154 related articles for article (PubMed ID: 29845113)
1. Determining the incidence of familiality in ALS: A study of temporal trends in Ireland from 1994 to 2016.
Ryan M; Heverin M; Doherty MA; Davis N; Corr EM; Vajda A; Pender N; McLaughlin R; Hardiman O
Neurol Genet; 2018 Jun; 4(3):e239. PubMed ID: 29845113
[TBL] [Abstract][Full Text] [Related]
2. Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: a population-based case-control cohort study of familial and sporadic amyotrophic lateral sclerosis.
Byrne S; Heverin M; Elamin M; Bede P; Lynch C; Kenna K; MacLaughlin R; Walsh C; Al Chalabi A; Hardiman O
Ann Neurol; 2013 Nov; 74(5):699-708. PubMed ID: 23836460
[TBL] [Abstract][Full Text] [Related]
3. Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis.
Byrne S; Walsh C; Lynch C; Bede P; Elamin M; Kenna K; McLaughlin R; Hardiman O
J Neurol Neurosurg Psychiatry; 2011 Jun; 82(6):623-7. PubMed ID: 21047878
[TBL] [Abstract][Full Text] [Related]
4. VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK.
Kwok CT; Wang HY; Morris AG; Smith B; Shaw C; de Belleroche J
J Neurol Sci; 2015 Feb; 349(1-2):209-13. PubMed ID: 25618255
[TBL] [Abstract][Full Text] [Related]
5. Amyotrophic lateral sclerosis in the Faroe Islands - a genealogical study.
Johansen M; Svenstrup K; Mortensen Ó; Andorsdóttir G; Á Steig B; Joensen P; Hansen T; Petersen MS
Amyotroph Lateral Scler Frontotemporal Degener; 2021 Nov; 22(7-8):571-575. PubMed ID: 32885668
[TBL] [Abstract][Full Text] [Related]
6. Clustering of Neuropsychiatric Disease in First-Degree and Second-Degree Relatives of Patients With Amyotrophic Lateral Sclerosis.
O'Brien M; Burke T; Heverin M; Vajda A; McLaughlin R; Gibbons J; Byrne S; Pinto-Grau M; Elamin M; Pender N; Hardiman O
JAMA Neurol; 2017 Dec; 74(12):1425-1430. PubMed ID: 29049464
[TBL] [Abstract][Full Text] [Related]
7. Pre-symptomatic diagnosis in ALS.
Corcia P; Lumbroso S; Cazeneuve C; Mouzat K; Camu W; Vourc'h P;
Rev Neurol (Paris); 2020 Mar; 176(3):166-169. PubMed ID: 31932031
[TBL] [Abstract][Full Text] [Related]
8. Incidence of pathogenic, likely pathogenic, and uncertain ALS variants in a clinic cohort.
Roggenbuck J; Palettas M; Vicini L; Patel R; Quick A; Kolb SJ
Neurol Genet; 2020 Feb; 6(1):e390. PubMed ID: 32042918
[TBL] [Abstract][Full Text] [Related]
9. TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations.
Maekawa S; Leigh PN; King A; Jones E; Steele JC; Bodi I; Shaw CE; Hortobagyi T; Al-Sarraj S
Neuropathology; 2009 Dec; 29(6):672-83. PubMed ID: 19496940
[TBL] [Abstract][Full Text] [Related]
10. Epidemiology and clinical features of amyotrophic lateral sclerosis in Ireland between 1995 and 2004.
O'Toole O; Traynor BJ; Brennan P; Sheehan C; Frost E; Corr B; Hardiman O
J Neurol Neurosurg Psychiatry; 2008 Jan; 79(1):30-2. PubMed ID: 17634215
[TBL] [Abstract][Full Text] [Related]
11. Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation.
Conte A; Lattante S; Luigetti M; Del Grande A; Romano A; Marcaccio A; Marangi G; Rossini PM; Neri G; Zollino M; Sabatelli M
J Neurol Neurosurg Psychiatry; 2012 Dec; 83(12):1201-3. PubMed ID: 22773853
[TBL] [Abstract][Full Text] [Related]
12. Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.
Yan J; Deng HX; Siddique N; Fecto F; Chen W; Yang Y; Liu E; Donkervoort S; Zheng JG; Shi Y; Ahmeti KB; Brooks B; Engel WK; Siddique T
Neurology; 2010 Aug; 75(9):807-14. PubMed ID: 20668259
[TBL] [Abstract][Full Text] [Related]
13. SOD1 and cognitive dysfunction in familial amyotrophic lateral sclerosis.
Wicks P; Abrahams S; Papps B; Al-Chalabi A; Shaw CE; Leigh PN; Goldstein LH
J Neurol; 2009 Feb; 256(2):234-41. PubMed ID: 19252762
[TBL] [Abstract][Full Text] [Related]
14. Estimated Familial Amyotrophic Lateral Sclerosis Proportion: A Literature Review and Meta-analysis.
Barberio J; Lally C; Kupelian V; Hardiman O; Flanders WD
Neurol Genet; 2023 Dec; 9(6):e200109. PubMed ID: 38045991
[TBL] [Abstract][Full Text] [Related]
15. Secular Trends of Amyotrophic Lateral Sclerosis: The Piemonte and Valle d'Aosta Register.
Chiò A; Mora G; Moglia C; Manera U; Canosa A; Cammarosano S; Ilardi A; Bertuzzo D; Bersano E; Cugnasco P; Grassano M; Pisano F; Mazzini L; Calvo A;
JAMA Neurol; 2017 Sep; 74(9):1097-1104. PubMed ID: 28692730
[TBL] [Abstract][Full Text] [Related]
16. FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis.
Deng HX; Zhai H; Bigio EH; Yan J; Fecto F; Ajroud K; Mishra M; Ajroud-Driss S; Heller S; Sufit R; Siddique N; Mugnaini E; Siddique T
Ann Neurol; 2010 Jun; 67(6):739-48. PubMed ID: 20517935
[TBL] [Abstract][Full Text] [Related]
17. De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China.
Zou ZY; Cui LY; Sun Q; Li XG; Liu MS; Xu Y; Zhou Y; Yang XZ
Neurobiol Aging; 2013 Apr; 34(4):1312.e1-8. PubMed ID: 23046859
[TBL] [Abstract][Full Text] [Related]
18. Age-period-cohort analysis of trends in amyotrophic lateral sclerosis incidence.
Tobin K; Gilthorpe MS; Rooney J; Heverin M; Vajda A; Staines A; Hardiman O
J Neurol; 2016 Oct; 263(10):1919-26. PubMed ID: 27372451
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Cognitive impairment in familial ALS.
Wheaton MW; Salamone AR; Mosnik DM; McDonald RO; Appel SH; Schmolck HI; Ringholz GM; Schulz PE
Neurology; 2007 Oct; 69(14):1411-7. PubMed ID: 17909153
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]