-
1
-
-
33644831390
-
Uncommon causes of dementia: Rare, but not marginal
-
DOI 10.1017/S1041610205001742, PII S1041610205001742
-
Almeida, O., Flicker, L. and Lautenschlager, N. T. (2005). Uncommon causes of dementia: rare, but not marginal. International Psychogeriatrics, 17 (Suppl.), S1-S2. (Pubitemid 44561751)
-
(2005)
International Psychogeriatrics
, vol.17
, Issue.SUPPL. 1
-
-
Almeida, O.P.1
Flicker, L.2
Lautenschlager, N.T.3
-
2
-
-
0033358526
-
A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease
-
DOI 10.1086/302374
-
Almqvist, E. W., Bloch, M., Brinkman, R., Craufurd, D. and Hayden, M. R. (1999). A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease. American Journal of Human Genetics, 64, 1293-1304. (Pubitemid 30468747)
-
(1999)
American Journal of Human Genetics
, vol.64
, Issue.5
, pp. 1293-1304
-
-
Almqvist, E.W.1
Bloch, M.2
Brinkman, R.3
Craufurd, D.4
Hayden, M.R.5
-
3
-
-
3042681436
-
-
Australian Law Reform Commission Sydney last accessed 20 April 2011
-
Australian Law Reform Commission (2003). Essentially Yours: The Protection of Human Genetic Information in Australia. Sydney. Available at: http://beta.austlii.edu.au/au/other/alrc/publications/reports/96/; last accessed 20 April 2011.
-
(2003)
Essentially Yours: The Protection of Human Genetic Information in Australia
-
-
-
4
-
-
84899598163
-
-
last accessed 20 April 2011
-
Docker, K. (2010). Explaining my DNA Results. Available at: http://hungrybeast.abc.net.au/stories/explaining-my-dnaresults; last accessed 20 April 2011.
-
(2010)
Explaining My DNA Results
-
-
Docker, K.1
-
5
-
-
0035666019
-
Psychological studies in Huntington's disease: Making up the balance [3]
-
Duisterhof, M., Trijsburg, R. W., Niermeijer, M. F., Roos, R. A. and Tibben, A. (2001). Psychological studies in Huntington's disease: making up the balance. Journal of Medical Genetics, 38, 852-861. (Pubitemid 34014211)
-
(2001)
Journal of Medical Genetics
, vol.38
, Issue.12
, pp. 852-861
-
-
Duisterhof, M.1
Trijsburg, R.W.2
Niermeijer, M.F.3
Roos, R.A.C.4
Tibben, A.5
-
6
-
-
84899613446
-
Genetic discrimination of individuals at risk of Huntington's disease: Further analysis of the RESPOND-HD data from Australia (site 144)
-
Goh, A., Yastrubetskaya, O. and Chiu, E. (2010). Genetic discrimination of individuals at risk of Huntington's disease: further analysis of the RESPOND-HD data from Australia (site 144). Neurotherapeutics, 7, 138.
-
(2010)
Neurotherapeutics
, vol.7
, pp. 138
-
-
Goh, A.1
Yastrubetskaya, O.2
Chiu, E.3
-
7
-
-
7944221966
-
Genetic association study of PINK1 coding polymorphisms in Parkinson's disease
-
DOI 10.1016/j.neulet.2004.09.043, PII S0304394004011772
-
Groen, J. L. et al. (2004). Genetic association study of PINK1 coding polymorphisms in Parkinson's disease. Neuroscience Letters, 372, 226-229. (Pubitemid 39470201)
-
(2004)
Neuroscience Letters
, vol.372
, Issue.3
, pp. 226-229
-
-
Groen, J.L.1
Kawarai, T.2
Toulina, A.3
Rivoiro, C.4
Salehi-Rad, S.5
Sato, C.6
Morgan, A.7
Liang, Y.8
Postuma, R.B.9
St George-Hyslop, P.10
Lang, A.E.11
Rogaeva, E.12
-
8
-
-
0021028244
-
A polymorphic DNA marker genetically linked to Huntington's disease
-
Gusella, J. F. et al. (1983). A polymorphic DNA marker genetically linked to Huntington's disease. Nature, 306, 234-238. (Pubitemid 14232350)
-
(1983)
Nature
, vol.306
, Issue.5940
, pp. 234-238
-
-
Gusella, J.F.1
Wexler, N.S.2
Conneally, P.M.3
-
11
-
-
0035479286
-
Mutation of the PRNP gene at codon 211 in familial CJD
-
Ladogana, A. et al. (2001). Mutation of the PRNP gene at codon 211 in familial CJD. American Journal of Medical Genetics, 103, 133-137.
