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Items: 1 to 20 of 22

1.

Automated Detection of High Frequency Oscillations in Human Scalp Electroencephalogram.

Charupanit K, Nunez MD, Bernardo D, Bebin M, Krueger DA, Northrup H, Sahin M, Wu JY, Lopour BA.

Conf Proc IEEE Eng Med Biol Soc. 2018 Jul;2018:3116-3119. doi: 10.1109/EMBC.2018.8513033.

PMID:
30441054
2.

High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.

Hamdan FF, Myers CT, Cossette P, Lemay P, Spiegelman D, Laporte AD, Nassif C, Diallo O, Monlong J, Cadieux-Dion M, Dobrzeniecka S, Meloche C, Retterer K, Cho MT, Rosenfeld JA, Bi W, Massicotte C, Miguet M, Brunga L, Regan BM, Mo K, Tam C, Schneider A, Hollingsworth G; Deciphering Developmental Disorders Study, FitzPatrick DR, Donaldson A, Canham N, Blair E, Kerr B, Fry AE, Thomas RH, Shelagh J, Hurst JA, Brittain H, Blyth M, Lebel RR, Gerkes EH, Davis-Keppen L, Stein Q, Chung WK, Dorison SJ, Benke PJ, Fassi E, Corsten-Janssen N, Kamsteeg EJ, Mau-Them FT, Bruel AL, Verloes A, Õunap K, Wojcik MH, Albert DVF, Venkateswaran S, Ware T, Jones D, Liu YC, Mohammad SS, Bizargity P, Bacino CA, Leuzzi V, Martinelli S, Dallapiccola B, Tartaglia M, Blumkin L, Wierenga KJ, Purcarin G, O'Byrne JJ, Stockler S, Lehman A, Keren B, Nougues MC, Mignot C, Auvin S, Nava C, Hiatt SM, Bebin M, Shao Y, Scaglia F, Lalani SR, Frye RE, Jarjour IT, Jacques S, Boucher RM, Riou E, Srour M, Carmant L, Lortie A, Major P, Diadori P, Dubeau F, D'Anjou G, Bourque G, Berkovic SF, Sadleir LG, Campeau PM, Kibar Z, Lafrenière RG, Girard SL, Mercimek-Mahmutoglu S, Boelman C, Rouleau GA, Scheffer IE, Mefford HC, Andrade DM, Rossignol E, Minassian BA, Michaud JL.

Am J Hum Genet. 2017 Nov 2;101(5):664-685. doi: 10.1016/j.ajhg.2017.09.008.

3.

MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus.

Blanchet P, Bebin M, Bruet S, Cooper GM, Thompson ML, Duban-Bedu B, Gerard B, Piton A, Suckno S, Deshpande C, Clowes V, Vogt J, Turnpenny P, Williamson MP, Alembik Y; Clinical Sequencing Exploratory Research Study Consortium; Deciphering Developmental Disorders Consortium, Glasgow E, McNeill A.

PLoS Genet. 2017 Aug 31;13(8):e1006957. doi: 10.1371/journal.pgen.1006957. eCollection 2017 Aug.

4.

Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism.

Harms FL, Girisha KM, Hardigan AA, Kortüm F, Shukla A, Alawi M, Dalal A, Brady L, Tarnopolsky M, Bird LM, Ceulemans S, Bebin M, Bowling KM, Hiatt SM, Lose EJ, Primiano M, Chung WK, Juusola J, Akdemir ZC, Bainbridge M, Charng WL, Drummond-Borg M, Eldomery MK, El-Hattab AW, Saleh MAM, Bézieau S, Cogné B, Isidor B, Küry S, Lupski JR, Myers RM, Cooper GM, Kutsche K.

Am J Hum Genet. 2017 Jan 5;100(1):117-127. doi: 10.1016/j.ajhg.2016.11.012. Epub 2016 Dec 22.

5.

UBQLN2 mutation causing heterogeneous X-linked dominant neurodegeneration.

Fahed AC, McDonough B, Gouvion CM, Newell KL, Dure LS, Bebin M, Bick AG, Seidman JG, Harter DH, Seidman CE.

Ann Neurol. 2014 May;75(5):793-798. doi: 10.1002/ana.24164. Epub 2014 May 9.

6.

Functional assessment of TSC2 variants identified in individuals with tuberous sclerosis complex.

Hoogeveen-Westerveld M, Ekong R, Povey S, Mayer K, Lannoy N, Elmslie F, Bebin M, Dies K, Thompson C, Sparagana SP, Davies P, van Eeghen AM, Thiele EA, van den Ouweland A, Halley D, Nellist M.

