Figlewicz DA - Search Results

1

A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS.

Wills AM, Cronin S, Slowik A, Kasperaviciute D, Van Es MA, Morahan JM, Valdmanis PN, Meininger V, Melki J, Shaw CE, Rouleau GA, Fisher EM, Shaw PJ, Morrison KE, Pamphlett R, Van den Berg LH, Figlewicz DA, Andersen PM, Al-Chalabi A, Hardiman O, Purcell S, Landers JE, Brown RH Jr. Wills AM, et al. Among authors: figlewicz da. Neurology. 2009 Jul 7;73(1):16-24. doi: 10.1212/WNL.0b013e3181a18674. Epub 2009 Mar 25. Neurology. 2009. PMID: 19321847 Free PMC article.

2

Analysis of the KSP repeat of the neurofilament heavy subunit in familiar amyotrophic lateral sclerosis.

Rooke K, Figlewicz DA, Han FY, Rouleau GA. Rooke K, et al. Among authors: figlewicz da. Neurology. 1996 Mar;46(3):789-90. doi: 10.1212/wnl.46.3.789. Neurology. 1996. PMID: 8618684

3

Spinobulbar muscular atrophy can mimic ALS: the importance of genetic testing in male patients with atypical ALS.

Parboosingh JS, Figlewicz DA, Krizus A, Meininger V, Azad NA, Newman DS, Rouleau GA. Parboosingh JS, et al. Among authors: figlewicz da. Neurology. 1997 Aug;49(2):568-72. doi: 10.1212/wnl.49.2.568. Neurology. 1997. PMID: 9270598

4

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. Among authors: figlewicz da. Adv Neurol. 1991;56:215-26. Adv Neurol. 1991. PMID: 1853758 No abstract available.

5

Paraoxonase gene polymorphisms and sporadic ALS.

Slowik A, Tomik B, Wolkow PP, Partyka D, Turaj W, Malecki MT, Pera J, Dziedzic T, Szczudlik A, Figlewicz DA. Slowik A, et al. Among authors: figlewicz da. Neurology. 2006 Sep 12;67(5):766-70. doi: 10.1212/01.wnl.0000219565.32247.11. Epub 2006 Jul 5. Neurology. 2006. PMID: 16822965

6

The expansions of ALS.

Hardiman O, Figlewicz DA. Hardiman O, et al. Among authors: figlewicz da. Neurology. 2012 Aug 28;79(9):842-3. doi: 10.1212/WNL.0b013e3182662031. Epub 2012 Jul 25. Neurology. 2012. PMID: 22843260 No abstract available.

7

Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia.

Meijer IA, Hand CK, Cossette P, Figlewicz DA, Rouleau GA. Meijer IA, et al. Among authors: figlewicz da. Arch Neurol. 2002 Feb;59(2):281-6. doi: 10.1001/archneur.59.2.281. Arch Neurol. 2002. PMID: 11843700

8

Lack of association between VEGF gene polymorphisms and plasma VEGF levels and sporadic AL.

Golenia A, Tomik B, Zawislak D, Wolkow P, Dziubek A, Sado M, Szczudlik A, Figlewicz DA, Slowik A. Golenia A, et al. Among authors: figlewicz da. Neurology. 2010 Nov 30;75(22):2035-7. doi: 10.1212/WNL.0b013e3181ff9658. Neurology. 2010. PMID: 21115961 No abstract available.

9

Androgen receptor gene polymorphisms in amyotrophic lateral sclerosis.

Garofalo O, Figlewicz DA, Leigh PN, Powell JF, Meininger V, Dib M, Rouleau GA. Garofalo O, et al. Among authors: figlewicz da. Neuromuscul Disord. 1993 May;3(3):195-9. doi: 10.1016/0960-8966(93)90059-s. Neuromuscul Disord. 1993. PMID: 8400860

10

SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis.

Rouleau GA, Clark AW, Rooke K, Pramatarova A, Krizus A, Suchowersky O, Julien JP, Figlewicz D. Rouleau GA, et al. Ann Neurol. 1996 Jan;39(1):128-31. doi: 10.1002/ana.410390119. Ann Neurol. 1996. PMID: 8572658

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