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43 results

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Dravet Syndrome: Diagnosis and Long-Term Course.
Connolly MB. Connolly MB. Can J Neurol Sci. 2016 Jun;43 Suppl 3:S3-8. doi: 10.1017/cjn.2016.243. Can J Neurol Sci. 2016. PMID: 27264139 Review.
Dravet syndrome is one of the most severe epilepsy syndromes of early childhood, and it comes with very high morbidity and mortality. ...It is likely that Dravet syndrome is underdiagnosed in adults with treatment-resistant epilepsy. Early diagnosis …
Dravet syndrome is one of the most severe epilepsy syndromes of early childhood, and it comes with very high morbidity and mor …
Diagnosis and long-term course of Dravet syndrome.
Scheffer IE. Scheffer IE. Eur J Paediatr Neurol. 2012 Sep;16 Suppl 1:S5-8. doi: 10.1016/j.ejpn.2012.04.007. Epub 2012 Jun 16. Eur J Paediatr Neurol. 2012. PMID: 22704920 Review.
Dravet syndrome is a severe infantile-onset epilepsy syndrome with a distinctive but complex electroclinical presentation. ...Rare patients have normal intellect. The long-term course involves ongoing, brief nocturnal convulsions and a ch …
Dravet syndrome is a severe infantile-onset epilepsy syndrome with a distinctive but complex electroclinical presentati …
Dravet syndrome: the long-term outcome.
Genton P, Velizarova R, Dravet C. Genton P, et al. Epilepsia. 2011 Apr;52 Suppl 2:44-9. doi: 10.1111/j.1528-1167.2011.03001.x. Epilepsia. 2011. PMID: 21463279 Review.
Few studies focused on the long-term outcome of Dravet syndrome in adulthood are available in the literature, but all are concordant. ...Fever sensitivity (temperature variations) persists throughout the clinical course of DS, but its impact on …
Few studies focused on the long-term outcome of Dravet syndrome in adulthood are available in the literature, bu …
Long-term course of Dravet syndrome: a study from an epilepsy center in Japan.
Takayama R, Fujiwara T, Shigematsu H, Imai K, Takahashi Y, Yamakawa K, Inoue Y. Takayama R, et al. Epilepsia. 2014 Apr;55(4):528-38. doi: 10.1111/epi.12532. Epub 2014 Feb 6. Epilepsia. 2014. PMID: 24502503
OBJECTIVE: This study attempted to clarify the long-term course of Dravet syndrome (DS). METHODS: Sixty-four patients diagnosed with DS (44 with typical DS, and 20 with atypical DS) were studied. ...Epilepsy phenotype may influence lon …
OBJECTIVE: This study attempted to clarify the long-term course of Dravet syndrome (DS). METHODS: Sixty-f …
Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.
Catarino CB, Liu JY, Liagkouras I, Gibbons VS, Labrum RW, Ellis R, Woodward C, Davis MB, Smith SJ, Cross JH, Appleton RE, Yendle SC, McMahon JM, Bellows ST, Jacques TS, Zuberi SM, Koepp MJ, Martinian L, Scheffer IE, Thom M, Sisodiya SM. Catarino CB, et al. Brain. 2011 Oct;134(Pt 10):2982-3010. doi: 10.1093/brain/awr129. Epub 2011 Jun 29. Brain. 2011. PMID: 21719429 Free PMC article.
Dravet syndrome is an epilepsy syndrome of infantile onset, frequently caused by SCN1A mutations or deletions. Its prevalence, long-term evolution in adults and neuropathology are not well known. We identified a series of 22 adult patients, incl …
Dravet syndrome is an epilepsy syndrome of infantile onset, frequently caused by SCN1A mutations or deletions. Its prev …
Difficulty of Early Diagnosis and Requirement of Long-Term Follow-Up in Benign Infantile Seizures.
Kikuchi K, Hamano S, Higurashi N, Matsuura R, Suzuki K, Tanaka M, Minamitani M. Kikuchi K, et al. Pediatr Neurol. 2015 Aug;53(2):157-62. doi: 10.1016/j.pediatrneurol.2015.03.025. Epub 2015 Apr 10. Pediatr Neurol. 2015. PMID: 26096618
CONCLUSION: About 30% of patients initially diagnosed as having benign infantile seizures did not experience a benign clinical course. Our findings suggest that clinical features in the acute phase are not helpful for predicting benign outcomes in benign infantile s …
CONCLUSION: About 30% of patients initially diagnosed as having benign infantile seizures did not experience a benign clinical cou …
Juvenile myoclonic epilepsy: Long-term prognosis and risk factors.
Pietrafusa N, La Neve A, de Palma L, Boero G, Luisi C, Vigevano F, Specchio N. Pietrafusa N, et al. Brain Dev. 2021 Jun;43(6):688-697. doi: 10.1016/j.braindev.2021.02.005. Epub 2021 Mar 27. Brain Dev. 2021. PMID: 33781581 Review.
OBJECTIVE: Our goal was to investigate the long-term clinical course of juvenile myoclonic epilepsy (JME) in a cohort of patients and to identify prognostic factors for refractoriness and seizure relapse after anti-seizure medications (ASMs) withdrawal …
OBJECTIVE: Our goal was to investigate the long-term clinical course of juvenile myoclonic epilepsy (JME) in a c …
Early and long-term electroclinical features of patients with epilepsy and PCDH19 mutation.
Chemaly N, Losito E, Pinard JM, Gautier A, Villeneuve N, Arbues AS, An I, Desguerre I, Dulac O, Chiron C, Kaminska A, Nabbout R. Chemaly N, et al. Epileptic Disord. 2018 Dec 1;20(6):457-467. doi: 10.1684/epd.2018.1009. Epileptic Disord. 2018. PMID: 30530412
Protocadherin 19 (PCDH19) mutations have been identified in epilepsy in females with mental retardation as well as patients with a "Dravet-like" phenotype. We aimed to elucidate the electroclinical phenotype associated with PCDH19 mutation, which is currently difficult to …
Protocadherin 19 (PCDH19) mutations have been identified in epilepsy in females with mental retardation as well as patients with a "Drave …
A long-term follow-up study of Dravet syndrome up to adulthood.
Akiyama M, Kobayashi K, Yoshinaga H, Ohtsuka Y. Akiyama M, et al. Epilepsia. 2010 Jun;51(6):1043-52. doi: 10.1111/j.1528-1167.2009.02466.x. Epub 2009 Dec 22. Epilepsia. 2010. PMID: 20041943
PURPOSE: We intended to elucidate the whole clinical course of Dravet syndrome (DS) comprehensively, from infancy through adulthood. METHODS: Subjects were 31 patients with DS (14 with typical DS, and 17 with borderline DS) who were followed from childhood to …
PURPOSE: We intended to elucidate the whole clinical course of Dravet syndrome (DS) comprehensively, from infancy throu …
Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings.
Wolff M, Cassé-Perrot C, Dravet C. Wolff M, et al. Epilepsia. 2006;47 Suppl 2:45-8. doi: 10.1111/j.1528-1167.2006.00688.x. Epilepsia. 2006. PMID: 17105460
Severe Myoclonic Epilepsy in infancy (SMEI, or Dravet syndrome) is a drug-resistant epilepsy that occurs in the first year of life of previously healthy children. ...Global mental retardation, attention deficit and psychotic behavior have been reported but th …
Severe Myoclonic Epilepsy in infancy (SMEI, or Dravet syndrome) is a drug-resistant epilepsy that occurs in the first y …
43 results