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Pathophysiology of Conversion to Symptomatic Leber Hereditary Optic Neuropathy and Therapeutic Implications: a Review.
Curr Neurol Neurosci Rep. 2020 Apr 15;20(5):11. doi: 10.1007/s11910-020-01032-8.
Curr Neurol Neurosci Rep. 2020.
PMID: 32296973
Review.
OCT retinal nerve fiber layer thickness differentiates acute optic neuritis from MOG antibody-associated disease and Multiple Sclerosis: RNFL thickening in acute optic neuritis from MOGAD vs MS.
Chen JJ, Sotirchos ES, Henderson AD, Vasileiou ES, Flanagan EP, Bhatti MT, Jamali S, Eggenberger ER, Dinome M, Frohman LP, Arnold AC, Bonelli L, Seleme N, Mejia-Vergara AJ, Moss HE, Padungkiatsagul T, Stiebel-Kalish H, Lotan I, Hellmann MA, Hodge D, Oertel FC, Paul F, Saidha S, Calabresi PA, Pittock SJ.
Chen JJ, et al. Among authors: seleme n.
Mult Scler Relat Disord. 2022 Feb;58:103525. doi: 10.1016/j.msard.2022.103525. Epub 2022 Jan 11.
Mult Scler Relat Disord. 2022.
PMID: 35038647
Free PMC article.
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Details and outcomes of a large cohort of MOG-IgG associated optic neuritis.
Chen JJ, Flanagan EP, Bhatti MT, Tisavipat N, Jamali S, Kunchok A, Eggenberger ER, Nome MD, Sotirchos ES, Vasileiou ES, Henderson AD, Arnold AC, Bonelli L, Seleme N, Mejia-Vergara AJ, Moss HE, Padungkiatsagul T, Stiebel-Kalish H, Lotan I, Wilf-Yarkoni A, Hellmann MA, Vuppala A, Hodge D, Pittock SJ.
Chen JJ, et al. Among authors: seleme n.
Mult Scler Relat Disord. 2022 Dec;68:104237. doi: 10.1016/j.msard.2022.104237. Epub 2022 Oct 10.
Mult Scler Relat Disord. 2022.
PMID: 36252317
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Leber Hereditary Optic Neuropathy Conversion in a Patient With Idiopathic Intracranial Hypertension.
Araya J, Araya C, Conrads T, Sadun A, Seleme N.
Araya J, et al. Among authors: seleme n.
J Neuroophthalmol. 2023 Dec 1;43(4):e139-e141. doi: 10.1097/WNO.0000000000001572. Epub 2022 Nov 23.
J Neuroophthalmol. 2023.
PMID: 36730072
No abstract available.
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Pan-American mDNA haplogroups in Chilean patients with Leber's hereditary optic neuropathy.
Romero P, Fernández V, Slabaugh M, Seleme N, Reyes N, Gallardo P, Herrera L, Peña L, Pezo P, Moraga M.
Romero P, et al. Among authors: seleme n.
Mol Vis. 2014 Mar 14;20:334-40. eCollection 2014.
Mol Vis. 2014.
PMID: 24672219
Free PMC article.
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Clinical spectrum of Kufor-Rakeb syndrome in the Chilean kindred with ATP13A2 mutations.
Behrens MI, Brüggemann N, Chana P, Venegas P, Kägi M, Parrao T, Orellana P, Garrido C, Rojas CV, Hauke J, Hahnen E, González R, Seleme N, Fernández V, Schmidt A, Binkofski F, Kömpf D, Kubisch C, Hagenah J, Klein C, Ramirez A.
Behrens MI, et al. Among authors: seleme n.
Mov Disord. 2010 Sep 15;25(12):1929-37. doi: 10.1002/mds.22996.
Mov Disord. 2010.
PMID: 20683840
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Neuro-Ophthalmic Complications in Patients Treated With CTLA-4 and PD-1/PD-L1 Checkpoint Blockade.
Sun MM, Seleme N, Chen JJ, Zekeridou A, Sechi E, Walsh RD, Beebe JD, Sabbagh O, Mejico LJ, Gratton S, Skidd PM, Bellows DA, Falardeau J, Fraser CL, Cappelen-Smith C, Haines SR, Hassanzadeh B, Seay MD, Subramanian PS, Williams Z, Gordon LK.
Sun MM, et al. Among authors: seleme n.
J Neuroophthalmol. 2021 Dec 1;41(4):519-530. doi: 10.1097/WNO.0000000000001148.
J Neuroophthalmol. 2021.
PMID: 33136674
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[Cost-benefit in the study of the dissemination of stage I and II in breast cancer].
Camacho J, Barriga C, Escobar P, Seleme N, Schwartz R.
Camacho J, et al. Among authors: seleme n.
Rev Med Chil. 2003 Feb;131(2):155-7.
Rev Med Chil. 2003.
PMID: 12708253
Spanish.
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