189 related articles for article (PubMed ID: 22154821)
1. Exome sequencing reveals SPG11 mutations causing juvenile ALS.
Daoud H; Zhou S; Noreau A; Sabbagh M; Belzil V; Dionne-Laporte A; Tranchant C; Dion P; Rouleau GA
Neurobiol Aging; 2012 Apr; 33(4):839.e5-9. PubMed ID: 22154821
[TBL] [Abstract][Full Text] [Related]
2. Exome sequencing reveals novel SPG11 mutation in hereditary spastic paraplegia with complicated phenotypes.
Li YS; Mao CY; Shi CH; Song B; Wu J; Qin J; Ji Y; Niu HX; Luo HY; Shang DD; Sun SL; Xu YM
J Clin Neurosci; 2015 Jul; 22(7):1150-4. PubMed ID: 26003865
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. VCP mutations in familial and sporadic amyotrophic lateral sclerosis.
Koppers M; van Blitterswijk MM; Vlam L; Rowicka PA; van Vught PW; Groen EJ; Spliet WG; Engelen-Lee J; Schelhaas HJ; de Visser M; van der Kooi AJ; van der Pol WL; Pasterkamp RJ; Veldink JH; van den Berg LH
Neurobiol Aging; 2012 Apr; 33(4):837.e7-13. PubMed ID: 22078486
[TBL] [Abstract][Full Text] [Related]
5. SPG11 compound mutations in spastic paraparesis with thin corpus callosum.
Samaranch L; Riverol M; Masdeu JC; Lorenzo E; Vidal-Taboada JM; Irigoyen J; Pastor MA; de Castro P; Pastor P
Neurology; 2008 Jul; 71(5):332-6. PubMed ID: 18663179
[TBL] [Abstract][Full Text] [Related]
6. Progranulin genetic variability contributes to amyotrophic lateral sclerosis.
Sleegers K; Brouwers N; Maurer-Stroh S; van Es MA; Van Damme P; van Vught PW; van der Zee J; Serneels S; De Pooter T; Van den Broeck M; Cruts M; Schymkowitz J; De Jonghe P; Rousseau F; van den Berg LH; Robberecht W; Van Broeckhoven C
Neurology; 2008 Jul; 71(4):253-9. PubMed ID: 18184915
[TBL] [Abstract][Full Text] [Related]
7. VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient.
van Blitterswijk M; van Es MA; Koppers M; van Rheenen W; Medic J; Schelhaas HJ; van der Kooi AJ; de Visser M; Veldink JH; van den Berg LH
Neurobiol Aging; 2012 Dec; 33(12):2950.e1-4. PubMed ID: 22878164
[TBL] [Abstract][Full Text] [Related]
8. A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient.
Corrado L; Carlomagno Y; Falasco L; Mellone S; Godi M; Cova E; Cereda C; Testa L; Mazzini L; D'Alfonso S
Neurobiol Aging; 2011 Mar; 32(3):552.e1-6. PubMed ID: 20363051
[TBL] [Abstract][Full Text] [Related]
9. Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Gijselinck I; Engelborghs S; Maes G; Cuijt I; Peeters K; Mattheijssens M; Joris G; Cras P; Martin JJ; De Deyn PP; Kumar-Singh S; Van Broeckhoven C; Cruts M
Arch Neurol; 2010 May; 67(5):606-16. PubMed ID: 20457961
[TBL] [Abstract][Full Text] [Related]
10. P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis.
Conte A; Lattante S; Zollino M; Marangi G; Luigetti M; Del Grande A; Servidei S; Trombetta F; Sabatelli M
Neuromuscul Disord; 2012 Jan; 22(1):73-5. PubMed ID: 21907581
[TBL] [Abstract][Full Text] [Related]
11. Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis.
Millecamps S; Corcia P; Cazeneuve C; Boillée S; Seilhean D; Danel-Brunaud V; Vandenberghe N; Pradat PF; Le Forestier N; Lacomblez L; Bruneteau G; Camu W; Brice A; Meininger V; LeGuern E; Salachas F
Neurobiol Aging; 2012 Apr; 33(4):839.e1-3. PubMed ID: 22169395
[TBL] [Abstract][Full Text] [Related]
12. Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11.
Chen X; Liu J; Wei QQ; Ou RW; Cao B; Yuan X; Hou Y; Zhang L; Shang H
BMC Neurol; 2020 Jan; 20(1):2. PubMed ID: 31900114
[TBL] [Abstract][Full Text] [Related]
13. Genotype-phenotype correlation in seven motor neuron disease families with novel ALS2 mutations.
Sprute R; Jergas H; Ölmez A; Alawbathani S; Karasoy H; Dafsari HS; Becker K; Daimagüler HS; Nürnberg P; Muntoni F; Topaloglu H; Uyanik G; Cirak S
Am J Med Genet A; 2021 Feb; 185(2):344-354. PubMed ID: 33155358
[TBL] [Abstract][Full Text] [Related]
14. Mutation analysis of PFN1 in familial amyotrophic lateral sclerosis patients.
Daoud H; Dobrzeniecka S; Camu W; Meininger V; Dupré N; Dion PA; Rouleau GA
Neurobiol Aging; 2013 Apr; 34(4):1311.e1-2. PubMed ID: 23062600
[TBL] [Abstract][Full Text] [Related]
15. Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis.
Hand CK; Devon RS; Gros-Louis F; Rochefort D; Khoris J; Meininger V; Bouchard JP; Camu W; Hayden MR; Rouleau GA
Arch Neurol; 2003 Dec; 60(12):1768-71. PubMed ID: 14676054
[TBL] [Abstract][Full Text] [Related]
16. Hot-spot KIF5A mutations cause familial ALS.
Brenner D; Yilmaz R; Müller K; Grehl T; Petri S; Meyer T; Grosskreutz J; Weydt P; Ruf W; Neuwirth C; Weber M; Pinto S; Claeys KG; Schrank B; Jordan B; Knehr A; Günther K; Hübers A; Zeller D; Kubisch C; Jablonka S; Sendtner M; Klopstock T; de Carvalho M; Sperfeld A; Borck G; Volk AE; Dorst J; Weis J; Otto M; Schuster J; Del Tredici K; Braak H; Danzer KM; Freischmidt A; Meitinger T; Strom TM; Ludolph AC; Andersen PM; Weishaupt JH;
Brain; 2018 Mar; 141(3):688-697. PubMed ID: 29342275
[TBL] [Abstract][Full Text] [Related]
17. A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy.
Conforti FL; Sprovieri T; Mazzei R; Ungaro C; La Bella V; Tessitore A; Patitucci A; Magariello A; Gabriele AL; Tedeschi G; Simone IL; Majorana G; Valentino P; Condino F; Bono F; Monsurrò MR; Muglia M; Quattrone A
Neuromuscul Disord; 2008 Jan; 18(1):68-70. PubMed ID: 17703939
[TBL] [Abstract][Full Text] [Related]
18. Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis.
Paubel A; Violette J; Amy M; Praline J; Meininger V; Camu W; Corcia P; Andres CR; Vourc'h P;
Arch Neurol; 2008 Oct; 65(10):1333-6. PubMed ID: 18852347
[TBL] [Abstract][Full Text] [Related]
19. C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany.
Drepper C; Herrmann T; Wessig C; Beck M; Sendtner M
Neurobiol Aging; 2011 Mar; 32(3):548.e1-4. PubMed ID: 20018407
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
