-
1
-
-
31544466502
-
Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene
-
COI: 1:CAS:528:DC%2BD28XhsFSrsrw%3D, PID: 16469270
-
Andersen PM. Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene. Curr Neurol Neurosci Rep 2006;6:37-46.
-
(2006)
Curr Neurol Neurosci Rep
, vol.6
, pp. 37-46
-
-
Andersen, P.M.1
-
2
-
-
84893649256
-
State of play in amyotrophic lateral sclerosis genetics
-
COI: 1:CAS:528:DC%2BC3sXhvFylsrbM, PID: 24369373
-
Renton AE, Chio A, Traynor BJ. State of play in amyotrophic lateral sclerosis genetics. Nat Neurosci 2014;17:17-23.
-
(2014)
Nat Neurosci
, vol.17
, pp. 17-23
-
-
Renton, A.E.1
Chio, A.2
Traynor, B.J.3
-
3
-
-
77956877621
-
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study
-
COI: 1:CAS:528:DC%2BC3cXhtFOntbjM, PID: 20801717
-
Shatunov A, Mok K, Newhouse S, et al. Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. Lancet Neurol 2010;9:986-994.
-
(2010)
Lancet Neurol
, vol.9
, pp. 986-994
-
-
Shatunov, A.1
Mok, K.2
Newhouse, S.3
-
4
-
-
77952115084
-
Identification of 2 loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
PID: 20457961
-
Gijselinck I, Engelborghs S, Maes G, et al. Identification of 2 loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Arch Neurol 2010;67:606-616.
-
(2010)
Arch Neurol
, vol.67
, pp. 606-616
-
-
Gijselinck, I.1
Engelborghs, S.2
Maes, G.3
-
5
-
-
33645069660
-
Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3
-
PID: 16495328
-
Vance C, Al-Chalabi A, Ruddy D, et al. Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3. Brain 2006;129:868-876.
-
(2006)
Brain
, vol.129
, pp. 868-876
-
-
Vance, C.1
Al-Chalabi, A.2
Ruddy, D.3
-
6
-
-
33645062075
-
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia
-
COI: 1:STN:280:DC%2BD287nsVeltA%3D%3D, PID: 16421333
-
Morita M, Al-Chalabi A, Andersen PM, et al. A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia. Neurology 2006;66:839-844.
-
(2006)
Neurology
, vol.66
, pp. 839-844
-
-
Morita, M.1
Al-Chalabi, A.2
Andersen, P.M.3
-
7
-
-
78751478222
-
Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family
-
PID: 20562461
-
Boxer AL, Mackenzie IR, Boeve BF, et al. Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family. J Neurol Neurosurg Psychiatry 2011;82:196-203.
-
(2011)
J Neurol Neurosurg Psychiatry
, vol.82
, pp. 196-203
-
-
Boxer, A.L.1
Mackenzie, I.R.2
Boeve, B.F.3
-
8
-
-
33846945446
-
Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p
-
PID: 17296840
-
Valdmanis PN, Dupre N, Bouchard JP, et al. Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p. Arch Neurol 2007;64:240-245.
-
(2007)
Arch Neurol
, vol.64
, pp. 240-245
-
-
Valdmanis, P.N.1
Dupre, N.2
Bouchard, J.P.3
-
9
-
-
80054832080
-
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
-
COI: 1:CAS:528:DC%2BC3MXhtlKrtL%2FP, PID: 21944778
-
DeJesus-Hernandez M, Mackenzie IR, Boeve BF, et al. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 2011;72:245-256.
-
(2011)
Neuron
, vol.72
, pp. 245-256
-
-
DeJesus-Hernandez, M.1
Mackenzie, I.R.2
Boeve, B.F.3
-
10
-
-
80054837386
-
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
-
COI: 1:CAS:528:DC%2BC3MXhtlKrtL%2FI, PID: 21944779
-
Renton AE, Majounie E, Waite A, et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 2011;72:257-268.
-
(2011)
Neuron
, vol.72
, pp. 257-268
-
-
Renton, A.E.1
Majounie, E.2
Waite, A.3
-
11
-
-
84858622829
-
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
-
COI: 1:CAS:528:DC%2BC38XksFWltbo%3D, PID: 22406228
-
Majounie E, Renton AE, Mok K, et al. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. Lancet Neurol 2012;11:323-330.
-
(2012)
Lancet Neurol
, vol.11
, pp. 323-330
-
-
Majounie, E.1
Renton, A.E.2
Mok, K.3
-
12
-
-
84871219249
-
The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder
-
COI: 1:CAS:528:DC%2BC38XhvVClt7%2FK, PID: 22692064
-
Smith BN, Newhouse S, Shatunov A, et al. The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder. Eur J Hum Genet 2013;21:102-108.
-
(2013)
Eur J Hum Genet
, vol.21
, pp. 102-108
-
-
Smith, B.N.1
Newhouse, S.2
Shatunov, A.3
-
13
-
-
84866093352
-
C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts
-
PID: 22875086
-
Dobson-Stone C, Hallupp M, Bartley L, et al. C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts. Neurology 2012;79:995-1001.
-
(2012)
Neurology
, vol.79
, pp. 995-1001
-
-
Dobson-Stone, C.1
Hallupp, M.2
Bartley, L.3
-
14
-
-
84876411369
-
Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population
-
COI: 1:CAS:528:DC%2BC3sXivF2qtrg%3D, PID: 23434116
-
Beck J, Poulter M, Hensman D, et al. Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population. Am J Hum Genet 2013;92:345-353.
-
(2013)
Am J Hum Genet
, vol.92
, pp. 345-353
-
-
Beck, J.1
Poulter, M.2
Hensman, D.3
-
15
-
-
84896699287
-
The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype
-
COI: 1:CAS:528:DC%2BC2cXitFCmsbc%3D, PID: 24493408
-
Cooper-Knock J, Shaw PJ, Kirby J. The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype. Acta Neuropathol 2014;127:333-345.
-
(2014)
Acta Neuropathol
, vol.127
, pp. 333-345
-
-
Cooper-Knock, J.1
Shaw, P.J.2
Kirby, J.3
-
16
-
-
84857054634
-
Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72
-
PID: 22366792
-
Cooper-Knock J, Hewitt C, Highley JR, et al. Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72. Brain 2012;135:751-764.
-
(2012)
Brain
, vol.135
, pp. 751-764
-
-
Cooper-Knock, J.1
Hewitt, C.2
Highley, J.R.3
-
17
-
-
84875226784
-
Japanese amyotrophic lateral sclerosis patients with GGGGCC hexanucleotide repeat expansion in C9ORF72
-
PID: 23012445
-
Konno T, Shiga A, Tsujino A, et al. Japanese amyotrophic lateral sclerosis patients with GGGGCC hexanucleotide repeat expansion in C9ORF72. J Neurol Neurosurg Psychiatry 2013;84:398-401.
