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Items: 1 to 20 of 89


Epilepsy in autism is associated with intellectual disability and gender: evidence from a meta-analysis.

Amiet C, Gourfinkel-An I, Bouzamondo A, Tordjman S, Baulac M, Lechat P, Mottron L, Cohen D.

Biol Psychiatry. 2008 Oct 1;64(7):577-82. doi: 10.1016/j.biopsych.2008.04.030. Epub 2008 Jun 20.


Childhood absence epilepsy: behavioral, cognitive, and linguistic comorbidities.

Caplan R, Siddarth P, Stahl L, Lanphier E, Vona P, Gurbani S, Koh S, Sankar R, Shields WD.

Epilepsia. 2008 Nov;49(11):1838-46. doi: 10.1111/j.1528-1167.2008.01680.x. Epub 2008 Jun 13.


Risk of autism spectrum disorders after infantile spasms: a population-based study nested in a cohort with seizures in the first year of life.

Saemundsen E, Ludvigsson P, Rafnsson V.

Epilepsia. 2008 Nov;49(11):1865-70. doi: 10.1111/j.1528-1167.2008.01688.x. Epub 2008 Jun 13.


An investigation of sleep characteristics, EEG abnormalities and epilepsy in developmentally regressed and non-regressed children with autism.

Giannotti F, Cortesi F, Cerquiglini A, Miraglia D, Vagnoni C, Sebastiani T, Bernabei P.

J Autism Dev Disord. 2008 Nov;38(10):1888-97. doi: 10.1007/s10803-008-0584-4. Epub 2008 May 16.


Advances in autism genetics: on the threshold of a new neurobiology.

Abrahams BS, Geschwind DH.

Nat Rev Genet. 2008 May;9(5):341-55. doi: 10.1038/nrg2346. Review. Erratum in: Nat Rev Genet. 2008 Jun;9(6):493.


Attention impairment in rolandic epilepsy: systematic review.

Kavros PM, Clarke T, Strug LJ, Halperin JM, Dorta NJ, Pal DK.

Epilepsia. 2008 Sep;49(9):1570-80. doi: 10.1111/j.1528-1167.2008.01610.x. Epub 2008 Apr 11. Review.


Academic performance in children with rolandic epilepsy.

Piccinelli P, Borgatti R, Aldini A, Bindelli D, Ferri M, Perna S, Pitillo G, Termine C, Zambonin F, Balottin U.

Dev Med Child Neurol. 2008 May;50(5):353-6. doi: 10.1111/j.1469-8749.2007.02040.x.


Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.

Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek AG, Stillman AA, Tanriover G, Abrahams BS, Duvall JA, Robbins EM, Geschwind DH, Biederer T, Gunel M, Lifton RP, State MW.

Am J Hum Genet. 2008 Jan;82(1):165-73. doi: 10.1016/j.ajhg.2007.09.017.


A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.

Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH, Chakravarti A.

Am J Hum Genet. 2008 Jan;82(1):160-4. doi: 10.1016/j.ajhg.2007.09.015.


Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.

Alarcón M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH.

Am J Hum Genet. 2008 Jan;82(1):150-9. doi: 10.1016/j.ajhg.2007.09.005.


Epilepsy in patients with pervasive developmental disorder not otherwise specified.

Parmeggiani A, Posar A, Antolini C, Scaduto MC, Santucci M, Giovanardi-Rossi P.

J Child Neurol. 2007 Oct;22(10):1198-203.


Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions.

Oliveira G, Ataíde A, Marques C, Miguel TS, Coutinho AM, Mota-Vieira L, Gonçalves E, Lopes NM, Rodrigues V, Carmona da Mota H, Vicente AM.

Dev Med Child Neurol. 2007 Oct;49(10):726-33.


Prevalence of epileptiform activity in healthy children during sleep.

Capdevila OS, Dayyat E, Kheirandish-Gozal L, Gozal D.

Sleep Med. 2008 Mar;9(3):303-9. Epub 2007 Jul 16.


Seizures in Rett syndrome: an overview from a one-year calendar study.

Jian L, Nagarajan L, de Klerk N, Ravine D, Christodoulou J, Leonard H.

Eur J Paediatr Neurol. 2007 Sep;11(5):310-7. Epub 2007 Apr 11.


Tuberous sclerosis complex and epilepsy: recent developments and future challenges.

Holmes GL, Stafstrom CE; Tuberous Sclerosis Study Group.

Epilepsia. 2007 Apr;48(4):617-30. Epub 2007 Mar 26. Review.


Autism and epilepsy: a retrospective follow-up study.

Hara H.

Brain Dev. 2007 Sep;29(8):486-90. Epub 2007 Feb 26.


EEG abnormalities in West syndrome: correlation with the emergence of autistic features.

Kayaalp L, Dervent A, Saltik S, Uluduz D, Kayaalp IV, Demirbilek V, Ghaziuddin M.

Brain Dev. 2007 Jul;29(6):336-45. Epub 2006 Nov 17.


Seizures and electroencephalographic findings in CDKL5 mutations: case report and review.

Grosso S, Brogna A, Bazzotti S, Renieri A, Morgese G, Balestri P.

Brain Dev. 2007 May;29(4):239-42. Epub 2006 Oct 16. Review.


Abnormalities on the neurological examination and EEG in young children with pervasive developmental disorders.

Akshoomoff N, Farid N, Courchesne E, Haas R.

J Autism Dev Disord. 2007 May;37(5):887-93.

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