-
1
-
-
0036189675
-
Progression-free rate as the principal end-point for phase II trials in soft-tissue sarcomas
-
Van Glabbeke, M. et al. Progression-free rate as the principal end-point for phase II trials in soft-tissue sarcomas. Eur. J. Cancer 38, 543-549 (2002).
-
(2002)
Eur. J. Cancer
, vol.38
, pp. 543-549
-
-
Van Glabbeke, M.1
-
2
-
-
0035970795
-
Sample size tables for exact single-stage phase II designs
-
A'Hern, R. P. Sample size tables for exact single-stage phase II designs. Stat. Med. 20, 859-866 (2001).
-
(2001)
Stat. Med.
, vol.20
, pp. 859-866
-
-
A'Hern, R.P.1
-
3
-
-
50549174560
-
The determination of the number of patients required in a preliminary and a follow-up trial of a new chemotherapeutic agent
-
Gehan, E. A. The determination of the number of patients required in a preliminary and a follow-up trial of a new chemotherapeutic agent. J. Chronic Dis. 13, 346-353 (1961).
-
(1961)
J. Chronic Dis.
, vol.13
, pp. 346-353
-
-
Gehan, E.A.1
-
4
-
-
0020108590
-
One-sample multiple testing procedure for phase II clinical trials
-
Fleming, T. R. One-sample multiple testing procedure for phase II clinical trials. Biometrics 38, 143-151 (1982).
-
(1982)
Biometrics
, vol.38
, pp. 143-151
-
-
Fleming, T.R.1
-
5
-
-
0024536437
-
Optimal two-stage designs for phase II clinical trials
-
Simon, R. Optimal two-stage designs for phase II clinical trials. Control. Clin. Trials 10, 1-10 (1989).
-
(1989)
Control. Clin. Trials
, vol.10
, pp. 1-10
-
-
Simon, R.1
-
6
-
-
33645894705
-
A randomized, double-blind, futility clinical trial of creatine and minocycline in early Parkinson disease
-
NINDS NET-PD Investigators. A randomized, double-blind, futility clinical trial of creatine and minocycline in early Parkinson disease. Neurology 66, 664-671 (2006).
-
(2006)
Neurology
, vol.66
, pp. 664-671
-
-
-
7
-
-
0000224448
-
-
eds Fahn, S. et al. Macmillan Healthcare Information
-
Fahn, S. et al. in Recent Developments in Parkinson's Disease Vol. 2 (eds Fahn, S. et al.) 153-163 (Macmillan Healthcare Information, 1987).
-
(1987)
Recent Developments in Parkinson's Disease
, vol.2
, pp. 153-163
-
-
Fahn, S.1
-
8
-
-
0024457355
-
DATATOP: A multicenter controlled clinical trial in early Parkinson's disease
-
No authors listed Parkinson Study Group
-
[No authors listed] DATATOP: a multicenter controlled clinical trial in early Parkinson's disease. Parkinson Study Group. Arch. Neurol. 46, 1052-1060 (1989).
-
(1989)
Arch. Neurol.
, vol.46
, pp. 1052-1060
-
-
-
9
-
-
19944433460
-
A responsive outcome for Parkinson's disease neuroprotection futility studies
-
Elm, J. J. et al. A responsive outcome for Parkinson's disease neuroprotection futility studies. Ann. Neurol. 57, 197-203 (2005).
-
(2005)
Ann. Neurol.
, vol.57
, pp. 197-203
-
-
Elm, J.J.1
-
10
-
-
33645864949
-
Optimizing the ongoing search for new treatments for Parkinson disease: Using futility designs
-
Tilley, B. C. et al. Optimizing the ongoing search for new treatments for Parkinson disease: using futility designs. Neurology 66, 628-633 (2006).
-
(2006)
Neurology
, vol.66
, pp. 628-633
-
-
Tilley, B.C.1
-
11
-
-
33947625905
-
The appropriateness of some common procedures for testing the equality of two independent binomial populations
-
D'Agostino, R., Chase, W. & Belanger, A. The appropriateness of some common procedures for testing the equality of two independent binomial populations. The American Statistician 42, 198-202 (1988).
-
(1988)
The American Statistician
, vol.42
, pp. 198-202
-
-
D'Agostino, R.1
Chase, W.2
Belanger, A.3
-
12
-
-
33645864950
-
Futility studies: Spending a little to save a lot
-
Schwid, S. R. & Cutter, G. R. Futility studies: spending a little to save a lot. Neurology 66, 626-627 (2006).