-
(2013)
J Neurol Neurosurg Psychiatry
, vol.84
, pp. 398-401
-
-
Konno, T.1
Shiga, A.2
Tsujino, A.3
-
18
-
-
84878919243
-
Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat
-
Jones AR, Woollacott I, Shatunov A, et al. Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. Neurobiol Aging 2013;34:2234 e1-e7
-
(2013)
Neurobiol Aging
, vol.34
, pp. 2234 e1-e7
-
-
Jones, A.R.1
Woollacott, I.2
Shatunov, A.3
-
21
-
-
84155172791
-
The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study
-
PID: 21836033
-
Phukan J, Elamin M, Bede P, et al. The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study. J Neurol Neurosurg Psychiatry 2012;83:102-108
-
(2012)
J Neurol Neurosurg Psychiatry
, vol.83
, pp. 102-108
-
-
Phukan, J.1
Elamin, M.2
Bede, P.3
-
22
-
-
84921403905
-
Cognitive correlates in amyotrophic lateral sclerosis: a population-based study in Italy
-
PID: 24769471
-
Montuschi A, Iazzolino B, Calvo A, et al. Cognitive correlates in amyotrophic lateral sclerosis: a population-based study in Italy. J Neurol Neurosurg Psychiatry 2015;86:168-173.
-
(2015)
J Neurol Neurosurg Psychiatry
, vol.86
, pp. 168-173
-
-
Montuschi, A.1
Iazzolino, B.2
Calvo, A.3
-
23
-
-
85138842172
-
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population
-
Sabatelli M, Conforti FL, Zollino M, et al. C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population. Neurobiol Aging 2012;33:1848 e15-e20.
-
(1848)
Neurobiol Aging
, vol.2012
, Issue.33
, pp. e15-e20
-
-
Sabatelli, M.1
Conforti, F.L.2
Zollino, M.3
-
24
-
-
84857921617
-
Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p
-
COI: 1:CAS:528:DC%2BC38Xisl2ktbg%3D, PID: 22228244
-
Stewart H, Rutherford NJ, Briemberg H, et al. Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p. Acta Neuropathol 2012;123:409-417.
-
(2012)
Acta Neuropathol
, vol.123
, pp. 409-417
-
-
Stewart, H.1
Rutherford, N.J.2
Briemberg, H.3
-
25
-
-
84857050135
-
Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
-
COI: 1:CAS:528:DC%2BC38XislSqsrk%3D, PID: 22305801
-
Byrne S, Elamin M, Bede P, et al. Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study. Lancet Neurol 2012;11:232-240.
-
(2012)
Lancet Neurol
, vol.11
, pp. 232-240
-
-
Byrne, S.1
Elamin, M.2
Bede, P.3
-
26
-
-
84857522741
-
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72
-
PID: 22366794
-
Chio A, Borghero G, Restagno G, et al. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. Brain 2012;135:784-793
-
(2012)
Brain
, vol.135
, pp. 784-793
-
-
Chio, A.1
Borghero, G.2
Restagno, G.3
-
27
-
-
84871610298
-
Analysis of the C9orf72 gene in patients with amyotrophic lateral sclerosis in Spain and different populations worldwide
-
COI: 1:CAS:528:DC%2BC3sXit1Wk, PID: 22936364
-
Garcia-Redondo A, Dols-Icardo O, Rojas-Garcia R, et al. Analysis of the C9orf72 gene in patients with amyotrophic lateral sclerosis in Spain and different populations worldwide. Hum Mutat 2013;34:79-82.
-
(2013)
Hum Mutat
, vol.34
, pp. 79-82
-
-
Garcia-Redondo, A.1
Dols-Icardo, O.2
Rojas-Garcia, R.3
-
28
-
-
0034605478
-
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22
-
COI: 1:CAS:528:DC%2BD3cXnt1Ort78%3D, PID: 11015796
-
Hosler BA, Siddique T, Sapp PC, et al. Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22. JAMA 2000;284:1664-1669.
-
(2000)
JAMA
, vol.284
, pp. 1664-1669
-
-
Hosler, B.A.1
Siddique, T.2
Sapp, P.C.3
-
29
-
-
81355146748
-
Chromosome 9 ALS and FTD locus is probably derived from a single founder
-
Mok K, Traynor BJ, Schymick J, et al. Chromosome 9 ALS and FTD locus is probably derived from a single founder. Neurobiol Aging 2012;33:209 e3-e8.
-
(2012)
Neurobiol Aging
, vol.33
, pp. 209 e3-e8
-
-
Mok, K.1
Traynor, B.J.2
Schymick, J.3
-
30
-
-
84865068311
-
Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases
-
PID: 22843265
-
van Rheenen W, van Blitterswijk M, Huisman MH, et al. Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases. Neurology 2012;79:878-882.
-
(2012)
Neurology
, vol.79
, pp. 878-882
-
-
van Rheenen, W.1
van Blitterswijk, M.2
Huisman, M.H.3
-
31
-
-
84884159557
-
Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort study
-
Debray S, Race V, Crabbe V, et al. Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort study. Neurobiol Aging 2013;34:2890 e7-e90 e12.
-
(2013)
Neurobiol Aging
, vol.34
, pp. 2890 e7-e90 e12
-
-
Debray, S.1
Race, V.2
Crabbe, V.3
-
32
-
-
84864083825
-
Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes
-
COI: 1:CAS:528:DC%2BC38Xpt1yjtL8%3D, PID: 22499346
-
Millecamps S, Boillee S, Le Ber I, et al. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes. J Med Genet 2012;49:258-263.
-
(2012)
J Med Genet
, vol.49
, pp. 258-263
-
-
Millecamps, S.1
Boillee, S.2
Le Ber, I.3
-
33
-
-
84863393788
-
Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
-
PID: 22366793
-
Boeve BF, Boylan KB, Graff-Radford NR, et al. Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72. Brain 2012;135:765-783.
-
(2012)
Brain
, vol.135
, pp. 765-783
-
-
Boeve, B.F.1
Boylan, K.B.2
Graff-Radford, N.R.3
-
34
-
-
83555166183
-
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
-
COI: 1:CAS:528:DC%2BC3MXhs1CisLzJ, PID: 22154785
-
Gijselinck I, Van Langenhove T, van der Zee J, et al. A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study. Lancet Neurol 2012;11:54-65.
-
(2012)
Lancet Neurol
, vol.11
, pp. 54-65
-
-
Gijselinck, I.1
Van Langenhove, T.2
van der Zee, J.3
-
35
-
-
84857587514
-
Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p
-
PID: 22344582
-
Hsiung GY, DeJesus-Hernandez M, Feldman HH, et al. Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p. Brain 2012;135:709-722.
-
(2012)
Brain
, vol.135
, pp. 709-722
-
-
Hsiung, G.Y.1
DeJesus-Hernandez, M.2
Feldman, H.H.3
-
36
-
-
84896738352
-
Clinical characteristics of C9ORF72-linked frontotemporal lobar degeneration
-
PID: 24052799
-
Kaivorinne AL, Bode MK, Paavola L, et al. Clinical characteristics of C9ORF72-linked frontotemporal lobar degeneration. Dement Geriatr Cogn Dis Extra 2013;3:251-262.
-
(2013)
Dement Geriatr Cogn Dis Extra
, vol.3
, pp. 251-262
-
-
Kaivorinne, A.L.1
Bode, M.K.2
Paavola, L.3
-
37
-
-
84866109396
-
C9ORF72 hexanucleotide repeat expansions in patients with ALS from the Coriell Cell Repository
-
PID: 22815561
-
Rutherford NJ, DeJesus-Hernandez M, Baker MC, et al. C9ORF72 hexanucleotide repeat expansions in patients with ALS from the Coriell Cell Repository. Neurology 2012;79:482-483.
-
(2012)
Neurology
, vol.79
, pp. 482-483
-
-
Rutherford, N.J.1
DeJesus-Hernandez, M.2
Baker, M.C.3
-
38
-
-
84884486165
-
C9ORF72 expansions, parkinsonism, and Parkinson disease: a clinicopathologic study
-
COI: 1:CAS:528:DC%2BC3sXhtlagu73O, PID: 23884045
-
Cooper-Knock J, Frolov A, Highley JR, et al. C9ORF72 expansions, parkinsonism, and Parkinson disease: a clinicopathologic study. Neurology 2013;81:808-811.
