-
2
-
-
0025344047
-
Olivopontocerebellar atrophy: MR diagnosis and relationship to multisystem atrophy
-
Savoiardo M, Strada L, Girotti F, et al. Olivopontocerebellar atrophy: MR diagnosis and relationship to multisystem atrophy. Radiology 1990;174:693-696
-
(1990)
Radiology
, vol.174
, pp. 693-696
-
-
Savoiardo, M.1
Strada, L.2
Girotti, F.3
-
3
-
-
0028238767
-
Friedreich's ataxia: MR findings involving the cervical portion of the spinal cord
-
Mascalchi M, Salvi F, Piacentini S, Bartolozzi C. Friedreich's ataxia: MR findings involving the cervical portion of the spinal cord. AJR 1994;163:187-191
-
(1994)
AJR
, vol.163
, pp. 187-191
-
-
Mascalchi, M.1
Salvi, F.2
Piacentini, S.3
Bartolozzi, C.4
-
5
-
-
0027405101
-
Magnetic resonance imaging in hereditary and idiopathic ataxia
-
Wullner U, Klockgethet T, Petersen D, et al. Magnetic resonance imaging in hereditary and idiopathic ataxia. Neurology 1993;43:318-326
-
(1993)
Neurology
, vol.43
, pp. 318-326
-
-
Wullner, U.1
Klockgethet, T.2
Petersen, D.3
-
6
-
-
0029042435
-
Added value of automated clinical proton MR spectroscopy of the brain
-
Moats TA, Watson L, Schonl T, et al. Added value of automated clinical proton MR spectroscopy of the brain. J Comput Assist Tomogr 1995;19:480-491
-
(1995)
J Comput Assist Tomogr
, vol.19
, pp. 480-491
-
-
Moats, T.A.1
Watson, L.2
Schonl, T.3
-
8
-
-
0027257734
-
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci
-
Jodice C, Frontali M, Persichetti F, et al. The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci. Hum Mol Genet 1993; 2:1383-1387
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1383-1387
-
-
Jodice, C.1
Frontali, M.2
Persichetti, F.3
-
9
-
-
0028037806
-
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias
-
Giunti P, Sweeney MG, Spadaro M, et al. The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias. Brain 1994;117:645-649
-
(1994)
Brain
, vol.117
, pp. 645-649
-
-
Giunti, P.1
Sweeney, M.G.2
Spadaro, M.3
-
10
-
-
0028224243
-
Automated single-voxel proton MRS: Technical development and multisite verification
-
Webb PG, Sailasuta N, Kohler SJ, et al. Automated single-voxel proton MRS: technical development and multisite verification. Magn Reson Med 1994;31:365-373
-
(1994)
Magn Reson Med
, vol.31
, pp. 365-373
-
-
Webb, P.G.1
Sailasuta, N.2
Kohler, S.J.3
-
11
-
-
0027164698
-
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
-
Orr HT, Chung M, Banfi S, et al. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet 1993;4:221-226
-
(1993)
Nat Genet
, vol.4
, pp. 221-226
-
-
Orr, H.T.1
Chung, M.2
Banfi, S.3
-
12
-
-
0027162192
-
Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to human chromosome 12q23-24.1
-
Gispert S, Twells R, Oroczo G, et al. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to human chromosome 12q23-24.1. Nat Genet 1993; 4:295-299
-
(1993)
Nat Genet
, vol.4
, pp. 295-299
-
-
Gispert, S.1
Twells, R.2
Oroczo, G.3
-
13
-
-
0027279503
-
The gene for Machado-Joseph disease maps to chromosome 14q
-
Takiyama Y, Nishizawa M, Tanaka H, et al. The gene for Machado-Joseph disease maps to chromosome 14q. Nat Genet 1993;4:300-304
-
(1993)
Nat Genet
, vol.4
, pp. 300-304
-
-
Takiyama, Y.1
Nishizawa, M.2
Tanaka, H.3
-
14
-
-
0001172320
-
Autosomal dominant spinocerebellar ataxia: Clinical description of a distinct hereditary ataxia and genetic localization to chromosome 16 (SCA4) in a Utah kindred
-
Abstract
-
Gardner K, Alderson K, Galster B, et al. Autosomal dominant spinocerebellar ataxia: clinical description of a distinct hereditary ataxia and genetic localization to chromosome 16 (SCA4) in a Utah kindred. Neurology 1994;44(suppl 2):921S (Abstract)
-
(1994)
Neurology
, vol.44
, Issue.2 SUPPL.