-
(2006)
Neurology
, vol.66
, pp. 626-627
-
-
Schwid, S.R.1
Cutter, G.R.2
-
13
-
-
83555173501
-
Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: Analysis of 24 month observational data
-
Tabrizi, S. J. et al. 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 (2012).
-
(2012)
Lancet Neurol.
, vol.11
, pp. 42-53
-
-
Tabrizi, S.J.1
-
14
-
-
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, S. J. 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. 12, 637-649 (2013).
-
(2013)
Lancet Neurol.
, vol.12
, pp. 637-649
-
-
Tabrizi, S.J.1
-
15
-
-
84884724757
-
A randomized, double-blind, placebo-controlled trial of pridopidine in Huntington's disease
-
Huntington Study Group HART Investigators. A randomized, double-blind, placebo-controlled trial of pridopidine in Huntington's disease. Mov. Disord. 28, 1407-1415 (2013).
-
(2013)
Mov. Disord.
, vol.28
, pp. 1407-1415
-
-
-
16
-
-
33846225133
-
Huntington's disease
-
Walker, F. O. Huntington's disease. Lancet 369, 218-228 (2007).
-
(2007)
Lancet
, vol.369
, pp. 218-228
-
-
Walker, F.O.1
-
17
-
-
0033589692
-
Prevalence of progressive supranuclear palsy and multiple system atrophy: A cross-sectional study
-
Schrag, A., Ben-Shlomo, Y. & Quinn, N. P. Prevalence of progressive supranuclear palsy and multiple system atrophy: a cross-sectional study. Lancet 354, 1771-1775 (1999).
-
(1999)
Lancet
, vol.354
, pp. 1771-1775
-
-
Schrag, A.1
Ben-Shlomo, Y.2
Quinn, N.P.3
-
18
-
-
33644818304
-
1,026 Experimental treatments in acute stroke
-
O'Collins, V. E. et al. 1,026 experimental treatments in acute stroke. Ann. Neurol. 59, 467-477 (2006).
-
(2006)
Ann. Neurol.
, vol.59
, pp. 467-477
-
-
O'Collins, V.E.1
-
19
-
-
46249131138
-
NXY-059 for the treatment of acute stroke: Pooled analysis of the SAINT I and II Trials
-
Diener, H. C. et al. NXY-059 for the treatment of acute stroke: pooled analysis of the SAINT I and II Trials. Stroke 39, 1751-1758 (2008).
-
(2008)
Stroke
, vol.39
, pp. 1751-1758
-
-
Diener, H.C.1
-
20
-
-
33745955359
-
Therapeutic strategies for the treatment of stroke
-
Green, A. R. & Shuaib, A. Therapeutic strategies for the treatment of stroke. Drug Discov. Today 11, 681-693 (2006).
-
(2006)
Drug Discov. Today
, vol.11
, pp. 681-693
-
-
Green, A.R.1
Shuaib, A.2
-
21
-
-
46249110404
-
Is it time to definitely abandon neuroprotection in acute ischemic stroke?
-
Sacchetti, M. L. Is it time to definitely abandon neuroprotection in acute ischemic stroke? Stroke 39, 1659-1660 (2008).
-
(2008)
Stroke
, vol.39
, pp. 1659-1660
-
-
Sacchetti, M.L.1
-
22
-
-
84900478304
-
Importance of preclinical research in the development of neuroprotective strategies for ischemic stroke
-
Neuhaus, A. A. et al. Importance of preclinical research in the development of neuroprotective strategies for ischemic stroke. JAMA Neurol. 71, 634-639 (2014).
-
(2014)
JAMA Neurol.
, vol.71
, pp. 634-639
-
-
Neuhaus, A.A.1
-
23
-
-
84888384968
-
Novel approaches to neuroprotection trials in acute ischemic stroke
-
Tymianski, M. Novel approaches to neuroprotection trials in acute ischemic stroke. Stroke 44, 2942-2950 (2013).
-
(2013)
Stroke
, vol.44
, pp. 2942-2950
-
-
Tymianski, M.1
-
24
-
-
0024328055
-
Measurements of acute cerebral infarction: A clinical examination scale
-
Brott, T. et al. Measurements of acute cerebral infarction: a clinical examination scale. Stroke 20, 864-870 (1989).
