170 related articles for article (PubMed ID: 10751268)
1. Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p.
Byrne PC; Mc Monagle P; Webb S; Fitzgerald B; Parfrey NA; Hutchinson M
Neurology; 2000 Apr; 54(7):1510-7. PubMed ID: 10751268
[TBL] [Abstract][Full Text] [Related]
2. Linkage of AD HSP and cognitive impairment to chromosome 2p: haplotype and phenotype analysis indicates variable expression and low or delayed penetrance.
Byrne PC; Webb S; McSweeney F; Burke T; Hutchinson M; Parfrey NA
Eur J Hum Genet; 1998; 6(3):275-82. PubMed ID: 9781032
[TBL] [Abstract][Full Text] [Related]
3. Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p.
Webb S; Coleman D; Byrne P; Parfrey N; Burke T; Hutchinson J; Hutchinson M
Brain; 1998 Apr; 121 ( Pt 4)():601-9. PubMed ID: 9577388
[TBL] [Abstract][Full Text] [Related]
4. Further evidence of dementia in SPG4-linked autosomal dominant hereditary spastic paraplegia.
McMonagle P; Byrne P; Hutchinson M
Neurology; 2004 Feb; 62(3):407-10. PubMed ID: 14872021
[TBL] [Abstract][Full Text] [Related]
5. Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2.
Raskind WH; Pericak-Vance MA; Lennon F; Wolff J; Lipe HP; Bird TD
Am J Med Genet; 1997 Feb; 74(1):26-36. PubMed ID: 9034002
[TBL] [Abstract][Full Text] [Related]
6. Dementia in SPG4 hereditary spastic paraplegia: clinical, genetic, and neuropathologic evidence.
Murphy S; Gorman G; Beetz C; Byrne P; Dytko M; McMonagle P; Kinsella K; Farrell M; Hutchinson M
Neurology; 2009 Aug; 73(5):378-84. PubMed ID: 19652142
[TBL] [Abstract][Full Text] [Related]
7. Cognitive impairment in families with pure autosomal dominant hereditary spastic paraparesis.
Webb S; Hutchinson M
Brain; 1998 May; 121 ( Pt 5)():923-9. PubMed ID: 9619194
[TBL] [Abstract][Full Text] [Related]
8. Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q.
Hedera P; DiMauro S; Bonilla E; Wald J; Eldevik OP; Fink JK
Neurology; 1999 Jul; 53(1):44-50. PubMed ID: 10408535
[TBL] [Abstract][Full Text] [Related]
9. A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.
Fontaine B; Davoine CS; Dürr A; Paternotte C; Feki I; Weissenbach J; Hazan J; Brice A
Am J Hum Genet; 2000 Feb; 66(2):702-7. PubMed ID: 10677329
[TBL] [Abstract][Full Text] [Related]
10. Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.
Heinzlef O; Paternotte C; Mahieux F; Prud'homme JF; Dien J; Madigand M; Pouget J; Weissenbach J; Roullet E; Hazan J
J Med Genet; 1998 Feb; 35(2):89-93. PubMed ID: 9507385
[TBL] [Abstract][Full Text] [Related]
11. Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study.
Nielsen JE; Krabbe K; Jennum P; Koefoed P; Jensen LN; Fenger K; Eiberg H; Hasholt L; Werdelin L; Sørensen SA
J Neurol Neurosurg Psychiatry; 1998 Jan; 64(1):61-6. PubMed ID: 9436729
[TBL] [Abstract][Full Text] [Related]
12. Clinical heterogeneity of familial spastic paraplegia linked to chromosome 2p21.
Nance MA; Raabe WA; Midani H; Kolodny EH; David WS; Megna L; Pericak-Vance MA; Haines JL
Hum Hered; 1998; 48(3):169-78. PubMed ID: 9618065
[TBL] [Abstract][Full Text] [Related]
13. 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
Am J Med Genet A; 2005 Feb; 133A(1):13-7. PubMed ID: 15637712
[TBL] [Abstract][Full Text] [Related]
14. Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation.
White KD; Ince PG; Lusher M; Lindsey J; Cookson M; Bashir R; Shaw PJ; Bushby KM
Neurology; 2000 Jul; 55(1):89-94. PubMed ID: 10891911
[TBL] [Abstract][Full Text] [Related]
15. 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
Eur J Neurol; 2004 Dec; 11(12):817-24. PubMed ID: 15667412
[TBL] [Abstract][Full Text] [Related]
16. Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q.
Hedera P; Rainier S; Alvarado D; Zhao X; Williamson J; Otterud B; Leppert M; Fink JK
Am J Hum Genet; 1999 Feb; 64(2):563-9. PubMed ID: 9973294
[TBL] [Abstract][Full Text] [Related]
17. Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.
Dürr A; Davoine CS; Paternotte C; von Fellenberg J; Cogilinicean S; Coutinho P; Lamy C; Bourgeois S; Prud'homme JF; Penet C; Mas JL; Burgunder JM; Hazan J; Weissenbach J; Brice A; Fontaine B
Brain; 1996 Oct; 119 ( Pt 5)():1487-96. PubMed ID: 8931574
[TBL] [Abstract][Full Text] [Related]
18. Phenotype of AD-HSP due to mutations in the SPAST gene: comparison with AD-HSP without mutations.
McMonagle P; Byrne PC; Fitzgerald B; Webb S; Parfrey NA; Hutchinson M
Neurology; 2000 Dec; 55(12):1794-800. PubMed ID: 11134375
[TBL] [Abstract][Full Text] [Related]
19. 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
Eur J Hum Genet; 2008 Jan; 16(1):97-104. PubMed ID: 17957230
[TBL] [Abstract][Full Text] [Related]
20. A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.
Hanein S; Dürr A; Ribai P; Forlani S; Leutenegger AL; Nelson I; Babron MC; Elleuch N; Depienne C; Charon C; Brice A; Stevanin G
Hum Genet; 2007 Nov; 122(3-4):261-73. PubMed ID: 17605047
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
