-
1
-
-
0026339303
-
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
-
Oberlè I, Rousseau F, Heitz D, et al. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome. Science. 1991;252:1097-1102.
-
(1991)
Science
, vol.252
, pp. 1097-1102
-
-
Oberlè, I.1
Rousseau, F.2
Heitz, D.3
-
2
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk AJ, Pieretti M, Sutcliffe JS, et al. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell. 1991;65:905-914.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.1
Pieretti, M.2
Sutcliffe, J.S.3
-
3
-
-
0002908947
-
The molecular biology of the fragile X mutation
-
Hagerman RJ, Cronister A, eds. Baltimore: Johns Hopkins University Press
-
Brown WT. The molecular biology of the fragile X mutation. In: Hagerman RJ, Cronister A, eds. Fragile X Syndrome: Diagnosis, Treatment, and Research, 2nd ed. Baltimore: Johns Hopkins University Press; 1996:88-113.
-
(1996)
Fragile X Syndrome: Diagnosis, Treatment, and Research, 2nd Ed.
, pp. 88-113
-
-
Brown, W.T.1
-
5
-
-
0001966753
-
Physical and behavioral phenotype
-
Hagerman RJ, Cronister A, eds. Baltimore: Johns Hopkins University Press
-
Hagerman RJ. Physical and behavioral phenotype. In: Hagerman RJ, Cronister A, eds. Fragile X Syndrome: Diagnosis, Treatment, and Research, 2nd ed. Baltimore: Johns Hopkins University Press; 1996:3-87.
-
(1996)
Fragile X Syndrome: Diagnosis, Treatment, and Research, 2nd Ed.
, pp. 3-87
-
-
Hagerman, R.J.1
-
6
-
-
0036591683
-
The fragile X premutation: Into the phenotypic fold
-
Hagerman RJ, Hagerman PJ. The fragile X premutation: into the phenotypic fold. Curr Opin Genet Dev. 2002;12:278-283.
-
(2002)
Curr Opin Genet Dev
, vol.12
, pp. 278-283
-
-
Hagerman, R.J.1
Hagerman, P.J.2
-
7
-
-
0028799833
-
Prevalence of carriers of premutation-size alleles of the FMRI gene - And implications for the population genetics of the fragile X syndrome
-
Rousseau F, Rouillard P, Morel ML, et al. Prevalence of carriers of premutation-size alleles of the FMRI gene - and implications for the population genetics of the fragile X syndrome. Am J Hum Genet. 1995;57:1006-1018.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1006-1018
-
-
Rousseau, F.1
Rouillard, P.2
Morel, M.L.3
-
8
-
-
0027674521
-
The neurocognitive phenotype of female carriers of fragile X: Additional evidence for specificity
-
Mazzocco MM, Pennington BF, Hagerman RJ. The neurocognitive phenotype of female carriers of fragile X: additional evidence for specificity. J Dev Behav Pediatr. 1993;14:328-335.
-
(1993)
J Dev Behav Pediatr
, vol.14
, pp. 328-335
-
-
Mazzocco, M.M.1
Pennington, B.F.2
Hagerman, R.J.3
-
9
-
-
0027482074
-
Neurobehavioral effects of the fragile X premutation in adult women: A controlled study
-
Reiss AL, Freund L, Abrams MT, et al. Neurobehavioral effects of the fragile X premutation in adult women: a controlled study. Am J Hum Genet. 1993;52:884-894.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 884-894
-
-
Reiss, A.L.1
Freund, L.2
Abrams, M.T.3
-
11
-
-
0030054149
-
Learning-disabled males with a fragile X CGG expansion in the upper premutation size range
-
Hagerman RJ, Staley LW, O'Connor R, et al. Learning-disabled males with a fragile X CGG expansion in the upper premutation size range. Pediatrics. 1996;97:122-126.