-
(2001)
American Journal of Medical Genetics
, vol.103
, pp. 133-137
-
-
Ladogana, A.1
-
13
-
-
0030744876
-
Mutation in the α-synuclein gene identified in families with Parkinson's disease
-
DOI 10.1126/science.276.5321.2045
-
Polymeropoulos, M. H. et al. (1997). Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science, 276, 2045-2047. (Pubitemid 27443610)
-
(1997)
Science
, vol.276
, Issue.5321
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
Ide, S.E.4
Dehejia, A.5
Dutra, A.6
Pike, B.7
Root, H.8
Rubenstein, J.9
Boyer, R.10
Stenroos, E.S.11
Chandrasekharappa, S.12
Athanassiadou, A.13
Papapetropoulos, T.14
Johnson, W.G.15
Lazzarini, A.M.16
Duvoisin, R.C.17
Di Iorio, G.18
Golbe, L.I.19
Nussbaum, R.L.20
more..
-
14
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
-
Sherrington, R. et al. (1995). Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature, 375, 754-760.
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
-
15
-
-
0022209882
-
Genetic jeopardy and the new clairvoyance
-
A. Bearn, A. Motulsky and B. Childs (eds.) New York: Praeger
-
Wexler, N. S. (1985). Genetic jeopardy and the new clairvoyance. In A. Bearn, A. Motulsky and B. Childs (eds.), Progress in Medical Genetics, vol. 6, Genetics of Neurological Disorders (pp. 277-304). New York: Praeger.
-
(1985)
Progress in Medical Genetics Vol. 6, Genetics of Neurological Disorders
, pp. 277-304
-
-
Wexler, N.S.1
-
16
-
-
12144288251
-
Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset
-
DOI 10.1073/pnas.0308679101
-
Wexler, N. S. et al. (2004). Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. Proceedings of the National Academy of Sciences of the United States of America, 101, 3498-3503. (Pubitemid 38338224)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.10
, pp. 3498-3503
-
-
Wexler, N.S.1
Lorimer, J.2
Porter, J.3
Gomez, F.4
Moskowitz, C.5
Shackell, E.6
Marder, K.7
Penchaszadeh, G.8
Roberts, S.A.9
Gayan, J.10
Brocklebank, D.11
Cherny, S.S.12
Cardon, L.R.13
Gray, J.14
Dlouhy, S.R.15
Wiktorski, S.16
Hodes, M.E.17
Conneally, P.M.18
Penney, J.B.19
Gusella, J.20
Cha, J.-H.21
Irizarry, M.22
Rosas, D.23
Hersch, S.24
Hollingsworth, Z.25
MacDonald, M.26
Young, A.B.27
Andresen, J.M.28
Housman, D.E.29
Mieja De Young, M.30
Bonilla, E.31
Stillings, T.32
Negrette, A.33
Snodgrass, S.R.34
Martinez-Jaurrieta, M.D.35
Ramos-Arroyo, M.A.36
Bickham, J.37
Ramos, J.S.38
Marshall, F.39
Shoulson, I.40
Rey, G.J.41
Feigin, A.42
Arnheim, N.43
Acevedo-Cruz, A.44
Acosta, L.45
Alvir, J.46
Fischbeck, K.47
Thompson, L.M.48
Young, A.49
Dure, L.50
O'Brien, C.J.51
Paulsen, J.52
Brickman, A.53
Krch, D.54
Peery, S.55
Hogarth, P.56
Higgins Jr., D.S.57
Landwehrmeyeri, B.58
more..
-
17
-
-
0041833569
-
Tau protein in frontotemporal dementia linked to chromosome 3 (FTD-3)
-
Yancopoulou, D., Crowther, R. A., Chakrabartil, L., Gydesen, S., Brown, J. M. and Spillantini, M. G. (2003). Tau protein in frontotemporal dementia linked to chromosome 3 (FTD-3). Journal of Neuropathology and Experimental Neurology, 62, 878-882. (Pubitemid 37082781)
-
(2003)
Journal of Neuropathology and Experimental Neurology
, vol.62
, Issue.8
, pp. 878-882
-
-
Yancopoulou, D.1
Crowther, R.A.2
Chakrabarti, L.3
Gydesen, S.4
Brown, J.M.5
Spillantini, M.G.6
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