-
-
Gardner, K.1
Alderson, K.2
Galster, B.3
-
15
-
-
0028020605
-
Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11
-
Ranum LPW, Schut LJ, Lundgren J, et al. Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11. Nat Genet 1994; 8:280-284
-
(1994)
Nat Genet
, vol.8
, pp. 280-284
-
-
Ranum, L.P.W.1
Schut, L.J.2
Lundgren, J.3
-
16
-
-
0029842513
-
DNA-triplet repeats and neurologic disease
-
Rosenberg RN. DNA-triplet repeats and neurologic disease. N Engl J Med 1996;335:221-226
-
(1996)
N Engl J Med
, vol.335
, pp. 221-226
-
-
Rosenberg, R.N.1
-
17
-
-
0024273067
-
Low leukocyte glutamate dehydrogenase activity does not correlate with a particular type of multiple system atrophy
-
Duvoisin RC, Nicklas WJ, Ritchie V, et al. Low leukocyte glutamate dehydrogenase activity does not correlate with a particular type of multiple system atrophy. J Neurol Neurosurg Psychiatry 1988;51:1508-1511
-
(1988)
J Neurol Neurosurg Psychiatry
, vol.51
, pp. 1508-1511
-
-
Duvoisin, R.C.1
Nicklas, W.J.2
Ritchie, V.3
-
18
-
-
0022506793
-
Glutamate dehydrogenase in olivopontocerebellar atrophies: Leukocytes, fibroblasts and muscle mitochondria
-
Finocchiaro G, Taroni F, DiDonato S. Glutamate dehydrogenase in olivopontocerebellar atrophies: leukocytes, fibroblasts and muscle mitochondria. Neurology 1985;36:550-553
-
(1985)
Neurology
, vol.36
, pp. 550-553
-
-
Finocchiaro, G.1
Taroni, F.2
DiDonato, S.3
-
19
-
-
0024364966
-
Normal cerebellar glutamate dehydrogenase protein in spinocerebellar degeneration
-
Rosenberg RN, Banner C. Normal cerebellar glutamate dehydrogenase protein in spinocerebellar degeneration. J Neurol Neurosurg Psychiatry 1989;52:666-668
-
(1989)
J Neurol Neurosurg Psychiatry
, vol.52
, pp. 666-668
-
-
Rosenberg, R.N.1
Banner, C.2
-
20
-
-
0002402978
-
Diseases of the basal ganglia, cerebellum and motor neurons
-
Hume Adams J, Corsellis JAN, Duchen LW, eds. New York: Wiley
-
Oppenheimer DR. Diseases of the basal ganglia, cerebellum and motor neurons. In: Hume Adams J, Corsellis JAN, Duchen LW, eds. Greenfield's neuropathology. 4th ed. New York: Wiley 1984;699-747
-
(1984)
Greenfield's Neuropathology. 4th Ed.
, pp. 699-747
-
-
Oppenheimer, D.R.1
-
21
-
-
0028819081
-
n expansion and early premonitory signs and symptoms
-
n expansion and early premonitory signs and symptoms. Neurology 1995;45:24-30
-
(1995)
Neurology
, vol.45
, pp. 24-30
-
-
Genis, D.1
Matilla, T.2
Volpini, V.3
-
22
-
-
0026582590
-
HLA-linked spinocerebellar ataxia: A clinical and genetic study of large Italian kindreds
-
Spadaro M, Giunti P, Lulli P, et al. HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds. Acta Neurol Scand 1992;85:257-265
-
(1992)
Acta Neurol Scand
, vol.85
, pp. 257-265
-
-
Spadaro, M.1
Giunti, P.2
Lulli, P.3
-
23
-
-
0014577403
-
Subcellular location of N-acetyl-aspartyl-glutamate, N-acetyl-glutamate and glutathione in brain
-
Reichelt KL, Fonnum F. Subcellular location of N-acetyl-aspartyl-glutamate, N-acetyl-glutamate and glutathione in brain. J Neurochem 1969;16:1409-1416
-
(1969)
J Neurochem
, vol.16
, pp. 1409-1416
-
-
Reichelt, K.L.1
Fonnum, F.2
-
24
-
-
0026000851
-
Immunocytochemical localization of N-acetyl-aspartate with monoclonal antibodies
-
Simmons MI, Frondoza CG, Coyle JT. Immunocytochemical localization of N-acetyl-aspartate with monoclonal antibodies. Neuroscience 1991;45:37-45
-
(1991)
Neuroscience
, vol.45
, pp. 37-45
-
-
Simmons, M.I.1
Frondoza, C.G.2
Coyle, J.T.3