-
(1989)
Stroke
, vol.20
, pp. 864-870
-
-
Brott, T.1
-
25
-
-
0023889706
-
Interobserver agreement for the assessment of handicap in stroke patients
-
Van Swieten, J. C., Koudstaal, P. J., Visser, M. C., Schouten, H. J. & van Gijn, J. Interobserver agreement for the assessment of handicap in stroke patients. Stroke 19, 604-607 (1988).
-
(1988)
Stroke
, vol.19
, pp. 604-607
-
-
Van Swieten, J.C.1
Koudstaal, P.J.2
Visser, M.C.3
Schouten, H.J.4
Van Gijn, J.5
-
26
-
-
70450195021
-
Functional evaluation: The Barthel Index
-
Mahoney, F. I. & Barthel, D. W. Functional evaluation: the Barthel Index. Md State Med. J. 14, 61-65 (1965).
-
(1965)
Md State Med. J.
, vol.14
, pp. 61-65
-
-
Mahoney, F.I.1
Barthel, D.W.2
-
27
-
-
33846641246
-
Screening potential therapies: Lessons learned from new paradigms used in Parkinson disease
-
Tilley, B. C. & Galpern, W. R. Screening potential therapies: lessons learned from new paradigms used in Parkinson disease. Stroke 38, 800-803 (2007).
-
(2007)
Stroke
, vol.38
, pp. 800-803
-
-
Tilley, B.C.1
Galpern, W.R.2
-
28
-
-
0028783948
-
Tissue plasminogen activator for acute ischemic stroke
-
No authors listed The National Institute of Neurological Disorders and Stroke rt-PA Stroke Study Group
-
[No authors listed] Tissue plasminogen activator for acute ischemic stroke. The National Institute of Neurological Disorders and Stroke rt-PA Stroke Study Group. N. Engl. J. Med. 333, 1581-1587 (1995).
-
(1995)
N. Engl. J. Med.
, vol.333
, pp. 1581-1587
-
-
-
29
-
-
27644481285
-
Applying a phase II futility study design to therapeutic stroke trials
-
Palesch, Y. Y., Tilley, B. C., Sackett, D. L., Johnston, K. C. & Woolson, R. Applying a phase II futility study design to therapeutic stroke trials. Stroke 36, 2410-2414 (2005).
-
(2005)
Stroke
, vol.36
, pp. 2410-2414
-
-
Palesch, Y.Y.1
Tilley, B.C.2
Sackett, D.L.3
Johnston, K.C.4
Woolson, R.5
-
30
-
-
79952486262
-
Amyotrophic lateral sclerosis
-
Kiernan, M. C. et al. Amyotrophic lateral sclerosis. Lancet 377, 942-955 (2011).
-
(2011)
Lancet
, vol.377
, pp. 942-955
-
-
Kiernan, M.C.1
-
31
-
-
0028097839
-
A controlled trial of riluzole in amyotrophic lateral sclerosis
-
ALS/Riluzole Study Group
-
Bensimon, G., Lacomblez, L. & Meininger, V. A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group. N. Engl. J. Med. 330, 585-591 (1994).
-
(1994)
N. Engl. J. Med.
, vol.330
, pp. 585-591
-
-
Bensimon, G.1
Lacomblez, L.2
Meininger, V.3
-
32
-
-
84885388013
-
Dexpramipexole versus placebo for patients with amyotrophic lateral sclerosis (EMPOWER): A randomised, double-blind, phase 3 trial
-
Cudkowicz, M. E. et al. Dexpramipexole versus placebo for patients with amyotrophic lateral sclerosis (EMPOWER): a randomised, double-blind, phase 3 trial. Lancet Neurol. 12, 1059-1067 (2013).
-
(2013)
Lancet Neurol.
, vol.12
, pp. 1059-1067
-
-
Cudkowicz, M.E.1
-
33
-
-
84875273042
-
Lithium in patients with amyotrophic lateral sclerosis (LiCALS): A phase 3 multicentre, randomised, double-blind, placebo-controlled trial
-
UKMND-LiCALS Study Group et al. Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial. Lancet Neurol. 12, 339-345 (2013).
-
(2013)
Lancet Neurol.
, vol.12
, pp. 339-345
-
-
-
34
-
-
36148960127
-
Efficacy of minocycline in patients with amyotrophic lateral sclerosis: A phase III randomised trial
-
Gordon, P. H. et al. Efficacy of minocycline in patients with amyotrophic lateral sclerosis: a phase III randomised trial. Lancet Neurol. 6, 1045-1053 (2007).
