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Items: 16

1.

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.

Patel H, Cross H, Proukakis C, Hershberger R, Bork P, Ciccarelli FD, Patton MA, McKusick VA, Crosby AH.

Nat Genet. 2002 Aug;31(4):347-8. Epub 2002 Jul 22.

PMID:
12134148
2.

[From gene to disease; spastin and hereditary spastic paraparesis].

Bruyn RP, Frants RR.

Ned Tijdschr Geneeskd. 2004 Jan 24;148(4):179-81. Review. Dutch.

PMID:
14974310
3.

Hereditary spastic paraplegia: spastin phenotype and function.

Fink JK, Rainier S.

Arch Neurol. 2004 Jun;61(6):830-3. Review. No abstract available.

PMID:
15210518
4.

[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
5.

[Recent progress in genetic study of hereditary spastic paraplegia].

Takano H, Kasuga K, Kobayashi H, Nishizawa M.

No To Shinkei. 2003 Sep;55(9):757-63. Review. Japanese. No abstract available.

PMID:
14571837
6.

[Hereditary spastic paraplegia].

Kanda T, Kobayashi H.

Nihon Rinsho. 2002 Apr;60 Suppl 4:429-32. Review. Japanese. No abstract available.

PMID:
12013904
7.

Hereditary spastic paraplegia: mitochondrial metalloproteases of yeast.

Pearce DA.

Hum Genet. 1999 Jun;104(6):443-8. Review.

PMID:
10453730
8.

[Classification of hereditary spastic paraplegia (HSP)].

Utsumi H, Yuasa T.

No To Shinkei. 2003 Sep;55(9):739-47. Review. Japanese. No abstract available.

PMID:
14571835
9.

Molecular basis of inherited spastic paraplegias.

Casari G, Rugarli E.

Curr Opin Genet Dev. 2001 Jun;11(3):336-42. Review.

PMID:
11377972
10.

"Pure" hereditary spastic paraplegias: the story becomes complicated.

Figlewicz DA, Bird TD.

Neurology. 1999 Jul 13;53(1):5-7. Review. No abstract available.

PMID:
10408527
11.

Hereditary spastic paraplegia: clues from a rare disorder for a common problem?

Burgunder JM, Hunziker W.

IUBMB Life. 2003 Jun;55(6):347-52. Review.

12.

[Molecular genetics of familial spastic paraplegia].

Shibasaki Y, Kobayashi H.

Ryoikibetsu Shokogun Shirizu. 1999;(27 Pt 2):224-6. Review. Japanese. No abstract available.

PMID:
10434637
13.

[Familial spastic paraplegia (FSP)].

Shibasaki Y, Kobayashi H.

Ryoikibetsu Shokogun Shirizu. 1999;(27 Pt 2):221-3. Review. Japanese. No abstract available.

PMID:
10434636
14.

[Diseases and developmental disorders caused by mutations in genes encoding AAA and AAA+ proteins].

Ogura T.

Seikagaku. 2001 Sep;73(9):1159-62. Review. Japanese. No abstract available.

PMID:
11676001
15.

[Paraplegia, familial spastic].

Fukuda T, Sugie H.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):476-7. Review. Japanese. No abstract available.

PMID:
11528848
16.

Troyer Syndrome: report of the first "non-Amish" sibship and review.

Farag TI, El-Badramany MH, Al-Sharkawy S.

Am J Med Genet. 1994 Dec 1;53(4):383-5. Review. No abstract available.

PMID:
7864052

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