-
1
-
-
0014310582
-
Progressive proximal spinal and bulbar muscular atrophy of late onset: A sex-linked recessive trait
-
Kennedy, W.R. and Alter, M. and Sung, J.H. (1968) Progressive proximal spinal and bulbar muscular atrophy of late onset: A sex-linked recessive trait. Neurology, 18, pp. 671-680.
-
(1968)
Neurology
, vol.18
, pp. 671-680
-
-
Kennedy, W.R.1
Alter, M.2
Sung, J.H.3
-
2
-
-
0020584152
-
A family with adult spinal and bulbar muscular atrophy, X-linked inheritance and associated testicular failure
-
Arbizu, T. and Santamaria, J. and Gomez, J.M. and Quilez, A. and Serra, J.P. (1983) A family with adult spinal and bulbar muscular atrophy, X-linked inheritance and associated testicular failure. J Neurol Sci, 59, pp. 371-382.
-
(1983)
J. Neurol. Sci.
, vol.59
, pp. 371-382
-
-
Arbizu, T.1
Santamaria, J.2
Gomez, J.M.3
Quilez, A.4
Serra, J.P.5
-
3
-
-
0020457362
-
X-linked recessive bulbospinal neuronopathy: A report of ten cases
-
Harding, A.E. and Thomas, P.K. and Baraitser, M. and Bradbury, P.G. and Morgan-Hughes, J.A. and Ponsford, J.R. (1982) X-linked recessive bulbospinal neuronopathy: A report of ten cases. J Neurol Neurosurg Psychiatry, 45, pp. 1012-1019.
-
(1982)
J. Neurol. Neurosurg. Psychiatry
, vol.45
, pp. 1012-1019
-
-
Harding, A.E.1
Thomas, P.K.2
Baraitser, M.3
Bradbury, P.G.4
Morgan-Hughes, J.A.5
Ponsford, J.R.6
-
4
-
-
0030066136
-
Spinal and bulbar muscular atrophy: Androgen receptor dysfunction caused by a trinucleotide repeat expansion
-
MacLean, H.E. and Warne, G.L. and Zajac, J.D. (1996) Spinal and bulbar muscular atrophy: Androgen receptor dysfunction caused by a trinucleotide repeat expansion. J Neurol Sci, 135, pp. 149-157.
-
(1996)
J. Neurol. Sci.
, vol.135
, pp. 149-157
-
-
MacLean, H.E.1
Warne, G.L.2
Zajac, J.D.3
-
5
-
-
0343975426
-
Hereditary proximal spinal muscular atrophy of late onset
-
Kennedy, W.R. and Alter, M. and Foreman, R.T. (1966) Hereditary proximal spinal muscular atrophy of late onset. Neurology, 16, pp. 306-307.
-
(1966)
Neurology
, vol.16
, pp. 306-307
-
-
Kennedy, W.R.1
Alter, M.2
Foreman, R.T.3
-
6
-
-
0032772394
-
Cognition, language and behaviour in motor neuron disease: Evidence of frontotemporal dysfunction
-
Bak, T.H. and Hodges, J.R. (1999) Cognition, language and behaviour in motor neuron disease: Evidence of frontotemporal dysfunction. Dement Geriatr Cogn Disord, 10, pp. 29-32.
-
(1999)
Dement Geriatr. Cogn. Disord.
, vol.10
, pp. 29-32
-
-
Bak, T.H.1
Hodges, J.R.2
-
7
-
-
0017662179
-
Amyotrophic lateral sclerosis in Finland
-
Jokelainen, M. (1977) Amyotrophic lateral sclerosis in Finland. Acta Neurol Scand, 56, pp. 194-204.
-
(1977)
Acta Neurol. Scand.
, vol.56
, pp. 194-204
-
-
Jokelainen, M.1
-
8
-
-
0029026756
-
Inter-relation between 'classic' motor neuron disease and frontotemporal dementia: Neuropsychological and single photon emission computed tomography study
-
Talbot, P.R. and Goulding, P.J. and Lloyd, J.J. and Snowden, J.S. and Neary, D. and Testa, H.J. (1995) Inter-relation between 'classic' motor neuron disease and frontotemporal dementia: Neuropsychological and single photon emission computed tomography study. J Neurol Neurosurg Psychiatry, 58, pp. 541-547
-
(1995)
J. Neurol. Neurosurg. Psychiatry
, vol.58
, pp. 541-547
-
-
Talbot, P.R.1
Goulding, P.J.2
Lloyd, J.J.3
Snowden, J.S.4
Neary, D.5
Testa, H.J.6
-
9
-
-
0034326242
-
Cognitive change in motor neuron disease/amyotrophic lateral sclerosis (MND/ALS)
-
Neary, D. and Snowden, J.S. and Mann, D.M.A. (2000) Cognitive change in motor neuron disease/amyotrophic lateral sclerosis (MND/ALS). J Neurol Sci, 180, pp. 15-20.
