McKenna-Yasek D - Search Results

1

Randomized trial of l-serine in patients with hereditary sensory and autonomic neuropathy type 1.

Fridman V, Suriyanarayanan S, Novak P, David W, Macklin EA, McKenna-Yasek D, Walsh K, Aziz-Bose R, Oaklander AL, Brown R, Hornemann T, Eichler F. Fridman V, et al. Neurology. 2019 Jan 22;92(4):e359-e370. doi: 10.1212/WNL.0000000000006811. Epub 2019 Jan 9. Neurology. 2019. PMID: 30626650 Free PMC article. Clinical Trial.

2

Apolipoprotein E epsilon 4 allele is not associated with earlier age at onset in amyotrophic lateral sclerosis.

Mui S, Rebeck GW, McKenna-Yasek D, Hyman BT, Brown RH Jr. Mui S, et al. Ann Neurol. 1995 Sep;38(3):460-3. doi: 10.1002/ana.410380318. Ann Neurol. 1995. PMID: 7668834

3

Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene.

Cudkowicz ME, McKenna-Yasek D, Chen C, Hedley-Whyte ET, Brown RH Jr. Cudkowicz ME, et al. Ann Neurol. 1998 Jun;43(6):703-10. doi: 10.1002/ana.410430604. Ann Neurol. 1998. PMID: 9629839

4

Pilot study of myoblast transfer in the treatment of Becker muscular dystrophy.

Neumeyer AM, Cros D, McKenna-Yasek D, Zawadzka A, Hoffman EP, Pegoraro E, Hunter RG, Munsat TL, Brown RH Jr. Neumeyer AM, et al. Neurology. 1998 Aug;51(2):589-92. doi: 10.1212/wnl.51.2.589. Neurology. 1998. PMID: 9710042 Clinical Trial.

5

Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22.

Bejaoui K, McKenna-Yasek D, Hosler BA, Burns-Deater E, Deater LM, O'Neill G, Haines JL, Brown RH Jr. Bejaoui K, et al. Neurology. 1999 Feb;52(3):510-5. doi: 10.1212/wnl.52.3.510. Neurology. 1999. PMID: 10025779

6

A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathy.

Ho M, Gallardo E, McKenna-Yasek D, De Luna N, Illa I, Brown RH Jr. Ho M, et al. Ann Neurol. 2002 Jan;51(1):129-33. doi: 10.1002/ana.10080. Ann Neurol. 2002. PMID: 11782994

7

Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort.

Ticozzi N, Silani V, LeClerc AL, Keagle P, Gellera C, Ratti A, Taroni F, Kwiatkowski TJ Jr, McKenna-Yasek DM, Sapp PC, Brown RH Jr, Landers JE. Ticozzi N, et al. Neurology. 2009 Oct 13;73(15):1180-5. doi: 10.1212/WNL.0b013e3181bbff05. Epub 2009 Sep 9. Neurology. 2009. PMID: 19741215 Free PMC article.

8

Paraoxonase gene mutations in amyotrophic lateral sclerosis.

Ticozzi N, LeClerc AL, Keagle PJ, Glass JD, Wills AM, van Blitterswijk M, Bosco DA, Rodriguez-Leyva I, Gellera C, Ratti A, Taroni F, McKenna-Yasek D, Sapp PC, Silani V, Furlong CE, Brown RH Jr, Landers JE. Ticozzi N, et al. Ann Neurol. 2010 Jul;68(1):102-7. doi: 10.1002/ana.21993. Ann Neurol. 2010. PMID: 20582942 Free PMC article.

9

Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis.

González-Pérez P, Cirulli ET, Drory VE, Dabby R, Nisipeanu P, Carasso RL, Sadeh M, Fox A, Festoff BW, Sapp PC, McKenna-Yasek D, Goldstein DB, Brown RH Jr, Blumen SC. González-Pérez P, et al. Neurology. 2012 Nov 27;79(22):2201-8. doi: 10.1212/WNL.0b013e318275963b. Epub 2012 Nov 14. Neurology. 2012. PMID: 23152587 Free PMC article.

10

A novel dysferlin mutant pseudoexon bypassed with antisense oligonucleotides.

Dominov JA, Uyan O, Sapp PC, McKenna-Yasek D, Nallamilli BR, Hegde M, Brown RH Jr. Dominov JA, et al. Ann Clin Transl Neurol. 2014 Sep;1(9):703-20. doi: 10.1002/acn3.96. Epub 2014 Sep 27. Ann Clin Transl Neurol. 2014. PMID: 25493284 Free PMC article.

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