120 related articles for article (PubMed ID: 10797436)
1. Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin.
Rocco P; Vainzof M; Froehner SC; Peters MF; Marie SK; Passos-Bueno MR; Zatz M
Am J Med Genet; 2000 May; 92(2):122-7. PubMed ID: 10797436
[TBL] [Abstract][Full Text] [Related]
2. Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity.
Reid E; Dearlove AM; Whiteford ML; Rhodes M; Rubinsztein DC
Neurology; 1999 Nov; 53(8):1844-9. PubMed ID: 10563637
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13.
Reid E; Dearlove AM; Osborn O; Rogers MT; Rubinsztein DC
Am J Hum Genet; 2000 Feb; 66(2):728-32. PubMed ID: 10677333
[TBL] [Abstract][Full Text] [Related]
6. A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity.
Reid E; Dearlove AM; Rhodes M; Rubinsztein DC
Am J Hum Genet; 1999 Sep; 65(3):757-63. PubMed ID: 10441583
[TBL] [Abstract][Full Text] [Related]
7. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.
Ashley-Koch A; Bonner ER; Gaskell PC; West SG; Tim R; Wolpert CM; Jones R; Farrell CD; Nance M; Svenson IK; Marchuk DA; Boustany RM; Vance JM; Scott WK; Pericak-Vance MA
Neurogenetics; 2001 Mar; 3(2):91-7. PubMed ID: 11354831
[TBL] [Abstract][Full Text] [Related]
8. Hereditary spastic paraplegia: LOD-score considerations for confirmation of linkage in a heterogeneous trait.
Dubé MP; Mlodzienski MA; Kibar Z; Farlow MR; Ebers G; Harper P; Kolodny EH; Rouleau GA; Figlewicz DA
Am J Hum Genet; 1997 Mar; 60(3):625-9. PubMed ID: 9042923
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia.
Zhao GH; Hu ZM; Shen L; Jiang H; Ren ZJ; Liu XM; Xia K; Guo P; Pan Q; Tang BS
Chin Med J (Engl); 2008 Mar; 121(5):430-4. PubMed ID: 18364116
[TBL] [Abstract][Full Text] [Related]
12. Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.
Scott WK; Gaskell PC; Lennon F; Wolpert CM; Menold MM; Aylsworth AS; Warner C; Farrell CD; Boustany RM; Albright SG; Boyd E; Kingston HM; Cumming WJ; Vance JM; Pericak-Vance MA
Neurogenetics; 1997 Sep; 1(2):95-102. PubMed ID: 10732810
[TBL] [Abstract][Full Text] [Related]
13. Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation.
Del-Favero J; Goossens D; De Jonghe P; Benson K; Michalik A; Van den Bossche D; Horwitz M; Van Broeckhoven C
Hum Genet; 1999 Sep; 105(3):217-25. PubMed ID: 10987648
[TBL] [Abstract][Full Text] [Related]
14. Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.
Fonknechten N; Mavel D; Byrne P; Davoine CS; Cruaud C; Bönsch D; Samson D; Coutinho P; Hutchinson M; McMonagle P; Burgunder JM; Tartaglione A; Heinzlef O; Feki I; Deufel T; Parfrey N; Brice A; Fontaine B; Prud'homme JF; Weissenbach J; Dürr A; Hazan J
Hum Mol Genet; 2000 Mar; 9(4):637-44. PubMed ID: 10699187
[TBL] [Abstract][Full Text] [Related]
15. A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3.
De Michele G; De Fusco M; Cavalcanti F; Filla A; Marconi R; Volpe G; Monticelli A; Ballabio A; Casari G; Cocozza S
Am J Hum Genet; 1998 Jul; 63(1):135-9. PubMed ID: 9634528
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family.
Bürger J; Metzke H; Paternotte C; Schilling F; Hazan J; Reis A
Hum Genet; 1996 Sep; 98(3):371-5. PubMed ID: 8707310
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A novel missense mutation (I344K) in the SPG4gene in a Korean family with autosomal-dominant hereditary spastic paraplegia.
Ki CS; Lee WY; Han DH; Sung DH; Lee KB; Lee KA; Cho SS; Cho S; Hwang H; Sohn KM; Choi YJ; Kim JW
J Hum Genet; 2002; 47(9):473-7. PubMed ID: 12202986
[TBL] [Abstract][Full Text] [Related]
20. Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.
Hentati A; Pericak-Vance MA; Lennon F; Wasserman B; Hentati F; Juneja T; Angrist MH; Hung WY; Boustany RM; Bohlega S
Hum Mol Genet; 1994 Oct; 3(10):1867-71. PubMed ID: 7849714
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
