-
1
-
-
0014310582
-
Progressive proximal spinal and bulbar muscular atrophy of late onset: A sex-link recessive trait
-
Kennedy WR, Alter M, Sung JH. Progressive proximal spinal and bulbar muscular atrophy of late onset: a sex-link recessive trait. Neurology 1968;18:671-680.
-
(1968)
Neurology
, vol.18
, pp. 671-680
-
-
Kennedy, W.R.1
Alter, M.2
Sung, J.H.3
-
2
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
La Spada AR, Wilson EM, Lubahn DB, Harding AE, Fischbeck KH Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 1991;352 77-79.
-
(1991)
Nature
, vol.352
, pp. 77-79
-
-
La Spada, A.R.1
Wilson, E.M.2
Lubahn, D.B.3
Harding, A.E.4
Fischbeck, K.H.5
-
3
-
-
0028596054
-
Étude génétique moléculaire d'une famille atteinte su syndrome de Kennedy avec une hétérozygote symptomatique
-
Paris
-
Ferion E, Le Roux MG, Pascal O, Moisan JP, Fève JR. Étude génétique moléculaire d'une famille atteinte su syndrome de Kennedy avec une hétérozygote symptomatique. Rev Neurol (Paris) 1994,150.854-857.
-
(1994)
Rev Neurol
, vol.150
, pp. 854-857
-
-
Ferion, E.1
Le Roux, M.G.2
Pascal, O.3
Moisan, J.P.4
Fève, J.R.5
-
4
-
-
84865894462
-
Princípios teóricos e básicos em biologia molecular
-
Andrade LEC. Princípios teóricos e básicos em biologia molecular. Rev Bras Reumatol 1993;33:31-41.
-
(1993)
Rev Bras Reumatol
, vol.33
, pp. 31-41
-
-
Andrade, L.E.C.1
-
6
-
-
0030077323
-
Triplet repeats and human diseases
-
Singer RH Triplet repeats and human diseases. Mol Med Today 1996;2:65-69
-
(1996)
Mol Med Today
, vol.2
, pp. 65-69
-
-
Singer, R.H.1
-
7
-
-
0030477621
-
Trinucleotide repeat disorders in humans: Discussions of mechanism and medical issues
-
Timchenko LT, Caskey CT Trinucleotide repeat disorders in humans: discussions of mechanism and medical issues. FASEB J 1996,10.1589-1597
-
(1996)
FASEB J
, vol.10
, pp. 1589-1597
-
-
Timchenko, L.T.1
Caskey, C.T.2
-
9
-
-
0028309533
-
Genes with triplet repeats: A new classes of mutations causing neurological diseases
-
Plassart E, Fontaine B Genes with triplet repeats: a new classes of mutations causing neurological diseases. Biomed Pharmacother 1994,48:191-197
-
(1994)
Biomed Pharmacother
, vol.48
, pp. 191-197
-
-
Plassart, E.1
Fontaine, B.2
-
10
-
-
0029744077
-
Analysis of polyglutamine-coding repeats in the TATA-binding protein in diferent human populations and in patients with schizophrenia and bipolar affective disorder
-
Rubinztein DC, Leggo J, Crow TJ, et al Analysis of polyglutamine-coding repeats in the TATA-binding protein in diferent human populations and in patients with schizophrenia and bipolar affective disorder Am J Med Genet 1996 67:495-498
-
(1996)
Am J Med Genet
, vol.67
, pp. 495-498
-
-
Rubinztein, D.C.1
Leggo, J.2
Crow, T.J.3
-
11
-
-
0030712094
-
Transgenic mouse models of neurodegenerative disease caused by CAG/polyglutamine expansions
-
Bates GP, Davies SW Transgenic mouse models of neurodegenerative disease caused by CAG/polyglutamine expansions. Mol Med Today 1997,3:508-515
-
(1997)
Mol Med Today
, vol.3
, pp. 508-515
-
-
Bates, G.P.1
Davies, S.W.2
-
12
-
-
18744437622
-
Doença de Kennedy: Relato de dois casos
-
Seefeld M, Cunha FM, Feriaz LE, Scola RH, Werneck LC. Doença de Kennedy: relato de dois casos. Arq Neuropsiquiatr 1995;53:471-474
-
(1995)
Arq Neuropsiquiatr
, vol.53
, pp. 471-474
-
-
Seefeld, M.1
Cunha, F.M.2
Feriaz, L.E.3
Scola, R.H.4
Werneck, L.C.5
-
13
-
-
0030798569
-
Spinobulbar muscular atrophy can mimic ALS the importance of genetic testing in male patients with atypical ALS
-
Parboosingh JS, Figlewicz DA, Krizus A, et al. Spinobulbar muscular atrophy can mimic ALS the importance of genetic testing in male patients with atypical ALS Neurology 1997;49:568-572.
-
(1997)
Neurology
, vol.49
, pp. 568-572
-
-
Parboosingh, J.S.1
Figlewicz, D.A.2
Krizus, A.3
-
14
-
-
0025260440
-
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromossome 5q11.2-13 3
-
Brzustowicz LM, Lehner T, Castilla LH et al. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromossome 5q11.2-13 3 Nature 1990,344 540-541
-
(1990)
Nature
, vol.344
, pp. 540-541
-
-
Brzustowicz, L.M.1
Lehner, T.2
Castilla, L.H.3
-
15
-
-
0029129227
-
Spinal and bulbar muscular atrophy: A trinucleotide-repeat expansion neurodegenetative disease
-
Brooks BP, Fischbeck KH Spinal and bulbar muscular atrophy: a trinucleotide-repeat expansion neurodegenetative disease. Trends Neurosci 1995;18:459-461.
-
(1995)
Trends Neurosci
, vol.18
, pp. 459-461
-
-
Brooks, B.P.1
Fischbeck, K.H.2
-
16
-
-
0026456909
-
Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy
-
Belsham DD, Woon-Chee Y, Greenberg CR, Wrogemann K. Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy. J Neurol Sci 1992,112:133-138
-
(1992)
J Neurol Sci
, vol.112
, pp. 133-138
-
-
Belsham, D.D.1
Woon-Chee, Y.2
Greenberg, C.R.3
Wrogemann, K.4
-
17
-
-
0028952350
-
Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disorders
-
Ferlini A, Patrosso MC, Guidetti D, et al Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disorders. Am J Med Gen 1995,55 105-111.
-
(1995)
Am J Med Gen
, vol.55
, pp. 105-111
-
-
Ferlini, A.1
Patrosso, M.C.2
Guidetti, D.3
-
18
-
-
0030023666
-
Testosterone therapy and the pathogenesis of Kennedy's disease (X-linked bulbospinal muscular atrophy)
-
Goldenberg JN, Bradley WG Testosterone therapy and the pathogenesis of Kennedy's disease (X-linked bulbospinal muscular atrophy) J Neurol Sci 1996,135.158-161
-
(1996)
J Neurol Sci
, vol.135
, pp. 158-161
-
-
Goldenberg, J.N.1
Bradley, W.G.2
|