120 related articles for article (PubMed ID: 8707310)
1. 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]
2. Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p.
Hazan J; Fontaine B; Bruyn RP; Lamy C; van Deutekom JC; Rime CS; Dürr A; Melki J; Lyon-Caen O; Agid Y
Hum Mol Genet; 1994 Sep; 3(9):1569-73. PubMed ID: 7833913
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Molecular genetics of familial spastic paraplegia: a multitude of responsible genes.
Kobayashi H; Garcia CA; Alfonso G; Marks HG; Hoffman EP
J Neurol Sci; 1996 May; 137(2):131-8. PubMed ID: 8782167
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. Another pedigree with pure autosomal dominant spastic paraplegia (AD-FSP) from Tibet mapping to 14q11.2-q24.3.
Huang S; Zhuyu ; Li H; Labu ; Baizhu ; Lo WH; Fischer C; Vogel F
Hum Genet; 1997 Oct; 100(5-6):620-3. PubMed ID: 9341882
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
