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2. 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]
3. 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]
4. Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity. Hentati A; Pericak-Vance MA; Hung WY; Belal S; Laing N; Boustany RM; Hentati F; Ben Hamida M; Siddique T Hum Mol Genet; 1994 Aug; 3(8):1263-7. PubMed ID: 7987300 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q. Hughes CA; Byrne PC; Webb S; McMonagle P; Patterson V; Hutchinson M; Parfrey NA Neurology; 2001 May; 56(9):1230-3. PubMed ID: 11342696 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15. Shibasaki Y; Tanaka H; Iwabuchi K; Kawasaki S; Kondo H; Uekawa K; Ueda M; Kamiya T; Katayama Y; Nakamura A; Takashima H; Nakagawa M; Masuda M; Utsumi H; Nakamuro T; Tada K; Kurohara K; Inoue K; Koike F; Sakai T; Tsuji S; Kobayashi H Ann Neurol; 2000 Jul; 48(1):108-12. PubMed ID: 10894224 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]