-
(2013)
Neurology
, vol.81
, pp. 808-811
-
-
Cooper-Knock, J.1
Frolov, A.2
Highley, J.R.3
-
39
-
-
84874318643
-
C9orf72 repeat expansions are a rare genetic cause of parkinsonism
-
PID: 23413259
-
Lesage S, Le Ber I, Condroyer C, et al. C9orf72 repeat expansions are a rare genetic cause of parkinsonism. Brain 2013;136:385-391.
-
(2013)
Brain
, vol.136
, pp. 385-391
-
-
Lesage, S.1
Le Ber, I.2
Condroyer, C.3
-
40
-
-
84874019770
-
Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease
-
COI: 1:CAS:528:DC%2BC3sXlsF2qtL4%3D, PID: 22650353
-
Lindquist SG, Duno M, Batbayli M, et al. Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease. Clin Genet 2013;83:279-283.
-
(2013)
Clin Genet
, vol.83
, pp. 279-283
-
-
Lindquist, S.G.1
Duno, M.2
Batbayli, M.3
-
41
-
-
84878803626
-
C9orf72 hexanucleotide repeat expansion and Guam amyotrophic lateral sclerosis-Parkinsonism-dementia complex
-
PID: 23588498
-
Dombroski BA, Galasko DR, Mata IF, et al. C9orf72 hexanucleotide repeat expansion and Guam amyotrophic lateral sclerosis-Parkinsonism-dementia complex. JAMA Neurol 2013;70:742-745.
-
(2013)
JAMA Neurol
, vol.70
, pp. 742-745
-
-
Dombroski, B.A.1
Galasko, D.R.2
Mata, I.F.3
-
42
-
-
84866058216
-
C9ORF72 repeat expansion in amyotrophic lateral sclerosis in the Kii peninsula of Japan
-
PID: 22637429
-
Ishiura H, Takahashi Y, Mitsui J, et al. C9ORF72 repeat expansion in amyotrophic lateral sclerosis in the Kii peninsula of Japan. Arch Neurol 2012;69:1154-1158.
-
(2012)
Arch Neurol
, vol.69
, pp. 1154-1158
-
-
Ishiura, H.1
Takahashi, Y.2
Mitsui, J.3
-
43
-
-
84885047459
-
C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China
-
PID: 24068985
-
Jiao B, Guo JF, Wang YQ, et al. C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China. Front Cell Neurosci 2013;7:164.
-
(2013)
Front Cell Neurosci
, vol.7
, pp. 164
-
-
Jiao, B.1
Guo, J.F.2
Wang, Y.Q.3
-
44
-
-
84892998754
-
C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease
-
COI: 1:CAS:528:DC%2BC3sXhsFCrtb7O, PID: 23845100
-
Nuytemans K, Bademci G, Kohli MM, et al. C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease. Ann Hum Genet 2013;77:351-363.
-
(2013)
Ann Hum Genet
, vol.77
, pp. 351-363
-
-
Nuytemans, K.1
Bademci, G.2
Kohli, M.M.3
-
45
-
-
84893718348
-
Polymerase chain reaction and Southern blot-based analysis of the C9orf72 hexanucleotide repeat in different motor neuron diseases
-
Hubers A, Marroquin N, Schmoll B, et al. Polymerase chain reaction and Southern blot-based analysis of the C9orf72 hexanucleotide repeat in different motor neuron diseases. Neurobiol Aging 2014;35:1214 e1-e6.
-
(2014)
Neurobiol Aging
, vol.35
, pp. 1214 e1-e6
-
-
Hubers, A.1
Marroquin, N.2
Schmoll, B.3
-
46
-
-
84891738058
-
Hereditary spastic paraplegia is not associated with C9ORF72 repeat expansions in a Danish cohort
-
COI: 1:STN:280:DC%2BC2c%2FkvFWisQ%3D%3D, PID: 24126854
-
Nielsen TT, Svenstrup K, Duno M, Nielsen JE. Hereditary spastic paraplegia is not associated with C9ORF72 repeat expansions in a Danish cohort. Spinal Cord 2014;52:77-79.
-
(2014)
Spinal Cord
, vol.52
, pp. 77-79
-
-
Nielsen, T.T.1
Svenstrup, K.2
Duno, M.3
Nielsen, J.E.4
-
48
-
-
84895768608
-
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies
-
COI: 1:CAS:528:DC%2BC2cXhs1yhu7Y%3D, PID: 24363131
-
Hensman Moss DJ, Poulter M, Beck J, et al. C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies. Neurology 2014;82:292-299.
-
(2014)
Neurology
, vol.82
, pp. 292-299
-
-
Hensman Moss, D.J.1
Poulter, M.2
Beck, J.3
-
49
-
-
84871780700
-
C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia
-
PID: 23080112
-
Fogel BL, Pribadi M, Pi S, Perlman SL, Geschwind DH, Coppola G. C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia. Mov Disord 2012;27:1832-1833.
-
(2012)
Mov Disord
, vol.27
, pp. 1832-1833
-
-
Fogel, B.L.1
Pribadi, M.2
Pi, S.3
Perlman, S.L.4
Geschwind, D.H.5
Coppola, G.6
-
50
-
-
84902203309
-
Multiple system atrophy and amyotrophic lateral sclerosis in a family with hexanucleotide repeat expansions in C9orf72
-
PID: 24733620
-
Goldman JS, Quinzii C, Dunning-Broadbent J, et al. Multiple system atrophy and amyotrophic lateral sclerosis in a family with hexanucleotide repeat expansions in C9orf72. JAMA Neurol 2014;71:771-774.
-
(2014)
JAMA Neurol
, vol.71
, pp. 771-774
-
-
Goldman, J.S.1
Quinzii, C.2
Dunning-Broadbent, J.3
-
51
-
-
84863393065
-
Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
-
PID: 22300873
-
Snowden JS, Rollinson S, Thompson JC, et al. Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations. Brain 2012;135:693-708.
-
(2012)
Brain
, vol.135
, pp. 693-708
-
-
Snowden, J.S.1
Rollinson, S.2
Thompson, J.C.3
-
52
-
-
84866081962
-
Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features
-
PID: 22875087
-
Sha SJ, Takada LT, Rankin KP, et al. Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features. Neurology 2012;79:1002-1011.
-
(2012)
Neurology
, vol.79
, pp. 1002-1011
-
-
Sha, S.J.1
Takada, L.T.2
Rankin, K.P.3
-
53
-
-
84857516402
-
The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions
-
PID: 22300876
-
Simon-Sanchez J, Dopper EG, Cohn-Hokke PE, et al. The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions. Brain 2012;135:723-735.
-
(2012)
Brain
, vol.135
, pp. 723-735
-
-
Simon-Sanchez, J.1
Dopper, E.G.2
Cohn-Hokke, P.E.3
-
54
-
-
84873457052
-
Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians
-
Kohli MA, John-Williams K, Rajbhandary R, et al. Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians. Neurobiol Aging 2013;34:1519 e5-e12.