-
25
-
-
0027450301
-
Proton nuclear magnetic resonance spectroscopy unambiguously identifies different neuronal cell types
-
Urenjak J, Williams SR, Gadian DG, Noble M. Proton nuclear magnetic resonance spectroscopy unambiguously identifies different neuronal cell types. J Neurosci 1993;13:981-989
-
(1993)
J Neurosci
, vol.13
, pp. 981-989
-
-
Urenjak, J.1
Williams, S.R.2
Gadian, D.G.3
Noble, M.4
-
26
-
-
0028146216
-
Transsynaptic reduction in N-acetyl-aspartate in cerebellar diaschisis: A proton MR spectroscopic imaging study
-
Fulham MJ, Dietz MJ, Duyn JH, et al. Transsynaptic reduction in N-acetyl-aspartate in cerebellar diaschisis: a proton MR spectroscopic imaging study. J Comput Assist Tomogr 1994; 18:697-704
-
(1994)
J Comput Assist Tomogr
, vol.18
, pp. 697-704
-
-
Fulham, M.J.1
Dietz, M.J.2
Duyn, J.H.3
-
27
-
-
0028817270
-
Reversal of brain metabolic alterations with zidovudine detected by proton localized magnetic resonance spectroscopy
-
Vion-Dury J, Nicoli P, Salvan AM, et al. Reversal of brain metabolic alterations with zidovudine detected by proton localized magnetic resonance spectroscopy. Lancet 1995;345:60-61
-
(1995)
Lancet
, vol.345
, pp. 60-61
-
-
Vion-Dury, J.1
Nicoli, P.2
Salvan, A.M.3
-
28
-
-
0024810311
-
Brain metabolites as 1HNMR markers of neuronal and glial disorders
-
Gill SS, Small RK, Thomas DG, et al. Brain metabolites as 1HNMR markers of neuronal and glial disorders. NMR Biomed 1989;2:196-200
-
(1989)
NMR Biomed
, vol.2
, pp. 196-200
-
-
Gill, S.S.1
Small, R.K.2
Thomas, D.G.3
-
29
-
-
0027535032
-
Absolute concentrations of metabolites in the adult human brain in vivo: Quantification of localized proton MR spectra
-
Michaelis T, Merboldt KD, Bruhn H, et al. Absolute concentrations of metabolites in the adult human brain in vivo: quantification of localized proton MR spectra. Radiology 1993;187: 219-227
-
(1993)
Radiology
, vol.187
, pp. 219-227
-
-
Michaelis, T.1
Merboldt, K.D.2
Bruhn, H.3
-
30
-
-
0027943105
-
Subclinical hepatic encephalopathy: Proton MR spectroscopic abnormalities
-
Ross BD, Jacobson S, Villamil F, et al. Subclinical hepatic encephalopathy: proton MR spectroscopic abnormalities. Radiology 1994;193:457-463
-
(1994)
Radiology
, vol.193
, pp. 457-463
-
-
Ross, B.D.1
Jacobson, S.2
Villamil, F.3
-
31
-
-
0027722281
-
Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitocondrial encephalopathies
-
Matthews PM, Andermann F, Silver K, et al. Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitocondrial encephalopathies. Neurology 43;1993:2484-2490
-
(1993)
Neurology
, vol.43
, pp. 2484-2490
-
-
Matthews, P.M.1
Andermann, F.2
Silver, K.3
-
33
-
-
0344402998
-
Proton magnetic resonance spectroscopy of the cerebellum in sporadic adult-onset ataxia
-
Abstract
-
Graham GD, Hwang JH, Rothman DL, et al. Proton magnetic resonance spectroscopy of the cerebellum in sporadic adult-onset ataxia. Neurology 1995;45(suppl 4):A186 (Abstract)
-
(1995)
Neurology
, vol.45
, Issue.4 SUPPL.
-
-
Graham, G.D.1
Hwang, J.H.2
Rothman, D.L.3
-
34
-
-
0030031817
-
Proton magnetic resonance spectroscopic imaging in patients with cerebellar degeneration
-
Tedeschi G, Bertolino A, Massaquoi SG, et al. Proton magnetic resonance spectroscopic imaging in patients with cerebellar degeneration. Ann Neurol 1996;39:71-78
-
(1996)
Ann Neurol
, vol.39
, pp. 71-78
-
-
Tedeschi, G.1
Bertolino, A.2
Massaquoi, S.G.3
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