Similar articles for PMID: 16931506

Year	Number of Results
1991	1
1998	1
2001	4
2002	13
2003	8
2004	8
2005	21
2006	22
2007	33
2008	22
2009	6
2010	8
2011	8
2012	15
2013	5
2014	4
2015	5
2016	4
2018	1
2019	1
2021	2
2023	1
2024	0

1

SMN1 gene, but not SMN2, is a risk factor for sporadic ALS.

Corcia P, Camu W, Halimi JM, Vourc'h P, Antar C, Vedrine S, Giraudeau B, de Toffol B, Andres CR; French ALS Study Group. Corcia P, et al. Neurology. 2006 Oct 10;67(7):1147-50. doi: 10.1212/01.wnl.0000233830.85206.1e. Epub 2006 Aug 23. Neurology. 2006. PMID: 16931506 Clinical Trial.

2

SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS.

Veldink JH, Kalmijn S, Van der Hout AH, Lemmink HH, Groeneveld GJ, Lummen C, Scheffer H, Wokke JH, Van den Berg LH. Veldink JH, et al. Neurology. 2005 Sep 27;65(6):820-5. doi: 10.1212/01.wnl.0000174472.03292.dd. Epub 2005 Aug 10. Neurology. 2005. PMID: 16093455

3

Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patients.

Gamez J, Also E, Alias L, Corbera-Bellalta M, Barceló MJ, Centeno M, Raguer N, Gratacós M, Baiget M, Tizzano EF. Gamez J, et al. Clin Neurol Neurosurg. 2007 Dec;109(10):844-8. doi: 10.1016/j.clineuro.2007.07.019. Epub 2007 Sep 11. Clin Neurol Neurosurg. 2007. PMID: 17850955

4

Inverse correlation between SMN1 and SMN2 copy numbers: evidence for gene conversion from SMN2 to SMN1.

Ogino S, Gao S, Leonard DG, Paessler M, Wilson RB. Ogino S, et al. Eur J Hum Genet. 2003 Mar;11(3):275-7. doi: 10.1038/sj.ejhg.5200957. Eur J Hum Genet. 2003. PMID: 12673282

5

Spinal muscular atrophy diagnostics.

Prior TW. Prior TW. J Child Neurol. 2007 Aug;22(8):952-6. doi: 10.1177/0883073807305668. J Child Neurol. 2007. PMID: 17761649 Review.

6

Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: a highly efficient and reliable carrier-screening test.

Su YN, Hung CC, Li H, Lee CN, Cheng WF, Tsao PN, Chang MC, Yu CL, Hsieh WS, Lin WL, Hsu SM. Su YN, et al. Hum Mutat. 2005 May;25(5):460-7. doi: 10.1002/humu.20160. Hum Mutat. 2005. PMID: 15832310

7

The importance of the SMN genes in the genetics of sporadic ALS.

Corcia P, Camu W, Praline J, Gordon PH, Vourch P, Andres C. Corcia P, et al. Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):436-40. doi: 10.3109/17482960902759162. Amyotroph Lateral Scler. 2009. PMID: 19922137

8

Analysis of point mutations in the SMN1 gene in SMA patients bearing a single SMN1 copy.

Zapletalová E, Hedvicáková P, Kozák L, Vondrácek P, Gaillyová R, Maríková T, Kalina Z, Jüttnerová V, Fajkus J, Fajkusová L. Zapletalová E, et al. Neuromuscul Disord. 2007 Jun;17(6):476-81. doi: 10.1016/j.nmd.2007.03.003. Epub 2007 May 1. Neuromuscul Disord. 2007. PMID: 17475491

9

Determination of SMN1 and SMN2 copy number using TaqMan technology.

Anhuf D, Eggermann T, Rudnik-Schöneborn S, Zerres K. Anhuf D, et al. Hum Mutat. 2003 Jul;22(1):74-8. doi: 10.1002/humu.10221. Hum Mutat. 2003. PMID: 12815596

10

New insights on the evolution of the SMN1 and SMN2 region: simulation and meta-analysis for allele and haplotype frequency calculations.

Ogino S, Wilson RB, Gold B. Ogino S, et al. Eur J Hum Genet. 2004 Dec;12(12):1015-23. doi: 10.1038/sj.ejhg.5201288. Eur J Hum Genet. 2004. PMID: 15470363

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