-
(2013)
Neurobiol Aging
, vol.34
, pp. 1519 e5-e12
-
-
Kohli, M.A.1
John-Williams, K.2
Rajbhandary, R.3
-
55
-
-
84878782299
-
C9orf72 hexanucleotide repeat expansions in clinical Alzheimer disease
-
PID: 23588422
-
Harms M, Benitez BA, Cairns N, et al. C9orf72 hexanucleotide repeat expansions in clinical Alzheimer disease. JAMA Neurol 2013;70:736-741.
-
(2013)
JAMA Neurol
, vol.70
, pp. 736-741
-
-
Harms, M.1
Benitez, B.A.2
Cairns, N.3
-
56
-
-
84875267247
-
C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment
-
Cacace R, Van Cauwenberghe C, Bettens K, et al. C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment. Neurobiol Aging 2013;34:1712 e1-e7.
-
(2013)
Neurobiol Aging
, vol.34
, pp. 1712 e1-e7
-
-
Cacace, R.1
Van Cauwenberghe, C.2
Bettens, K.3
-
57
-
-
85058205773
-
C9orf72 repeat expansions are restricted to the ALS-FTD spectrum
-
Ticozzi N, Tiloca C, Calini D, et al. C9orf72 repeat expansions are restricted to the ALS-FTD spectrum. Neurobiol Aging 2014;35:936 e13-e17.
-
(2014)
Neurobiol Aging
, vol.35
, pp. 936 e13-e17
-
-
Ticozzi, N.1
Tiloca, C.2
Calini, D.3
-
58
-
-
84856132922
-
Repeat expansion in C9ORF72 in Alzheimer's disease
-
COI: 1:CAS:528:DC%2BC38Xht1Gmsbo%3D, PID: 22216764
-
Majounie E, Abramzon Y, Renton AE, et al. Repeat expansion in C9ORF72 in Alzheimer's disease. N Engl J Med 2012;366:283-284.
-
(2012)
N Engl J Med
, vol.366
, pp. 283-284
-
-
Majounie, E.1
Abramzon, Y.2
Renton, A.E.3
-
59
-
-
84872301861
-
C9ORF72 repeat expansions not detected in a group of patients with schizophrenia
-
Huey ED, Nagy PL, Rodriguez-Murillo L, et al. C9ORF72 repeat expansions not detected in a group of patients with schizophrenia. Neurobiol Aging 2013;34:1309 e9-e10
-
(2013)
Neurobiol Aging
, vol.34
, pp. 1309 e9-e10
-
-
Huey, E.D.1
Nagy, P.L.2
Rodriguez-Murillo, L.3
-
60
-
-
84903366205
-
Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample
-
Fahey C, Byrne S, McLaughlin R, et al. Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample. Neurobiol Aging 2014;35:1510 e1-e5.
-
(2014)
Neurobiol Aging
, vol.35
, pp. 1510 e1-e5
-
-
Fahey, C.1
Byrne, S.2
McLaughlin, R.3
-
61
-
-
84893790427
-
The C9ORF72 hexanucleotide repeat expansion is a rare cause of schizophrenia
-
Galimberti D, Reif A, Dell'osso B, et al. The C9ORF72 hexanucleotide repeat expansion is a rare cause of schizophrenia. Neurobiol Aging 2014;35:1214 e7-14 e10.
-
(2014)
Neurobiol Aging
, vol.35
, pp. 1214 e7-14 e10
-
-
Galimberti, D.1
Reif, A.2
Dell'osso, B.3
-
62
-
-
84877344506
-
C9ORF72 expansion in a family with bipolar disorder
-
COI: 1:CAS:528:DC%2BC3sXpsVymsLk%3D, PID: 23551834
-
Meisler MH, Grant AE, Jones JM, et al. C9ORF72 expansion in a family with bipolar disorder. Bipolar Disord 2013;15:326-332.
-
(2013)
Bipolar Disord
, vol.15
, pp. 326-332
-
-
Meisler, M.H.1
Grant, A.E.2
Jones, J.M.3
-
63
-
-
84892737893
-
Incomplete penetrance of the C9ORF72 hexanucleotide repeat expansions: frequency in a cohort of geriatric non-demented subjects
-
COI: 1:CAS:528:DC%2BC2cXislKqtg%3D%3D, PID: 24121957
-
Galimberti D, Arosio B, Fenoglio C, et al. Incomplete penetrance of the C9ORF72 hexanucleotide repeat expansions: frequency in a cohort of geriatric non-demented subjects. J Alzheimers Dis 2014;39:19-22.
-
(2014)
J Alzheimers Dis
, vol.39
, pp. 19-22
-
-
Galimberti, D.1
Arosio, B.2
Fenoglio, C.3
-
64
-
-
82355180849
-
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
-
COI: 1:CAS:528:DC%2BC3MXhsFCms77K, PID: 22083254
-
Murray ME, Dejesus-Hernandez M, Rutherford NJ, et al. Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72. Acta Neuropathol 2011;122:673-690.
-
(2011)
Acta Neuropathol
, vol.122
, pp. 673-690
-
-
Murray, M.E.1
Dejesus-Hernandez, M.2
Rutherford, N.J.3
-
65
-
-
82355180826
-
p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS
-
COI: 1:CAS:528:DC%2BC3MXhsFCms77F, PID: 22101323
-
Al-Sarraj S, King A, Troakes C, et al. p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS. Acta Neuropathol 2011;122:691-702.
-
(2011)
Acta Neuropathol
, vol.122
, pp. 691-702
-
-
Al-Sarraj, S.1
King, A.2
Troakes, C.3
-
66
-
-
41949141411
-
Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions visualized with ubiquitin-binding protein p62 immunohistochemistry
-
PID: 18379439
-
Pikkarainen M, Hartikainen P, Alafuzoff I. Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions visualized with ubiquitin-binding protein p62 immunohistochemistry. J Neuropathol Exp Neurol 2008;67:280-298.
-
(2008)
J Neuropathol Exp Neurol
, vol.67
, pp. 280-298
-
-
Pikkarainen, M.1
Hartikainen, P.2
Alafuzoff, I.3
-
67
-
-
67651243804
-
Frontotemporal lobar degeneration with ubiquitinated tau-negative inclusions and additional alpha-synuclein pathology but also unusual cerebellar ubiquitinated p62-positive, TDP-43-negative inclusions
-
PID: 18715271
-
King A, Al-Sarraj S, Shaw C. Frontotemporal lobar degeneration with ubiquitinated tau-negative inclusions and additional alpha-synuclein pathology but also unusual cerebellar ubiquitinated p62-positive, TDP-43-negative inclusions. Neuropathology 2009;29:466-471.
-
(2009)
Neuropathology
, vol.29
, pp. 466-471
-
-
King, A.1
Al-Sarraj, S.2
Shaw, C.3
-
68
-
-
79957562827
-
Ubiquitinated, p62 immunopositive cerebellar cortical neuronal inclusions are evident across the spectrum of TDP-43 proteinopathies but are only rarely additionally immunopositive for phosphorylation-dependent TDP-43
-
PID: 21118398
-
King A, Maekawa S, Bodi I, Troakes C, Al-Sarraj S. Ubiquitinated, p62 immunopositive cerebellar cortical neuronal inclusions are evident across the spectrum of TDP-43 proteinopathies but are only rarely additionally immunopositive for phosphorylation-dependent TDP-43. Neuropathology 2011;31:239-249.
-
(2011)
Neuropathology
, vol.31
, pp. 239-249
-
-
King, A.1
Maekawa, S.2
Bodi, I.3
Troakes, C.4
Al-Sarraj, S.5
-
69
-
-
85005915306
-
Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72
-
PID: 24252525
-
Mann DM, Rollinson S, Robinson A, et al. Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72. Acta Neuropathol Commun 2013;1:68.
