Similar articles for PMID: 15024734

Year	Number of Results
1954	2
1963	1
1988	1
1994	1
1998	1
1999	1
2001	2
2002	3
2003	2
2004	8
2005	11
2006	8
2007	15
2008	7
2009	1
2011	1
2024	0

1

Importance of standard nomenclature for SMN1 small intragenic ("subtle") mutations.

Ogino S, Wilson RB. Ogino S, et al. Hum Mutat. 2004 Apr;23(4):392-3. doi: 10.1002/humu.20013. Hum Mutat. 2004. PMID: 15024734 No abstract available.

2

Molecular analysis of SMA patients without homozygous SMN1 deletions using a new strategy for identification of SMN1 subtle mutations.

Clermont O, Burlet P, Benit P, Chanterau D, Saugier-Veber P, Munnich A, Cusin V. Clermont O, et al. Hum Mutat. 2004 Nov;24(5):417-27. doi: 10.1002/humu.20092. Hum Mutat. 2004. PMID: 15459957

3

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 Sep;11(9):723. doi: 10.1038/sj.ejhg.5201032. Eur J Hum Genet. 2003. PMID: 12939662 No abstract available.

4

Nucleotide differences in SMN1 and SMN2 gene.

Kesari A, Mittal B. Kesari A, et al. Prenat Diagn. 2004 May;24(5):398. doi: 10.1002/pd.843. Prenat Diagn. 2004. PMID: 15164419 No abstract available.

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

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

7

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

8

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

9

Synthesis and biological evaluation of novel 2,4-diaminoquinazoline derivatives as SMN2 promoter activators for the potential treatment of spinal muscular atrophy.

Thurmond J, Butchbach ME, Palomo M, Pease B, Rao M, Bedell L, Keyvan M, Pai G, Mishra R, Haraldsson M, Andresson T, Bragason G, Thosteinsdottir M, Bjornsson JM, Coovert DD, Burghes AH, Gurney ME, Singh J. Thurmond J, et al. J Med Chem. 2008 Feb 14;51(3):449-69. doi: 10.1021/jm061475p. Epub 2008 Jan 19. J Med Chem. 2008. PMID: 18205293

10

Case report: birth after preimplantation genetic diagnosis of a subtle mutation in SMN1 gene.

Moutou C, Machev N, Gardes N, Viville S. Moutou C, et al. Prenat Diagn. 2006 Nov;26(11):1037-41. doi: 10.1002/pd.1551. Prenat Diagn. 2006. PMID: 16941715

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