-Escueta AV. Minassian BA, et al. Clin Neurosci. 1995-1996;3(4):223-35. Clin Neurosci. 1995. PMID: 8891396 Review.
Mendelian forms of benign myoclonic epilepsies where a chromosomal locus has been defined include (1) the autosomal dominant (AD) juvenile myoclonic epilepsy (JME) in chr. 6p11, (2) the autosomal dominant childhood absence epilepsy which …
Mendelian forms of benign myoclonic epilepsies where a chromosomal locus has been defined include (1) the autosomal dominant ( …
Complex inheritance and parent-of-origin effect in juvenile myoclonic epilepsy.
Pal DK, Durner M, Klotz I, Dicker E, Shinnar S, Resor S, Cohen J, Harden C, Moshé SL, Ballaban-Gill K, Bromfield EB, Greenberg DA. Pal DK, et al. Brain Dev. 2006 Mar;28(2):92-8. doi: 10.1016/j.braindev.2005.05.009. Epub 2006 Jan 18. Brain Dev. 2006. PMID: 16414227 Free PMC article.
BACKGROUND: Juvenile myoclonic epilepsy (JME) is an idiopathic generalized epilepsy (IGE) with complex inheritance. ...The adjusted female: male risk ratio was very high in JME (RR=12.5; 95% CI: 1.9-83.7). Absence seizures in JME probands increa …
BACKGROUND: Juvenile myoclonic epilepsy (JME) is an idiopathic generalized epilepsy (IGE) with complex inheritan …
DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians.
Pathak S, Miller J, Morris EC, Stewart WCL, Greenberg DA. Pathak S, et al. Epilepsia. 2018 May;59(5):1011-1019. doi: 10.1111/epi.14058. Epub 2018 Apr 2. Epilepsia. 2018. PMID: 29608786 Free PMC article.
OBJECTIVE: Juvenile myoclonic epilepsy (JME) is a common adolescent-onset genetic generalized epilepsy (GGE) syndrome. ...In families with non-JME GGE, we found no relationship between promoter methylation and epilepsy. In non-Caucasian JME fami …
OBJECTIVE: Juvenile myoclonic epilepsy (JME) is a common adolescent-onset genetic generalized epilepsy (GGE) syn …
The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1".
Sander T, Hildmann T, Janz D, Wienker TF, Neitzel H, Bianchi A, Bauer G, Sailer U, Berek K, Schmitz B, et al. Sander T, et al. Ann Neurol. 1995 Aug;38(2):210-7. doi: 10.1002/ana.410380213. Ann Neurol. 1995. PMID: 7654068
Linkage studies of families ascertained through patients with juvenile myoclonic epilepsy (JME) suggest that an HLA-linked susceptibility gene on chromosome 6, designated "EJM1," predisposes to a group of idiopathic generalized epilepsies (IGEs) compri …
Linkage studies of families ascertained through patients with juvenile myoclonic epilepsy (JME) suggest that an HLA-lin …
Case-control pharmacogenetic study of HCN1/HCN2 variants and genetic generalized epilepsies.
Wu SZ, Ye H, Yang XG, Lu ZL, Qu Q, Qu J. Wu SZ, et al. Clin Exp Pharmacol Physiol. 2018 Mar;45(3):226-233. doi: 10.1111/1440-1681.12877. Epub 2017 Nov 28. Clin Exp Pharmacol Physiol. 2018. PMID: 29047147
The frequency of the HCN1 rs10462087 CC+CT genotype was lower in patients with childhood absence epilepsy (CAE) than controls (P = .047). Rs7255568 was associated with the risk of CAE (P = .028) and juvenile myoclonic epilepsy (JME) (P = .02). ...After …
The frequency of the HCN1 rs10462087 CC+CT genotype was lower in patients with childhood absence epilepsy (CAE) than controls (P = .0 …
The 1674+11C>T polymorphism of CHRNA4 is associated with juvenile myoclonic epilepsy.
Rozycka A, Steinborn B, Trzeciak WH. Rozycka A, et al. Seizure. 2009 Oct;18(8):601-3. doi: 10.1016/j.seizure.2009.06.007. Epub 2009 Jul 3. Seizure. 2009. PMID: 19577488 Free article.
The alpha4 subunit gene (CHRNA4) of the neuronal nicotinic acetylcholine receptor (nAChR), linked to an idiopathic partial epilepsy, autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), may also play a key role in the development of the idiopathic generalize …
The alpha4 subunit gene (CHRNA4) of the neuronal nicotinic acetylcholine receptor (nAChR), linked to an idiopathic partial epilepsy, …
Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q.
Elmslie FV, Rees M, Williamson MP, Kerr M, Kjeldsen MJ, Pang KA, Sundqvist A, Friis ML, Chadwick D, Richens A, Covanis A, Santos M, Arzimanoglou A, Panayiotopoulos CP, Curtis D, Whitehouse WP, Gardiner RM. Elmslie FV, et al. Hum Mol Genet. 1997 Aug;6(8):1329-34. doi: 10.1093/hmg/6.8.1329. Hum Mol Genet. 1997. PMID: 9259280
These are categorised as idiopathic in the absence of detectable structural or metabolic abnormalities. Juvenile myoclonic epilepsy (JME) is a distinctive and common variety of familial idiopathic generalised epilepsy (IGE) with a prevalence of 0.5- …
These are categorised as idiopathic in the absence of detectable structural or metabolic abnormalities. Juvenile myoclonic …
Self-perception of factors that precipitate or inhibit seizures in juvenile myoclonic epilepsy.
da Silva Sousa P, Lin K, Garzon E, Sakamoto AC, Yacubian EM. da Silva Sousa P, et al. Seizure. 2005 Jul;14(5):340-6. doi: 10.1016/j.seizure.2005.04.007. Seizure. 2005. PMID: 15955714 Free article.
PURPOSE: To assess self-perception of factors that precipitate or inhibit seizures in patients with juvenile myoclonic epilepsy (JME). PATIENTS AND METHODS: Thirty-six males and 39 females with JME and mean age of 25.8+/-8.7 years were analysed. ...In order o …
PURPOSE: To assess self-perception of factors that precipitate or inhibit seizures in patients with juvenile myoclonic epil …
21 results