165 related articles for article (PubMed ID: 29493298)
1. Phenotypic and genotypic studies of ALS cases in ALS-SMA families.
Corcia P; Vourc'h P; Blasco H; Couratier P; Dangoumau A; Bellance R; Desnuelle C; Viader F; Pautot V; Millecamps S; Bakkouche S; Salachas F; Andres CR; Meininger V; Camu W
Amyotroph Lateral Scler Frontotemporal Degener; 2018 Aug; 19(5-6):432-437. PubMed ID: 29493298
[TBL] [Abstract][Full Text] [Related]
2. SMN1 gene study in three families in which ALS and spinal muscular atrophy co-exist.
Corcia P; Khoris J; Couratier P; Mayeux-Portas V; Bieth E; De Toffol B; Autret A; Müh JP; Andres C; Camu W
Neurology; 2002 Nov; 59(9):1464-6. PubMed ID: 12427909
[TBL] [Abstract][Full Text] [Related]
3. Pathogenic commonalities between spinal muscular atrophy and amyotrophic lateral sclerosis: Converging roads to therapeutic development.
Bowerman M; Murray LM; Scamps F; Schneider BL; Kothary R; Raoul C
Eur J Med Genet; 2018 Nov; 61(11):685-698. PubMed ID: 29313812
[TBL] [Abstract][Full Text] [Related]
4. Effect of familial clustering in the genetic screening of 235 French ALS families.
Corcia P; Camu W; Brulard C; Marouillat S; Couratier P; Camdessanché JP; Cintas P; Verschueren A; Soriani MH; Desnuelle C; Fleury MC; Guy N; Cassereau J; Viader F; Pittion-Vouyovitch S; Danel V; Kolev I; Le Masson G; Beltran S; Salachas F; Bernard E; Pradat PF; Blasco H; Lanznaster D; Hergesheimer R; Laumonnier F; Andres CR; Meininger V; Vourc'h P
J Neurol Neurosurg Psychiatry; 2021 May; 92(5):479-484. PubMed ID: 33408239
[TBL] [Abstract][Full Text] [Related]
5. Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies.
Kariya S; Re DB; Jacquier A; Nelson K; Przedborski S; Monani UR
Hum Mol Genet; 2012 Aug; 21(15):3421-34. PubMed ID: 22581780
[TBL] [Abstract][Full Text] [Related]
6. The genotype-phenotype landscape of familial amyotrophic lateral sclerosis in Australia.
McCann EP; Williams KL; Fifita JA; Tarr IS; O'Connor J; Rowe DB; Nicholson GA; Blair IP
Clin Genet; 2017 Sep; 92(3):259-266. PubMed ID: 28105640
[TBL] [Abstract][Full Text] [Related]
7. The relationship of spinal muscular atrophy to motor neuron disease: investigation of SMN and NAIP gene deletions in sporadic and familial ALS.
Orrell RW; Habgood JJ; de Belleroche JS; Lane RJ
J Neurol Sci; 1997 Jan; 145(1):55-61. PubMed ID: 9073029
[TBL] [Abstract][Full Text] [Related]
8. The importance of the SMN genes in the genetics of sporadic ALS.
Corcia P; Camu W; Praline J; Gordon PH; Vourch P; Andres C
Amyotroph Lateral Scler; 2009; 10(5-6):436-40. PubMed ID: 19922137
[TBL] [Abstract][Full Text] [Related]
9. Genetics of amyotrophic lateral sclerosis.
Corcia P; Couratier P; Blasco H; Andres CR; Beltran S; Meininger V; Vourc'h P
Rev Neurol (Paris); 2017 May; 173(5):254-262. PubMed ID: 28449881
[TBL] [Abstract][Full Text] [Related]
10. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
Millecamps S; Boillée S; Le Ber I; Seilhean D; Teyssou E; Giraudeau M; Moigneu C; Vandenberghe N; Danel-Brunaud V; Corcia P; Pradat PF; Le Forestier N; Lacomblez L; Bruneteau G; Camu W; Brice A; Cazeneuve C; Leguern E; Meininger V; Salachas F
J Med Genet; 2012 Apr; 49(4):258-63. PubMed ID: 22499346
[TBL] [Abstract][Full Text] [Related]
11. [Familial Amyotrophic Lateral Sclerosis].
