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Transition into adulthood: Tuberous sclerosis complex, S turge‐ W eber syndrome, and R asmussen encephalitis
dc.contributor.authorThiele, Elizabeth A.en_US
dc.contributor.authorGranata, Tizianaen_US
dc.contributor.authorMatricardi, Saraen_US
dc.contributor.authorChugani, Harry T.en_US
dc.date.accessioned2014-10-07T16:09:08Z
dc.date.availableWITHHELD_11_MONTHSen_US
dc.date.available2014-10-07T16:09:08Z
dc.date.issued2014-08en_US
dc.identifier.citationThiele, Elizabeth A.; Granata, Tiziana; Matricardi, Sara; Chugani, Harry T. (2014). "Transition into adulthood: Tuberous sclerosis complex, S turge‐ W eber syndrome, and R asmussen encephalitis." Epilepsia : 29-33.en_US
dc.identifier.issn0013-9580en_US
dc.identifier.issn1528-1167en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/108590
dc.publisherWiley‐Blackwellen_US
dc.subject.otherR Asmussen's Encephalitisen_US
dc.subject.otherS Turge W Eberen_US
dc.subject.otherTuberous Sclerosisen_US
dc.titleTransition into adulthood: Tuberous sclerosis complex, S turge‐ W eber syndrome, and R asmussen encephalitisen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMedicine (General)en_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/108590/1/epi12722.pdf
dc.identifier.doi10.1111/epi.12722en_US
dc.identifier.sourceEpilepsiaen_US
dc.identifier.citedreferenceNorthrup H, Krueger DA, International Tuberous Sclerosis Complex Consensus Group. TSC diagnostic criteria update: recommendations of the 2012 international Tuberous Sclerosis Complex Consensus conference. Pediatr Neurol 2013; 49: 243 – 254.en_US
dc.identifier.citedreferenceShirley MD, Tang H, Gallione CJ, et al. Sturge–Weber syndrome and port‐wine stains caused by somatic mutation in GNAQ. N Engl J Med 2013; 368: 1971 – 1979.en_US
dc.identifier.citedreferenceChu‐Shore CJ, Major P, Camposano S, et al. The natural history of epilepsy in TSC. Epilepsia 2010; 51: 1239 – 1241.en_US
dc.identifier.citedreferenceKwiatkowski DJ, Whittemore VH, Thiele EA (Ed). Tuberous sclerosis complex: genes, clinical features and therapeutics. London, UK: Wiley‐Blackwell; 2011.en_US
dc.identifier.citedreferenceVining EP, Freeman JM, Pillas DJ, et al. Why would you remove half a brain? The outcome of children after hemispherectomy‐the Johns Hopkins experience: 1968 to 1996. Pediatrics 1997; 100: 163 – 171.en_US
dc.identifier.citedreferenceGranata T. Rasmussen's syndrome. Neurol Sci 2003; 24 ( Suppl. 4 ): S239 – S243.en_US
dc.identifier.citedreferenceKossoff EH, Balasta M, Hatfield LM, et al. Self‐reported treatment patterns in patients with Sturge–Weber syndrome and migraines. J Child Neurol 2007; 22: 720 – 726.en_US
dc.identifier.citedreferenceSujansky E, Conradi S. Outcome of Sturge–Weber syndrome in 52 adults. Am J Med Genet 1995; 57: 35 – 45.en_US
dc.identifier.citedreferenceBehen ME, Juhasz C, Wolfe‐Christensen C, et al. Brain damage and IQ in unilateral Sturge–Weber syndrome: support for a “fresh start” hypothesis. Epilepsy Behav 2011; 22: 352 – 357.en_US
dc.identifier.citedreferencePascual‐Castroviejo I, Pascual‐Pascual SI, Velazquez‐Fragua R, et al. Sturge–Weber syndrome: study of 55 patients. Can J Neurol Sci 2008; 35: 301 – 307.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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