-
1
-
-
0027023516
-
Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy
-
La Spada AR, Roling DB, Harding AE, et al. Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy. Nat Genet 1992;2:301-4.
-
(1992)
Nat Genet
, vol.2
, pp. 301-304
-
-
La Spada, A.R.1
Roling, D.B.2
Harding, A.E.3
-
2
-
-
0036894940
-
X-linked bulbospinal neuronopathy: Kennedy disease
-
Sperfeld AD, Karitzky J, Brummer D, et al. X-linked bulbospinal neuronopathy: Kennedy disease. Arch Neurol 2002;59:1921-6.
-
(2002)
Arch Neurol
, vol.59
, pp. 1921-1926
-
-
Sperfeld, A.D.1
Karitzky, J.2
Brummer, D.3
-
3
-
-
0033911038
-
Sensory ataxia as the initial clinical symptom in X-linked recessive bulbospinal neuronopathy
-
Buecking A, Pfister R. Sensory ataxia as the initial clinical symptom in X-linked recessive bulbospinal neuronopathy. J Neurol Neurosurg Psychiatry 2000;69:277.
-
(2000)
J Neurol Neurosurg Psychiatry
, vol.69
, pp. 277
-
-
Buecking, A.1
Pfister, R.2
-
4
-
-
0030049356
-
-
Guidetti D, Vescovini E, Motti L, et al. X-linked bulbar and spinal muscular atrophy or Kennedy disease: clinical, neurophysiological, neuropathological, neuropsychological and molecular study of a large family. J Neurol Sci 1996;135:140-8.
-
Guidetti D, Vescovini E, Motti L, et al. X-linked bulbar and spinal muscular atrophy or Kennedy disease: clinical, neurophysiological, neuropathological, neuropsychological and molecular study of a large family. J Neurol Sci 1996;135:140-8.
-
-
-
-
5
-
-
0034973141
-
A voxel-based morphometric study of ageing in 465 normal adult human brains
-
Good CD, Johnsrude IS, Ashburner J, et al. A voxel-based morphometric study of ageing in 465 normal adult human brains. Neuroimage 2001;14:21-36.
-
(2001)
Neuroimage
, vol.14
, pp. 21-36
-
-
Good, C.D.1
Johnsrude, I.S.2
Ashburner, J.3
-
7
-
-
0031867908
-
Kennedy's disease: Unusual molecular pathologic and clinical features
-
Shaw PJ, Thagesen H, Tomkins J, et al. Kennedy's disease: unusual molecular pathologic and clinical features. Neurology 1998;51:252-5.
-
(1998)
Neurology
, vol.51
, pp. 252-255
-
-
Shaw, P.J.1
Thagesen, H.2
Tomkins, J.3
-
8
-
-
0036021684
-
Proton MRS in Kennedy disease: Absolute metabolite and macromolecular concentrations
-
Mader I, Karitzky J, Klose U, et al. Proton MRS in Kennedy disease: absolute metabolite and macromolecular concentrations. J Magn Reson Imaging 2002;16:160-7.
-
(2002)
J Magn Reson Imaging
, vol.16
, pp. 160-167
-
-
Mader, I.1
Karitzky, J.2
Klose, U.3
-
9
-
-
29244468268
-
Global brain atrophy and corticospinal tract alterations in ALS, as investigated by voxel-based morphometry of 3-D MRI
-
Kassubek J, Unrath A, Huppertz HJ, et al. Global brain atrophy and corticospinal tract alterations in ALS, as investigated by voxel-based morphometry of 3-D MRI. Amyotroph Lateral Scler Other Motor Neuron Disord 2005;6:213-20.
-
(2005)
Amyotroph Lateral Scler Other Motor Neuron Disord
, vol.6
, pp. 213-220
-
-
Kassubek, J.1
Unrath, A.2
Huppertz, H.J.3
-
10
-
-
20544476698
-
MR-pathologic comparison of the upper spinal cord in different motor neuron diseases
-
Sperfeld AD, Bretschneider V, Flaith L, et al. MR-pathologic comparison of the upper spinal cord in different motor neuron diseases. Eur Neurol 2005;53:74-7.
-
(2005)
Eur Neurol
, vol.53
, pp. 74-77
-
-
Sperfeld, A.D.1
Bretschneider, V.2
Flaith, L.3
-
11
-
-
20144362557
-
Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients
-
Adachi H, Katsuno M, Minamiyama M, et al. Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients. Brain 2005;128:659-70.
-
(2005)
Brain
, vol.128
, pp. 659-670
-
-
Adachi, H.1
Katsuno, M.2
Minamiyama, M.3
-
12
-
-
0024586435
-
X-linked recessive bulbospinal neuronopathy. A clinicopathological study
-
Sobue G, Hashizume Y, Mukai E, et al. X-linked recessive bulbospinal neuronopathy. A clinicopathological study. Brain 1989;112:209-32.
-
(1989)
Brain
, vol.112
, pp. 209-232
-
-
Sobue, G.1
Hashizume, Y.2
Mukai, E.3
-
13
-
-
0038714285
-
Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy
-
Katsuno M, Adachi H, Doyu M, et al. Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy. Nat Med 2003;9:768-73.
-
(2003)
Nat Med
, vol.9
, pp. 768-773
-
-
Katsuno, M.1
Adachi, H.2
Doyu, M.3
-
14
-
-
0009744392
-
Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLA
-
Schilling G, Wood JD, Duan K, et al. Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLA. Neuron 1999;24:275-86.
-
(1999)
Neuron
, vol.24
, pp. 275-286
-
-
Schilling, G.1
Wood, J.D.2
Duan, K.3
-
15
-
-
0037444446
-
Heat shock protein 70 chaperone overexpression ameliorates phenotypes of the spinal and bulbar muscular atrophy transgenic mouse model by reducing nuclear-localized mutant androgen receptor protein
-
Adachi H, Katsuno M, Minamiyama M, et al. Heat shock protein 70 chaperone overexpression ameliorates phenotypes of the spinal and bulbar muscular atrophy transgenic mouse model by reducing nuclear-localized mutant androgen receptor protein. J Neurosci 2003;23:2203-11.
-
(2003)
J Neurosci
, vol.23
, pp. 2203-2211
-
-
Adachi, H.1
Katsuno, M.2
Minamiyama, M.3
|