Hum Mutat. 2013 Jan;34(1):167-75. doi: 10.1002/humu.22202. Epub 2012 Oct 11. Erratum in: Hum Mutat. 2013 Feb;34(2):408-10. van Eeghen, Agnies M [added]; Thiele, Elizabeth A [added].

PMID:
22903760
7.

Monosomy1p36.3 and trisomy 19p13.3 in a child with periventricular nodular heterotopia.

Descartes M, Mikhail FM, Franklin JC, McGrath TM, Bebin M.

Pediatr Neurol. 2011 Oct;45(4):274-8. doi: 10.1016/j.pediatrneurol.2011.06.002.

PMID:
21907895
8.

Magnetic resonance imaging abnormalities associated with vigabatrin in patients with epilepsy.

Wheless JW, Carmant L, Bebin M, Conry JA, Chiron C, Elterman RD, Frost M, Paolicchi JM, Donald Shields W, Thiele EA, Zupanc ML, Collins SD.

Epilepsia. 2009 Feb;50(2):195-205. doi: 10.1111/j.1528-1167.2008.01896.x. Epub 2008 Nov 17.

9.

Pharmacokinetics of levetiracetam in infants and young children with epilepsy.

Glauser TA, Mitchell WG, Weinstock A, Bebin M, Chen D, Coupez R, Stockis A, Lu ZS.

Epilepsia. 2007 Jun;48(6):1117-22. Epub 2007 Apr 18.

10.

Vagus nerve stimulation in children less than 5 years old.

Blount JP, Tubbs RS, Kankirawatana P, Kiel S, Knowlton R, Grabb PA, Bebin M.

Childs Nerv Syst. 2006 Sep;22(9):1167-9. Epub 2006 May 23.

PMID:
16718501
11.

Electroclinical and magnetoencephalographic studies in epilepsy patients with polymicrogyria.

Burneo JG, Bebin M, Kuzniecky RI, Knowlton RC.

Epilepsy Res. 2004 Dec;62(2-3):125-33.

PMID:
15579301
12.

Cortical reorganization in malformations of cortical development: a magnetoencephalographic study.

Burneo JG, Kuzniecky RI, Bebin M, Knowlton RC.

Neurology. 2004 Nov 23;63(10):1818-24.

PMID:
15557496
13.

Temporal lobectomy in congenital porencephaly associated with hippocampal sclerosis.

Burneo JG, Faught E, Knowlton RC, Martin RC, Bebin M, Morawetz R, Kuzniecky R.

Arch Neurol. 2003 Jun;60(6):830-4.

PMID:
12810487
14.

Pediatric partial and generalized seizures.

Bebin M.

J Child Neurol. 2002 Jan;17 Suppl 1:S65-9. Review.

PMID:
11918466
15.

Histological appearance of a chronically stimulated vagus nerve in a pediatric patient.

Tubbs RS, Patwardhan R, Palmer CA, Kelly DR, Elton S, Blount JP, Bebin M, Grabb PA.

Pediatr Neurosurg. 2001 Aug;35(2):99-102.

PMID:
11549921
16.

The acute management of seizures.

Bebin M.

Pediatr Ann. 1999 Apr;28(4):225-9.

PMID:
10224615
17.

Congenital porencephaly: MR features and relationship to hippocampal sclerosis.

Ho SS, Kuzniecky RI, Gilliam F, Faught E, Bebin M, Morawetz R.

AJNR Am J Neuroradiol. 1998 Jan;19(1):135-41.

18.

Congenital porencephaly and hippocampal sclerosis. Clinical features and epileptic spectrum.

Ho SS, Kuzniecky RI, Gilliam F, Faught E, Bebin M, Morawetz R.

Neurology. 1997 Nov;49(5):1382-8.

PMID:
9371926
19.

Intrinsic epileptogenesis of hypothalamic hamartomas in gelastic epilepsy.

Kuzniecky R, Guthrie B, Mountz J, Bebin M, Faught E, Gilliam F, Liu HG.

Ann Neurol. 1997 Jul;42(1):60-7.

PMID:
9225686
20.

Supplementary sensorimotor area epilepsy. Seizure localization, cortical propagation and subcortical activation pathways using ictal SPECT.

Laich E, Kuzniecky R, Mountz J, Liu HG, Gilliam F, Bebin M, Faught E, Morawetz R.

Brain. 1997 May;120 ( Pt 5):855-64.

PMID:
9183255

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