124 related articles for article (PubMed ID: 9736780)
21. Analysis of ERDA1, CTG18.1, and uncloned CAG/CTG repeat sequences in familial Parkinson's disease with anticipation.
Schraen-Maschke S; Brique S; Chartier-Harlin MC; Brique E; Destée A; Sablonnière B
Am J Med Genet; 1999 Dec; 88(6):738-41. PubMed ID: 10581499
[TBL] [Abstract][Full Text] [Related]
22. Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia.
Bowen T; Guy CA; Cardno AG; Vincent JB; Kennedy JL; Jones LA; Gray M; Sanders RD; McCarthy G; Murphy KC; Owen MJ; O'Donovan MC
Psychiatr Genet; 2000 Mar; 10(1):33-7. PubMed ID: 10909126
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Extensive genetic heterogeneity in the "pure" form of autosomal dominant familial spastic paraplegia (Strümpell's disease).
Kobayashi H; Garcia CA; Tay PN; Hoffman EP
Muscle Nerve; 1996 Nov; 19(11):1435-8. PubMed ID: 8874401
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15.
Martínez Murillo F; Kobayashi H; Pegoraro E; Galluzzi G; Creel G; Mariani C; Farina E; Ricci E; Alfonso G; Pauli RM; Hoffman EP
Neurology; 1999 Jul; 53(1):50-6. PubMed ID: 10408536
[TBL] [Abstract][Full Text] [Related]
28. Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q.
Hazan J; Lamy C; Melki J; Munnich A; de Recondo J; Weissenbach J
Nat Genet; 1993 Oct; 5(2):163-7. PubMed ID: 8252041
[TBL] [Abstract][Full Text] [Related]
29. Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees.
De Jonghe P; Krols L; Michalik A; Hazan J; Smeyers G; Löfgren A; Weissenbach J; Martin JJ; Van Broeckhoven C
Eur J Hum Genet; 1996; 4(5):260-6. PubMed ID: 8946171
[TBL] [Abstract][Full Text] [Related]
30. CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.
Fujigasaki H; Martin JJ; De Deyn PP; Camuzat A; Deffond D; Stevanin G; Dermaut B; Van Broeckhoven C; Dürr A; Brice A
Brain; 2001 Oct; 124(Pt 10):1939-47. PubMed ID: 11571212
[TBL] [Abstract][Full Text] [Related]
31. A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection array.
Holmes SE; Wentzell JS; Seixas AI; Callahan C; Silveira I; Ross CA; Margolis RL
Hum Genet; 2006 Sep; 120(2):193-200. PubMed ID: 16783570
[TBL] [Abstract][Full Text] [Related]
32. Spastic paraplegia, ataxia, mental retardation (SPAR): a novel genetic disorder.
Hedera P; Rainier S; Zhao XP; Schalling M; Lindblad K; Yuan QP; Ikeuchi T; Trobe J; Wald JJ; Eldevik OP; Kluin K; Fink JK
Neurology; 2002 Feb; 58(3):411-6. PubMed ID: 11839840
[TBL] [Abstract][Full Text] [Related]
33. Uncloned expanded CAG/CTG repeat sequences in autosomal dominant cerebellar ataxia (ADCA) detected by the repeat expansion detection (RED) method.
Pujana MA; Volpini V; Gratacós M; Corral J; Banchs I; Sánchez A; Genís D; Cervera C; Estivill X
J Med Genet; 1998 Feb; 35(2):99-102. PubMed ID: 9507387
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Intergenerational CAG repeat expansion at ERDA1 in a family with childhood-onset depression, schizoaffective disorder, and recurrent major depression.
Vincent JB; Kovacs M; Krol R; Barr CL; Kennedy JL
Am J Med Genet; 1999 Feb; 88(1):79-82. PubMed ID: 10050972
[TBL] [Abstract][Full Text] [Related]
36. Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.
Paternotte C; Rudnicki D; Fizames C; Davoine CS; Mavel D; Dürr A; Samson D; Marquette C; Muselet D; Vega-Czarny N; Drouot N; Voit T; Fontaine B; Gyapay G; Auburger G; Weissenbach J; Hazan J
Genome Res; 1998 Nov; 8(11):1216-27. PubMed ID: 9847083
[TBL] [Abstract][Full Text] [Related]
37. Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.
Fink JK; Wu CT; Jones SM; Sharp GB; Lange BM; Lesicki A; Reinglass T; Varvil T; Otterud B; Leppert M
Am J Hum Genet; 1995 Jan; 56(1):188-92. PubMed ID: 7825577
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. A CAG trinucleotide repeat expansion and familial schizophrenia.
Ohara1 K; Ikeuchi T; Suzuki Y; Ohtani M; Ohara K; Tsuji S
Psychiatry Res; 2000 Jul; 94(3):257-62. PubMed ID: 10889290
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
