Epilepsy [NEW TOPIC PAGE]

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From PubMed Clinical Queries

PubMed Clinical Queries is an utility offered by PubMed to search scientific literature in specific clinical research areas

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• Search PubMed Clinical Queries for "Epilepsy" 

Results: 5 of 40309

• Asynchronous, bilateral, and biphasic temporally unstructured electrical stimulation of amygdalae enhances the suppression of pentylenetetrazole-induced seizures in rats.
  de Oliveira JC, Maciel RM, Moraes MFD, Rosa Cota V.Epilepsy Res. 2018 Jul 20; 146:1-8. Epub 2018 Jul 20.
• Nodding syndrome: recent insights into etiology, pathophysiology, and treatment.
  Mwaka AD, Semakula JR, Abbo C, Idro R.Res Rep Trop Med. 2018; 9:89-93. Epub 2018 May 24.
• Patient-reported outcome (PRO) measure-based algorithm for clinical decision support in epilepsy outpatient follow-up: a test-retest reliability study.
  Schougaard LMV, de Thurah A, Christiansen DH, Sidenius P, Hjollund NH.BMJ Open. 2018 Jul 25; 8(7):e021337. Epub 2018 Jul 25.
• Perampanel in routine clinical use across Europe: Pooled, multicenter, observational data.
  Rohracher A, Zimmermann G, Villanueva V, Garamendi I, Sander JW, Wehner T, Shankar R, Ben-Menachem E, Brodie MJ, Pensel MC, et al.Epilepsia. 2018 Jul 25; . Epub 2018 Jul 25.
• Clinical Outcomes of Posterolateral Fusion vs. Posterior Lumbar Interbody Fusion in Patients with Lumbar Spinal Stenosis and Degenerative Instability.
  Farrokhi MR, Yadollahikhales G, Gholami M, Mousavi SR, Mesbahi AR, Asadi-Pooya AA.Pain Physician. 2018 Jul; 21(4):383-406.

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This column displays citations filtered to a specific clinical study category and scope. These search filters were developed by Haynes RB et al. See more filter information.

Systematic Reviews

Results: 5 of 2374

• Lacosamide in children with drug-resistant epilepsy.
  Rüegger AD, Freeman JL, Harvey AS.J Paediatr Child Health. 2018 Jul 27; . Epub 2018 Jul 27.
• The role of hydroxychloroquine in catastrophic antiphospholipid syndrome case: Series of two case reports and review of literature.
  Hindi Z, Hussein M, Gad A, Khaled AA, Zahoor T.SAGE Open Med Case Rep. 2018; 6:2050313X18782808. Epub 2018 Jun 26.
• Current behavioral assessments of movement disorders in children.
  Asakawa T, Sugiyama K, Nozaki T, Sameshima T, Kobayashi S, Wang L, Hong Z, Chen SJ, Li CD, Ding D, et al.CNS Neurosci Ther. 2018 Jul 24; . Epub 2018 Jul 24.
• The quality of life of older adults with epilepsy: A systematic review.
  Baranowski CJ.Seizure. 2018 Jun 4; 60:190-197. Epub 2018 Jun 4.
• Updated evidence of the association between toxocariasis and epilepsy: Systematic review and meta-analysis.
  Luna J, Cicero CE, Rateau G, Quattrocchi G, Marin B, Bruno E, Dalmay F, Druet-Cabanac M, Nicoletti A, Preux PM.PLoS Negl Trop Dis. 2018 Jul 20; 12(7):e0006665. Epub 2018 Jul 20.

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This column displays citations for systematic reviews, meta-analyses, reviews of clinical trials, evidence-based medicine, consensus development conferences, and guidelines. See filter information or additional related sources.

Medical Genetics

Topic:AllDiagnosisDifferential DiagnosisClinical DescriptionManagementGenetic CounselingMolecular GeneticsGenetic Testing

Results: 5 of 16491

• De novo KCNA1 variants in the PVP motif cause infantile epileptic encephalopathy and cognitive impairment similar to recurrent KCNA2 variants.
  Rogers A, Golumbek P, Cellini E, Doccini V, Guerrini R, Wallgren-Pettersson C, Thuresson AC, Gurnett CA.Am J Med Genet A. 2018 Jul 28; . Epub 2018 Jul 28.
• Thrombospondin receptor α2δ-1 promotes synaptogenesis and spinogenesis via postsynaptic Rac1.
  Risher WC, Kim N, Koh S, Choi JE, Mitev P, Spence EF, Pilaz LJ, Wang D, Feng G, Silver DL, et al.J Cell Biol. 2018 Jul 27; . Epub 2018 Jul 27.
• The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders.
  Willsey AJ, Morris MT, Wang S, Willsey HR, Sun N, Teerikorpi N, Baum TB, Cagney G, Bender KJ, Desai TA, et al.Cell. 2018 Jul 26; 174(3):505-520.
• Genetics Sheds New Light on Congenital Hydrocephalus Biology.
  Lal D, Palotie A.Neuron. 2018 Jul 25; 99(2):246-247.
• The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: a common epileptic encephalopathy.
  Coughlin CR 2nd, Swanson MA, Spector E, Meeks NJL, Kronquist KE, Aslamy M, Wempe MF, van Karnebeek CDM, Gospe SM Jr, Aziz VG, et al.J Inherit Metab Dis. 2018 Jul 24; . Epub 2018 Jul 24.

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This column displays citations pertaining to topics in medical genetics. See more filter information.