-
(1996)
Pediatrics
, vol.97
, pp. 122-126
-
-
Hagerman, R.J.1
Staley, L.W.2
O'Connor, R.3
-
12
-
-
0028237294
-
Transmitting males and carrier females in fragile X - Revisited
-
Loesch DZ, Hay DA, Mulley J. Transmitting males and carrier females in fragile X - revisited. Am J Med Genet. 1994;51:392-399.
-
(1994)
Am J Med Genet
, vol.51
, pp. 392-399
-
-
Loesch, D.Z.1
Hay, D.A.2
Mulley, J.3
-
13
-
-
0031978146
-
Phenotypic involvement in females with the FMR1 gene mutation
-
Riddle JE, Cheema A, Sobesky WE, et al. Phenotypic involvement in females with the FMR1 gene mutation. Am J Ment Retard. 1998;102:590-601.
-
(1998)
Am J Ment Retard
, vol.102
, pp. 590-601
-
-
Riddle, J.E.1
Cheema, A.2
Sobesky, W.E.3
-
14
-
-
0028283366
-
Prediction of mental status in carriers of the fragile X mutation using CGG repeat length
-
Smits A, Smeets D, Hamel B, et al. Prediction of mental status in carriers of the fragile X mutation using CGG repeat length. Am J Med Genet. 1994;51:497-500.
-
(1994)
Am J Med Genet
, vol.51
, pp. 497-500
-
-
Smits, A.1
Smeets, D.2
Hamel, B.3
-
15
-
-
0033940157
-
Elevated levels of FMR1 messenger RNA in carrier males: A new mechanism of involvement in the fragile X syndrome
-
Tassone F, Hagerman RJ, Taylor AK, et al. Elevated levels of FMR1 messenger RNA in carrier males: a new mechanism of involvement in the fragile X syndrome. Am J Hum Genet. 2000;66:6-15.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 6-15
-
-
Tassone, F.1
Hagerman, R.J.2
Taylor, A.K.3
-
16
-
-
0034016083
-
Clinical involvement and protein expression in individuals with the FMR1 premutation
-
Tassone F, Hagerman RJ, Taylor AK, et al. Clinical involvement and protein expression in individuals with the FMR1 premutation. Am J Med Genet. 2000;91:44-152.
-
(2000)
Am J Med Genet
, vol.91
, pp. 44-152
-
-
Tassone, F.1
Hagerman, R.J.2
Taylor, A.K.3
-
17
-
-
0032541268
-
Genotype-phenotype relationship in female carriers of the premutation and full mutation of FMR-1
-
Franke P, Leboyer M, Gansicke M, et al. Genotype-phenotype relationship in female carriers of the premutation and full mutation of FMR-1. Psychiatry Res. 1998;80:113-127.
-
(1998)
Psychiatry Res
, vol.80
, pp. 113-127
-
-
Franke, P.1
Leboyer, M.2
Gansicke, M.3
-
18
-
-
0242467602
-
Effect of the fragile X status categories and the FMRP levels on executive functioning in fragile X males and females
-
Loesch DZ, Bui QM, Grigsby J, et al. Effect of the fragile X status categories and the FMRP levels on executive functioning in fragile X males and females. Neuropsychology. 2003;17:646-657.
-
(2003)
Neuropsychology
, vol.17
, pp. 646-657
-
-
Loesch, D.Z.1
Bui, Q.M.2
Grigsby, J.3
-
19
-
-
13044266376
-
Premutation female carriers of fragile X syndrome: A pilot study on brain anatomy and metabolism
-
Murphy DGM, Mentis MJ, Pietrini P, et al. Premutation female carriers of fragile X syndrome: a pilot study on brain anatomy and metabolism. J Am Acad Child Adolesc Psychiatry. 1999;38:1294-1301.
-
(1999)
J Am Acad Child Adolesc Psychiatry
, vol.38
, pp. 1294-1301
-
-
Murphy, D.G.M.1
Mentis, M.J.2
Pietrini, P.3
-
20
-
-
0035838379
-
Intention tremor, parkinsonism and generalized brain atrophy in older male carriers of fragile X
-
Hagerman RJ, Leehey M, Heinrichs W, et al. Intention tremor, parkinsonism and generalized brain atrophy in older male carriers of fragile X. Neurology. 1991;57:127-130.