-
(2000)
J. Neurol. Sci.
, vol.180
, pp. 15-20
-
-
Neary, D.1
Snowden, J.S.2
Mann, D.M.A.3
-
10
-
-
0021823269
-
Cognitive impairment in motor neuron disease
-
Gallassi, R. and Montagna, P. and Ciardulli, C. and Lorusso, S. and Mussuto, V. and Stracciari, A. (1985) Cognitive impairment in motor neuron disease. Acta Neurol Scand, 71, pp. 480-484.
-
(1985)
Acta Neurol. Scand.
, vol.71
, pp. 480-484
-
-
Gallassi, R.1
Montagna, P.2
Ciardulli, C.3
Lorusso, S.4
Mussuto, V.5
Stracciari, A.6
-
11
-
-
0029941595
-
Cognition, language and speech in amyotrophic lateral sclerosis: A review
-
Strong, M.J. and Grace, G.M. and Orange, J.B. and Leeper, H.A. (1996) Cognition, language and speech in amyotrophic lateral sclerosis: A review. J Clin Exp Neuropsychol, 18, pp. 291-303.
-
(1996)
J. Clin. Exp. Neuropsychol.
, vol.18
, pp. 291-303
-
-
Strong, M.J.1
Grace, G.M.2
Orange, J.B.3
Leeper, H.A.4
-
12
-
-
0037044240
-
The overlap of amyotrophic lateral sclerosis and frontotemporal dementia
-
Lomen-Hoerth, C. and Anderson, T. and Miller, B. (2002) The overlap of amyotrophic lateral sclerosis and frontotemporal dementia. Neurology, 59, pp. 1077-1079.
-
(2002)
Neurology
, vol.59
, pp. 1077-1079
-
-
Lomen-Hoerth, C.1
Anderson, T.2
Miller, B.3
-
13
-
-
0030926838
-
Relation between cognitive dysfunction and pseudobulbar palsy in amyotrophic lateral sclerosis
-
Abrahams, S. and Goldstein, L.H. and Al Chalabi, A. and Pickering, A. and Morris, R.G. and Passingham, R.E. et al (1997) Relation between cognitive dysfunction and pseudobulbar palsy in amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry, 62, pp. 464-472.
-
(1997)
J. Neurol. Neurosurg. Psychiatry
, vol.62
, pp. 464-472
-
-
Abrahams, S.1
Goldstein, L.H.2
Al Chalabi, A.3
Pickering, A.4
Morris, R.G.5
Passingham, R.E.6
-
14
-
-
0031867908
-
Kennedy's disease: Unusual molecular pathological and clinical features
-
Shaw, P.J. and Thagesen, H. and Tomkins, J. and Slade, J.Y. and Usher, P. and Jackson, A. et al (1998) Kennedy's disease: Unusual molecular pathological and clinical features. Neurology, 51, pp. 252-255.
-
(1998)
Neurology
, vol.51
, pp. 252-255
-
-
Shaw, P.J.1
Thagesen, H.2
Tomkins, J.3
Slade, J.Y.4
Usher, P.5
Jackson, A.6
-
15
-
-
0030049356
-
X-linked bulbar and spinal muscular atrophy, or Kennedy's disease: Clinical, neurophysiological, neuropathological, neuropsychological and molecular study of a large family
-
Guidetti, D. and Vescovini, E. and Motti, L. and Ghidoni, E. and Gemignani, F. and Marbini, A. et al (1996) X-linked bulbar and spinal muscular atrophy, or Kennedy's disease: Clinical, neurophysiological, neuropathological, neuropsychological and molecular study of a large family. J Neurol Sci, 135, pp. 140-148.
-
(1996)
J. Neurol. Sci.
, vol.135
, pp. 140-148
-
-
Guidetti, D.1
Vescovini, E.2
Motti, L.3
Ghidoni, E.4
Gemignani, F.5
Marbini, A.6
-
16
-
-
0034605478
-
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22
-
Hosler, B.A. and Siddique, T. and Sapp, P.C. and Sailor, W. and Huang, M.C. and Hossain, A. et al (2000) Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22. JAMA, 284, pp. 1664-1669.
-
(2000)
JAMA
, vol.284
, pp. 1664-1669
-
-
Hosler, B.A.1
Siddique, T.2
Sapp, P.C.3
Sailor, W.4
Huang, M.C.5
Hossain, A.6
-
17
-
-
9144253222
-
Chromosomal translocation t (18;21)(q23;q22.1) indicates novel susceptibility loci for frontotemporal dementia with ALS
-
Prudlo, J. and Alber, B. and Kalscheuer, V.M. and Roemer, K. and Martin, T. and Dullinger, J. et al (2004) Chromosomal translocation t (18;21)(q23;q22.1) indicates novel susceptibility loci for frontotemporal dementia with ALS. Ann Neurol, 55, pp. 134-138.
-
(2004)
Ann. Neurol.
, vol.55
, pp. 134-138
-
-
Prudlo, J.1
Alber, B.2
Kalscheuer, V.M.3
Roemer, K.4
Martin, T.5
Dullinger, J.6
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