-
1
-
-
34250815039
-
Genetics of essential tremor
-
Deng H., Le W., Jankovic J. Genetics of essential tremor. Brain 2007, 130:1456-1464.
-
(2007)
Brain
, vol.130
, pp. 1456-1464
-
-
Deng, H.1
Le, W.2
Jankovic, J.3
-
2
-
-
27144517403
-
Analysis of LRRK2 functional domains in nondominant Parkinson disease
-
Skipper L., Shen H., Chua E., Bonnard C., Kolatkar P., Tan L.C., et al. Analysis of LRRK2 functional domains in nondominant Parkinson disease. Neurology 2005, 65:1319-1321.
-
(2005)
Neurology
, vol.65
, pp. 1319-1321
-
-
Skipper, L.1
Shen, H.2
Chua, E.3
Bonnard, C.4
Kolatkar, P.5
Tan, L.C.6
-
3
-
-
34247191920
-
Parkinsonism and essential tremor in a family with pseudo-dominant inheritance of PARK2: an FP-CIT SPECT study
-
Pellecchia M.T., Varrone A., Annesi G., Amboni M., Cicarelli G., Sansone V., et al. Parkinsonism and essential tremor in a family with pseudo-dominant inheritance of PARK2: an FP-CIT SPECT study. Mov Disord 2007, 22:559-563.
-
(2007)
Mov Disord
, vol.22
, pp. 559-563
-
-
Pellecchia, M.T.1
Varrone, A.2
Annesi, G.3
Amboni, M.4
Cicarelli, G.5
Sansone, V.6
-
4
-
-
33947192873
-
Afamily with Parkinson disease, essential tremor, bell palsy, and parkin mutations
-
Deng H., Le W.D., Hunter C.B., Mejia N., Xie W.J., Jankovic J. Afamily with Parkinson disease, essential tremor, bell palsy, and parkin mutations. Arch Neurol 2007, 64:421-424.
-
(2007)
Arch Neurol
, vol.64
, pp. 421-424
-
-
Deng, H.1
Le, W.D.2
Hunter, C.B.3
Mejia, N.4
Xie, W.J.5
Jankovic, J.6
-
5
-
-
84155187234
-
LINGO1 variants in essential tremor and Parkinson's disease
-
Deng H., Gu S., Jankovic J. LINGO1 variants in essential tremor and Parkinson's disease. Acta Neurol Scand 2012, 125:1-7.
-
(2012)
Acta Neurol Scand
, vol.125
, pp. 1-7
-
-
Deng, H.1
Gu, S.2
Jankovic, J.3
-
6
-
-
84864931903
-
Exome sequencing identifies FUS mutations as a cause of essential tremor
-
Merner N.D., Girard S.L., Catoire H., Bourassa C.V., Belzil V.V., Riviere J.B., et al. Exome sequencing identifies FUS mutations as a cause of essential tremor. Am J Hum Genet 2012, 91:313-319.
-
(2012)
Am J Hum Genet
, vol.91
, pp. 313-319
-
-
Merner, N.D.1
Girard, S.L.2
Catoire, H.3
Bourassa, C.V.4
Belzil, V.V.5
Riviere, J.B.6
-
7
-
-
84877589178
-
Genetic analysis of the fused in sarcoma gene in Chinese Han patients with essential tremor
-
2078.e3-e4
-
Zheng W., Deng X., Liang H., Song Z., Gao K., Yang Y., et al. Genetic analysis of the fused in sarcoma gene in Chinese Han patients with essential tremor. Neurobiol Aging 2013, 34. 2078.e3-e4.
-
(2013)
Neurobiol Aging
, vol.34
-
-
Zheng, W.1
Deng, X.2
Liang, H.3
Song, Z.4
Gao, K.5
Yang, Y.6
-
8
-
-
84884545450
-
Identification of a novel risk variant in the FUS gene in essential tremor
-
Wu Y.R., Foo J.N., Tan L.C., Chen C.M., Prakash K.M., Chen Y.C., et al. Identification of a novel risk variant in the FUS gene in essential tremor. Neurology 2013, 81:541-544.
-
(2013)
Neurology
, vol.81
, pp. 541-544
-
-
Wu, Y.R.1
Foo, J.N.2
Tan, L.C.3
Chen, C.M.4
Prakash, K.M.5
Chen, Y.C.6
-
9
-
-
77956357112
-
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia
-
Yan J., Deng H.X., Siddique N., Fecto F., Chen W., Yang Y., et al. Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia. Neurology 2010, 75:807-814.
-
(2010)
Neurology
, vol.75
, pp. 807-814
-
-
Yan, J.1
Deng, H.X.2
Siddique, N.3
Fecto, F.4
Chen, W.5
Yang, Y.6
-
10
-
-
41149163183
-
Parkinson's disease: clinical features and diagnosis
-
Jankovic J. Parkinson's disease: clinical features and diagnosis. JNeurol Neurosurg Psychiatr 2008, 79:368-376.
-
(2008)
JNeurol Neurosurg Psychiatr
, vol.79
, pp. 368-376
-
-
Jankovic, J.1
-
11
-
-
77953890823
-
TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
-
Lagier-Tourenne C., Polymenidou M., Cleveland D.W. TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration. Hum Mol Genet 2010, 19:R46-R64.
-
(2010)
Hum Mol Genet
, vol.19
-
-
Lagier-Tourenne, C.1
Polymenidou, M.2
Cleveland, D.W.3
-
12
-
-
79951740192
-
Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis
-
Belzil V.V., Daoud H., St-Onge J., Desjarlais A., Bouchard J.P., Dupre N., et al. Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis. Amyotroph Lateral Scler 2011, 12:113-117.
-
(2011)
Amyotroph Lateral Scler
, vol.12
, pp. 113-117
-
-
Belzil, V.V.1
Daoud, H.2
St-Onge, J.3
Desjarlais, A.4
Bouchard, J.P.5
Dupre, N.6
|