epilepsy

Variations in EEG discharges predict ADHD severity within individual Smith-Lemli-Opitz patients.

Schreiber JM, Lanham DC, Trescher WH, Sparks SE, Wassif CA, Caffo BS, et al. Variations in EEG discharges predict ADHD severity within individual Smith-Lemli-Opitz patients. Neurology. 2014;83(2):151-9. DOI: 10.1212/WNL.0000000000000565. PubMed PMID: 24920862.

Risk of epilepsy among patients with atopic dermatitis: a nationwide longitudinal study.

Chen M-H, Wu Y-H, Su T-P, Chen Y-S, Hsu J-W, Huang K-L, et al. Risk of epilepsy among patients with atopic dermatitis: a nationwide longitudinal study. Epilepsia. 2014;55(8):1307-12. DOI: 10.1111/epi.12667. PubMed PMID: 24917387.

Psychiatric and neurologic risk factors for incident cases of new-onset epilepsy in older adults: data from U.S. Medicare beneficiaries.

Martin RC, Faught E, Richman J, Funkhouser E, Kim Y, Clements K, et al. Psychiatric and neurologic risk factors for incident cases of new-onset epilepsy in older adults: data from U.S. Medicare beneficiaries. Epilepsia. 2014;55(7):1120-7. DOI: 10.1111/epi.12649. PubMed PMID: 24902475.

Lennox-Gastaut syndrome and phenotype: secondary network epilepsies.

Archer JS, Warren AEL, Stagnitti MR, Masterton RAJ, Abbott DF, Jackson GD. Lennox-Gastaut syndrome and phenotype: secondary network epilepsies. Epilepsia. 2014;55(8):1245-54. DOI: 10.1111/epi.12682. PubMed PMID: 24902608.

Co-occurring malformations of cortical development and SCN1A gene mutations.

Barba C, Parrini E, Coras R, Galuppi A, Craiu D, Kluger G, et al. Co-occurring malformations of cortical development and SCN1A gene mutations. Epilepsia. 2014;55(7):1009-19. DOI: 10.1111/epi.12658. PubMed PMID: 24902755.

IDH1 mutation is associated with seizures and protoplasmic subtype in patients with low-grade gliomas.

Liubinas SV, D'Abaco GM, Moffat BM, Gonzales M, Feleppa F, Nowell CJ, et al. IDH1 mutation is associated with seizures and protoplasmic subtype in patients with low-grade gliomas. Epilepsia. 2014;55(9):1438-43. DOI: 10.1111/epi.12662. PubMed PMID: 24903073.

Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation.

Venkateswaran S, Myers KA, Smith AC, Beaulieu CL, Schwartzentruber JA, Majewski J, et al. Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation. Epilepsia. 2014;55(7):e75-9. DOI: 10.1111/epi.12663. PubMed PMID: 24903190.

Sofie's journey.

Levy C, Levy B. Sofie's journey. Epilepsia. 2014;55(9):1329-30. DOI: 10.1111/epi.12664. PubMed PMID: 24903458.

Sudden unexpected death in epilepsy: assessing the public health burden.

Thurman DJ, Hesdorffer DC, French JA. Sudden unexpected death in epilepsy: assessing the public health burden. Epilepsia. 2014;55(10):1479-85. DOI: 10.1111/epi.12666. PubMed PMID: 24903551.

Seizure frequency and patient-centered outcome assessment in epilepsy.

Choi H, Hamberger MJ, Munger Clary H, Loeb R, Onchiri FM, Baker G, et al. Seizure frequency and patient-centered outcome assessment in epilepsy. Epilepsia. 2014;55(8):1205-12. DOI: 10.1111/epi.12672. PubMed PMID: 24903898.