-
(1991)
Neurology
, vol.57
, pp. 127-130
-
-
Hagerman, R.J.1
Leehey, M.2
Heinrichs, W.3
-
21
-
-
33748530578
-
Neurodegeneration among older male premutation carriers of Fragile X syndrome
-
Poster Session No. 431.8
-
Grigsby J, Leehey M, Hagerman RJ, et al. Neurodegeneration among older male premutation carriers of Fragile X syndrome. Soc Neurosci Abstr. 2001;27. Poster Session No. 431.8.
-
(2001)
Soc Neurosci Abstr
, vol.27
-
-
Grigsby, J.1
Leehey, M.2
Hagerman, R.J.3
-
22
-
-
0038521838
-
Tremor/ataxia syndrome in fragile X carrier males
-
Leehey MA, Hagerman R, Landau W, et al. Tremor/ataxia syndrome in fragile X carrier males. Mov Disord. 2002;17:744.
-
(2002)
Mov Disord
, vol.17
, pp. 744
-
-
Leehey, M.A.1
Hagerman, R.2
Landau, W.3
-
23
-
-
0037229944
-
The fragile X premutation presenting as essential tremor
-
Leehey MA, Munhoz RP, Lang AE, et al. The fragile X premutation presenting as essential tremor. Arch Neurol. 2003;60:117-121.
-
(2003)
Arch Neurol
, vol.60
, pp. 117-121
-
-
Leehey, M.A.1
Munhoz, R.P.2
Lang, A.E.3
-
24
-
-
0036846189
-
Fragile X premutation carriers: Characteristic MR imaging findings in adult males with progressive cerebellar and cognitive dysfunction
-
Brunberg JA, Jacquemont S, Hagerman RJ, et al. Fragile X premutation carriers: characteristic MR imaging findings in adult males with progressive cerebellar and cognitive dysfunction. AJNR Am J Neuroradiol. 2002;23:1757-1766.
-
(2002)
AJNR Am J Neuroradiol
, vol.23
, pp. 1757-1766
-
-
Brunberg, J.A.1
Jacquemont, S.2
Hagerman, R.J.3
-
25
-
-
0036345801
-
Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers
-
Greco CM, Hagerman RJ, Tassone F, et al. Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers. Brain. 2002;125:1760-1771.
-
(2002)
Brain
, vol.125
, pp. 1760-1771
-
-
Greco, C.M.1
Hagerman, R.J.2
Tassone, F.3
-
26
-
-
1642403699
-
Dysexecutive syndrome in older men with action tremor and the Fragile X premutation
-
Grigsby J, Hills J, Wilson R, et al. Dysexecutive syndrome in older men with action tremor and the Fragile X premutation. J Int Neuropsychol Soc. 2002;8:282.
-
(2002)
J Int Neuropsychol Soc
, vol.8
, pp. 282
-
-
Grigsby, J.1
Hills, J.2
Wilson, R.3
-
27
-
-
33748559336
-
Cognitive impairment among males with the fragile X tremor-ataxia syndrome (FXTAS)
-
Program No. 95.8. Online
-
Grigsby J, Brega A, Jacquemont S, et al. Cognitive impairment among males with the fragile X tremor-ataxia syndrome (FXTAS). Soc Neurosci Abstr. 2004; Program No. 95.8. Online.
-
(2004)
Soc Neurosci Abstr
-
-
Grigsby, J.1
Brega, A.2
Jacquemont, S.3
-
28
-
-
0037384643
-
Fragile X premutation tremor/ataxia syndrome: Molecular, clinical, and neuroimaging correlates
-
Jacquemont S, Hagerman RJ, Leehey M, et al. Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates. Am J Hum Genet. 2003;72:869-878.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 869-878
-
-
Jacquemont, S.1
Hagerman, R.J.2
Leehey, M.3
-
29
-
-
9144252520
-
Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population: Initial results from a California family-based study
-
Jacquemont S, Hagerman RJ, Leehey MA, et al. Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population: Initial results from a California family-based study. JAMA. 2004;291:460-469.