-
(2013)
Acta Neuropathol Commun
, vol.1
, pp. 68
-
-
Mann, D.M.1
Rollinson, S.2
Robinson, A.3
-
70
-
-
84892590289
-
Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS
-
COI: 1:CAS:528:DC%2BC3sXhs1ehtLbF, PID: 24129584
-
Gendron TF, Bieniek KF, Zhang YJ, et al. Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS. Acta Neuropathol 2013;126:829-844.
-
(2013)
Acta Neuropathol
, vol.126
, pp. 829-844
-
-
Gendron, T.F.1
Bieniek, K.F.2
Zhang, Y.J.3
-
71
-
-
84892585689
-
Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins
-
COI: 1:CAS:528:DC%2BC3sXhs1Kisb3K, PID: 24132570
-
Mori K, Arzberger T, Grasser FA, et al. Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins. Acta Neuropathol 2013;126:881-893.
-
(2013)
Acta Neuropathol
, vol.126
, pp. 881-893
-
-
Mori, K.1
Arzberger, T.2
Grasser, F.A.3
-
72
-
-
84903513101
-
Sequestration of multiple RNA Recognition Motif-containing proteins by C9ORF72 repeat expansions
-
PID: 24866055
-
Cooper-Knock J, Walsh MJ, Higginbottom A, et al. Sequestration of multiple RNA Recognition Motif-containing proteins by C9ORF72 repeat expansions. Brain 2014;137:2040-2051.
-
(2014)
Brain
, vol.137
, pp. 2040-2051
-
-
Cooper-Knock, J.1
Walsh, M.J.2
Higginbottom, A.3
-
73
-
-
84888098632
-
Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration
-
COI: 1:CAS:528:DC%2BC3sXhvFCisL3N, PID: 24170860
-
Lagier-Tourenne C, Baughn M, Rigo F, et al. Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration. Proc Natl Acad Sci U S A 2013;110:E4530-E4539.
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. E4530-E4539
-
-
Lagier-Tourenne, C.1
Baughn, M.2
Rigo, F.3
-
74
-
-
84892585908
-
C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci
-
COI: 1:CAS:528:DC%2BC3sXhs1yru73E, PID: 24170096
-
Mizielinska S, Lashley T, Norona FE, et al. C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci. Acta Neuropathol 2013;126:845-857.
-
(2013)
Acta Neuropathol
, vol.126
, pp. 845-857
-
-
Mizielinska, S.1
Lashley, T.2
Norona, F.E.3
-
75
-
-
84874246696
-
The product of C9orf72, a gene strongly implicated in neurodegeneration, is structurally related to DENN Rab-GEFs
-
COI: 1:CAS:528:DC%2BC3sXis1Ojsbk%3D, PID: 23329412
-
Levine TP, Daniels RD, Gatta AT, Wong LH, Hayes MJ. The product of C9orf72, a gene strongly implicated in neurodegeneration, is structurally related to DENN Rab-GEFs. Bioinformatics 2013;29:499-503.
-
(2013)
Bioinformatics
, vol.29
, pp. 499-503
-
-
Levine, T.P.1
Daniels, R.D.2
Gatta, A.T.3
Wong, L.H.4
Hayes, M.J.5
-
76
-
-
84901038797
-
C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal trafficking
-
COI: 1:CAS:528:DC%2BC2cXpvV2rs70%3D, PID: 24549040
-
Farg MA, Sundaramoorthy V, Sultana JM, et al. C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal trafficking. Hum Mol Genet 2014;23:3579-3595.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 3579-3595
-
-
Farg, M.A.1
Sundaramoorthy, V.2
Sultana, J.M.3
-
77
-
-
77956274512
-
Loss of ALS2/Alsin exacerbates motor dysfunction in a SOD1-expressing mouse ALS model by disturbing endolysosomal trafficking
-
PID: 20339559
-
Hadano S, Otomo A, Kunita R, et al. Loss of ALS2/Alsin exacerbates motor dysfunction in a SOD1-expressing mouse ALS model by disturbing endolysosomal trafficking. PLoS ONE 2010;5:e9805.
-
(2010)
PLoS ONE
, vol.5
, pp. e9805
-
-
Hadano, S.1
Otomo, A.2
Kunita, R.3
-
78
-
-
84888369415
-
The mouse C9ORF72 ortholog is enriched in neurons known to degenerate in ALS and FTD
-
COI: 1:CAS:528:DC%2BC3sXhslWjur%2FK, PID: 24185425
-
Suzuki N, Maroof AM, Merkle FT, et al. The mouse C9ORF72 ortholog is enriched in neurons known to degenerate in ALS and FTD. Nat Neurosci 2013;16:1725-1727.
-
(2013)
Nat Neurosci
, vol.16
, pp. 1725-1727
-
-
Suzuki, N.1
Maroof, A.M.2
Merkle, F.T.3
-
79
-
-
77649136250
-
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
-
PID: 20154673
-
Van Deerlin VM, Sleiman PM, Martinez-Lage M, et al. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nat Genet 2010;42:234-239.
-
(2010)
Nat Genet
, vol.42
, pp. 234-239
-
-
Van Deerlin, V.M.1
Sleiman, P.M.2
Martinez-Lage, M.3
-
80
-
-
84896738170
-
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions
-
COI: 1:CAS:528:DC%2BC2cXpvVCktw%3D%3D, PID: 24442578
-
Gallagher MD, Suh E, Grossman M, et al. TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions. Acta Neuropathol 2014;127:407-418.
-
(2014)
Acta Neuropathol
, vol.127
, pp. 407-418
-
-
Gallagher, M.D.1
Suh, E.2
Grossman, M.3
-
81
-
-
84883742170
-
TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia
-
COI: 1:CAS:528:DC%2BC3sXhtl2lt7%2FF, PID: 23742080
-
Nicholson AM, Finch NA, Wojtas A, et al. TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia. J Neurochem 2013;126:781-791.
-
(2013)
J Neurochem
, vol.126
, pp. 781-791
-
-
Nicholson, A.M.1
Finch, N.A.2
Wojtas, A.3
-
82
-
-
84896718565
-
TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia
-
PID: 24385136
-
van Blitterswijk M, Mullen B, Nicholson AM, et al. TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia. Acta Neuropathol 2014;127:397-406.
-
(2014)
Acta Neuropathol
, vol.127
, pp. 397-406
-
-
van Blitterswijk, M.1
Mullen, B.2
Nicholson, A.M.3
-
83
-
-
84903819005
-
Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers
-
van Blitterswijk M, Mullen B, Heckman MG, et al. Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers. Neurobiol Aging 2014;35:2421 e13-e17.
-
(2014)
Neurobiol Aging
, vol.35
, pp. 2421 e13-e17
-
-
van Blitterswijk, M.1
Mullen, B.2
Heckman, M.G.3
-
84
-
-
77956155218
-
Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS
-
COI: 1:CAS:528:DC%2BC3cXhtVOnurvF, PID: 20740007
-
Elden AC, Kim HJ, Hart MP, et al. Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS. Nature 2010;466:1069-1075.
-
(2010)
Nature
, vol.466
, pp. 1069-1075
-
-
Elden, A.C.1
Kim, H.J.2
Hart, M.P.3
-
85
-
-
84908320047
-
Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders
-
COI: 1:CAS:528:DC%2BC2cXhsFert7bE, PID: 25098532
-
Lattante S, Millecamps S, Stevanin G, et al. Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders. Neurology 2014;83:990-995.
