-
1
-
-
79952740327
-
Longitudinal change in regional brain volumes in prodromal Huntington disease
-
doi: 10.1136/jnnp.2010.208264
-
Aylward, E. H., Nopoulos, P. C., Ross, C. A., Langbehn, D. R., Pierson, R. K., Mills, J. A., et al. (2011). Longitudinal change in regional brain volumes in prodromal Huntington disease. J. Neurol. Neurosurg. Psychiatr. 82, 405-410. doi: 10.1136/jnnp.2010.208264
-
(2011)
J. Neurol. Neurosurg. Psychiatr
, vol.82
, pp. 405-410
-
-
Aylward, E.H.1
Nopoulos, P.C.2
Ross, C.A.3
Langbehn, D.R.4
Pierson, R.K.5
Mills, J.A.6
-
2
-
-
70449931956
-
Motor abnormalities in premanifest persons with Huntington's disease: the PREDICT-HD study
-
doi:10.1002/mds.22601
-
Biglan, K. M., Ross, C. A., Langbehn, D. R., Aylward, E. H., Stout, J. C., Queller, S., et al. (2009). Motor abnormalities in premanifest persons with Huntington's disease: the PREDICT-HD study. Mov. Disord. 24, 1763-1772. doi:10.1002/mds.22601
-
(2009)
Mov. Disord.
, vol.24
, pp. 1763-1772
-
-
Biglan, K.M.1
Ross, C.A.2
Langbehn, D.R.3
Aylward, E.H.4
Stout, J.C.5
Queller, S.6
-
3
-
-
33845430355
-
The value of database controls in pilot or futility studies in ALS
-
doi:10.1212/01.wnl.0000244415.48221.81
-
Czaplinski, A., Haverkamp, L. J., Yen, A. A., Simpson, E. P., Lai, E. C., and Appel, S. H. (2006). The value of database controls in pilot or futility studies in ALS. Neurology 67, 1827-1832. doi:10.1212/01.wnl.0000244415.48221.81
-
(2006)
Neurology
, vol.67
, pp. 1827-1832
-
-
Czaplinski, A.1
Haverkamp, L.J.2
Yen, A.A.3
Simpson, E.P.4
Lai, E.C.5
Appel, S.H.6
-
4
-
-
36549036813
-
Psychiatric symptoms in Huntington's disease before diagnosis: the Predict-HD study
-
and PREDICT-HD Investigators of the Huntington Study Group
-
Duff, K., Paulsen, J. S., Beglinger, L. J., Langbehn, D. R., Stout, J. C., and PREDICT-HD Investigators of the Huntington Study Group. (2007). Psychiatric symptoms in Huntington's disease before diagnosis: the Predict-HD study. Biol. Psychiatry 62, 1341-1346. doi:10.1016/j.biopsych.2006.11.034
-
(2007)
Biol. Psychiatry
, vol.62
, pp. 1341-1346
-
-
Duff, K.1
Paulsen, J.S.2
Beglinger, L.J.3
Langbehn, D.R.4
Stout, J.C.5
-
5
-
-
19944433460
-
A responsive outcome for Parkinson's disease neuroprotection futility studies
-
doi:10.1002/ana.20361
-
Elm, J. J., Goetz, C. G., Ravina, B., Shannon, K., Wooten, G. F., Tanner, C. M., et al. (2005). A responsive outcome for Parkinson's disease neuroprotection futility studies. Ann. Neurol. 57, 197-203. doi:10.1002/ana.20361
-
(2005)
Ann. Neurol.
