-
1
-
-
33846225133
-
Huntington's disease
-
Walker FO. Huntington's disease. Lancet 2007;369:218-228.
-
(2007)
Lancet
, vol.369
, pp. 218-228
-
-
Walker, F.O.1
-
2
-
-
84855922033
-
Pharmacologic approaches to the treatment of Huntington's disease
-
Venuto CS, McGarry A, Ma Q, Kieburtz K. Pharmacologic approaches to the treatment of Huntington's disease. Mov Disord 2012;27:31-41.
-
(2012)
Mov Disord
, vol.27
, pp. 31-41
-
-
Venuto, C.S.1
McGarry, A.2
Ma, Q.3
Kieburtz, K.4
-
3
-
-
84898017417
-
Huntington disease: natural history, biomarkers and prospects for therapeutics
-
Ross CA, Aylward EH, Wild EJ, et al. Huntington disease: natural history, biomarkers and prospects for therapeutics. Nat Rev Neurol 2014;10:204-216.
-
(2014)
Nat Rev Neurol
, vol.10
, pp. 204-216
-
-
Ross, C.A.1
Aylward, E.H.2
Wild, E.J.3
-
5
-
-
81255195330
-
Pridopidine for the treatment of motor function in patients with Huntington's disease (MermaiHD): a phase 3, randomised, double-blind, placebo-controlled trial
-
de Yebenes JG, Landwehrmeyer B, Squitieri F, et al. Pridopidine for the treatment of motor function in patients with Huntington's disease (MermaiHD): a phase 3, randomised, double-blind, placebo-controlled trial. Lancet Neurol 2011;10:1049-1057.
-
(2011)
Lancet Neurol
, vol.10
, pp. 1049-1057
-
-
de Yebenes, J.G.1
Landwehrmeyer, B.2
Squitieri, F.3
-
6
-
-
84884724757
-
A randomized, double-blind, placebo-controlled trial of pridopidine in Huntington's disease
-
The Huntington Study Group HI. A randomized, double-blind, placebo-controlled trial of pridopidine in Huntington's disease. Mov Disord 2013;28:1407-1415.
-
(2013)
Mov Disord
, vol.28
, pp. 1407-1415
-
-
-
7
-
-
84884720110
-
The pridopidine paradox in Huntington's disease
-
Reilmann R. The pridopidine paradox in Huntington's disease. Mov Disord 2013;28:1321-1324.
-
(2013)
Mov Disord
, vol.28
, pp. 1321-1324
-
-
Reilmann, R.1
-
8
-
-
78650026297
-
Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis
-
Tabrizi SJ, Scahill RI, Durr A, et al. Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis. Lancet Neurol 2011;10:31-42.
-
(2011)
Lancet Neurol
, vol.10
, pp. 31-42
-
-
Tabrizi, S.J.1
Scahill, R.I.2
Durr, A.3
-
9
-
-
68249113963
-
Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data
-
Tabrizi SJ, Langbehn DR, Leavitt BR, et al. Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data. Lancet Neurol 2009;8:791-801.
-
(2009)
Lancet Neurol
, vol.8
, pp. 791-801
-
-
Tabrizi, S.J.1
Langbehn, D.R.2
Leavitt, B.R.3
-
10
-
-
78650850960
-
Tapping linked to function and structure in premanifest and symptomatic Huntington disease
-
Bechtel N, Scahill RI, Rosas HD, et al. Tapping linked to function and structure in premanifest and symptomatic Huntington disease. Neurology 2010;75:2150-2160.
-
(2010)
Neurology
, vol.75
, pp. 2150-2160
-
-
Bechtel, N.1
Scahill, R.I.2
Rosas, H.D.3
-
11
-
-
84879032355
-
Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational data
-
Tabrizi SJ, Scahill RI, Owen G, et al. Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational data. Lancet Neurol 2013;12:637-649.
