211 related articles for article (PubMed ID: 17895902)
21. Clinical features of hereditary spastic paraplegia due to spastin mutation.
McDermott CJ; Burness CE; Kirby J; Cox LE; Rao DG; Hewamadduma C; Sharrack B; Hadjivassiliou M; Chinnery PF; Dalton A; Shaw PJ;
Neurology; 2006 Jul; 67(1):45-51. PubMed ID: 16832076
[TBL] [Abstract][Full Text] [Related]
22. Compound heterozygosity in the SPG4 gene causes hereditary spastic paraplegia.
Pantakani DV; Zechner U; Arygriou L; Pauli S; Sauter SM; Mannan AU
Clin Genet; 2008 Mar; 73(3):268-72. PubMed ID: 18190593
[TBL] [Abstract][Full Text] [Related]
23. Three novel spastin (SPG4) mutations in families with autosomal dominant hereditary spastic paraplegia.
Proukakis C; Hart PE; Cornish A; Warner TT; Crosby AH
J Neurol Sci; 2002 Sep; 201(1-2):65-9. PubMed ID: 12163196
[TBL] [Abstract][Full Text] [Related]
24. Posterior fossa abnormalities in hereditary spastic paraparesis with spastin mutations.
Scuderi C; Fichera M; Calabrese G; Elia M; Amato C; Savio M; Borgione E; Vitello GA; Musumeci SA
J Neurol Neurosurg Psychiatry; 2009 Apr; 80(4):440-3. PubMed ID: 19289482
[TBL] [Abstract][Full Text] [Related]
25. Mutation analysis of SPG4 and SPG3A genes and its implication in molecular diagnosis of Korean patients with hereditary spastic paraplegia.
Park SY; Ki CS; Kim HJ; Kim JW; Sung DH; Kim BJ; Lee WY
Arch Neurol; 2005 Jul; 62(7):1118-21. PubMed ID: 16009769
[TBL] [Abstract][Full Text] [Related]
26. A large Japanese SPG4 family with a novel insertion mutation of the SPG4 gene: a clinical and genetic study.
Namekawa M; Takiyama Y; Sakoe K; Shimazaki H; Amaike M; Niijima K; Nakano I; Nishizawa M
J Neurol Sci; 2001 Mar; 185(1):63-8. PubMed ID: 11266693
[TBL] [Abstract][Full Text] [Related]
27. Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia.
Dürr A; Camuzat A; Colin E; Tallaksen C; Hannequin D; Coutinho P; Fontaine B; Rossi A; Gil R; Rousselle C; Ruberg M; Stevanin G; Brice A
Arch Neurol; 2004 Dec; 61(12):1867-72. PubMed ID: 15596607
[TBL] [Abstract][Full Text] [Related]
28. Exon 8-17 deletions of SPAST in a Chinese family with hereditary spastic paraplegia: a case report and literature review.
Wang K; Zhao G
J Neurol Sci; 2015 Oct; 357(1-2):282-4. PubMed ID: 26165777
[TBL] [Abstract][Full Text] [Related]
29. Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia.
Crippa F; Panzeri C; Martinuzzi A; Arnoldi A; Redaelli F; Tonelli A; Baschirotto C; Vazza G; Mostacciuolo ML; Daga A; Orso G; Profice P; Trabacca A; D'Angelo MG; Comi GP; Galbiati S; Lamperti C; Bonato S; Pandolfo M; Meola G; Musumeci O; Toscano A; Trevisan CP; Bresolin N; Bassi MT
Arch Neurol; 2006 May; 63(5):750-5. PubMed ID: 16682546
[TBL] [Abstract][Full Text] [Related]
30. Motor system abnormalities in hereditary spastic paraparesis type 4 (SPG4) depend on the type of mutation in the spastin gene.
Bönsch D; Schwindt A; Navratil P; Palm D; Neumann C; Klimpe S; Schickel J; Hazan J; Weiller C; Deufel T; Liepert J
J Neurol Neurosurg Psychiatry; 2003 Aug; 74(8):1109-12. PubMed ID: 12876245
[TBL] [Abstract][Full Text] [Related]
31. A Japanese SPG4 family with a novel missense mutation of the SPG4 gene: intrafamilial variability in age at onset and clinical severity.