-
(2007)
Lancet Neurol.
, vol.6
, pp. 1045-1053
-
-
Gordon, P.H.1
-
36
-
-
0028904953
-
Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classifications
-
Zerres, K. & Rudnik-Schöneborn, S. Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classifications. Arch. Neurol. 52, 518-523 (1995).
-
(1995)
Arch. Neurol.
, vol.52
, pp. 518-523
-
-
Zerres, K.1
Rudnik-Schöneborn, S.2
-
37
-
-
84925946878
-
Observational study of spinal muscular atrophy type I and implications for clinical trials
-
Finkel, R. S. et al. Observational study of spinal muscular atrophy type I and implications for clinical trials. Neurology 83, 810-817 (2014).
-
(2014)
Neurology
, vol.83
, pp. 810-817
-
-
Finkel, R.S.1
-
38
-
-
84555218229
-
Spinal muscular atrophy: A clinical and research update
-
Markowitz, J. A., Singh, P. & Darras, B. T. Spinal muscular atrophy: a clinical and research update. Pediatr. Neurol. 46, 1-12 (2012).
-
(2012)
Pediatr. Neurol.
, vol.46
, pp. 1-12
-
-
Markowitz, J.A.1
Singh, P.2
Darras, B.T.3
-
39
-
-
27644537716
-
Challenges and opportunities in clinical trials for spinal muscular atrophy
-
Hirtz, D. et al. Challenges and opportunities in clinical trials for spinal muscular atrophy. Neurology 65, 1352-1357 (2005).
-
(2005)
Neurology
, vol.65
, pp. 1352-1357
-
-
Hirtz, D.1
-
40
-
-
34548154298
-
Perspectives on clinical trials in spinal muscular atrophy
-
Swoboda, K. J. et al. Perspectives on clinical trials in spinal muscular atrophy. J. Child Neurol. 22, 957-966 (2007).
-
(2007)
J. Child Neurol.
, vol.22
, pp. 957-966
-
-
Swoboda, K.J.1
-
41
-
-
84859816485
-
Childhood spinal muscular atrophy: Controversies and challenges
-
Mercuri, E., Bertini, E. & Iannaccone, S. T. Childhood spinal muscular atrophy: controversies and challenges. Lancet Neurol. 11, 443-452 (2012).
-
(2012)
Lancet Neurol.
, vol.11
, pp. 443-452
-
-
Mercuri, E.1
Bertini, E.2
Iannaccone, S.T.3
-
42
-
-
0024504359
-
The natural history of multiple sclerosis: A geographically based study. I. Clinical course and disability
-
Weinshenker, B. G. et al. The natural history of multiple sclerosis: a geographically based study. I. Clinical course and disability. Brain 112, 133-146 (1989).
-
(1989)
Brain
, vol.112
, pp. 133-146
-
-
Weinshenker, B.G.1
-
43
-
-
84883742744
-
Treatment trials in progressive MS-current challenges and future directions
-
Koch, M. W., Cutter, G., Stys, P. K., Yong, V. W. & Metz, L. M. Treatment trials in progressive MS-current challenges and future directions. Nat. Rev. Neurol. 9, 496-503 (2013).
-
(2013)
Nat. Rev. Neurol.
, vol.9
, pp. 496-503
-
-
Koch, M.W.1
Cutter, G.2
Stys, P.K.3
Yong, V.W.4
Metz, L.M.5
-
44
-
-
0021035886
-
Rating neurologic impairment in multiple sclerosis: An expanded disability status scale (EDSS)
-
Kurtzke, J. F. Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS). Neurology 33, 1444-1452 (1983).
-
(1983)
Neurology
, vol.33
, pp. 1444-1452
-
-
Kurtzke, J.F.1
-
45
-
-
84864149880
-
Revisiting the multiple sclerosis functional composite: Proceedings from the National Multiple Sclerosis Society (NMSS) Task Force on Clinical Disability Measures
-
Ontaneda, D. et al. Revisiting the multiple sclerosis functional composite: proceedings from the National Multiple Sclerosis Society (NMSS) Task Force on Clinical Disability Measures. Mult. Scler. 18, 1074-1080 (2012).
-
(2012)
Mult. Scler.
, vol.18
, pp. 1074-1080
-
-
Ontaneda, D.1
-
46
-
-
0032919071
-
Development of a multiple sclerosis functional composite as a clinical trial outcome measure
-
Cutter, G. R. et al. Development of a multiple sclerosis functional composite as a clinical trial outcome measure. Brain 122, 871-882 (1999).
