McKenna-Yasek DM - Search Results

1

SOD1 Suppression with Adeno-Associated Virus and MicroRNA in Familial ALS.

Mueller C, Berry JD, McKenna-Yasek DM, Gernoux G, Owegi MA, Pothier LM, Douthwright CL, Gelevski D, Luppino SD, Blackwood M, Wightman NS, Oakley DH, Frosch MP, Flotte TR, Cudkowicz ME, Brown RH Jr. Mueller C, et al. Among authors: mckenna yasek dm. N Engl J Med. 2020 Jul 9;383(2):151-158. doi: 10.1056/NEJMoa2005056. N Engl J Med. 2020. PMID: 32640133

2

Gene linkage in familial amyotrophic lateral sclerosis: a progress report.

Brown RH Jr, Horvitz HR, Rouleau GA, McKenna-Yasek D, Beard C, Sapp P, Haines JL, Gusella JF, Figlewicz DA. Brown RH Jr, et al. Adv Neurol. 1991;56:215-26. Adv Neurol. 1991. PMID: 1853758 No abstract available.

3

Identification of three novel mutations in the gene for Cu/Zn superoxide dismutase in patients with familial amyotrophic lateral sclerosis.

Sapp PC, Rosen DR, Hosler BA, Esteban J, McKenna-Yasek D, O'Regan JP, Horvitz HR, Brown RH Jr. Sapp PC, et al. Neuromuscul Disord. 1995 Sep;5(5):353-7. doi: 10.1016/0960-8966(95)00007-a. Neuromuscul Disord. 1995. PMID: 7496169

4

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

5

Absence of mutations in the Mn superoxide dismutase or catalase genes in familial amyotrophic lateral sclerosis.

Parboosingh JS, Rouleau GA, Meninger V, McKenna-Yasek D, Brown RH Jr, Figlewicz DA. Parboosingh JS, et al. Neuromuscul Disord. 1995 Jan;5(1):7-10. doi: 10.1016/0960-8966(94)e0022-z. Neuromuscul Disord. 1995. PMID: 7719145 Free article.

6

Superoxide dismutase concentration and activity in familial amyotrophic lateral sclerosis.

Bowling AC, Barkowski EE, McKenna-Yasek D, Sapp P, Horvitz HR, Beal MF, Brown RH Jr. Bowling AC, et al. J Neurochem. 1995 May;64(5):2366-9. doi: 10.1046/j.1471-4159.1995.64052366.x. J Neurochem. 1995. PMID: 7722523

7

Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers.

Rosen DR, Sapp P, O'Regan J, McKenna-Yasek D, Schlumpf KS, Haines JL, Gusella JF, Horvitz HR, Brown RH Jr. Rosen DR, et al. Am J Med Genet. 1994 May 15;51(1):61-9. doi: 10.1002/ajmg.1320510114. Am J Med Genet. 1994. PMID: 7913294

8

Identification of two novel mutations and a new polymorphism in the gene for Cu/Zn superoxide dismutase in patients with amyotrophic lateral sclerosis.

Esteban J, Rosen DR, Bowling AC, Sapp P, McKenna-Yasek D, O'Regan JP, Beal MF, Horvitz HR, Brown RH Jr. Esteban J, et al. Hum Mol Genet. 1994 Jun;3(6):997-8. doi: 10.1093/hmg/3.6.997. Hum Mol Genet. 1994. PMID: 7951252 No abstract available.

9

Cu/Zn superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosis.

Robberecht W, Sapp P, Viaene MK, Rosen D, McKenna-Yasek D, Haines J, Horvitz R, Theys P, Brown R Jr. Robberecht W, et al. J Neurochem. 1994 Jan;62(1):384-7. doi: 10.1046/j.1471-4159.1994.62010384.x. J Neurochem. 1994. PMID: 8263541

10

Blood superoxide dismutase, catalase and glutathione peroxidase activities in familial and sporadic amyotrophic lateral sclerosis.

Przedborski S, Donaldson DM, Murphy PL, Hirsch O, Lange D, Naini AB, McKenna-Yasek D, Brown RH Jr. Przedborski S, et al. Neurodegeneration. 1996 Mar;5(1):57-64. doi: 10.1006/neur.1996.0008. Neurodegeneration. 1996. PMID: 8731383 Free article. Clinical Trial.

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