-
(2013)
Lancet Neurol
, vol.12
, pp. 637-649
-
-
Tabrizi, S.J.1
Scahill, R.I.2
Owen, G.3
-
12
-
-
84893636639
-
A 5-year follow-up of deep brain stimulation in Huntington's disease
-
López-Sendón Moreno JL, García-Caldentey J, Regidor I, del Álamo M, García de Yébenes J. A 5-year follow-up of deep brain stimulation in Huntington's disease. Parkinsonism Relat Disord 2014;20:260-261.
-
(2014)
Parkinsonism Relat Disord
, vol.20
, pp. 260-261
-
-
López-Sendón Moreno, J.L.1
García-Caldentey, J.2
Regidor, I.3
del Álamo, M.4
García5
Yébenes, J.6
-
13
-
-
84903892559
-
Deep brain stimulation for Huntington's disease: long-term results of a prospective open-label study
-
Gonzalez V, Cif L, Biolsi B, et al. Deep brain stimulation for Huntington's disease: long-term results of a prospective open-label study. J Neurosurg 2014;121:114-122.
-
(2014)
J Neurosurg
, vol.121
, pp. 114-122
-
-
Gonzalez, V.1
Cif, L.2
Biolsi, B.3
-
14
-
-
84907928730
-
-
Overview of device regulation. Available at:
-
U.S. Food and Drug Administration. Overview of device regulation. 2014. Available at: http://wwwfdagov/MedicalDevices/DeviceRegulationandGuidance/Overview/defaulthtm.
-
(2014)
-
-
-
15
-
-
84907928729
-
-
A prospective pilot trial for pallidal deep brain stimulation in Huntington's disease
-
Vesper J. A prospective pilot trial for pallidal deep brain stimulation in Huntington's disease. 2014. http://chdifoundationorg/2014-conference/.
-
(2014)
-
-
Vesper, J.1
-
16
-
-
84892153139
-
Clinical development success rates for investigational drugs
-
Rosenthal MH, David WT, John LC, Celia E, Jesse . Clinical development success rates for investigational drugs. Nat Biotechnol 2014;32:40-51.
-
(2014)
Nat Biotechnol
, vol.32
, pp. 40-51
-
-
Rosenthal, M.H.1
David, W.T.2
John, L.C.3
Celia, E.4
Jesse5
-
17
-
-
84860690620
-
Can the flow of medicines be improved? Fundamental pharmacokinetic and pharmacological principles toward improving phase II survival
-
Morgan P, Van Der Graaf PH, Arrowsmith J, Feltner DE, Drummond KS, Wegner CD, Street SD. Can the flow of medicines be improved? Fundamental pharmacokinetic and pharmacological principles toward improving phase II survival. Drug Discov Today 2012;17:419-424.
-
(2012)
Drug Discov Today
, vol.17
, pp. 419-424
-
-
Morgan, P.1
Van Der Graaf, P.H.2
Arrowsmith, J.3
Feltner, D.E.4
Drummond, K.S.5
Wegner, C.D.6
Street, S.D.7
-
18
-
-
84903947419
-
Alzheimer's disease drug-development pipeline: few candidates, frequent failures
-
Cummings JL, Morstorf T, Zhong K. Alzheimer's disease drug-development pipeline: few candidates, frequent failures. Alzheimers Res Ther 2013;6:37.
-
(2013)
Alzheimers Res Ther
, vol.6
, pp. 37
-
-
Cummings, J.L.1
Morstorf, T.2
Zhong, K.3
-
19
-
-
84907928728
-
-
PBT2. Accessed 23 July
-
ALZFORUM. PBT2. http://wwwalzforumorg/therapeutics/pbt2_br. Accessed 23 July 2014.
-
(2014)
-
-
-
20
-
-
0022536654
-
Huntington's disease: effect of cysteamine, a somatostatin-depleting agent
-
Shults C, Steardo L, Barone P, et al. Huntington's disease: effect of cysteamine, a somatostatin-depleting agent. Neurology 1986;36:1099-1102.
-
(1986)
Neurology
, vol.36
, pp. 1099-1102
-
-
Shults, C.1
Steardo, L.2
Barone, P.3
-
21
-
-
79952898732
-
Potential of cystamine and cysteamine in the treatment of neurodegenerative diseases
-
Gibrat C, Cicchetti F. Potential of cystamine and cysteamine in the treatment of neurodegenerative diseases. Prog Neuropsychopharmacol Biol Psychiatry 2011;35:380-389.
