-
1
-
-
77954122221
-
Genome-wide association studies: the key to unlocking neurodegeneration?
-
COI: 1:CAS:528:DC%2BC3cXnvFSnsLw%3D, PID: 20581814
-
Gandhi S, Wood NW (2010) Genome-wide association studies: the key to unlocking neurodegeneration? Nat Neurosci 13:789–794. doi:10.1038/nn.2584
-
(2010)
Nat Neurosci
, vol.13
, pp. 789-794
-
-
Gandhi, S.1
Wood, N.W.2
-
2
-
-
84980053612
-
Pathways to neurodegeneration: mechanistic insights from GWAS in Alzheimer’s disease, Parkinson’s disease, and related disorders
-
PID: 24093081
-
Ramanan VK, Saykin AJ (2013) Pathways to neurodegeneration: mechanistic insights from GWAS in Alzheimer’s disease, Parkinson’s disease, and related disorders. Am J Neurodegener Dis 2:145–175
-
(2013)
Am J Neurodegener Dis
, vol.2
, pp. 145-175
-
-
Ramanan, V.K.1
Saykin, A.J.2
-
3
-
-
84866121057
-
For Alzheimer disease GWAS, pulling needles from the haystack is just the first step
-
PID: 22722635
-
Swerdlow RH, Corder EH (2012) For Alzheimer disease GWAS, pulling needles from the haystack is just the first step. Neurology 79:204–205. doi:10.1212/WNL.0b013e318260581d
-
(2012)
Neurology
, vol.79
, pp. 204-205
-
-
Swerdlow, R.H.1
Corder, E.H.2
-
4
-
-
0037062609
-
The prevalence of frontotemporal dementia
-
COI: 1:STN:280:DC%2BD38zhsFWguw%3D%3D, PID: 12058088
-
Ratnavalli E, Brayne C, Dawson K, Hodges JR (2002) The prevalence of frontotemporal dementia. Neurology 58:1615–1621
-
(2002)
Neurology
, vol.58
, pp. 1615-1621
-
-
Ratnavalli, E.1
Brayne, C.2
Dawson, K.3
Hodges, J.R.4
-
5
-
-
33645078169
-
Comparison of family histories in FTLD subtypes and related tauopathies
-
COI: 1:STN:280:DC%2BD2Mnmt1Gmtg%3D%3D, PID: 16344531
-
Goldman JS, Farmer JM, Wood EM et al (2005) Comparison of family histories in FTLD subtypes and related tauopathies. Neurology 65:1817–1819
-
(2005)
Neurology
, vol.65
, pp. 1817-1819
-
-
Goldman, J.S.1
Farmer, J.M.2
Wood, E.M.3
-
6
-
-
0041320789
-
Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study
-
PID: 12876142
-
Rosso SM, Kaat LD, Baks T et al (2003) Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study. Brain 126:2016–2022. doi:10.1093/brain/awg204
-
(2003)
Brain
, vol.126
, pp. 2016-2022
-
-
Rosso, S.M.1
Kaat, L.D.2
Baks, T.3
-
7
-
-
70449365115
-
The heritability and genetics of frontotemporal lobar degeneration
-
COI: 1:CAS:528:DC%2BD1MXhtlCmsrjP, PID: 19884572
-
Rohrer JD, Guerreiro R, Vandrovcova J et al (2009) The heritability and genetics of frontotemporal lobar degeneration. Neurology 73:1451–1456. doi:10.1212/WNL.0b013e3181bf997a
-
(2009)
Neurology
, vol.73
, pp. 1451-1456
-
-
Rohrer, J.D.1
Guerreiro, R.2
Vandrovcova, J.3
-
8
-
-
33750601024
-
Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementia
-
PID: 17071924
-
Le Ber I, Guedj E, Gabelle A et al (2006) Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementia. Brain 129:3051–3065
-
(2006)
Brain
, vol.129
, pp. 3051-3065
-
-
Le Ber, I.1
Guedj, E.2
Gabelle, A.3
-
9
-
-
84896697357
-
The neuropathology associated with repeat expansions in the C9ORF72 gene
-
COI: 1:CAS:528:DC%2BC3sXitVWjtLvO, PID: 24356984
-
Mackenzie IRA, Frick P, Neumann M (2014) The neuropathology associated with repeat expansions in the C9ORF72 gene. Acta Neuropathol 127:347–357. doi:10.1007/s00401-013-1232-4
-
(2014)
Acta Neuropathol
, vol.127
, pp. 347-357
-
-
Mackenzie, I.R.A.1
Frick, P.2
Neumann, M.3
-
10
-
-
84865862939
-
