These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
22. [Myoclonic epilepsies in infancy]. Palencia R. Rev Neurol; 2000 Jun 21; 30 Suppl 1():S15-24. PubMed ID: 10904965 [Abstract] [Full Text] [Related]
23. [Benign myoclonic epilepsy in infant]. Prats-Viñas JM, Garaizar C, Ruiz-Espinoza C. Rev Neurol; 2000 Jun 21; 34(3):201-4. PubMed ID: 12022064 [Abstract] [Full Text] [Related]
24. [Severe myoclonic epilepsy in infancy. Clinical and paraclinical aspects]. Martínez-Bermejo A, López-Martín V, Arcas J, Tendero A, Roche Herrero MC, Merino M. Rev Neurol; 2000 Jun 21; 37(1):55-9. PubMed ID: 12861510 [Abstract] [Full Text] [Related]
25. Benign myoclonic epilepsy of infancy evolving to Jeavons syndrome. Moutaouakil F, El Otmani H, Fadel H, El Moutawakkil B, Slassi I. Pediatr Neurol; 2010 Sep 21; 43(3):213-6. PubMed ID: 20691946 [Abstract] [Full Text] [Related]
26. Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients. Ragona F, Brazzo D, De Giorgi I, Morbi M, Freri E, Teutonico F, Gennaro E, Zara F, Binelli S, Veggiotti P, Granata T. Brain Dev; 2010 Jan 21; 32(1):71-7. PubMed ID: 19854600 [Abstract] [Full Text] [Related]
27. Benign myoclonic epilepsy in infants: video-EEG features and long-term follow-up. Lin Y, Itomi K, Takada H, Kuboda T, Okumura A, Aso K, Negoro T, Watanabe K. Neuropediatrics; 1998 Oct 21; 29(5):268-71. PubMed ID: 9810563 [Abstract] [Full Text] [Related]
28. SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures. Ebach K, Joos H, Doose H, Stephani U, Kurlemann G, Fiedler B, Hahn A, Hauser E, Hundt K, Holthausen H, Müller U, Neubauer BA. Neuropediatrics; 2005 Jun 21; 36(3):210-3. PubMed ID: 15944908 [Abstract] [Full Text] [Related]
29. Reflex myoclonic epilepsy in infancy: a multicenter clinical study. Verrotti A, Matricardi S, Capovilla G, D'Egidio C, Cusmai R, Romeo A, Pruna D, Pavone P, Cappanera S, Granata T, Gobbi G, Striano P, Grosso S, Parisi P, Franzoni E, Striano S, Spalice A, Marino R, Vigevano F, Coppola G. Epilepsy Res; 2013 Feb 21; 103(2-3):237-44. PubMed ID: 22819072 [Abstract] [Full Text] [Related]
30. Myoclonic epilepsy in infancy: an electroclinical study and long-term follow-up of 38 patients. Caraballo RH, Flesler S, Pasteris MC, Lopez Avaria MF, Fortini S, Vilte C. Epilepsia; 2013 Sep 21; 54(9):1605-12. PubMed ID: 23889608 [Abstract] [Full Text] [Related]
31. [Reflex benign myoclonic epilepsy of childhood. Apropos of a new case]. Fernández-Lorente J, Pastor J, Carbonell J, Aparicio-Meix JM. Rev Neurol; 2013 Sep 21; 29(1):39-42. PubMed ID: 10528309 [Abstract] [Full Text] [Related]
32. Benign pediatric localization-related epilepsies. Part I. Syndromes in infancy. Chahine LM, Mikati MA. Epileptic Disord; 2006 Sep 21; 8(3):169-83. PubMed ID: 16987737 [Abstract] [Full Text] [Related]
33. Early development in Dravet syndrome; visual function impairment precedes cognitive decline. Chieffo D, Ricci D, Baranello G, Martinelli D, Veredice C, Lettori D, Battaglia D, Dravet C, Mercuri E, Guzzetta F. Epilepsy Res; 2011 Jan 21; 93(1):73-9. PubMed ID: 21109403 [Abstract] [Full Text] [Related]
34. Cognitive and behavioral outcomes of epileptic syndromes: implications for education and clinical practice. Besag FM. Epilepsia; 2006 Jan 21; 47 Suppl 2():119-25. PubMed ID: 17105481 [Abstract] [Full Text] [Related]
36. The spectrum of benign infantile seizures. Specchio N, Vigevano F. Epilepsy Res; 2006 Aug 21; 70 Suppl 1():S156-67. PubMed ID: 16837167 [Abstract] [Full Text] [Related]
37. [Severe myoclonic epilepsy in childhood. Epidemiologic analytical study]. Nieto-Barrera M, Lillo MM, Rodríguez-Collado C, Candau R, Correa A. Rev Neurol; 2006 Aug 21; 30(7):620-4. PubMed ID: 10859739 [Abstract] [Full Text] [Related]
38. Overall management of patients with Dravet syndrome. Ceulemans B. Dev Med Child Neurol; 2011 Apr 21; 53 Suppl 2():19-23. PubMed ID: 21504428 [Abstract] [Full Text] [Related]
39. Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy. Kearney JA, Wiste AK, Stephani U, Trudeau MM, Siegel A, RamachandranNair R, Elterman RD, Muhle H, Reinsdorf J, Shields WD, Meisler MH, Escayg A. Pediatr Neurol; 2006 Feb 21; 34(2):116-20. PubMed ID: 16458823 [Abstract] [Full Text] [Related]
40. Clinical evaluation and diagnosis of severe epilepsy syndromes of early childhood. Zupanc ML. J Child Neurol; 2009 Aug 21; 24(8 Suppl):6S-14S. PubMed ID: 19666878 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]