672 related articles for article (PubMed ID: 16672289)
1. A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.
Thiffault I; Rioux MF; Tetreault M; Jarry J; Loiselle L; Poirier J; Gros-Louis F; Mathieu J; Vanasse M; Rouleau GA; Bouchard JP; Lesage J; Brais B
Brain; 2006 Sep; 129(Pt 9):2332-40. PubMed ID: 16672289
[TBL] [Abstract][Full Text] [Related]
2. Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3.
Klebe S; Azzedine H; Durr A; Bastien P; Bouslam N; Elleuch N; Forlani S; Charon C; Koenig M; Melki J; Brice A; Stevanin G
Brain; 2006 Jun; 129(Pt 6):1456-62. PubMed ID: 16434418
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum.
França MC; D'Abreu A; Maurer-Morelli CV; Seccolin R; Appenzeller S; Alessio A; Damasceno BP; Nucci A; Cendes F; Lopes-Cendes I
Mov Disord; 2007 Aug; 22(11):1556-62. PubMed ID: 17516453
[TBL] [Abstract][Full Text] [Related]
6. A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12.
Jarry J; Rioux MF; Bolduc V; Robitaille Y; Khoury V; Thiffault I; Tétreault M; Loisel L; Bouchard JP; Brais B
Brain; 2007 Feb; 130(Pt 2):368-80. PubMed ID: 17008331
[TBL] [Abstract][Full Text] [Related]
7. Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset.
Brockmann K; Simpson MA; Faber A; Bönnemann C; Crosby AH; Gärtner J
Neuropediatrics; 2005 Aug; 36(4):274-8. PubMed ID: 16138254
[TBL] [Abstract][Full Text] [Related]
8. Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11).
Winner B; Uyanik G; Gross C; Lange M; Schulte-Mattler W; Schuierer G; Marienhagen J; Hehr U; Winkler J
Arch Neurol; 2004 Jan; 61(1):117-21. PubMed ID: 14732628
[TBL] [Abstract][Full Text] [Related]
9. [A case of autosomal dominant, pure form spastic paraplegia with thinning of the corpus callosum].
Tomiyasu H; Hayashi R; Watanabe R; Honda M; Yoshii F
Rinsho Shinkeigaku; 1998 May; 38(5):435-9. PubMed ID: 9805990
[TBL] [Abstract][Full Text] [Related]
10. Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia.
Le Ber I; Clot F; Vercueil L; Camuzat A; Viémont M; Benamar N; De Liège P; Ouvrard-Hernandez AM; Pollak P; Stevanin G; Brice A; Dürr A
Neurology; 2006 Nov; 67(10):1769-73. PubMed ID: 17130408
[TBL] [Abstract][Full Text] [Related]
11. Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum.
Olmez A; Uyanik G; Ozgül RK; Gross C; Cirak S; Elibol B; Anlar B; Winner B; Hehr U; Topaloglu H; Winkler J
Neuropediatrics; 2006 Apr; 37(2):59-66. PubMed ID: 16773502
[TBL] [Abstract][Full Text] [Related]
12. Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish families.
Gücüyener K; Ozgül K; Paternotte C; Erdem H; Prud'homme JF; Ozgüç M; Topaloğlu H
Neuropediatrics; 2001 Jun; 32(3):142-6. PubMed ID: 11521210
[TBL] [Abstract][Full Text] [Related]
13. Hereditary spastic paraplegia with hypoplastic corpus callosum in a Turkish family.
Gucuyener K; Hirfanoglu T; Ok I; Cansu A; Serdaroglu A
J Child Neurol; 2007 Feb; 22(2):214-7. PubMed ID: 17621486
[TBL] [Abstract][Full Text] [Related]
14. A new locus (SPG47) maps to 1p13.2-1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum.
Blumkin L; Lerman-Sagie T; Lev D; Yosovich K; Leshinsky-Silver E
J Neurol Sci; 2011 Jun; 305(1-2):67-70. PubMed ID: 21440262
[TBL] [Abstract][Full Text] [Related]
15. Clinical and genetic study of autosomal recessive cerebellar ataxia type 1.
Dupré N; Gros-Louis F; Chrestian N; Verreault S; Brunet D; de Verteuil D; Brais B; Bouchard JP; Rouleau GA
Ann Neurol; 2007 Jul; 62(1):93-8. PubMed ID: 17503513
[TBL] [Abstract][Full Text] [Related]
16. Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity.
Lossos A; Stevanin G; Meiner V; Argov Z; Bouslam N; Newman JP; Gomori JM; Klebe S; Lerer I; Elleuch N; Silverstein S; Durr A; Abramsky O; Ben-Nariah Z; Brice A
Arch Neurol; 2006 May; 63(5):756-60. PubMed ID: 16682547
[TBL] [Abstract][Full Text] [Related]
17. A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24-2q31.
Gilbert DL; Leslie EJ; Keddache M; Leslie ND
Mov Disord; 2009 Feb; 24(3):364-70. PubMed ID: 19006192
[TBL] [Abstract][Full Text] [Related]
18. Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis.
Wakil SM; Murad HN; Baz BM; Hagos ST; Al-Amr RA; Al-Yamani SA; Al-Wadaee SM; Meyer BF; Bohlega SA
Neurosciences (Riyadh); 2012 Jan; 17(1):48-52. PubMed ID: 22246010
[TBL] [Abstract][Full Text] [Related]
19. Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity.
Boukhris A; Stevanin G; Feki I; Denis E; Elleuch N; Miladi MI; Truchetto J; Denora P; Belal S; Mhiri C; Brice A
Arch Neurol; 2008 Mar; 65(3):393-402. PubMed ID: 18332254
[TBL] [Abstract][Full Text] [Related]
20. Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.
Stevanin G; Bouslam N; Thobois S; Azzedine H; Ravaux L; Boland A; Schalling M; Broussolle E; Dürr A; Brice A
Ann Neurol; 2004 Jan; 55(1):97-104. PubMed ID: 14705117
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