The genetics and neuropathology of frontotemporal lobar degeneration
-
COI: 1:CAS:528:DC%2BC38Xht1egt7vE, PID: 22890575
-
Sieben A, Van Langenhove T, Engelborghs S et al (2012) The genetics and neuropathology of frontotemporal lobar degeneration. Acta Neuropathol 124:353–372. doi:10.1007/s00401-012-1029-x
-
(2012)
Acta Neuropathol
, vol.124
, pp. 353-372
-
-
Sieben, A.1
Van Langenhove, T.2
Engelborghs, S.3
-
11
-
-
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 (2011) Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72:245–256. doi:10.1016/j.neuron.2011.09.011
-
(2011)
Neuron
, vol.72
, pp. 245-256
-
-
DeJesus-Hernandez, M.1
Mackenzie, I.R.2
Boeve, B.F.3
-
12
-
-
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 (2011) A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 72:257–268. doi:10.1016/j.neuron.2011.09.010
-
(2011)
Neuron
, vol.72
, pp. 257-268
-
-
Renton, A.E.1
Majounie, E.2
Waite, A.3
-
13
-
-
84861488289
-
Early onset Alzheimer’s disease is associated with a distinct neuropsychological profile
-
PID: 22366769
-
Smits LL, Pijnenburg YAL, Koedam ELGE et al (2012) Early onset Alzheimer’s disease is associated with a distinct neuropsychological profile. J Alzheimers Dis 30:101–108. doi:10.3233/JAD-2012-111934
-
(2012)
J Alzheimers Dis
, vol.30
, pp. 101-108
-
-
Smits, L.L.1
Pijnenburg, Y.A.L.2
Koedam, E.L.G.E.3
-
14
-
-
80052938441
-
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
-
PID: 21810890
-
Rascovsky K, Hodges JR, Knopman D et al (2011) Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain 134:2456–2477. doi:10.1093/brain/awr179
-
(2011)
Brain
, vol.134
, pp. 2456-2477
-
-
Rascovsky, K.1
Hodges, J.R.2
Knopman, D.3
-
15
-
-
79952823979
-
Classification of primary progressive aphasia and its variants
-
PID: 21325651
-
Gorno-Tempini ML, Hillis AE, Weintraub S et al (2011) Classification of primary progressive aphasia and its variants. Neurology 76:1006–1014
-
(2011)
Neurology
, vol.76
, pp. 1006-1014
-
-
Gorno-Tempini, M.L.1
Hillis, A.E.2
Weintraub, S.3
-
16
-
-
67651160559
-
Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis
-
PID: 19462523
-
Strong MJ, Grace GM, Freedman M et al (2009) Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis. Amyotroph Lateral Scler 10:131–146
-
(2009)
Amyotroph Lateral Scler
, vol.10
, pp. 131-146
-
-
Strong, M.J.1
Grace, G.M.2
Freedman, M.3
-
17
-
-
0021271971
-
Clinical diagnosis of Alzheimer’s disease: report of the NINCDS-ADRDA Work Group* under the auspices of Department of Health and Human Services Task Force on Alzheimer’s Disease
-
COI: 1:STN:280:DyaL2c3ks1altQ%3D%3D, PID: 6610841
-
McKhann G, Drachman D, Folstein M et al (1984) Clinical diagnosis of Alzheimer’s disease: report of the NINCDS-ADRDA Work Group* under the auspices of Department of Health and Human Services Task Force on Alzheimer’s Disease. Neurology 34:939
-
(1984)
Neurology
, vol.34
, pp. 939
-
-
McKhann, G.1
Drachman, D.2
Folstein, M.3
-
18
-
-
84857997213
-
Diagnostic criteria for corticobasal syndrome: a comparative study
-
PID: 22019546
-
Mathew R, Bak TH, Hodges JR (2012) Diagnostic criteria for corticobasal syndrome: a comparative study. J Neurol Neurosurg Psychiatr 83:405–410. doi:10.1136/jnnp-2011-300875
-
(2012)
J Neurol Neurosurg Psychiatr
, vol.83
, pp. 405-410
-
-
Mathew, R.1
Bak, T.H.2
Hodges, J.R.3
-
19
-
-
84875939750
-
Clinical profile of PiB-positive corticobasal syndrome
-
COI: 1:CAS:528:DC%2BC3sXmtlSgtbk%3D, PID: 23577184