-
(1999)
Brain
, vol.122
, pp. 871-882
-
-
Cutter, G.R.1
-
47
-
-
66149190708
-
The search for responsive clinical endpoints in primary progressive multiple sclerosis
-
Bosma, L. V. et al. The search for responsive clinical endpoints in primary progressive multiple sclerosis. Mult. Scler. 15, 715-720 (2009).
-
(2009)
Mult. Scler.
, vol.15
, pp. 715-720
-
-
Bosma, L.V.1
-
48
-
-
33846833929
-
Glatiramer acetate in primary progressive multiple sclerosis: Resultsof a multinational, multicenter, double-blind, placebo-controlled trial
-
Wolinsky, J. S. et al. Glatiramer acetate in primary progressive multiple sclerosis: resultsof a multinational, multicenter, double-blind, placebo-controlled trial. Ann. Neurol. 61, 14-24 (2007).
-
(2007)
Ann. Neurol.
, vol.61
, pp. 14-24
-
-
Wolinsky, J.S.1
-
49
-
-
0037056364
-
Benefit of interferon β-1a on MSFC progression in secondary progressive MS
-
Cohen, J. A. et al. Benefit of interferon β-1a on MSFC progression in secondary progressive MS. Neurology 59, 679-687 (2002).
-
(2002)
Neurology
, vol.59
, pp. 679-687
-
-
Cohen, J.A.1
-
50
-
-
82955198543
-
A phase III study evaluating the efficacy and safety of MBP8298 in secondary progressive MS
-
Freedman, M. S. et al. A phase III study evaluating the efficacy and safety of MBP8298 in secondary progressive MS. Neurology 77, 1551-1560 (2011).
-
(2011)
Neurology
, vol.77
, pp. 1551-1560
-
-
Freedman, M.S.1
-
51
-
-
48349143130
-
Fatigue, depression and progression in multiple sclerosis
-
Koch, M., Uyttenboogaart, M., van Harten, A., Heerings, M. & De Keyser, J. Fatigue, depression and progression in multiple sclerosis. Mult. Scler. 14, 815-822 (2008).
-
(2008)
Mult. Scler.
, vol.14
, pp. 815-822
-
-
Koch, M.1
Uyttenboogaart, M.2
Van Harten, A.3
Heerings, M.4
De Keyser, J.5
-
52
-
-
84922949404
-
Depression in multiple sclerosis: A long-term longitudinal study
-
Koch, M. W. et al. Depression in multiple sclerosis: a long-term longitudinal study. Mult. Scler. 21, 76-82 (2015).
-
(2015)
Mult. Scler.
, vol.21
, pp. 76-82
-
-
Koch, M.W.1
-
53
-
-
20444401893
-
Immediate versus deferred antiepileptic drug treatment for early epilepsy and single seizures: A randomised controlled trial
-
Marson, A. et al. Immediate versus deferred antiepileptic drug treatment for early epilepsy and single seizures: a randomised controlled trial. Lancet 365, 2007-2013 (2005).
-
(2005)
Lancet
, vol.365
, pp. 2007-2013
-
-
Marson, A.1
-
54
-
-
33947241772
-
The SANAD study of effectiveness of carbamazepine, gabapentin, lamotrigine, oxcarbazepine, or topiramate for treatment of partial epilepsy: An unblinded randomised controlled trial
-
Marson, A. G. et al. The SANAD study of effectiveness of carbamazepine, gabapentin, lamotrigine, oxcarbazepine, or topiramate for treatment of partial epilepsy: an unblinded randomised controlled trial. Lancet 369, 1000-1015 (2007).
-
(2007)
Lancet
, vol.369
, pp. 1000-1015
-
-
Marson, A.G.1
-
55
-
-
33947228816
-
The SANAD study of effectiveness of valproate, lamotrigine, or topiramate for generalised and unclassifiable epilepsy: An unblinded randomised controlled trial
-
Marson, A. G. et al. The SANAD study of effectiveness of valproate, lamotrigine, or topiramate for generalised and unclassifiable epilepsy: an unblinded randomised controlled trial. Lancet 369, 1016-1026 (2007).
-
(2007)
Lancet
, vol.369
, pp. 1016-1026
-
-
Marson, A.G.1
-
56
-
-
80052592003
-
Drug-resistant epilepsy
-
Kwan, P., Schachter, S. C. & Brodie, M. J. Drug-resistant epilepsy. N. Engl. J. Med. 365, 919-926 (2011).