, vol.57
, pp. 197-203
-
-
Elm, J.J.1
Goetz, C.G.2
Ravina, B.3
Shannon, K.4
Wooten, G.F.5
Tanner, C.M.6
-
6
-
-
84867459080
-
Seven-year clinical follow-up of premanifest carriers of Huntington's disease
-
doi:10.1371/currents.RRN1288.,RRN1288
-
Hart, E., Middelkoop, H., Jurgens, C. K., Witjes-Ane, M. N., and Roos, R. A. (2011). Seven-year clinical follow-up of premanifest carriers of Huntington's disease. PLoS Curr. 3:RRN1288. doi:10.1371/currents.RRN1288
-
(2011)
PLoS Curr
, vol.3
-
-
Hart, E.1
Middelkoop, H.2
Jurgens, C.K.3
Witjes-Ane, M.N.4
Roos, R.A.5
-
7
-
-
33645798913
-
Tetrabenazine as antichorea therapy in Huntington disease: a randomized controlled trial
-
doi:10.1212/01.wnl.0000198586.85250.13.,Huntington Study Group
-
Huntington Study Group. (2006). Tetrabenazine as antichorea therapy in Huntington disease: a randomized controlled trial. Neurology 66, 366-372. doi:10.1212/01.wnl.0000198586.85250.13
-
(2006)
Neurology
, vol.66
, pp. 366-372
-
-
-
8
-
-
0032916974
-
Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers
-
doi:10.1001/archneur.56.5.563
-
Kirkwood, S. C., Siemers, E., Stout, J. C., Hodes, M. E., Conneally, P. M., Christian, J. C., et al. (1999). Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers. Arch. Neurol. 56, 563-568. doi:10.1001/archneur.56.5.563
-
(1999)
Arch. Neurol.
, vol.56
, pp. 563-568
-
-
Kirkwood, S.C.1
Siemers, E.2
Stout, J.C.3
Hodes, M.E.4
Conneally, P.M.5
Christian, J.C.6
-
9
-
-
0036720678
-
Longitudinal study evaluating neuropsychological changes in so-called asymptomatic carriers of the Huntington's disease mutation after 1 year
-
doi:10.1034/j.1600-0404.2002.01192.x
-
Lemiere, J., Decruyenaere, M., Evers-Kiebooms, G., Vandenbussche, E., and Dom, R. (2002). Longitudinal study evaluating neuropsychological changes in so-called asymptomatic carriers of the Huntington's disease mutation after 1 year. Acta Neurol. Scand. 106, 131-141. doi:10.1034/j.1600-0404.2002.01192.x
-
(2002)
Acta Neurol. Scand.
, vol.106
, pp. 131-141
-
-
Lemiere, J.1
Decruyenaere, M.2
Evers-Kiebooms, G.3
Vandenbussche, E.4
Dom, R.5
-
10
-
-
4344669917
-
Cognitive changes in patients with Huntington's disease (HD) and asymptomatic carriers of the HD mutation - a longitudinal follow-up study
-
doi:10.1007/s00415-004-0461-9
-
Lemiere, J., Decruyenaere, M., Evers-Kiebooms, G., Vandenbussche, E., and Dom, R. (2004). Cognitive changes in patients with Huntington's disease (HD) and asymptomatic carriers of the HD mutation - a longitudinal follow-up study. J. Neurol. 251, 935-942. doi:10.1007/s00415-004-0461-9
-
(2004)
J. Neurol.
, vol.251
, pp. 935-942
-
-
Lemiere, J.1
Decruyenaere, M.2
Evers-Kiebooms, G.3
Vandenbussche, E.4
Dom, R.5
-
12
-
-
83555178500
-
Basal ganglia atrophy in prodromal Huntington's disease is detectable over one year using automated segmentation
-
doi:10.1002/mds.23912
-
Majid, D. S., Aron, A. R., Thompson, W., Sheldon, S., Hamza, S., Stoffers, D., et al. (2011). Basal ganglia atrophy in prodromal Huntington's disease is detectable over one year using automated segmentation. Mov. Disord. 26, 2544-2551. doi:10.1002/mds.23912
-
(2011)
Mov. Disord.