-
(2014)
Neurology
, vol.83
, pp. 990-995
-
-
Lattante, S.1
Millecamps, S.2
Stevanin, G.3
-
86
-
-
84886389563
-
Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion
-
PID: 24154603
-
Sareen D, O'Rourke JG, Meera P, et al. Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion. Sci Transl Med 2013;5:208ra149.
-
(2013)
Sci Transl Med
, vol.5
, pp. 208ra149
-
-
Sareen, D.1
O'Rourke, J.G.2
Meera, P.3
-
87
-
-
84885808774
-
RNA Toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention
-
COI: 1:CAS:528:DC%2BC3sXhs1CrurfK, PID: 24139042
-
Donnelly CJ, Zhang PW, Pham JT, et al. RNA Toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention. Neuron 2013;80:415-428.
-
(2013)
Neuron
, vol.80
, pp. 415-428
-
-
Donnelly, C.J.1
Zhang, P.W.2
Pham, J.T.3
-
88
-
-
84890233174
-
Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic
-
COI: 1:CAS:528:DC%2BC3sXhvVKjtbjO, PID: 24290757
-
Lee YB, Chen HJ, Peres JN, et al. Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic. Cell Rep 2013;5:1178-1186.
-
(2013)
Cell Rep
, vol.5
, pp. 1178-1186
-
-
Lee, Y.B.1
Chen, H.J.2
Peres, J.N.3
-
89
-
-
84896259966
-
C9orf72 nucleotide repeat structures initiate molecular cascades of disease
-
COI: 1:CAS:528:DC%2BC2cXktV2rt7s%3D, PID: 24598541
-
Haeusler AR, Donnelly CJ, Periz G, et al. C9orf72 nucleotide repeat structures initiate molecular cascades of disease. Nature 2014;507:195-200.
-
(2014)
Nature
, vol.507
, pp. 195-200
-
-
Haeusler, A.R.1
Donnelly, C.J.2
Periz, G.3
-
90
-
-
84862202857
-
Cause or effect: misregulation of microRNA pathways in neurodegeneration
-
PID: 22509148
-
Gascon E, Gao FB. Cause or effect: misregulation of microRNA pathways in neurodegeneration. Front Neurosci 2012;6:48.
-
(2012)
Front Neurosci
, vol.6
, pp. 48
-
-
Gascon, E.1
Gao, F.B.2
-
91
-
-
84875981640
-
The disease-associated r(GGGGCC)n repeat from the C9orf72 gene forms tract length-dependent uni- and multimolecular RNA G-quadruplex structures
-
COI: 1:CAS:528:DC%2BC3sXlsVGitLo%3D, PID: 23423380
-
Reddy K, Zamiri B, Stanley SY, Macgregor RB, Jr., Pearson CE. The disease-associated r(GGGGCC)n repeat from the C9orf72 gene forms tract length-dependent uni- and multimolecular RNA G-quadruplex structures. J Biol Chem 2013;288:9860-9866.
-
(2013)
J Biol Chem
, vol.288
, pp. 9860-9866
-
-
Reddy, K.1
Zamiri, B.2
Stanley, S.Y.3
Macgregor, R.B.4
Pearson, C.E.5
-
92
-
-
84908027765
-
Discovery of a biomarker and lead small molecules to target r(GGGGCC)-associated defects in c9FTD/ALS
-
COI: 1:CAS:528:DC%2BC2cXhtlKmtbvM, PID: 25132468
-
Su Z, Zhang Y, Gendron TF, et al. Discovery of a biomarker and lead small molecules to target r(GGGGCC)-associated defects in c9FTD/ALS. Neuron 2014;83:1043-1050.
-
(2014)
Neuron
, vol.83
, pp. 1043-1050
-
-
Su, Z.1
Zhang, Y.2
Gendron, T.F.3
-
93
-
-
84874962380
-
The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS
-
COI: 1:CAS:528:DC%2BC3sXjvVaqtLw%3D, PID: 23393093
-
Mori K, Weng SM, Arzberger T, et al. The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS. Science 2013;339:1335-1338.
-
(2013)
Science
, vol.339
, pp. 1335-1338
-
-
Mori, K.1
Weng, S.M.2
Arzberger, T.3
-
94
-
-
78651105614
-
Non-ATG-initiated translation directed by microsatellite expansions
-
COI: 1:CAS:528:DC%2BC3MXms1Kiuw%3D%3D, PID: 21173221
-
Zu T, Gibbens B, Doty NS, et al. Non-ATG-initiated translation directed by microsatellite expansions. Proc Natl Acad Sci U S A 2011;108:260-265.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 260-265
-
-
Zu, T.1
Gibbens, B.2
Doty, N.S.3
-
95
-
-
84890837640
-
RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia
-
COI: 1:CAS:528:DC%2BC2cXnsV2gtg%3D%3D, PID: 24248382
-
Zu T, Liu Y, Banez-Coronel M, et al. RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia. Proc Natl Acad Sci U S A 2013;110:E4968-E4977.
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. E4968-E4977
-
-
Zu, T.1
Liu, Y.2
Banez-Coronel, M.3
-
96
-
-
84907221451
-
Poly-dipeptides encoded by the C9ORF72 repeats bind nucleoli, impede RNA biogenesis, and kill cells
-
COI: 1:CAS:528:DC%2BC2cXhsVGhtbzM, PID: 25081482
-
Kwon I, Xiang S, Kato M, et al. Poly-dipeptides encoded by the C9ORF72 repeats bind nucleoli, impede RNA biogenesis, and kill cells. Science 2014;345:1139-1145.
-
(2014)
Science
, vol.345
, pp. 1139-1145
-
-
Kwon, I.1
Xiang, S.2
Kato, M.3
-
97
-
-
84907188956
-
C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins
-
COI: 1:CAS:528:DC%2BC2cXhsVGhtb%2FI, PID: 25103406
-
Mizielinska S, Gronke S, Niccoli T, et al. C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins. Science 2014;345:1192-1194.
-
(2014)
Science
, vol.345
, pp. 1192-1194
-
-
Mizielinska, S.1
Gronke, S.2
Niccoli, T.3
-
98
-
-
84921640769
-
Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72
-
PID: 24950788
-
Davidson YS, Barker H, Robinson AC, et al. Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72. Acta Neuropathol Commun 2014;2:70.
-
(2014)
Acta Neuropathol Commun
, vol.2
, pp. 70
-
-
Davidson, Y.S.1
Barker, H.2
Robinson, A.C.3
-
99
-
-
84883292041
-
Stages of pTDP-43 pathology in amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BC3sXhtlKku7jE, PID: 23686809
-
Brettschneider J, Del Tredici K, Toledo JB, et al. Stages of pTDP-43 pathology in amyotrophic lateral sclerosis. Ann Neurol 2013;74:20-38.
-
(2013)
Ann Neurol
, vol.74
, pp. 20-38
-
-
Brettschneider, J.1
Del Tredici, K.2
Toledo, J.B.3
-
100
-
-
5444269465
-
Hypophosphorylated SR splicing factors transiently localize around active nucleolar organizing regions in telophase daughter nuclei
-
COI: 1:CAS:528:DC%2BD2cXosVOiu7w%3D, PID: 15479736
-
Bubulya PA, Prasanth KV, Deerinck TJ, et al. Hypophosphorylated SR splicing factors transiently localize around active nucleolar organizing regions in telophase daughter nuclei. J Cell Biol 2004;167:51-63.
