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Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
Brain. 2010 Mar;133(Pt 3):655-70. doi: 10.1093/brain/awp336. Epub 2010 Feb 2.
Brain. 2010.
PMID: 20129935
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Vetro A, Nielsen HN, Holm R, Hevner RF, Parrini E, Powis Z, Møller RS, Bellan C, Simonati A, Lesca G, Helbig KL, Palmer EE, Mei D, Ballardini E, Van Haeringen A, Syrbe S, Leuzzi V, Cioni G, Curry CJ, Costain G, Santucci M, Chong K, Mancini GMS, Clayton-Smith J, Bigoni S, Scheffer IE, Dobyns WB, Vilsen B, Guerrini R; ATP1A2/A3-collaborators.
Vetro A, et al.
Brain. 2021 Jun 22;144(5):1435-1450. doi: 10.1093/brain/awab052.
Brain. 2021.
PMID: 33880529
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Sudden unexplained death in children with epilepsy.
Donner EJ, Smith CR, Snead OC 3rd.
Donner EJ, et al.
Neurology. 2001 Aug 14;57(3):430-4. doi: 10.1212/wnl.57.3.430.
Neurology. 2001.
PMID: 11502908
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Can children with hyperlipidemia receive ketogenic diet for medication-resistant epilepsy?
Liu YM, Lowe H, Zak MM, Kobayashi J, Chan VW, Donner EJ.
Liu YM, et al.
J Child Neurol. 2013 Apr;28(4):479-83. doi: 10.1177/0883073813476140. Epub 2013 Feb 20.
J Child Neurol. 2013.
PMID: 23427065
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Prevalence of Genetic Disorders and GLUT1 Deficiency in a Ketogenic Diet Clinic.
Hewson S, Brunga L, Ojeda MF, Imhof E, Patel J, Zak M, Donner EJ, Kobayashi J, Salomons GS, Mercimek-Andrews S.
Hewson S, et al. Among authors: donner ej.
Can J Neurol Sci. 2018 Jan;45(1):93-96. doi: 10.1017/cjn.2017.246. Epub 2017 Nov 16.
Can J Neurol Sci. 2018.
PMID: 29144225
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Prevalence of inherited neurotransmitter disorders in patients with movement disorders and epilepsy: a retrospective cohort study.
Mercimek-Mahmutoglu S, Sidky S, Hyland K, Patel J, Donner EJ, Logan W, Mendoza-Londono R, Moharir M, Raiman J, Schulze A, Siriwardena K, Yoon G, Kyriakopoulou L.
Mercimek-Mahmutoglu S, et al.
Orphanet J Rare Dis. 2015 Feb 8;10:12. doi: 10.1186/s13023-015-0234-9.
Orphanet J Rare Dis. 2015.
PMID: 25758715
Free PMC article.
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Practice guideline summary: Sudden unexpected death in epilepsy incidence rates and risk factors: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology and the American Epilepsy Society.
Harden C, Tomson T, Gloss D, Buchhalter J, Cross JH, Donner E, French JA, Gil-Nagel A, Hesdorffer DC, Smithson WH, Spitz MC, Walczak TS, Sander JW, Ryvlin P.
Harden C, et al. Among authors: donner e.
Neurology. 2017 Apr 25;88(17):1674-1680. doi: 10.1212/WNL.0000000000003685.
Neurology. 2017.
PMID: 28438841
Free article.
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Neutropenia in Children Treated With Ketogenic Diet Therapy.
Munro K, Keller AE, Lowe H, Ferrara E, Whitney R, Liu CYM, Zak M, Chan V, Kobayashi J, Donner EJ.
Munro K, et al. Among authors: donner ej.
J Child Neurol. 2021 Jun;36(7):525-529. doi: 10.1177/0883073820984067. Epub 2021 Jan 4.
J Child Neurol. 2021.
PMID: 33393840
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Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisone.
Tein I, Donner EJ, Hale DE, Murphy EG.
Tein I, et al. Among authors: donner ej.
Pediatr Neurol. 1995 Jan;12(1):68-76. doi: 10.1016/0887-8994(94)00109-f.
Pediatr Neurol. 1995.
PMID: 7748366
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Abbreviated report of the NIH/NINDS workshop on sudden unexpected death in epilepsy.
Hirsch LJ, Donner EJ, So EL, Jacobs M, Nashef L, Noebels JL, Buchhalter JR.
Hirsch LJ, et al. Among authors: donner ej.
Neurology. 2011 May 31;76(22):1932-8. doi: 10.1212/WNL.0b013e31821de7de. Epub 2011 May 4.
Neurology. 2011.
PMID: 21543734
Free PMC article.
Review.
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