-
(2011)
N. Engl. J. Med.
, vol.365
, pp. 919-926
-
-
Kwan, P.1
Schachter, S.C.2
Brodie, M.J.3
-
57
-
-
57249087382
-
Lennox-Gastaut syndrome: A consensus approach on diagnosis, assessment, management, and trial methodology
-
Arzimanoglou, A. et al. Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology. Lancet Neurol. 8, 82-93 (2009).
-
(2009)
Lancet Neurol.
, vol.8
, pp. 82-93
-
-
Arzimanoglou, A.1
-
59
-
-
79955022433
-
Current therapeutic procedures in Dravet syndrome
-
Chiron, C. Current therapeutic procedures in Dravet syndrome. Dev. Med. Child Neurol. 53 (Suppl. 2), 16-18 (2011).
-
(2011)
Dev. Med. Child Neurol.
, vol.53
, pp. 16-18
-
-
Chiron, C.1
-
60
-
-
29144451510
-
Management of Landau-Kleffner syndrome
-
Mikati, M. A. & Shamseddine, A. N. Management of Landau-Kleffner syndrome. Paediatr. Drugs 7, 377-389 (2005).
-
(2005)
Paediatr. Drugs
, vol.7
, pp. 377-389
-
-
Mikati, M.A.1
Shamseddine, A.N.2
-
61
-
-
0031873690
-
Considerations on designing clinical trials to evaluate the place of new antiepileptic drugs in the treatment of newly diagnosed and chronic patients with epilepsy
-
No authors listed
-
[No authors listed] Considerations on designing clinical trials to evaluate the place of new antiepileptic drugs in the treatment of newly diagnosed and chronic patients with epilepsy. Epilepsia 39, 799-803 (1998).
-
(1998)
Epilepsia
, vol.39
, pp. 799-803
-
-
-
62
-
-
0021520020
-
A new rating scale for Alzheimer's disease
-
Rosen, W. G., Mohs, R. C. & Davis, K. L. A new rating scale for Alzheimer's disease. Am. J. Psychiatry 141, 1356-1364 (1984).
-
(1984)
Am. J. Psychiatry
, vol.141
, pp. 1356-1364
-
-
Rosen, W.G.1
Mohs, R.C.2
Davis, K.L.3
-
63
-
-
42749100518
-
Cholinesterase inhibitors for Alzheimer's disease
-
Art.
-
Birks, J. Cholinesterase inhibitors for Alzheimer's disease. Cochrane Database of Systematic Reviews, Issue 1. Art. No.: CD005593. http://dx.doi.org/10.1002/ 14651858.CD005593.
-
Cochrane Database of Systematic Reviews
, Issue.1
-
-
Birks, J.1
-
64
-
-
84855598434
-
What is the clinically relevant change on the ADAS-cog?
-
Schrag, A. et al. What is the clinically relevant change on the ADAS-cog? J. Neurol. Neurosurg. Psychiatry 83, 171-173 (2012).
-
(2012)
J. Neurol. Neurosurg. Psychiatry
, vol.83
, pp. 171-173
-
-
Schrag, A.1
-
65
-
-
23244452355
-
Rate of progression differs in frontotemporal dementia and Alzheimer disease
-
Rascovsky, K. et al. Rate of progression differs in frontotemporal dementia and Alzheimer disease. Neurology 65, 397-403 (2005).
-
(2005)
Neurology
, vol.65
, pp. 397-403
-
-
Rascovsky, K.1
-
66
-
-
24644437283
-
Frontotemporal dementia progresses to death faster than Alzheimer disease
-
Roberson, E. D. et al. Frontotemporal dementia progresses to death faster than Alzheimer disease. Neurology 65, 719-725 (2005).
-
(2005)
Neurology
, vol.65
, pp. 719-725
-
-
Roberson, E.D.1
-
67
-
-
0031457078
-
Transmissible spongiform encephalopathies
-
Haywood, A. M. Transmissible spongiform encephalopathies. N. Engl. J. Med. 337, 1821-1828 (1997).
-
(1997)
N. Engl. J. Med.
, vol.337
, pp. 1821-1828
-
-
Haywood, A.M.1
-
68
-
-
4944246589
-
Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies
-
Pocchiari, M. et al. Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Brain 127, 2348-2359 (2004).
-
(2004)
Brain
, vol.127
, pp. 2348-2359
-
-
Pocchiari, M.1
|