Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 119

1.

Traffic accidents: molecular genetic insights into the pathogenesis of the hereditary spastic paraplegias.

Soderblom C, Blackstone C.

Pharmacol Ther. 2006 Jan;109(1-2):42-56. Epub 2005 Jul 7. Review.

PMID:
16005518
2.

Advances in the hereditary spastic paraplegias.

Fink JK.

Exp Neurol. 2003 Nov;184 Suppl 1:S106-10. Review.

PMID:
14597333
3.

The hereditary spastic paraplegias: nine genes and counting.

Fink JK.

Arch Neurol. 2003 Aug;60(8):1045-9. Review.

PMID:
12925358
4.

Hereditary spastic paraplegia: clinical genomics and pharmacogenetic perspectives.

Contino G, Novelli G.

Expert Opin Pharmacother. 2006 Oct;7(14):1849-56. Review.

PMID:
17020412
5.

Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.

Fink JK, Heiman-Patterson T, Bird T, Cambi F, Dubé MP, Figlewicz DA, Fink JK, Haines JL, Heiman-Patterson T, Hentati A, Pericak-Vance MA, Raskind W, Rouleau GA, Siddique T.

Neurology. 1996 Jun;46(6):1507-14. Review.

PMID:
8649538
6.

Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31.

Züchner S, Wang G, Tran-Viet KN, Nance MA, Gaskell PC, Vance JM, Ashley-Koch AE, Pericak-Vance MA.

Am J Hum Genet. 2006 Aug;79(2):365-9. Epub 2006 May 26.

7.

[AAA ATPases and hereditary spastic paraplegia].

Wang YG, Shen L.

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. Review. Chinese.

PMID:
19504443
8.

Molecular aspects of hereditary spastic paraplegia.

Noreau A, Dion PA, Rouleau GA.

Exp Cell Res. 2014 Jul 1;325(1):18-26. doi: 10.1016/j.yexcr.2014.02.021. Epub 2014 Mar 11. Review.

PMID:
24631291
9.

A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.

Dick KJ, Al-Mjeni R, Baskir W, Koul R, Simpson MA, Patton MA, Raeburn S, Crosby AH.

Neurology. 2008 Jul 22;71(4):248-52. doi: 10.1212/01.wnl.0000319610.29522.8a. Epub 2008 May 7.

PMID:
18463364
10.

Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum.

Olmez A, Uyanik G, Ozgül RK, Gross C, Cirak S, Elibol B, Anlar B, Winner B, Hehr U, Topaloglu H, Winkler J.

Neuropediatrics. 2006 Apr;37(2):59-66.

PMID:
16773502
11.

NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6).

Rainier S, Chai JH, Tokarz D, Nicholls RD, Fink JK.

Am J Hum Genet. 2003 Oct;73(4):967-71. Epub 2003 Sep 23.

12.

Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity.

Boukhris A, Stevanin G, Feki I, Denora P, Elleuch N, Miladi MI, Goizet C, Truchetto J, Belal S, Brice A, Mhiri C.

Clin Genet. 2009 Jun;75(6):527-36. doi: 10.1111/j.1399-0004.2009.01176.x. Epub 2009 May 5.

PMID:
19438933
13.

The genetics of hereditary spastic paraplegia and implications for drug therapy.

Züchner S.

Expert Opin Pharmacother. 2007 Jul;8(10):1433-9. Review.

PMID:
17661726
15.

Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset.

Brockmann K, Simpson MA, Faber A, Bönnemann C, Crosby AH, Gärtner J.

Neuropediatrics. 2005 Aug;36(4):274-8.

PMID:
16138254
16.

Pathogenesis of autosomal dominant hereditary spastic paraplegia (SPG6) revealed by a rat model.

Watanabe F, Arnold WD, Hammer RE, Ghodsizadeh O, Moti H, Schumer M, Hashmi A, Hernandez A, Sneh A, Sahenk Z, Kisanuki YY.

J Neuropathol Exp Neurol. 2013 Nov;72(11):1016-28. doi: 10.1097/NEN.0000000000000000. Erratum in: J Neuropathol Exp Neurol. 2014 Feb;73(2):190.

17.

Current insights into familial spastic paraparesis: new advances in an old disease.

Fortini D, Cricchi F, Di Fabio R, Damiano M, Comanducci G, Benedetti L, Valoppi M, Grieco GS, D'Eugenio O, Celato A, Santorelli F, Casali C, Amabile GA, Pierelli F.

Funct Neurol. 2003 Jan-Mar;18(1):43-9. Review.

PMID:
12760414
18.

Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum.

Liao SS, Shen L, Du J, Zhao GH, Wang XY, Yang Y, Xiao ZQ, Yuan Y, Jiang H, Li N, Sun HD, Wang JL, Wang CY, Zhou YF, Mo XY, Xia K, Tang BS.

J Neurol Sci. 2008 Dec 15;275(1-2):92-9. doi: 10.1016/j.jns.2008.07.038. Epub 2008 Oct 2.

PMID:
18835492
19.

Hereditary spastic paraplegia.

Fink JK.

Neurol Clin. 2002 Aug;20(3):711-26. Review.

PMID:
12432827
20.

Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54).

Gonzalez M, Nampoothiri S, Kornblum C, Oteyza AC, Walter J, Konidari I, Hulme W, Speziani F, Schöls L, Züchner S, Schüle R.

Eur J Hum Genet. 2013 Nov;21(11):1214-8. doi: 10.1038/ejhg.2013.29. Epub 2013 Mar 13.

Supplemental Content

Support Center