-
(2011)
Prog Neuropsychopharmacol Biol Psychiatry
, vol.35
, pp. 380-389
-
-
Gibrat, C.1
Cicchetti, F.2
-
22
-
-
84903539020
-
Genetic deletion of transglutaminase 2 does not rescue the phenotypic deficits observed in R6/2 and zQ175 mouse models of Huntington's disease
-
Menalled LB, Kudwa AE, Oakeshott S, et al. Genetic deletion of transglutaminase 2 does not rescue the phenotypic deficits observed in R6/2 and zQ175 mouse models of Huntington's disease. PloS One 2013;9:e99520.
-
(2013)
PloS One
, vol.9
, pp. e99520
-
-
Menalled, L.B.1
Kudwa, A.E.2
Oakeshott, S.3
-
23
-
-
33646421164
-
Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase
-
Borrell-Pagès M, Canals JM, Cordelières FP, et al. Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase. J Clin Invest 2006;116:1410-1424.
-
(2006)
J Clin Invest
, vol.116
, pp. 1410-1424
-
-
Borrell-Pagès, M.1
Canals, J.M.2
Cordelières, F.P.3
-
26
-
-
84899965665
-
A potent and selective Sirtuin 1 inhibitor alleviates pathology in multiple animal and cell models of Huntington's disease
-
Smith MR, Syed A, Lukacsovich T, et al. A potent and selective Sirtuin 1 inhibitor alleviates pathology in multiple animal and cell models of Huntington's disease. Hum Mol Genet 2014;23:2995-3007.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 2995-3007
-
-
Smith, M.R.1
Syed, A.2
Lukacsovich, T.3
-
27
-
-
84883553202
-
Q02 A randomised, double-blind, placebo-controlled phase IB pharmacodynamic study with selisistat (SEN0014196) in HD patients
-
Süssmuth S, Landwehrmeyer G, Tabrizi S, et al. Q02 A randomised, double-blind, placebo-controlled phase IB pharmacodynamic study with selisistat (SEN0014196) in HD patients. J Neurol Neurosurg Psychiatry 2012;83(Suppl 1):A55.
-
(2012)
J Neurol Neurosurg Psychiatry
, vol.83
, Issue.1 SUPPL
, pp. A55
-
-
Süssmuth, S.1
Landwehrmeyer, G.2
Tabrizi, S.3
-
28
-
-
84907928725
-
Safety and tolerability of selisistat for the treatment of Huntington's disease: results from a randomized, double-blind, placebo-controlled phase II trial (S47.004)
-
Reilmann R, Squitieri F, Priller J, et al. Safety and tolerability of selisistat for the treatment of Huntington's disease: results from a randomized, double-blind, placebo-controlled phase II trial (S47.004). Neurology 2014;82(10 Suppl):S47.004.
-
(2014)
Neurology
, vol.82
, Issue.10 SUPPL
-
-
Reilmann, R.1
Squitieri, F.2
Priller, J.3
-
30
-
-
78650779872
-
Chronic suppression of phosphodiesterase 10A alters striatal expression of genes responsible for neurotransmitter synthesis, neurotransmission, and signaling pathways implicated in Huntington's disease
-
Kleiman RJ, Kimmel LH, Bove SE, et al. Chronic suppression of phosphodiesterase 10A alters striatal expression of genes responsible for neurotransmitter synthesis, neurotransmission, and signaling pathways implicated in Huntington's disease. J Pharmacol Exp Ther 2010;336:64-76.
-
(2010)
J Pharmacol Exp Ther
, vol.336
, pp. 64-76
-
-
Kleiman, R.J.1
Kimmel, L.H.2
Bove, S.E.3
-
34
-
-
84907928722
-
-
SD-809: a VMAT-2 inhibitor for the agram (phase 3 ongoing). Accessed July
-
Pharmaceuticals Auspex. SD-809: a VMAT-2 inhibitor for the agram (phase 3 ongoing). http://www.auspexpharma.com/pipeline/. Accessed July 2014.