, vol.26
, pp. 2544-2551
-
-
Majid, D.S.1
Aron, A.R.2
Thompson, W.3
Sheldon, S.4
Hamza, S.5
Stoffers, D.6
-
13
-
-
80053539477
-
Modeling longitudinal change in motor and cognitive processing speed in presymptomatic Huntington's disease
-
doi:10.1080/13803395.2011.574606
-
Maroof, D. A., Gross, A. L., and Brandt, J. (2011). Modeling longitudinal change in motor and cognitive processing speed in presymptomatic Huntington's disease. J. Clin. Exp. Neuropsychol. 33, 901-909. doi:10.1080/13803395.2011.574606
-
(2011)
J. Clin. Exp. Neuropsychol.
, vol.33
, pp. 901-909
-
-
Maroof, D.A.1
Gross, A.L.2
Brandt, J.3
-
14
-
-
79958170933
-
The Trail Making Test in prodromal Huntington disease: contributions of disease progression to test performance
-
doi:10.1080/13803395.2010.541228
-
O'Rourke, J. J., Beglinger, L. J., Smith, M. M., Mills, J., Moser, D. J., Rowe, K. C., et al. (2011). The Trail Making Test in prodromal Huntington disease: contributions of disease progression to test performance. J. Clin. Exp. Neuropsychol. 33, 567-579. doi:10.1080/13803395.2010.541228
-
(2011)
J. Clin. Exp. Neuropsychol.
, vol.33
, pp. 567-579
-
-
O'Rourke, J.J.1
Beglinger, L.J.2
Smith, M.M.3
Mills, J.4
Moser, D.J.5
Rowe, K.C.6
-
15
-
-
84879147400
-
Measuring executive dysfunction longitudinally and in relation to genetic burden, brain volumetrics, and depression in prodromal Huntington disease
-
doi:10.1093/arclin/acs105
-
Papp, K. V., Snyder, P. J., Mills, J. A., Duff, K., Westervelt, H. J., Long, J. D., et al. (2013). Measuring executive dysfunction longitudinally and in relation to genetic burden, brain volumetrics, and depression in prodromal Huntington disease. Arch. Clin. Neuropsychol. 28, 156-168. doi:10.1093/arclin/acs105
-
(2013)
Arch. Clin. Neuropsychol.
, vol.28
, pp. 156-168
-
-
Papp, K.V.1
Snyder, P.J.2
Mills, J.A.3
Duff, K.4
Westervelt, H.J.5
Long, J.D.6
-
16
-
-
33745110056
-
Investigators of the Huntington Study Group preparing for preventive clinical trials: the Predict-HD study
-
doi:10.1001/archneur.63.6.883
-
Paulsen, J. S., Hayden, M., Stout, J. C., Langbehn, D. R., Aylward, E., Ross, C. A., et al. (2006). Investigators of the Huntington Study Group preparing for preventive clinical trials: the Predict-HD study. Arch. Neurol. 63, 883-890. doi:10.1001/archneur.63.6.883
-
(2006)
Arch. Neurol.
, vol.63
, pp. 883-890
-
-
Paulsen, J.S.1
Hayden, M.2
Stout, J.C.3
Langbehn, D.R.4
Aylward, E.5
Ross, C.A.6
-
17
-
-
48249114740
-
Detection of Huntington's disease decades before diagnosis: the Predict-HD study
-
doi:10.1136/jnnp. 2007. 128728
-
Paulsen, J. S., Langbehn, D. R., Stout, J. C., Aylward, E., Ross, C. A., Nance, M., et al. (2008). Detection of Huntington's disease decades before diagnosis: the Predict-HD study. J. Neurol. Neurosurg. Psychiatr. 79, 874-880. doi:10.1136/jnnp.2007.128728
-
(2008)
J. Neurol. Neurosurg. Psychiatr.
, vol.79
, pp. 874-880
-
-
Paulsen, J.S.1
Langbehn, D.R.2
Stout, J.C.3
Aylward, E.4
Ross, C.A.5
Nance, M.6
-
18
-
-
84885649254
-
Cognitive decline in prodromal Huntington disease: implications for clinical trials
-
doi:10.1136/jnnp-2013-305114., PREDICT-HD Investigators and Coordinators of the Huntington Study Group
-
Paulsen, J. S., Smith, M. M., Long, J. D., PREDICT-HD Investigators and Coordinators of the Huntington Study Group. (2013). Cognitive decline in prodromal Huntington disease: implications for clinical trials. J. Neurol. Neurosurg. Psychiatr. 84, 1233-1239. doi:10.1136/jnnp-2013-305114
-
(2013)
