Scheffer IE - Search Results

1

Sleep problems in Dravet syndrome: a modifiable comorbidity.

Licheni SH, Mcmahon JM, Schneider AL, Davey MJ, Scheffer IE. Licheni SH, et al. Among authors: scheffer ie. Dev Med Child Neurol. 2018 Feb;60(2):192-198. doi: 10.1111/dmcn.13601. Epub 2017 Nov 7. Dev Med Child Neurol. 2018. PMID: 29110313 Free article.

2

Autosomal dominant rolandic epilepsy and speech dyspraxia: a new syndrome with anticipation.

Scheffer IE, Jones L, Pozzebon M, Howell RA, Saling MM, Berkovic SF. Scheffer IE, et al. Ann Neurol. 1995 Oct;38(4):633-42. doi: 10.1002/ana.410380412. Ann Neurol. 1995. PMID: 7574460

3

Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome).

Scheffer IE, Wallace R, Mulley JC, Berkovic SF. Scheffer IE, et al. Brain Dev. 2001 Nov;23(7):732-5. doi: 10.1016/s0387-7604(01)00272-8. Brain Dev. 2001. PMID: 11701287 Review.

4

LGI1 mutations in temporal lobe epilepsies.

Berkovic SF, Izzillo P, McMahon JM, Harkin LA, McIntosh AM, Phillips HA, Briellmann RS, Wallace RH, Mazarib A, Neufeld MY, Korczyn AD, Scheffer IE, Mulley JC. Berkovic SF, et al. Among authors: scheffer ie. Neurology. 2004 Apr 13;62(7):1115-9. doi: 10.1212/01.wnl.0000118213.94650.81. Neurology. 2004. PMID: 15079010

5

Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.

Marini C, Scheffer IE, Crossland KM, Grinton BE, Phillips FL, McMahon JM, Turner SJ, Dean JT, Kivity S, Mazarib A, Neufeld MY, Korczyn AD, Harkin LA, Dibbens LM, Wallace RH, Mulley JC, Berkovic SF. Marini C, et al. Among authors: scheffer ie. Epilepsia. 2004 May;45(5):467-78. doi: 10.1111/j.0013-9580.2004.46803.x. Epilepsia. 2004. PMID: 15101828 Free article.

6

Failure to confirm association of a polymorphism in ABCB1 with multidrug-resistant epilepsy.

Tan NC, Heron SE, Scheffer IE, Pelekanos JT, McMahon JM, Vears DF, Mulley JC, Berkovic SF. Tan NC, et al. Among authors: scheffer ie. Neurology. 2004 Sep 28;63(6):1090-2. doi: 10.1212/01.wnl.0000137051.33486.c7. Neurology. 2004. PMID: 15452306

7

Distinguishing sleep disorders from seizures: diagnosing bumps in the night.

Derry CP, Davey M, Johns M, Kron K, Glencross D, Marini C, Scheffer IE, Berkovic SF. Derry CP, et al. Among authors: scheffer ie. Arch Neurol. 2006 May;63(5):705-9. doi: 10.1001/archneur.63.5.705. Arch Neurol. 2006. PMID: 16682539

8

De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study.

Berkovic SF, Harkin L, McMahon JM, Pelekanos JT, Zuberi SM, Wirrell EC, Gill DS, Iona X, Mulley JC, Scheffer IE. Berkovic SF, et al. Among authors: scheffer ie. Lancet Neurol. 2006 Jun;5(6):488-92. doi: 10.1016/S1474-4422(06)70446-X. Lancet Neurol. 2006. PMID: 16713920

9

A new molecular mechanism for severe myoclonic epilepsy of infancy: exonic deletions in SCN1A.

Mulley JC, Nelson P, Guerrero S, Dibbens L, Iona X, McMahon JM, Harkin L, Schouten J, Yu S, Berkovic SF, Scheffer IE. Mulley JC, et al. Among authors: scheffer ie. Neurology. 2006 Sep 26;67(6):1094-5. doi: 10.1212/01.wnl.0000237322.04338.2b. Neurology. 2006. PMID: 17000989

10

Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adults.

Jansen FE, Sadleir LG, Harkin LA, Vadlamudi L, McMahon JM, Mulley JC, Scheffer IE, Berkovic SF. Jansen FE, et al. Among authors: scheffer ie. Neurology. 2006 Dec 26;67(12):2224-6. doi: 10.1212/01.wnl.0000249312.73155.7d. Neurology. 2006. PMID: 17190949

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