Suzuki N; Nishiyama A; Kato M; Warita H; Aoki M
Brain Nerve; 2019 Nov; 71(11):1169-1181. PubMed ID: 31722303
[TBL] [Abstract][Full Text] [Related]
12. Estimated Prevalence and Incidence of Amyotrophic Lateral Sclerosis and SOD1 and C9orf72 Genetic Variants.
Brown CA; Lally C; Kupelian V; Flanders WD
Neuroepidemiology; 2021; 55(5):342-353. PubMed ID: 34247168
[TBL] [Abstract][Full Text] [Related]
13. TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy.
Turner BJ; Bäumer D; Parkinson NJ; Scaber J; Ansorge O; Talbot K
BMC Neurosci; 2008 Oct; 9():104. PubMed ID: 18957104
[TBL] [Abstract][Full Text] [Related]
14. SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS.
Veldink JH; Kalmijn S; Van der Hout AH; Lemmink HH; Groeneveld GJ; Lummen C; Scheffer H; Wokke JH; Van den Berg LH
Neurology; 2005 Sep; 65(6):820-5. PubMed ID: 16093455
[TBL] [Abstract][Full Text] [Related]
15. Clinical profile of motor neuron disease patients with lower urinary tract symptoms and neurogenic bladder.
Vázquez-Costa JF; Arlandis S; Hervas D; Martínez-Cuenca E; Cardona F; Pérez-Tur J; Broseta E; Sevilla T
J Neurol Sci; 2017 Jul; 378():130-136. PubMed ID: 28566149
[TBL] [Abstract][Full Text] [Related]
16. Analysis of the C9orf72 gene in spinal muscular atrophy patients.
Alías L; Bernal S; Barceló MJ; Martínez-Hernández R; Martínez E; Baiget M; Tizzano EF
Amyotroph Lateral Scler Frontotemporal Degener; 2014 Dec; 15(7-8):563-8. PubMed ID: 24998634
[TBL] [Abstract][Full Text] [Related]
17. Genetic analysis of the SOD1 and C9ORF72 genes in Hungarian patients with amyotrophic lateral sclerosis.
Tripolszki K; Csányi B; Nagy D; Ratti A; Tiloca C; Silani V; Kereszty É; Török N; Vécsei L; Engelhardt JI; Klivényi P; Nagy N; Széll M
Neurobiol Aging; 2017 May; 53():195.e1-195.e5. PubMed ID: 28222900
[TBL] [Abstract][Full Text] [Related]
18. Comprehensive analysis of the mutation spectrum in 301 German ALS families.
Müller K; Brenner D; Weydt P; Meyer T; Grehl T; Petri S; Grosskreutz J; Schuster J; Volk AE; Borck G; Kubisch C; Klopstock T; Zeller D; Jablonka S; Sendtner M; Klebe S; Knehr A; Günther K; Weis J; Claeys KG; Schrank B; Sperfeld AD; Hübers A; Otto M; Dorst J; Meitinger T; Strom TM; Andersen PM; Ludolph AC; Weishaupt JH;
J Neurol Neurosurg Psychiatry; 2018 Aug; 89(8):817-827. PubMed ID: 29650794
[TBL] [Abstract][Full Text] [Related]
19. Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases.
van Rheenen W; van Blitterswijk M; Huisman MH; Vlam L; van Doormaal PT; Seelen M; Medic J; Dooijes D; de Visser M; van der Kooi AJ; Raaphorst J; Schelhaas HJ; van der Pol WL; Veldink JH; van den Berg LH
Neurology; 2012 Aug; 79(9):878-82. PubMed ID: 22843265
[TBL] [Abstract][Full Text] [Related]
20. Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia.
Marjanović IV; Selak-Djokić B; Perić S; Janković M; Arsenijević V; Basta I; Lavrnić D; Stefanova E; Stević Z
J Neurol; 2017 Jun; 264(6):1091-1098. PubMed ID: 28444446
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]