J. Neurol. Neurosurg. Psychiatr.
, vol.84
, pp. 1233-1239
-
-
Paulsen, J.S.1
Smith, M.M.2
Long, J.D.3
-
19
-
-
0035964234
-
Clinical markers of early disease in persons near onset of Huntington's disease
-
doi:10.1212/WNL.57.4.658
-
Paulsen, J. S., Zhao, H., Stout, J. C., Brinkman, R. R., Guttman, M., Ross, C. A., et al. (2001). Clinical markers of early disease in persons near onset of Huntington's disease. Neurology 57, 658-662. doi:10.1212/WNL.57.4.658
-
(2001)
Neurology
, vol.57
, pp. 658-662
-
-
Paulsen, J.S.1
Zhao, H.2
Stout, J.C.3
Brinkman, R.R.4
Guttman, M.5
Ross, C.A.6
-
20
-
-
0030919726
-
CAG repeat number governs the development rate of pathology in Huntington's disease
-
doi:10.1002/ana.410410521
-
Penney, J. B. Jr., Vonsattel, J. P., Macdonald, M. E., Gusella, J. F., and Myers, R. H. (1997). CAG repeat number governs the development rate of pathology in Huntington's disease. Ann. Neurol. 41, 689-692. doi:10.1002/ana.410410521
-
(1997)
Ann. Neurol.
, vol.41
, pp. 689-692
-
-
Penney Jr., J.B.1
Vonsattel, J.P.2
Macdonald, M.E.3
Gusella, J.F.4
Myers, R.H.5
-
21
-
-
84898017417
-
Huntington disease: natural history, biomarkers and prospects for therapeutics
-
doi:10.1038/nrneurol.2014.24
-
Ross, C. A., Aylward, E. H., Wild, E. J., Langbehn, D. R., Long, J. D., Warner, J. H., et al. (2014). Huntington disease: natural history, biomarkers and prospects for therapeutics. Nat. Rev. Neurol. 10, 204-216. doi:10.1038/nrneurol.2014.24
-
(2014)
Nat. Rev. Neurol.
, vol.10
, pp. 204-216
-
-
Ross, C.A.1
Aylward, E.H.2
Wild, E.J.3
Langbehn, D.R.4
Long, J.D.5
Warner, J.H.6
-
22
-
-
78650031174
-
Huntington's disease: from molecular pathogenesis to clinical treatment
-
doi:10. 1016/S1474-4422(10) 70245-3
-
Ross, C. A., and Tabrizi, S. J. (2011). Huntington's disease: from molecular pathogenesis to clinical treatment. Lancet Neurol. 10, 83-98. doi:10.1016/S1474-4422(10)70245-3
-
(2011)
Lancet Neurol
, vol.10
, pp. 83-98
-
-
Ross, C.A.1
Tabrizi, S.J.2
-
23
-
-
77954629870
-
Self-paced timing detects and tracks change in prodromal Huntington disease
-
doi:10.1037/a0018905
-
Rowe, K. C., Paulsen, J. S., Langbehn, D. R., Duff, K., Beglinger, L. J., Wang, C., et al. (2010). Self-paced timing detects and tracks change in prodromal Huntington disease. Neuropsychology 24, 435-442. doi:10.1037/a0018905
-
(2010)
Neuropsychology
, vol.24
, pp. 435-442
-
-
Rowe, K.C.1
Paulsen, J.S.2
Langbehn, D.R.3
Duff, K.4
Beglinger, L.J.5
Wang, C.6
-
24
-
-
77950605609
-
Progression in prediagnostic Huntington disease
-
doi:10.1136/jnnp.2009.176982
-
Rupp, J., Blekher, T., Jackson, J., Beristain, X., Marshall, J., Hui, S., et al. (2010). Progression in prediagnostic Huntington disease. J. Neurol. Neurosurg. Psychiatr. 81, 379-384. doi:10.1136/jnnp.2009.176982
-
(2010)