-
(2014)
-
-
-
35
-
-
84907920445
-
Huntingtin-Lowering Strategies in Huntington's Disease: Antisense Oligonucleotides, Small RNAs, and Gene Editing.
-
Aronin N and DiFiglia M. Huntingtin-Lowering Strategies in Huntington's Disease: Antisense Oligonucleotides, Small RNAs, and Gene Editing. Mov Disord 2014;29:1455-1461.
-
(2014)
Mov Disord
, vol.29
, pp. 1455-1461
-
-
Aronin, N.1
DiFiglia, M.2
-
36
-
-
84876466100
-
An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study
-
Miller TM, Pestronk A, David W, et al. An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study. Lancet Neurol 2013;12:435-442.
-
(2013)
Lancet Neurol
, vol.12
, pp. 435-442
-
-
Miller, T.M.1
Pestronk, A.2
David, W.3
-
37
-
-
84907928721
-
Roche and Isis Pharmaceuticals form alliance for Huntington's Disease
-
consulted June 2014.
-
ISIS-ROCHE. Roche and Isis Pharmaceuticals form alliance for Huntington's Disease. 2013. http://www.roche.com/research_and_development/partnering/partnering-media/partnering_news-2013-04-08.htm, consulted June 2014.
-
(2013)
-
-
-
38
-
-
33645798913
-
Tetrabenazine as antichorea therapy in Huntington Disease
-
Huntington Study Group. Tetrabenazine as antichorea therapy in Huntington Disease. Neurology 2006;66(3):366-372.
-
(2006)
Neurology
, vol.66
, Issue.3
, pp. 366-372
-
-
-
39
-
-
84857136429
-
Huntington Study Group Cohort Investigators, Dorsey E. Characterization of a large group of individuals with huntington disease and their relatives enrolled in the COHORT study
-
Huntington Study Group Cohort Investigators, Dorsey E. Characterization of a large group of individuals with huntington disease and their relatives enrolled in the COHORT study. PloS One 2012;7:e29522.
-
(2012)
PloS One
, vol.7
, pp. e29522
-
-
-
40
-
-
84871183930
-
Investigators of the European Huntington's Disease Network. Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY
-
Orth M, Handley OJ, Schwenke C, et al.; Investigators of the European Huntington's Disease Network. Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY. PLoS Curr 2010;2:RRN1184.
-
(2010)
PLoS Curr
, vol.2
-
-
Orth, M.1
Handley, O.J.2
Schwenke, C.3
-
41
-
-
44949167557
-
Therapeutic interventions for symptomatic treatment in Huntington's disease
-
Mestre T, Ferreira J, Coelho MM, Rosa M, Sampaio C. Therapeutic interventions for symptomatic treatment in Huntington's disease. Cochrane Database Syst Rev 2009;3:CD006456.
-
(2009)
Cochrane Database Syst Rev
, vol.3
, pp. CD006456
-
-
Mestre, T.1
Ferreira, J.2
Coelho, M.M.3
Rosa, M.4
Sampaio, C.5
-
42
-
-
34948838383
-
Riluzole in Huntington's disease: a 3-year, randomized controlled study
-
Landwehrmeyer GB, Dubois B, de Yebenes JG, et al. Riluzole in Huntington's disease: a 3-year, randomized controlled study. Ann Neurol 2007;62:262-272.
-
(2007)
Ann Neurol
, vol.62
, pp. 262-272
-
-
Landwehrmeyer, G.B.1
Dubois, B.2
de Yebenes, J.G.3
-
43
-
-
84908089297
-
Research designs for proof-of-concept chronic pain clinical trials: IMMPACT recommendations
-
May 24. pii: -(14)00258-9. [Epub ahead of print].
-
Gewandter JS, Dworkin RH, Turk DC, et al. Research designs for proof-of-concept chronic pain clinical trials: IMMPACT recommendations. Pain 2014 May 24. pii: S0304-3959(14)00258-9. doi:10.1016/j.pain.2014.05.025. [Epub ahead of print].