-
(2004)
J Cell Biol
, vol.167
, pp. 51-63
-
-
Bubulya, P.A.1
Prasanth, K.V.2
Deerinck, T.J.3
-
101
-
-
0032032013
-
Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DyaK1cXit1GmsL4%3D, PID: 9539131
-
Lin CL, Bristol LA, Jin L, et al. Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis. Neuron 1998;20:589-602.
-
(1998)
Neuron
, vol.20
, pp. 589-602
-
-
Lin, C.L.1
Bristol, L.A.2
Jin, L.3
-
102
-
-
84930000577
-
C9orf72 FTLD/ALS-associated Gly-Ala dipeptide repeat proteins cause neuronal toxicity and Unc119 sequestration
-
COI: 1:CAS:528:DC%2BC2cXhtlKmt73I, PID: 25120191
-
May S, Hornburg D, Schludi MH, et al. C9orf72 FTLD/ALS-associated Gly-Ala dipeptide repeat proteins cause neuronal toxicity and Unc119 sequestration. Acta Neuropathol 2014;128:485-503.
-
(2014)
Acta Neuropathol
, vol.128
, pp. 485-503
-
-
May, S.1
Hornburg, D.2
Schludi, M.H.3
-
103
-
-
34249715853
-
Huntingtin interacting proteins are genetic modifiers of neurodegeneration
-
PID: 17500595
-
Kaltenbach LS, Romero E, Becklin RR, et al. Huntingtin interacting proteins are genetic modifiers of neurodegeneration. PLoS Genet 2007;3:e82.
-
(2007)
PLoS Genet
, vol.3
, pp. e82
-
-
Kaltenbach, L.S.1
Romero, E.2
Becklin, R.R.3
-
104
-
-
34249946466
-
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
-
COI: 1:CAS:528:DC%2BD2sXnsFKmtbc%3D, PID: 17469116
-
Mackenzie IR, Bigio EH, Ince PG, et al. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations. Ann Neurol 2007;61:427-434.
-
(2007)
Ann Neurol
, vol.61
, pp. 427-434
-
-
Mackenzie, I.R.1
Bigio, E.H.2
Ince, P.G.3
-
105
-
-
84921721593
-
Decoding the pathophysiological mechanisms that underlie RNA dysregulation in neurodegenerative disorders: a review of the current state of the art
-
Walsh MJ, Cooper-Knock J, Dodd JE, et al. Decoding the pathophysiological mechanisms that underlie RNA dysregulation in neurodegenerative disorders: a review of the current state of the art. Neuropathol Appl Neurobiol 2014;41:109-134.
-
(2014)
Neuropathol Appl Neurobiol
, vol.41
, pp. 109-134
-
-
Walsh, M.J.1
Cooper-Knock, J.2
Dodd, J.E.3
-
106
-
-
85056706559
-
Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion
-
Waite AJ, Baumer D, East S, et al. Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion. Neurobiol Aging 2014;35:1779 e5-e79 e13.
-
(2014)
Neurobiol Aging
, vol.35
, pp. 1779 e5-e79 e13
-
-
Waite, A.J.1
Baumer, D.2
East, S.3
-
107
-
-
84888223043
-
C9orf72 transcripton in a frontotemportal dementia case with two expanded alleles
-
PID: 24107864
-
Cooper-Knock J, Higginbottom A, Connor-Robson N, et al. C9orf72 transcripton in a frontotemportal dementia case with two expanded alleles. Neurology 2013;81:1719-1721.
-
(2013)
Neurology
, vol.81
, pp. 1719-1721
-
-
Cooper-Knock, J.1
Higginbottom, A.2
Connor-Robson, N.3
-
108
-
-
84911382953
-
Hypermethylation of the CpG-island near the C9orf72 G4C2-repeat expansion in FTLD patients
-
PID: 24908669
-
Xi Z, Rainero I, Rubino E, et al. Hypermethylation of the CpG-island near the C9orf72 G4C2-repeat expansion in FTLD patients. Hum Mol Genet 2014;23:5630-5637.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 5630-5637
-
-
Xi, Z.1
Rainero, I.2
Rubino, E.3
-
109
-
-
84878863605
-
Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion
-
COI: 1:CAS:528:DC%2BC3sXotlCqurY%3D, PID: 23731538
-
Xi Z, Zinman L, Moreno D, et al. Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion. Am J Hum Genet 2013;92:981-989.
-
(2013)
Am J Hum Genet
, vol.92
, pp. 981-989
-
-
Xi, Z.1
Zinman, L.2
Moreno, D.3
-
110
-
-
84873676245
-
C9ORF72 hexanucleotide expansions of 20–22 repeats are associated with frontotemporal deterioration
-
COI: 1:CAS:528:DC%2BC3sXhsFSnu7w%3D, PID: 23284068
-
Gomez-Tortosa E, Gallego J, Guerrero-Lopez R, et al. C9ORF72 hexanucleotide expansions of 20–22 repeats are associated with frontotemporal deterioration. Neurology 2013;80:366-370.
-
(2013)
Neurology
, vol.80
, pp. 366-370
-
-
Gomez-Tortosa, E.1
Gallego, J.2
Guerrero-Lopez, R.3
-
111
-
-
84894637352
-
Intermediate repeat expansion length in C9orf72 may be pathological in amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BC2cXjs1Khu7g%3D, PID: 24053774
-
Byrne S, Heverin M, Elamin M, Walsh C, Hardiman O. Intermediate repeat expansion length in C9orf72 may be pathological in amyotrophic lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener 2014;15:148-150.
-
(2014)
Amyotroph Lateral Scler Frontotemporal Degener
, vol.15
, pp. 148-150
-
-
Byrne, S.1
Heverin, M.2
Elamin, M.3
Walsh, C.4
Hardiman, O.5
-
112
-
-
84939886575
-
C9orf72 hypermethylation protects against repeat expansion-associated pathology in ALS/FTD
-
COI: 1:CAS:528:DC%2BC2cXnvVSrtr8%3D, PID: 24806409
-
Liu EY, Russ J, Wu K, et al. C9orf72 hypermethylation protects against repeat expansion-associated pathology in ALS/FTD. Acta Neuropathol 2014;128:525-541.
-
(2014)
Acta Neuropathol
, vol.128
, pp. 525-541
-
-
Liu, E.Y.1
Russ, J.2
Wu, K.3
-
113
-
-
84892596606
-
Reduced C9orf72 gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood
-
COI: 1:CAS:528:DC%2BC3sXhs1yrt7jM, PID: 24166615
-
Belzil VV, Bauer PO, Prudencio M, et al. Reduced C9orf72 gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood. Acta Neuropathol 2013;126:895-905.
-
(2013)
Acta Neuropathol
, vol.126
, pp. 895-905
-
-
Belzil, V.V.1
Bauer, P.O.2
Prudencio, M.3
-
114
-
-
33746795976
-
DNA sequence-specific polyamides alleviate transcription inhibition associated with long GAA.TTC repeats in Friedreich's ataxia
-
COI: 1:CAS:528:DC%2BD28XotFegtLc%3D, PID: 16857735
-
Burnett R, Melander C, Puckett JW, et al. DNA sequence-specific polyamides alleviate transcription inhibition associated with long GAA.TTC repeats in Friedreich's ataxia. Proc Natl Acad Sci U S A 2006;103:11497-11502.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 11497-11502
-
-
Burnett, R.1
Melander, C.2
Puckett, J.W.3
-
115
-
-
46149111652
-
Influence of Friedreich ataxia GAA noncoding repeat expansions on pre-mRNA processing
-
COI: 1:CAS:528:DC%2BD1cXos1Cisrg%3D, PID: 18597733
-
Baralle M, Pastor T, Bussani E, Pagani F. Influence of Friedreich ataxia GAA noncoding repeat expansions on pre-mRNA processing. Am J Hum Genet 2008;83:77-88.