J. Neurol. Neurosurg. Psychiatr.
, vol.81
, pp. 379-384
-
-
Rupp, J.1
Blekher, T.2
Jackson, J.3
Beristain, X.4
Marshall, J.5
Hui, S.6
-
25
-
-
0036257088
-
Psychomotor, executive, and memory function in preclinical Huntington's disease
-
doi:10.1076/jcen.24.2.133.998
-
Snowden, J. S., Craufurd, D., Thompson, J., and Neary, D. (2002). Psychomotor, executive, and memory function in preclinical Huntington's disease. J. Clin. Exp. Neuropsychol. 24, 133-145. doi:10.1076/jcen.24.2.133.998
-
(2002)
J. Clin. Exp. Neuropsychol.
, vol.24
, pp. 133-145
-
-
Snowden, J.S.1
Craufurd, D.2
Thompson, J.3
Neary, D.4
-
26
-
-
83555173501
-
Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data
-
doi:10. 1016/S1474-4422(11) 70263-0
-
Tabrizi, S. J., Reilmann, R., Roos, R. A., Durr, A., Leavitt, B., Owen, G., et al. (2012). Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data. Lancet Neurol. 11, 42-53. doi:10.1016/S1474-4422(11)70263-0
-
(2012)
Lancet Neurol
, vol.11
, pp. 42-53
-
-
Tabrizi, S.J.1
Reilmann, R.2
Roos, R.A.3
Durr, A.4
Leavitt, B.5
Owen, G.6
-
27
-
-
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
-
doi:10. 1016/S1474-4422(13) 70088-7
-
Tabrizi, S. J., Scahill, R. I., Owen, G., Durr, A., Leavitt, B. R., Roos, R. A., et al. (2013). 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. 12, 637-649. doi:10.1016/S1474-4422(13)70088-7
-
(2013)
Lancet Neurol
, vol.12
, pp. 637-649
-
-
Tabrizi, S.J.1
Scahill, R.I.2
Owen, G.3
Durr, A.4
Leavitt, B.R.5
Roos, R.A.6
-
28
-
-
84856000206
-
NeuroNEXT: accelerating drug development in neurology
-
doi:10.1016/S1474-4422(12)70008-X.,The Lancet Neurology
-
The Lancet Neurology. (2012). NeuroNEXT: accelerating drug development in neurology. Lancet Neurol. 11, 119. doi:10.1016/S1474-4422(12)70008-X
-
(2012)
Lancet Neurol
, vol.11
, pp. 119
-
-
-
30
-
-
57249086448
-
Allele-specific silencing of mutant Huntington's disease gene
-
doi:10.1111/j.1471-4159.2008.05734.x
-
Zhang, Y., Engelman, J., and Friedlander, R. M. (2009). Allele-specific silencing of mutant Huntington's disease gene. J. Neurochem. 108, 82-90. doi:10.1111/j.1471-4159.2008.05734.x
-
(2009)
J. Neurochem.
, vol.108
, pp. 82-90
-
-
Zhang, Y.1
Engelman, J.2
Friedlander, R.M.3
-
31
-
-
80052484592
-
Indexing disease progression at study entry with individuals at-risk for Huntington disease
-
doi:10.1002/Ajmg.B.31232
-
Zhang, Y., Long, J. D., Mills, J. A., Warner, J. H., Lu, W. J., and Paulsen, J. S. (2011). Indexing disease progression at study entry with individuals at-risk for Huntington disease. Am. J. Med. Genet. B Neuropsychiatr. Genet. 156B, 751-763. doi:10.1002/Ajmg.B.31232
-
(2011)
Am. J. Med. Genet. B Neuropsychiatr. Genet
, vol.156 B
, pp. 751-763
-
-
Zhang, Y.1
Long, J.D.2
Mills, J.A.3
Warner, J.H.4
Lu, W.J.5
Paulsen, J.S.6
|