Similar articles for PMID: 14985388

Year	Number of Results
1966	1
1973	1
1988	2
1989	3
1990	1
1991	3
1992	5
1993	8
1994	7
1995	8
1996	2
1997	4
1998	14
1999	4
2000	8
2001	3
2002	5
2003	3
2004	4
2005	8
2006	3
2007	1
2008	1
2009	2
2010	2
2011	3
2013	1
2014	1
2024	0

1

A new locus for recessive distal spinal muscular atrophy at Xq13.1-q21.

Takata RI, Speck Martins CE, Passosbueno MR, Abe KT, Nishimura AL, Da Silva MD, Monteiro A Jr, Lima MI, Kok F, Zatz M. Takata RI, et al. J Med Genet. 2004 Mar;41(3):224-9. doi: 10.1136/jmg.2003.013201. J Med Genet. 2004. PMID: 14985388 Free PMC article. No abstract available.

2

X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21.

Kennerson M, Nicholson G, Kowalski B, Krajewski K, El-Khechen D, Feely S, Chu S, Shy M, Garbern J. Kennerson M, et al. Neurology. 2009 Jan 20;72(3):246-52. doi: 10.1212/01.wnl.0000339483.86094.a5. Neurology. 2009. PMID: 19153371

3

Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14.

McEntagart M, Norton N, Williams H, Teare MD, Dunstan M, Baker P, Houlden H, Reilly M, Wood N, Harper PS, Futreal PA, Williams N, Rahman N. McEntagart M, et al. Am J Hum Genet. 2001 May;68(5):1270-6. doi: 10.1086/320122. Epub 2001 Apr 4. Am J Hum Genet. 2001. PMID: 11294660 Free PMC article.

4

Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.

Viollet L, Barois A, Rebeiz JG, Rifai Z, Burlet P, Zarhrate M, Vial E, Dessainte M, Estournet B, Kleinknecht B, Pearn J, Adams RD, Urtizberea JA, Cros DP, Bushby K, Munnich A, Lefebvre S. Viollet L, et al. Ann Neurol. 2002 May;51(5):585-92. doi: 10.1002/ana.10182. Ann Neurol. 2002. PMID: 12112104

5

Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families.

Viollet L, Zarhrate M, Maystadt I, Estournet-Mathiaut B, Barois A, Desguerre I, Mayer M, Chabrol B, LeHeup B, Cusin V, Billette De Villemeur T, Bonneau D, Saugier-Veber P, Touzery-De Villepin A, Delaubier A, Kaplan J, Jeanpierre M, Feingold J, Munnich A. Viollet L, et al. Eur J Hum Genet. 2004 Jun;12(6):483-8. doi: 10.1038/sj.ejhg.5201177. Eur J Hum Genet. 2004. PMID: 15054395

6

Transmission ratio distortion in the spinal muscular atrophy locus: data from 314 prenatal tests.

Botta A, Tacconelli A, Bagni I, Giardina E, Bonifazi E, Pietropolli A, Clementi M, Novelli G. Botta A, et al. Neurology. 2005 Nov 22;65(10):1631-5. doi: 10.1212/01.wnl.0000184506.61354.5b. Neurology. 2005. PMID: 16301493

7

Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p.

Christodoulou K, Kyriakides T, Hristova AH, Georgiou DM, Kalaydjieva L, Yshpekova B, Ivanova T, Weber JL, Middleton LT. Christodoulou K, et al. Hum Mol Genet. 1995 Sep;4(9):1629-32. doi: 10.1093/hmg/4.9.1629. Hum Mol Genet. 1995. PMID: 8541851

8

From enigmatic to problematic: the new molecular genetics of childhood spinal muscular atrophy.

Crawford TO. Crawford TO. Neurology. 1996 Feb;46(2):335-40. doi: 10.1212/wnl.46.2.335. Neurology. 1996. PMID: 8614490 Review. No abstract available.

9

Prenatal prediction of spinal muscular atrophy.

Daniels RJ, Suthers GK, Morrison KE, Thomas NH, Francis MJ, Mathew CG, Loughlin S, Heiberg A, Wood D, Dubowitz V, et al. Daniels RJ, et al. J Med Genet. 1992 Mar;29(3):165-70. doi: 10.1136/jmg.29.3.165. J Med Genet. 1992. PMID: 1348091 Free PMC article.

10

Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13.

Zara F, Gennaro E, Stabile M, Carbone I, Malacarne M, Majello L, Santangelo R, de Falco FA, Bricarelli FD. Zara F, et al. Am J Hum Genet. 2000 May;66(5):1552-7. doi: 10.1086/302876. Epub 2000 Mar 30. Am J Hum Genet. 2000. PMID: 10741954 Free PMC article.

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