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Multifocal myoclonus associated with mefloquine chemoprophylaxis.
Jiménez-Huete A, Gil-Nagel A, Franch O. Jiménez-Huete A, et al. Clin Neuropharmacol. 2002 Sep-Oct;25(5):243. doi: 10.1097/00002826-200209000-00002. Clin Neuropharmacol. 2002. PMID: 12410053 No abstract available.
Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest.
Johnson EW, Dubovsky J, Rich SS, O'Donovan CA, Orr HT, Anderson VE, Gil-Nagel A, Ahmann P, Dokken CG, Schneider DT, Weber JL. Johnson EW, et al. Hum Mol Genet. 1998 Jan;7(1):63-7. doi: 10.1093/hmg/7.1.63. Hum Mol Genet. 1998. PMID: 9384604
Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig.
Johnson EW, Iyer LM, Rich SS, Orr HT, Gil-Nagel A, Kurth JH, Zabramski JM, Marchuk DA, Weissenbach J, Clericuzio CL, Davis LE, Hart BL, Gusella JF, Kosofsky BE, Louis DN, Morrison LA, Green ED, Weber JL. Johnson EW, et al. Genome Res. 1995 Nov;5(4):368-80. doi: 10.1101/gr.5.4.368. Genome Res. 1995. PMID: 8750196
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1).
Sahoo T, Johnson EW, Thomas JW, Kuehl PM, Jones TL, Dokken CG, Touchman JW, Gallione CJ, Lee-Lin SQ, Kosofsky B, Kurth JH, Louis DN, Mettler G, Morrison L, Gil-Nagel A, Rich SS, Zabramski JM, Boguski MS, Green ED, Marchuk DA. Sahoo T, et al. Hum Mol Genet. 1999 Nov;8(12):2325-33. doi: 10.1093/hmg/8.12.2325. Hum Mol Genet. 1999. PMID: 10545614
Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Frontal Lobe Epilepsy: A New Clinico-Pathological Entity.
Schurr J, Coras R, Rössler K, Pieper T, Kudernatsch M, Holthausen H, Winkler P, Woermann F, Bien CG, Polster T, Schulz R, Kalbhenn T, Urbach H, Becker A, Grunwald T, Huppertz HJ, Gil-Nagel A, Toledano R, Feucht M, Mühlebner A, Czech T, Blümcke I. Schurr J, et al. Brain Pathol. 2017 Jan;27(1):26-35. doi: 10.1111/bpa.12347. Epub 2016 Feb 22. Brain Pathol. 2017. PMID: 26748554
Epilepsy in inherited metabolic disorders.
Pascual JM, Campistol J, Gil-Nagel A. Pascual JM, et al. Neurologist. 2008 Nov;14(6 Suppl 1):S2-S14. doi: 10.1097/01.nrl.0000340787.30542.41. Neurologist. 2008. PMID: 19225367 Review.
Praxis induction and its relationship with cognition in genetic generalized epilepsy.
Abarrategui B, Parejo-Carbonell B, García García ME, Gil-Nagel A, García-Morales I. Abarrategui B, et al. Epilepsy Behav. 2020 Jan;102:106638. doi: 10.1016/j.yebeh.2019.106638. Epub 2019 Dec 2. Epilepsy Behav. 2020. PMID: 31805510
Immunomodulated parkinsonism as a presenting symptom of LGI1 antibody encephalitis.
Kurtis MM, Toledano R, García-Morales I, Gil-Nagel A. Kurtis MM, et al. Parkinsonism Relat Disord. 2015 Oct;21(10):1286-7. doi: 10.1016/j.parkreldis.2015.08.014. Epub 2015 Aug 18. Parkinsonism Relat Disord. 2015. PMID: 26320889 No abstract available.
Editorial: challenges in the management of epilepsy.
Gil-Nagel A. Gil-Nagel A. Neurologist. 2008 Nov;14(6 Suppl 1):S1. doi: 10.1097/01.nrl.0000340786.30542.08. Neurologist. 2008. PMID: 19225365 No abstract available.
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