219 related articles for article (PubMed ID: 10677329)
21. Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34.
Valente EM; Brancati F; Caputo V; Bertini E; Patrono C; Costanti D; Dallapiccola B
Ann Neurol; 2002 Jun; 51(6):681-5. PubMed ID: 12112072
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. 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]
25. Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.
Gispert S; Santos N; Damen R; Voit T; Schulz J; Klockgether T; Orozco G; Kreuz F; Weissenbach J; Auburger G
Am J Hum Genet; 1995 Jan; 56(1):183-7. PubMed ID: 7825576
[TBL] [Abstract][Full Text] [Related]
26. Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.
Schüle R; Bonin M; Dürr A; Forlani S; Sperfeld AD; Klimpe S; Mueller JC; Seibel A; van de Warrenburg BP; Bauer P; Schöls L
Neurology; 2009 Jun; 72(22):1893-8. PubMed ID: 19357379
[TBL] [Abstract][Full Text] [Related]
27. A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3.
Muglia M; Magariello A; Nicoletti G; Patitucci A; Gabriele AL; Conforti FL; Mazzei R; Caracciolo M; Casari G; Ardito B; Lastilla M; Gambardella A; Quattrone A
J Neurol; 2002 Oct; 249(10):1413-6. PubMed ID: 12382159
[TBL] [Abstract][Full Text] [Related]
28. Familial spastic paraplegia: evidence for a fourth locus.
Bruyn RP; van Veen MM; Kremer H; Scheltens PH; Padberg GW
Clin Neurol Neurosurg; 1997 May; 99(2):87-90. PubMed ID: 9213050
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. 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]
31. Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus.
Muglia M; Criscuolo C; Magariello A; De Michele G; Scarano V; D'Adamo P; Ambrosio G; Gabriele AL; Patitucci A; Mazzei R; Conforti FL; Sprovieri T; Morgante L; Epifanio A; La Spina P; Valentino P; Gasparini P; Filla A; Quattrone A
Neurogenetics; 2004 Feb; 5(1):49-54. PubMed ID: 14658060
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. 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. PubMed ID: 8649538
[TBL] [Abstract][Full Text] [Related]
34. Autosomal dominant spastic paraplegia linked to chromosome 2p: clinical and genetic studies of a large Japanese pedigree.
Matsuura T; Sasaki H; Wakisaka A; Hamada T; Moriwaka F; Tashiro K
J Neurol Sci; 1997 Oct; 151(1):65-70. PubMed ID: 9335012
[TBL] [Abstract][Full Text] [Related]
35. Hereditary spastic paraplegia linked to chromosome 15q: Analysis of candidate genes.
Fink JK; Jones SM; Sharp GB; Lange BM; Otterud B; Leppert M
Neurology; 1996 Mar; 46(3):835-6. PubMed ID: 8618696
[TBL] [Abstract][Full Text] [Related]
36. Spastic paraplegia 15: linkage and clinical description of three Tunisian families.
Boukhris A; Feki I; Denis E; Miladi MI; Brice A; Mhiri C; Stevanin G
Mov Disord; 2008 Feb; 23(3):429-33. PubMed ID: 18098276
[TBL] [Abstract][Full Text] [Related]
37. The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype.
Patel H; Hart PE; Warner TT; Houlston RS; Patton MA; Jeffery S; Crosby AH
Am J Hum Genet; 2001 Jul; 69(1):209-15. PubMed ID: 11389484
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia.
Fontaine B; Rime CS; Hazan J; Dürr A; Stevanin G; Penet C; Reboul J; Agid Y; Lyon-Caen O; Baumann N
Neuromuscul Disord; 1995 Jan; 5(1):11-7. PubMed ID: 7719135
[TBL] [Abstract][Full Text] [Related]
40. A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28.
Vazza G; Zortea M; Boaretto F; Micaglio GF; Sartori V; Mostacciuolo ML
Am J Hum Genet; 2000 Aug; 67(2):504-9. PubMed ID: 10877981
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]