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Protean phenotypic features of the A3243G mitochondrial DNA mutation.
Kaufmann P, Engelstad K, Wei Y, Kulikova R, Oskoui M, Battista V, Koenigsberger DY, Pascual JM, Sano M, Hirano M, DiMauro S, Shungu DC, Mao X, De Vivo DC. Kaufmann P, et al. Among authors: wei y. Arch Neurol. 2009 Jan;66(1):85-91. doi: 10.1001/archneurol.2008.526. Arch Neurol. 2009. PMID: 19139304 Free PMC article.
Autonomic symptoms in carriers of the m.3243A>G mitochondrial DNA mutation.
Parsons T, Weimer L, Engelstad K, Linker A, Battista V, Wei Y, Hirano M, Dimauro S, De Vivo DC, Kaufmann P. Parsons T, et al. Among authors: wei y. Arch Neurol. 2010 Aug;67(8):976-9. doi: 10.1001/archneurol.2010.174. Arch Neurol. 2010. PMID: 20697048 Free PMC article.
Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype.
Kaufmann P, Engelstad K, Wei Y, Kulikova R, Oskoui M, Sproule DM, Battista V, Koenigsberger DY, Pascual JM, Shanske S, Sano M, Mao X, Hirano M, Shungu DC, Dimauro S, De Vivo DC. Kaufmann P, et al. Among authors: wei y. Neurology. 2011 Nov 29;77(22):1965-71. doi: 10.1212/WNL.0b013e31823a0c7f. Epub 2011 Nov 16. Neurology. 2011. PMID: 22094475 Free PMC article.
Glut1 deficiency syndrome and erythrocyte glucose uptake assay.
Yang H, Wang D, Engelstad K, Bagay L, Wei Y, Rotstein M, Aggarwal V, Levy B, Ma L, Chung WK, De Vivo DC. Yang H, et al. Among authors: wei y. Ann Neurol. 2011 Dec;70(6):996-1005. doi: 10.1002/ana.22640. Ann Neurol. 2011. PMID: 22190371
Does cognition improve following LVAD implantation?
Pavol MA, Willey JZ, Wei Y, Yuzefpolskaya M, Marshall RS, Marascalco PJ, Harwood J, Lazar RM. Pavol MA, et al. Among authors: wei y. Gen Thorac Cardiovasc Surg. 2018 Aug;66(8):456-463. doi: 10.1007/s11748-018-0947-5. Epub 2018 May 23. Gen Thorac Cardiovasc Surg. 2018. PMID: 29796750
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