Brown RH - Search Results

1

Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis.

Li YJ, Pericak-Vance MA, Haines JL, Siddique N, McKenna-Yasek D, Hung WY, Sapp P, Allen CI, Chen W, Hosler B, Saunders AM, Dellefave LM, Brown RH, Siddique T. Li YJ, et al. Among authors: brown rh. Neurogenetics. 2004 Dec;5(4):209-13. doi: 10.1007/s10048-004-0193-0. Epub 2004 Oct 2. Neurogenetics. 2004. PMID: 15657798

2

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

3

A novel mutation in the spastin gene in a family with spastic paraplegia.

Morita M, Ho M, Hosler BA, McKenna-Yasek D, Brown RH Jr. Morita M, et al. Among authors: brown rh jr. Neurosci Lett. 2002 May 31;325(1):57-61. doi: 10.1016/s0304-3940(02)00239-2. Neurosci Lett. 2002. PMID: 12023066

4

Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis.

Al-Chalabi A, Hansen VK, Simpson CL, Xi J, Hosler BA, Powell JF, McKenna-Yasek D, Shaw CE, Leigh PN, Brown RH Jr. Al-Chalabi A, et al. Among authors: brown rh jr. Neurogenetics. 2003 Aug;4(4):221-2. doi: 10.1007/s10048-003-0152-1. Epub 2003 May 27. Neurogenetics. 2003. PMID: 12768434 No abstract available.

5

Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis.

Sapp PC, Hosler BA, McKenna-Yasek D, Chin W, Gann A, Genise H, Gorenstein J, Huang M, Sailer W, Scheffler M, Valesky M, Haines JL, Pericak-Vance M, Siddique T, Horvitz HR, Brown RH Jr. Sapp PC, et al. Among authors: brown rh jr. Am J Hum Genet. 2003 Aug;73(2):397-403. doi: 10.1086/377158. Epub 2003 Jul 9. Am J Hum Genet. 2003. PMID: 12858291 Free PMC article.

6

Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis.

Garcia ML, Singleton AB, Hernandez D, Ward CM, Evey C, Sapp PA, Hardy J, Brown RH Jr, Cleveland DW. Garcia ML, et al. Among authors: brown rh jr. Neurobiol Dis. 2006 Jan;21(1):102-9. doi: 10.1016/j.nbd.2005.06.016. Epub 2005 Aug 3. Neurobiol Dis. 2006. PMID: 16084104

7

Variants in candidate ALS modifier genes linked to Cu/Zn superoxide dismutase do not explain divergent survival phenotypes.

Broom WJ, Russ C, Sapp PC, McKenna-Yasek D, Hosler BA, Andersen PM, Brown RH Jr. Broom WJ, et al. Among authors: brown rh jr. Neurosci Lett. 2006 Jan 9;392(1-2):52-7. doi: 10.1016/j.neulet.2005.08.058. Epub 2005 Sep 19. Neurosci Lett. 2006. PMID: 16174551

8

No association of DYNC1H1 with sporadic ALS in a case-control study of a northern European derived population: a tagging SNP approach.

Shah PR, Ahmad-Annuar A, Ahmadi KR, Russ C, Sapp PC, Horvitz HR, Brown RH Jr, Goldstein DB, Fisher EM. Shah PR, et al. Among authors: brown rh jr. Amyotroph Lateral Scler. 2006 Mar;7(1):46-56. doi: 10.1080/14660820500397057. Amyotroph Lateral Scler. 2006. PMID: 16546759

9

Age at onset in sod1-mediated amyotrophic lateral sclerosis shows familiality.

Fogh I, Rijsdijk F, Andersen PM, Sham PC, Knight J, Neale B, McKenna-Yasek D, Silani V, Brown RH Jr, Powell JF, Al-Chalabi A. Fogh I, et al. Among authors: brown rh jr. Neurogenetics. 2007 Aug;8(3):235-6. doi: 10.1007/s10048-007-0092-2. Epub 2007 Jun 5. Neurogenetics. 2007. PMID: 17549529 No abstract available.

10

Birth order and the genetics of amyotrophic lateral sclerosis.

Vivekananda U, Johnston C, McKenna-Yasek D, Shaw CE, Leigh PN, Brown RH, Al-Chalabi A. Vivekananda U, et al. Among authors: brown rh. J Neurol. 2008 Jan;255(1):99-102. doi: 10.1007/s00415-007-0709-2. Epub 2007 Dec 19. J Neurol. 2008. PMID: 18060566

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