-
(2014)
Pain
, pp. S0304-S3959
-
-
Gewandter, J.S.1
Dworkin, R.H.2
Turk, D.C.3
-
44
-
-
82255169270
-
Benefits, challenges and obstacles of adaptive clinical trial designs
-
Chow SC, Corey R. Benefits, challenges and obstacles of adaptive clinical trial designs. Orphanet J Rare Dis 2010;6:79.
-
(2010)
Orphanet J Rare Dis
, vol.6
, pp. 79
-
-
Chow, S.C.1
Corey, R.2
-
45
-
-
84898712203
-
PRECREST: a phase II prevention and biomarker trial of creatine in at-risk Huntington disease
-
Rosas HD, Doros G, Gevorkian S, et al. PRECREST: a phase II prevention and biomarker trial of creatine in at-risk Huntington disease. Neurology 2014;82:850-857.
-
(2014)
Neurology
, vol.82
, pp. 850-857
-
-
Rosas, H.D.1
Doros, G.2
Gevorkian, S.3
-
46
-
-
84878949241
-
Groundbreaking Alzheimer's disease prevention trial announced
-
consulted June 2014.
-
Banner Alzheimer Institute. Groundbreaking Alzheimer's disease prevention trial announced. 2012. http://banneralz.org/api-news-items/banner-alzheimers-partners-with-novartis.aspx, consulted June 2014.
-
(2012)
-
-
-
47
-
-
0018303366
-
Huntington disease: clinical care and evaluation
-
Shoulson I, Fahn S. Huntington disease: clinical care and evaluation. Neurology 1979;29:1-3.
-
(1979)
Neurology
, vol.29
, pp. 1-3
-
-
Shoulson, I.1
Fahn, S.2
-
48
-
-
0019444436
-
Huntington disease: functional capacities in patients treated with neuroleptic and antidepressant drugs
-
Shoulson I. Huntington disease: functional capacities in patients treated with neuroleptic and antidepressant drugs. Neurology 1981;31:1333-1335.
-
(1981)
Neurology
, vol.31
, pp. 1333-1335
-
-
Shoulson, I.1
-
49
-
-
85009332113
-
Unified Huntington's disease rating scale: reliability and consistency
-
The Huntington Study Group. Unified Huntington's disease rating scale: reliability and consistency. Mov Disord 1996;11:136-142.
-
(1996)
Mov Disord
, vol.11
, pp. 136-142
-
-
-
50
-
-
85009332113
-
Unified Huntington's Disease Rating Scale: reliability and consistency. Huntington Study Group
-
Unified Huntington's Disease Rating Scale: reliability and consistency. Huntington Study Group. Mov Disord 1996;11:136-142.
-
(1996)
Mov Disord
, vol.11
, pp. 136-142
-
-
-
51
-
-
0031740575
-
Unified Huntington's disease rating scale: a follow up
-
Siesling S, van Vugt JPP, Zwinderman KAH, Kieburtz K, Roos RAC. Unified Huntington's disease rating scale: a follow up. Mov Disord 1998;13:915-919.
-
(1998)
Mov Disord
, vol.13
, pp. 915-919
-
-
Siesling, S.1
van Vugt, J.P.P.2
Zwinderman, K.A.H.3
Kieburtz, K.4
Roos, R.A.C.5
-
52
-
-
80055092758
-
Assessment of involuntary choreatic movements in Huntington's disease-toward objective and quantitative measures
-
Reilmann R, Bohlen S, Kirsten F, Ringelstein EB, Lange HW. Assessment of involuntary choreatic movements in Huntington's disease-toward objective and quantitative measures. Mov Disord 2011;26:2267-2273.
-
(2011)
Mov Disord
, vol.26
, pp. 2267-2273
-
-
Reilmann, R.1
Bohlen, S.2
Kirsten, F.3
Ringelstein, E.B.4
Lange, H.W.5
-
53
-
-
78649376549
-
Tongue force analysis assesses motor phenotype in premanifest and symptomatic Huntington's disease
-
Reilmann R, Bohlen S, Klopstock T, et al. Tongue force analysis assesses motor phenotype in premanifest and symptomatic Huntington's disease. Mov Disord 2010;25:2195-2202.