-
Burrell JR, Hornberger M, Villemagne VL et al (2013) Clinical profile of PiB-positive corticobasal syndrome. PLoS One 8:e61025. doi:10.1371/journal.pone.0061025
-
(2013)
PLoS One
, vol.8
, pp. e61025
-
-
Burrell, J.R.1
Hornberger, M.2
Villemagne, V.L.3
-
20
-
-
84866093352
-
C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts
-
PID: 22875086
-
Dobson-Stone C, Hallupp M, Bartley L et al (2012) C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts. Neurology 79:995–1001. doi:10.1212/WNL.0b013e3182684634
-
(2012)
Neurology
, vol.79
, pp. 995-1001
-
-
Dobson-Stone, C.1
Hallupp, M.2
Bartley, L.3
-
21
-
-
84896781404
-
Frontotemporal dementia associated with the C9ORF72 mutation: a unique clinical profile
-
PID: 24445580
-
Devenney E, Hornberger M, Irish M et al (2014) Frontotemporal dementia associated with the C9ORF72 mutation: a unique clinical profile. JAMA Neurol 71:331–339. doi:10.1001/jamaneurol.2013.6002
-
(2014)
JAMA Neurol
, vol.71
, pp. 331-339
-
-
Devenney, E.1
Hornberger, M.2
Irish, M.3
-
22
-
-
84857517997
-
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features
-
PID: 22366791
-
Mahoney CJ, Beck J, Rohrer JD et al (2012) Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features. Brain 135:736–750. doi:10.1093/brain/awr361
-
(2012)
Brain
, vol.135
, pp. 736-750
-
-
Mahoney, C.J.1
Beck, J.2
Rohrer, J.D.3
-
23
-
-
84888875780
-
Development and validation of pedigree classification criteria for frontotemporal lobar degeneration
-
PID: 24081456
-
Wood EM, Falcone D, Suh E et al (2013) Development and validation of pedigree classification criteria for frontotemporal lobar degeneration. JAMA Neurol 70:1411–1417. doi:10.1001/jamaneurol.2013.3956
-
(2013)
JAMA Neurol
, vol.70
, pp. 1411-1417
-
-
Wood, E.M.1
Falcone, D.2
Suh, E.3
-
24
-
-
84867543551
-
SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
PID: 22972638
-
Rubino E, Rainero I, Chiò A et al (2012) SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Neurology 79:1556–1562. doi:10.1212/WNL.0b013e31826e25df
-
(2012)
Neurology
, vol.79
, pp. 1556-1562
-
-
Rubino, E.1
Rainero, I.2
Chiò, A.3
-
25
-
-
84906313820
-
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
-
Van der Zee J, Van Langenhove T, Kovacs GG et al (2014) Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration. Acta Neuropathol. doi:10.1007/s00401-014-1298-7
-
(2014)
Acta Neuropathol
-
-
Van der Zee, J.1
Van Langenhove, T.2
Kovacs, G.G.3
-
26
-
-
84874303411
-
C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing
-
PID: 23254636
-
Le Ber I, Camuzat A, Guillot-Noel L et al (2013) C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing. J Alzheimers Dis 34:485–499. doi:10.3233/JAD-121456
-
(2013)
J Alzheimers Dis
, vol.34
, pp. 485-499
-
-
Le Ber, I.1
Camuzat, A.2
Guillot-Noel, L.3
-
27
-
-
84863393065
-
Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
-
PID: 22300873
-
Snowden JS, Rollinson S, Thompson JC et al (2012) Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations. Brain 135:693–708. doi:10.1093/brain/awr355
-
(2012)
Brain
, vol.135
, pp. 693-708
-
-
Snowden, J.S.1
Rollinson, S.2
Thompson, J.C.3
-
28
-
-
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 (2012) Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. Lancet Neurol 11:323–330. doi:10.1016/S1474-4422(12)70043-1
-
(2012)
Lancet Neurol
, vol.11
, pp. 323-330
-
-
Majounie, E.1
Renton, A.E.2
Mok, K.3
-
29
-
-
