Similar articles for PMID: 12471215

Year	Number of Results
1976	1
1987	1
1989	1
1990	4
1991	2
1992	1
1993	2
1994	4
1995	5
1996	2
1997	8
1998	7
1999	7
2000	14
2001	16
2002	14
2003	11
2004	11
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2006	10
2007	15
2008	9
2009	8
2010	6
2011	4
2012	2
2013	4
2014	4
2015	1
2016	2
2020	1
2024	0

1

Autosomal dominant (AD) pure spastic paraplegia (HSP) linked to locus SPG4 affects almost exclusively males in a large pedigree.

Starling A, Rocco P, Passos-Bueno MR, Hazan J, Marie SK, Zatz M. Starling A, et al. J Med Genet. 2002 Dec;39(12):e77. doi: 10.1136/jmg.39.12.e77. J Med Genet. 2002. PMID: 12471215 Free PMC article. No abstract available.

2

Large deletion involving the 5'-UTR in the spastin gene caused mild phenotype of autosomal dominant hereditary spastic paraplegia.

Iwanaga H, Tsujino A, Shirabe S, Eguchi H, Fukushima N, Niikawa N, Yoshiura K, Eguchi K. Iwanaga H, et al. Am J Med Genet A. 2005 Feb 15;133A(1):13-7. doi: 10.1002/ajmg.a.30510. Am J Med Genet A. 2005. PMID: 15637712

3

Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia.

Sauter S, Miterski B, Klimpe S, Bönsch D, Schöls L, Visbeck A, Papke T, Hopf HC, Engel W, Deufel T, Epplen JT, Neesen J. Sauter S, et al. Hum Mutat. 2002 Aug;20(2):127-32. doi: 10.1002/humu.10105. Hum Mutat. 2002. PMID: 12124993

4

Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegia.

Ivanova N, Löfgren A, Tournev I, Rousev R, Andreeva A, Jordanova A, Georgieva V, Deconinck T, Timmerman V, Kremensky I, De Jonghe P, Mitev V. Ivanova N, et al. Clin Genet. 2006 Dec;70(6):490-5. doi: 10.1111/j.1399-0004.2006.00705.x. Clin Genet. 2006. PMID: 17100993

5

Hereditary spastic paraplegia caused by mutations in the SPG4 gene.

Bürger J, Fonknechten N, Hoeltzenbein M, Neumann L, Bratanoff E, Hazan J, Reis A. Bürger J, et al. Eur J Hum Genet. 2000 Oct;8(10):771-6. doi: 10.1038/sj.ejhg.5200528. Eur J Hum Genet. 2000. PMID: 11039577

6

Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.

Nielsen JE, Johnsen B, Koefoed P, Scheuer KH, Grønbech-Jensen M, Law I, Krabbe K, Nørremølle A, Eiberg H, Søndergård H, Dam M, Rehfeld JF, Krarup C, Paulson OB, Hasholt L, Sørensen SA. Nielsen JE, et al. Eur J Neurol. 2004 Dec;11(12):817-24. doi: 10.1111/j.1468-1331.2004.00888.x. Eur J Neurol. 2004. PMID: 15667412

7

[Hereditary spastic paraplegia type 4 (SPG4): clinical and molecular-genetic characteristics].

Rudenskaia GE, Sermiagina IG, Illarioshkin SN, Sidorova OP, Fedotov VP, Poliakov AV. Rudenskaia GE, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2010;110(6):12-9. Zh Nevrol Psikhiatr Im S S Korsakova. 2010. PMID: 20559269 Russian.

8

A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large Brazilian pedigree.

Mitne-Neto M, Kok F, Beetz C, Pessoa A, Bueno C, Graciani Z, Martyn M, Monteiro CB, Mitne G, Hubert P, Nygren AO, Valadares M, Cerqueira AM, Starling A, Deufel T, Zatz M. Mitne-Neto M, et al. Eur J Hum Genet. 2007 Dec;15(12):1276-9. doi: 10.1038/sj.ejhg.5201924. Epub 2007 Sep 26. Eur J Hum Genet. 2007. PMID: 17895902

9

Mental deficiency in three families with SPG4 spastic paraplegia.

Ribaï P, Depienne C, Fedirko E, Jothy AC, Viveweger C, Hahn-Barma V, Brice A, Durr A. Ribaï P, et al. Eur J Hum Genet. 2008 Jan;16(1):97-104. doi: 10.1038/sj.ejhg.5201922. Epub 2007 Oct 24. Eur J Hum Genet. 2008. PMID: 17957230

10

[AAA ATPases and hereditary spastic paraplegia].

Wang YG, Shen L. Wang YG, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Jun;26(3):298-301. doi: 10.3760/cma.j.issn.1003-9406.2009.03.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19504443 Review. Chinese.

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