-
(2008)
Am J Hum Genet
, vol.83
, pp. 77-88
-
-
Baralle, M.1
Pastor, T.2
Bussani, E.3
Pagani, F.4
-
116
-
-
84883460229
-
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia
-
COI: 1:CAS:528:DC%2BC3sXhtlyjtrjM, PID: 23818065
-
Fratta P, Poulter M, Lashley T, et al. Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia. Acta Neuropathol 2013;126:401-409.
-
(2013)
Acta Neuropathol
, vol.126
, pp. 401-409
-
-
Fratta, P.1
Poulter, M.2
Lashley, T.3
-
117
-
-
84875840045
-
Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisation
-
COI: 1:CAS:528:DC%2BC3sXnvVCjtbo%3D, PID: 23566336
-
Buchman VL, Cooper-Knock J, Connor-Robson N, et al. Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisation. Mol Neurodegener 2013;8:12.
-
(2013)
Mol Neurodegener
, vol.8
, pp. 12
-
-
Buchman, V.L.1
Cooper-Knock, J.2
Connor-Robson, N.3
-
118
-
-
84884163243
-
Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study
-
PID: 24011653
-
van Blitterswijk M, DeJesus-Hernandez M, Niemantsverdriet E, et al. Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study. Lancet Neurol 2013;12:978-988.
-
(2013)
Lancet Neurol
, vol.12
, pp. 978-988
-
-
van Blitterswijk, M.1
DeJesus-Hernandez, M.2
Niemantsverdriet, E.3
-
119
-
-
84892451456
-
Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia
-
COI: 1:CAS:528:DC%2BC2cXlvFeluw%3D%3D, PID: 24057670
-
Dols-Icardo O, Garcia-Redondo A, Rojas-Garcia R, et al. Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia. Hum Mol Genet 2014;23:749-754.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 749-754
-
-
Dols-Icardo, O.1
Garcia-Redondo, A.2
Rojas-Garcia, R.3
-
120
-
-
33845652267
-
The GAA triplet-repeat is unstable in the context of the human FXN locus and displays age-dependent expansions in cerebellum and DRG in a transgenic mouse model
-
COI: 1:CAS:528:DC%2BD28XhtlCjtrjE, PID: 17024371
-
Clark RM, De Biase I, Malykhina AP, Al-Mahdawi S, Pook M, Bidichandani SI. The GAA triplet-repeat is unstable in the context of the human FXN locus and displays age-dependent expansions in cerebellum and DRG in a transgenic mouse model. Hum Genet 2007;120:633-640.
-
(2007)
Hum Genet
, vol.120
, pp. 633-640
-
-
Clark, R.M.1
De Biase, I.2
Malykhina, A.P.3
Al-Mahdawi, S.4
Pook, M.5
Bidichandani, S.I.6
-
121
-
-
84890464112
-
C9ORF72 Hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype–phenotype correlation study
-
COI: 1:CAS:528:DC%2BC3sXhvV2iu77F, PID: 24064469
-
Benussi L, Rossi G, Glionna M, et al. C9ORF72 Hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype–phenotype correlation study. J Alzheimers Dis 2014;38:799-808.
-
(2014)
J Alzheimers Dis
, vol.38
, pp. 799-808
-
-
Benussi, L.1
Rossi, G.2
Glionna, M.3
-
122
-
-
84873093810
-
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats
-
PID: 23111906
-
van der Zee J, Gijselinck I, Dillen L, et al. A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats. Hum Mutat 2013;34:363-373.
-
(2013)
Hum Mutat
, vol.34
, pp. 363-373
-
-
van der Zee, J.1
Gijselinck, I.2
Dillen, L.3
-
123
-
-
84940008935
-
-
Beer AM, Cooper-Knock J, Higginbottom A, et al. Intermediate length C9orf72 expansion in an ALS patient without classical C9orf72 neuropathology. Amyotroph Lateral Scler Frontotemporal Degener 2014 Dec 1 [Epub ahead of print]
-
Beer AM, Cooper-Knock J, Higginbottom A, et al. Intermediate length C9orf72 expansion in an ALS patient without classical C9orf72 neuropathology. Amyotroph Lateral Scler Frontotemporal Degener 2014 Dec 1 [Epub ahead of print].
-
-
-
-
124
-
-
84901475610
-
A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
-
COI: 1:CAS:528:DC%2BC2cXhtFyns7rM, PID: 24706941
-
Akimoto C, Volk AE, van Blitterswijk M, et al. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories. J Med Genet 2014;51:419-424.
-
(2014)
J Med Genet
, vol.51
, pp. 419-424
-
-
Akimoto, C.1
Volk, A.E.2
van Blitterswijk, M.3
-
125
-
-
84863596527
-
Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion
-
COI: 1:CAS:528:DC%2BC38Xht1GnsrnK, PID: 22808918
-
Fong JC, Karydas AM, Goldman JS, et al. Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion. Alzheimers Res Ther 2012;4:27.
-
(2012)
Alzheimers Res Ther
, vol.4
, pp. 27
-
-
Fong, J.C.1
Karydas, A.M.2
Goldman, J.S.3
-
126
-
-
84898847400
-
Genetic counselling in ALS: facts, uncertainties and clinical suggestions
-
PID: 23833266
-
Chio A, Battistini S, Calvo A, et al. Genetic counselling in ALS: facts, uncertainties and clinical suggestions. J Neurol Neurosurg Psychiatry 2014;85:478-485.
-
(2014)
J Neurol Neurosurg Psychiatry
, vol.85
, pp. 478-485
-
-
Chio, A.1
Battistini, S.2
Calvo, A.3
-
127
-
-
84868152371
-
Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs
-
COI: 1:CAS:528:DC%2BC38XhsVaqt7fF, PID: 23023293
-
Lagier-Tourenne C, Polymenidou M, Hutt KR, et al. Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs. Nat Neurosci 2012;15:1488-1497.
-
(2012)
Nat Neurosci
, vol.15
, pp. 1488-1497
-
-
Lagier-Tourenne, C.1
Polymenidou, M.2
Hutt, K.R.3
-
128
-
-
84870572714
-
Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models
-
COI: 1:CAS:528:DC%2BC38XhsFOmt7jI, PID: 23104007
-
Armakola M, Higgins MJ, Figley MD, et al. Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models. Nat Genet 2012;44:1302-1309.
-
(2012)
Nat Genet
, vol.44
, pp. 1302-1309
-
-
Armakola, M.1
Higgins, M.J.2
Figley, M.D.3
-
129
-
-
80755163102
-
Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BC3MXhsVahur3O, PID: 22051914
-
Ferraiuolo L, Kirby J, Grierson AJ, Sendtner M, Shaw PJ. Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis. Nat Rev Neurol 2011;7:616-630.
-
(2011)
Nat Rev Neurol
, vol.7
, pp. 616-630
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-
Ferraiuolo, L.1
Kirby, J.2
Grierson, A.J.3
Sendtner, M.4
Shaw, P.J.5
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