-
(2010)
Mov Disord
, vol.25
, pp. 2195-2202
-
-
Reilmann, R.1
Bohlen, S.2
Klopstock, T.3
-
54
-
-
78650205712
-
Grasping premanifest Huntington's disease-shaping new endpoints for new trials
-
Reilmann R, Bohlen S, Klopstock T, et al. Grasping premanifest Huntington's disease-shaping new endpoints for new trials. Mov Disord 2010;25:2858-2862.
-
(2010)
Mov Disord
, vol.25
, pp. 2858-2862
-
-
Reilmann, R.1
Bohlen, S.2
Klopstock, T.3
-
55
-
-
84873455635
-
Clinical impairment in premanifest and early Huntington's disease is associated with regionally specific atrophy
-
Scahill RI, Hobbs NZ, Say MJ, et al. Clinical impairment in premanifest and early Huntington's disease is associated with regionally specific atrophy. Hum Brain Mapp 2013;34:519-529.
-
(2013)
Hum Brain Mapp
, vol.34
, pp. 519-529
-
-
Scahill, R.I.1
Hobbs, N.Z.2
Say, M.J.3
-
56
-
-
84862829257
-
PREDICT-HD Investigators of the Huntington Study Group. Cognitive domains that predict time to diagnosis in prodromal Huntington disease
-
Harrington DL, Smith MM, Zhang Y, Carlozzi NE, Paulsen JS; PREDICT-HD Investigators of the Huntington Study Group. Cognitive domains that predict time to diagnosis in prodromal Huntington disease. J Neurol Neurosurg Psychiatry 2012;83:612-619.
-
(2012)
J Neurol Neurosurg Psychiatry
, vol.83
, pp. 612-619
-
-
Harrington, D.L.1
Smith, M.M.2
Zhang, Y.3
Carlozzi, N.E.4
Paulsen, J.S.5
-
57
-
-
84861843888
-
Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's disease
-
Stout JC, Jones R, Labuschagne I, et al. Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's disease. J Neurol Neurosurg Psychiatry 2012;83:687-694.
-
(2012)
J Neurol Neurosurg Psychiatry
, vol.83
, pp. 687-694
-
-
Stout, J.C.1
Jones, R.2
Labuschagne, I.3
-
58
-
-
84907938672
-
HD-CAB: a cognitive assessment battery for clinical trials in Huntington's disease
-
Jul 7
-
Stout JC, Queller S, Baker KN, et al. HD-CAB: a cognitive assessment battery for clinical trials in Huntington's disease. Mov Disord 2014 Jul 7. doi: 10.1002/mds.25964.
-
(2014)
Mov Disord
-
-
Stout, J.C.1
Queller, S.2
Baker, K.N.3
-
59
-
-
79955100548
-
An item response analysis of the motor and behavioral subscales of the unified Huntington's disease rating scale in huntington disease gene expansion carriers
-
Vaccarino AL, Anderson K, Borowsky B, et al. An item response analysis of the motor and behavioral subscales of the unified Huntington's disease rating scale in huntington disease gene expansion carriers. Mov Disord 2011;26:877-884.
-
(2011)
Mov Disord
, vol.26
, pp. 877-884
-
-
Vaccarino, A.L.1
Anderson, K.2
Borowsky, B.3
-
60
-
-
84863399752
-
Longitudinal evaluation of neuropsychiatric symptoms in Huntington's disease
-
Thompson JC, Harris J, Sollom AC, et al. Longitudinal evaluation of neuropsychiatric symptoms in Huntington's disease. J Neuropsychiatry Clin Neurosci 2011;24:53-60.
-
(2011)
J Neuropsychiatry Clin Neurosci
, vol.24
, pp. 53-60
-
-
Thompson, J.C.1
Harris, J.2
Sollom, A.C.3
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