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Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.
Papadopoulou LC, Sue CM, Davidson MM, Tanji K, Nishino I, Sadlock JE, Krishna S, Walker W, Selby J, Glerum DM, Coster RV, Lyon G, Scalais E, Lebel R, Kaplan P, Shanske S, De Vivo DC, Bonilla E, Hirano M, DiMauro S, Schon EA. Papadopoulou LC, et al. Among authors: kaplan p. Nat Genet. 1999 Nov;23(3):333-7. doi: 10.1038/15513. Nat Genet. 1999. PMID: 10545952
Quantitative Electroencephalography Biomarkers in Patients With Anti-N-methyl-D-aspartate Receptor Encephalitis: A Case-Control Study.
David Cancino CA, Trenado C, Kaplan PW, Gómez Ávila FA, Fernández González-Aragón MDC, Moreno Avellán ÁJ, Soto Rincón CA, Quiñones Pesqueira GA, San-Juan D. David Cancino CA, et al. Among authors: kaplan pw. J Clin Neurophysiol. 2024 Oct 11. doi: 10.1097/WNP.0000000000001124. Online ahead of print. J Clin Neurophysiol. 2024. PMID: 39724935
Utility of CT perfusion in seizures and rhythmic and periodic patterns.
Ameen Ahmad S, Primiani C, Porambo M, Dang T, Kaplan PW, Yedavalli V, Husari KS. Ameen Ahmad S, et al. Among authors: kaplan pw. Clin Neurophysiol. 2024 Dec;168:121-128. doi: 10.1016/j.clinph.2024.10.008. Epub 2024 Oct 20. Clin Neurophysiol. 2024. PMID: 39489074
Choroid Plexus Volume in Pediatric-Onset Multiple Sclerosis.
Grasso EA, Bloy L, Kaplan P, Bar-Or A, Yeh EA, Arnold DL, Narayanan S, Marrie RA, Fadda G, Banwell BL; Canadian Demyelinating Disease Network. Grasso EA, et al. Among authors: kaplan p. Neurol Neuroimmunol Neuroinflamm. 2024 Nov;11(6):e200319. doi: 10.1212/NXI.0000000000200319. Epub 2024 Oct 23. Neurol Neuroimmunol Neuroinflamm. 2024. PMID: 39442038 Free PMC article.
1,071 results