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Quoted phrase not found in phrase index: "Benign partial infantile seizures"
Page 1
Idiopathic focal epilepsies.
Vigevano F, Specchio N, Fejerman N. Vigevano F, et al. Handb Clin Neurol. 2013;111:591-604. doi: 10.1016/B978-0-444-52891-9.00061-0. Handb Clin Neurol. 2013. PMID: 23622206 Review.
In the group with an autosomal dominant mode of inheritance we include benign familial infantile seizures and benign familial neonatal-infantile seizures. These entities are characterized by partial seizures in cluster, self …
In the group with an autosomal dominant mode of inheritance we include benign familial infantile seizures and benign …
Myoclonic-astatic epilepsy.
Doose H. Doose H. Epilepsy Res Suppl. 1992;6:163-8. Epilepsy Res Suppl. 1992. PMID: 1418479 Review.
Myoclonic-astatic epilepsy (MAE) belongs to the group of epilepsies with primarily generalized seizures as absence epilepsies, and juvenile myoclonic epilepsy, as well as infantile and juvenile idiopathic epilepsy with generalized tonic-clonic seizures. ...Th …
Myoclonic-astatic epilepsy (MAE) belongs to the group of epilepsies with primarily generalized seizures as absence epilepsies, and ju …
Pediatric focal epilepsy syndromes.
Sánchez Fernández I, Loddenkemper T. Sánchez Fernández I, et al. J Clin Neurophysiol. 2012 Oct;29(5):425-40. doi: 10.1097/WNP.0b013e31826bd943. J Clin Neurophysiol. 2012. PMID: 23027100 Review.
Benign epilepsy with centrotemporal spikes, early-onset childhood occipital epilepsy (Panayiotopoulos syndrome [PS]) and late-onset childhood occipital epilepsy (Gastaut type [LOCE-G]) are the principal pediatric focal epilepsy syndromes. ...Then, the initial description o …
Benign epilepsy with centrotemporal spikes, early-onset childhood occipital epilepsy (Panayiotopoulos syndrome [PS]) and late-onset c …
Benign infantile epilepsy with complex partial seizures.
Watanabe K, Yamamoto N, Negoro T, Takahashi I, Aso K, Maehara M. Watanabe K, et al. J Clin Neurophysiol. 1990 Jul;7(3):409-16. doi: 10.1097/00004691-199007000-00006. J Clin Neurophysiol. 1990. PMID: 2211995 Review.
Benign infantile epilepsy with complex partial seizures is characterized by a high incidence of family history of benign childhood convulsions, normal development prior to onset, infantile onset, no underlying disorders, no neurological a …
Benign infantile epilepsy with complex partial seizures is characterized by a high incidence of family history o …
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder.
Oates S, Absoud M, Goyal S, Bayley S, Baulcomb J, Sims A, Riddett A, Allis K, Brasch-Andersen C, Balasubramanian M, Bai R, Callewaert B, Hüffmeier U, Le Duc D, Radtke M, Korff C, Kennedy J, Low K, Møller RS, Nielsen JEK, Popp B, Quteineh L, Rønde G, Schönewolf-Greulich B, Shillington A, Taylor MR, Todd E, Torring PM, Tümer Z, Vasileiou G, Yates TM, Zweier C, Rosch R, Basson MA, Pal DK. Oates S, et al. Clin Genet. 2021 Oct;100(4):412-429. doi: 10.1111/cge.14023. Epub 2021 Jul 16. Clin Genet. 2021. PMID: 34216016 Free article.
Individuals with ZMYND11 associated epilepsy fell into three groups: (i) atypical benign partial epilepsy or idiopathic focal epilepsy (n = 8); (ii) generalised epilepsies/infantile epileptic encephalopathy (n = 4); (iii) unclassified (n = 8). Seizure …
Individuals with ZMYND11 associated epilepsy fell into three groups: (i) atypical benign partial epilepsy or idiopathic focal …
Treatment of benign focal epilepsies in children: when and how should be treated?
Oguni H. Oguni H. Brain Dev. 2011 Mar;33(3):207-12. doi: 10.1016/j.braindev.2010.10.024. Epub 2010 Nov 20. Brain Dev. 2011. PMID: 21095081 Review.
They include benign infantile seizures (BIS), Panayiotopoulos syndrome (PS), and benign childhood epilepsy with centrotemporal spikes (BCECTS) in this order of the onset age. ...We must remember that some patients with BCECTS may have an "atypical evol …
They include benign infantile seizures (BIS), Panayiotopoulos syndrome (PS), and benign childhood epilepsy with …
Genetics of the epilepsies: where are we and where are we going?
Helbig I, Lowenstein DH. Helbig I, et al. Curr Opin Neurol. 2013 Apr;26(2):179-85. doi: 10.1097/WCO.0b013e32835ee6ff. Curr Opin Neurol. 2013. PMID: 23429546 Free PMC article. Review.
Most importantly, PRRT2 was identified as the long-sought gene for benign familial infantile seizures. Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and se …
Most importantly, PRRT2 was identified as the long-sought gene for benign familial infantile seizures. Mutations in KCN …
Benign infantile seizures: a prospective study.
Espeche A. Espeche A. Epilepsy Res. 2010 Mar;89(1):96-103. doi: 10.1016/j.eplepsyres.2009.10.017. Epub 2009 Nov 30. Epilepsy Res. 2010. PMID: 19945823
INTRODUCTION: One idiopathic focal epileptic syndrome with onset during infancy is recognized, the benign infantile seizures (BIS). OBJECTIVE: To analyze the electroclinical features and evolution in patients with BIS and assess the difference between familia …
INTRODUCTION: One idiopathic focal epileptic syndrome with onset during infancy is recognized, the benign infantile seizure …
Genetics of idiopathic epilepsies.
Hirose S, Mitsudome A, Okada M, Kaneko S; Epilepsy Genetic Study Group, Japan. Hirose S, et al. Epilepsia. 2005;46 Suppl 1:38-43. doi: 10.1111/j.0013-9580.2005.461011.x. Epilepsia. 2005. PMID: 15816978 Free article. Review.
RESULTS: Mutations of the genes encoding two subunits of the neuronal nicotinic acetylcholine receptor were found in autosomal dominant nocturnal frontal lobe epilepsy. Mutations of two K(+)-channel genes were identified in benign familial neonatal convulsions. Mutations o …
RESULTS: Mutations of the genes encoding two subunits of the neuronal nicotinic acetylcholine receptor were found in autosomal dominant noct …
Seizures in Sotos syndrome: Phenotyping in 49 patients.
Fortin O, Vincelette C, Khan AQ, Berrahmoune S, Dassi C, Karimi M, Scheffer IE, Lu J, Davis K, Myers KA. Fortin O, et al. Epilepsia Open. 2021 Jun;6(2):425-430. doi: 10.1002/epi4.12484. Epub 2021 Apr 9. Epilepsia Open. 2021. PMID: 34033256 Free PMC article.
Most patients (33/49; 67%) had multiple seizure types. The majority (33/49; 67%) had seizures controlled on a single antiseizure medication or no medication. ...The seizure phenotype in Sotos syndrome most commonly involves staring spells, afebrile tonic-clon …
Most patients (33/49; 67%) had multiple seizure types. The majority (33/49; 67%) had seizures controlled on a single antiseizu …
36 results