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Items: 1 to 20 of 332

1.

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, et al.

Hum Mol Genet. 1994 Sep;3(9):1569-73.

PMID:
7833913
2.

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.

PMID:
8707310
3.

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.

4.

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.

PMID:
8874401
5.

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. Review.

PMID:
8782167
6.

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.

PMID:
10732810
7.

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.

PMID:
8252041
8.

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.

PMID:
9341882
9.

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.

10.

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 13;53(1):50-6.

PMID:
10408536
11.

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.

PMID:
7987300
12.

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.

13.

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.

PMID:
11354831
14.

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.

PMID:
9213050
15.

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 May-Jun;48(3):169-78.

PMID:
9618065
16.

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, et al.

Hum Mol Genet. 1994 Oct;3(10):1867-71.

PMID:
7849714
17.

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 3;151(1):65-70.

PMID:
9335012
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.

19.

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, et al.

Neuromuscul Disord. 1995 Jan;5(1):11-7.

PMID:
7719135
20.

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.

PMID:
12112072
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