Engelstad K - Search Results

1

Attitudes toward prevention of mtDNA-related diseases through oocyte mitochondrial replacement therapy.

Engelstad K, Sklerov M, Kriger J, Sanford A, Grier J, Ash D, Egli D, DiMauro S, Thompson JL, Sauer MV, Hirano M. Engelstad K, et al. Hum Reprod. 2016 May;31(5):1058-65. doi: 10.1093/humrep/dew033. Epub 2016 Mar 2. Hum Reprod. 2016. PMID: 26936885 Free PMC article.

2

Mitochondrial DNA abnormalities and autistic spectrum disorders.

Pons R, Andreu AL, Checcarelli N, Vilà MR, Engelstad K, Sue CM, Shungu D, Haggerty R, de Vivo DC, DiMauro S. Pons R, et al. Among authors: engelstad k. J Pediatr. 2004 Jan;144(1):81-5. doi: 10.1016/j.jpeds.2003.10.023. J Pediatr. 2004. PMID: 14722523

3

Varying loads of the mitochondrial DNA A3243G mutation in different tissues: implications for diagnosis.

Shanske S, Pancrudo J, Kaufmann P, Engelstad K, Jhung S, Lu J, Naini A, DiMauro S, De Vivo DC. Shanske S, et al. Among authors: engelstad k. Am J Med Genet A. 2004 Oct 1;130A(2):134-7. doi: 10.1002/ajmg.a.30220. Am J Med Genet A. 2004. PMID: 15372523

4

Nerve conduction abnormalities in patients with MELAS and the A3243G mutation.

Kaufmann P, Pascual JM, Anziska Y, Gooch CL, Engelstad K, Jhung S, DiMauro S, De Vivo DC. Kaufmann P, et al. Among authors: engelstad k. Arch Neurol. 2006 May;63(5):746-8. doi: 10.1001/archneur.63.5.746. Arch Neurol. 2006. PMID: 16682545

5

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: engelstad k. Arch Neurol. 2009 Jan;66(1):85-91. doi: 10.1001/archneurol.2008.526. Arch Neurol. 2009. PMID: 19139304 Free PMC article.

6

Longitudinal changes of mtDNA A3243G mutation load and level of functioning in MELAS.

Mehrazin M, Shanske S, Kaufmann P, Wei Y, Coku J, Engelstad K, Naini A, De Vivo DC, DiMauro S. Mehrazin M, et al. Among authors: engelstad k. Am J Med Genet A. 2009 Feb 15;149A(4):584-7. doi: 10.1002/ajmg.a.32703. Am J Med Genet A. 2009. PMID: 19253345 Free PMC article.

7

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: engelstad k. Arch Neurol. 2010 Aug;67(8):976-9. doi: 10.1001/archneurol.2010.174. Arch Neurol. 2010. PMID: 20697048 Free PMC article.

8

Decreased hippocampal expression of calbindin D28K and cognitive impairment in MELAS.

Emmanuele V, Garcia-Cazorla A, Huang HB, Coku J, Dorado B, Cortes EP, Engelstad K, De Vivo DC, Dimauro S, Bonilla E, Tanji K. Emmanuele V, et al. Among authors: engelstad k. J Neurol Sci. 2012 Jun 15;317(1-2):29-34. doi: 10.1016/j.jns.2012.03.005. Epub 2012 Apr 5. J Neurol Sci. 2012. PMID: 22483853 Free PMC article.

9

Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.

Weiduschat N, Kaufmann P, Mao X, Engelstad KM, Hinton V, DiMauro S, De Vivo D, Shungu D. Weiduschat N, et al. Neurology. 2014 Mar 4;82(9):798-805. doi: 10.1212/WNL.0000000000000169. Epub 2014 Jan 29. Neurology. 2014. PMID: 24477106 Free PMC article.

10

CoQ₁₀ Deficiency Is Not a Common Finding in GLUT1 Deficiency Syndrome.

Barca E, Tang M, Kleiner G, Engelstad K, DiMauro S, Quinzii CM, De Vivo DC. Barca E, et al. Among authors: engelstad k. JIMD Rep. 2016;29:47-52. doi: 10.1007/8904_2015_493. Epub 2015 Nov 29. JIMD Rep. 2016. PMID: 26615598 Free PMC article.

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