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 (2012) Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72. Brain 135:765–783. doi:10.1093/brain/aws004
-
(2012)
Brain
, vol.135
, pp. 765-783
-
-
Boeve, B.F.1
Boylan, K.B.2
Graff-Radford, N.R.3
-
30
-
-
33746910649
-
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
-
COI: 1:CAS:528:DC%2BD28XosVOgu74%3D, PID: 16862115
-
Cruts M, Gijselinck I, van der Zee J et al (2006) Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 442:920–924. doi:10.1038/nature05017
-
(2006)
Nature
, vol.442
, pp. 920-924
-
-
Cruts, M.1
Gijselinck, I.2
van der Zee, J.3
-
31
-
-
33749568019
-
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
-
COI: 1:CAS:528:DC%2BD28XhtVOgt77J, PID: 16950801
-
Gass J, Cannon A, Mackenzie IR et al (2006) Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. Hum Mol Genet 15:2988–3001. doi:10.1093/hmg/ddl241
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2988-3001
-
-
Gass, J.1
Cannon, A.2
Mackenzie, I.R.3
-
32
-
-
39749187585
-
Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations
-
PID: 18192287
-
Pickering-Brown SM, Rollinson S, Du Plessis D et al (2008) Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations. Brain 131:721–731. doi:10.1093/brain/awm331
-
(2008)
Brain
, vol.131
, pp. 721-731
-
-
Pickering-Brown, S.M.1
Rollinson, S.2
Du Plessis, D.3
-
33
-
-
79951722994
-
Early-onset versus late-onset Alzheimer’s disease: the case of the missing APOE ɛ4 allele
-
PID: 21185234
-
Van der Flier WM, Pijnenburg YA, Fox NC, Scheltens P (2011) Early-onset versus late-onset Alzheimer’s disease: the case of the missing APOE ɛ4 allele. Lancet Neurol 10:280–288. doi:10.1016/S1474-4422(10)70306-9
-
(2011)
Lancet Neurol
, vol.10
, pp. 280-288
-
-
Van der Flier, W.M.1
Pijnenburg, Y.A.2
Fox, N.C.3
Scheltens, P.4
-
34
-
-
77951694945
-
Correlating familial Alzheimer’s disease gene mutations with clinical phenotype
-
COI: 1:CAS:528:DC%2BC3cXhsFCnurg%3D, PID: 20387306
-
Ryan NS, Rossor MN (2010) Correlating familial Alzheimer’s disease gene mutations with clinical phenotype. Biomark Med 4:99–112. doi:10.2217/bmm.09.92
-
(2010)
Biomark Med
, vol.4
, pp. 99-112
-
-
Ryan, N.S.1
Rossor, M.N.2
-
35
-
-
32844465332
-
Clinical phenotypic heterogeneity of Alzheimer’s disease associated with mutations of the presenilin-1 gene
-
COI: 1:CAS:528:DC%2BD28XjtFegtb8%3D, PID: 16267640
-
Larner AJ, Doran M (2006) Clinical phenotypic heterogeneity of Alzheimer’s disease associated with mutations of the presenilin-1 gene. J Neurol 253:139–158. doi:10.1007/s00415-005-0019-5
-
(2006)
J Neurol
, vol.253
, pp. 139-158
-
-
Larner, A.J.1
Doran, M.2
-
36
-
-
8644276394
-
A presenilin 1 R278I mutation presenting with language impairment
-
COI: 1:STN:280:DC%2BD2crmt1ensQ%3D%3D, PID: 15534260
-
Godbolt AK, Beck JA, Collinge J et al (2004) A presenilin 1 R278I mutation presenting with language impairment. Neurology 63:1702–1704
-
(2004)
Neurology
, vol.63
, pp. 1702-1704
-
-
Godbolt, A.K.1
Beck, J.A.2
Collinge, J.3
-
37
-
-
84888235194
-
C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
-
PID: 24027057
-
Van Blitterswijk M, Baker MC, DeJesus-Hernandez M et al (2013) C9ORF72 repeat expansions in cases with previously identified pathogenic mutations. Neurology 81:1332–1341. doi:10.1212/WNL.0b013e3182a8250c
-
(2013)
Neurology
, vol.81
, pp. 1332-1341
-
-
Van Blitterswijk, M.1
Baker, M.C.2
DeJesus-Hernandez, M.3
|