Namekawa M; Takiyama Y; Sakoe K; Nagaki H; Shimazaki H; Yoshimura M; Ikeguchi K; Nakano I; Nishizawa M
Acta Neurol Scand; 2002 Dec; 106(6):387-91. PubMed ID: 12460147
[TBL] [Abstract][Full Text] [Related]
32. Hereditary spastic paraplegia: clinical genetic study of 15 families.
Orlacchio A; Kawarai T; Totaro A; Errico A; St George-Hyslop PH; Rugarli EI; Bernardi G
Arch Neurol; 2004 Jun; 61(6):849-55. PubMed ID: 15210521
[TBL] [Abstract][Full Text] [Related]
33. Hereditary spastic paraplegias.
Lau KK; Ching CK; Mak CM; Chan YW
Hong Kong Med J; 2009 Jun; 15(3):217-20. PubMed ID: 19494379
[TBL] [Abstract][Full Text] [Related]
34. [Hereditary spastic paraplegia type 4 (SPG4) in Russian patients].
Rudenskaya GE; Kadnikova VA; Sidorova OP; Beetz C; Illarioshkin SN; Dadaly EL; Proskokova TN; Ryzhkova OP
Zh Nevrol Psikhiatr Im S S Korsakova; 2019; 119(11):11-20. PubMed ID: 31851166
[TBL] [Abstract][Full Text] [Related]
35. A novel splicing mutation (c.870+3A>G) in SPG4 in a Korean family with hereditary spastic paraplegia.
Lim JS; Sung JJ; Hong YH; Park SS; Park KS; Cha JI; Lee JY; Lee KW
J Neurol Sci; 2010 Mar; 290(1-2):186-9. PubMed ID: 19939411
[TBL] [Abstract][Full Text] [Related]
36. SPG4-related hereditary spastic paraplegia: frequency and mutation spectrum in Brazil.
França MC; Dogini DB; D'Abreu A; Teive HA; Munhoz RP; Raskin S; Moro A; Melo CC; Gomes AP; Saute JA; Jardim LB; Lopes-Cendes I
Clin Genet; 2014 Aug; 86(2):194-6. PubMed ID: 24033003
[No Abstract] [Full Text] [Related]
37. Clinical and genetic analysis of four Taiwanese families with autosomal dominant hereditary spastic paraplegia.
Lan MY; Fu SC; Chang YY; Wu-Chou YH; Lai SC; Chen RS; Lu CS
J Formos Med Assoc; 2012 Jul; 111(7):380-5. PubMed ID: 22817815
[TBL] [Abstract][Full Text] [Related]
38. High frequency of SPG4 in Taiwanese families with autosomal dominant hereditary spastic paraplegia.
Lan MY; Chang YY; Yeh TH; Lai SC; Liou CW; Kuo HC; Wu YR; Lyu RK; Hung JW; Chang YC; Lu CS
BMC Neurol; 2014 Nov; 14():216. PubMed ID: 25421405
[TBL] [Abstract][Full Text] [Related]
39. Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex.
Parodi L; Fenu S; Barbier M; Banneau G; Duyckaerts C; Tezenas du Montcel S; Monin ML; Ait Said S; Guegan J; Tallaksen CME; Sablonniere B; Brice A; Stevanin G; Depienne C; Durr A;
Brain; 2018 Dec; 141(12):3331-3342. PubMed ID: 30476002
[TBL] [Abstract][Full Text] [Related]
40. A de novo SPAST mutation leading to somatic mosaicism is associated with a later age at onset in HSP.
Depienne C; Fedirko E; Faucheux JM; Forlani S; Bricka B; Goizet C; Lesourd S; Stevanin G; Ruberg M; Durr A; Brice A
Neurogenetics; 2007 Aug; 8(3):231-3. PubMed ID: 17597328
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