-
(2004)
JAMA
, vol.291
, pp. 460-469
-
-
Jacquemont, S.1
Hagerman, R.J.2
Leehey, M.A.3
-
30
-
-
33750343705
-
Impairment in the cognitive functioning of men with Fragile X Tremor-Ataxia Syndrome (FXTAS)
-
In press
-
Grigsby J, Brega AG, Jacquemont S, et al. Impairment in the cognitive functioning of men with Fragile X Tremor-Ataxia Syndrome (FXTAS). J Neurol Sci. In press.
-
J Neurol Sci
-
-
Grigsby, J.1
Brega, A.G.2
Jacquemont, S.3
-
31
-
-
2342635196
-
Fragile X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation
-
Hagerman RJ, Leavitt BR, Farzin F, et al. Fragile X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation. Am J Hum Genet. 2004;74:805-816.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 805-816
-
-
Hagerman, R.J.1
Leavitt, B.R.2
Farzin, F.3
-
32
-
-
0001161811
-
(2001b) Neuropathology and neurodegenerative features in some older male premutation carriers of fragile X syndrome
-
A8
-
Hagerman RJ, Greco C, Chudley A, et al. (2001b) Neuropathology and neurodegenerative features in some older male premutation carriers of fragile X syndrome. (Abstract). Am J Hum Genet. 2001;69(Suppl);A8:177.
-
(2001)
Am J Hum Genet
, vol.69
, Issue.SUPPL.
, pp. 177
-
-
Hagerman, R.J.1
Greco, C.2
Chudley, A.3
-
36
-
-
33749169804
-
A simple objective technique for measuring flexibility in thinking
-
Berg EA. A simple objective technique for measuring flexibility in thinking. J Gen Psychol. 1948;39:15-22.
-
(1948)
J Gen Psychol
, vol.39
, pp. 15-22
-
-
Berg, E.A.1
-
38
-
-
0026874607
-
Reliabilities, norms, and factor structure of the Behavioral Dyscontrol Scale
-
Grigsby J, Kaye K, Robbins LJ. Reliabilities, norms, and factor structure of the Behavioral Dyscontrol Scale. Percept Mot Skills. 1992;74:883-892.
-
(1992)
Percept Mot Skills
, vol.74
, pp. 883-892
-
-
Grigsby, J.1
Kaye, K.2
Robbins, L.J.3
-
39
-
-
0025637667
-
Prediction of independent functioning and behavior problems in geriatric patients
-
Kaye K, Grigsby J, Robbins LJ, et al. Prediction of independent functioning and behavior problems in geriatric patients. J Am Geriatr Soc. 1990;38:1304-1310.
-
(1990)
J Am Geriatr Soc
, vol.38
, pp. 1304-1310
-
-
Kaye, K.1
Grigsby, J.2
Robbins, L.J.3
-
41
-
-
0002608236
-
The Symbol Digit Modalities Test: A neuropsychologic test for economic screening of learning and other cerebral disorders
-
Smith A. The Symbol Digit Modalities Test: a neuropsychologic test for economic screening of learning and other cerebral disorders. Learn Disord. 1968;3:83-91.
-
(1968)
Learn Disord
, vol.3
, pp. 83-91
-
-
Smith, A.1
-
43
-
-
0001990813
-
Some tests of the decay theory of immediate memory
-
Brown J. Some tests of the decay theory of immediate memory. Q J Exp Psychol. 1958;10:12-21.
-
(1958)
Q J Exp Psychol
, vol.10
, pp. 12-21
-
-
Brown, J.1
-
44
-
-
58149454829
-
Short-term retention of individual verbal items
-
Peterson LR, Peterson MJ. Short-term retention of individual verbal items. J Exp Psychol. 1959;58:193-198.
-
(1959)
J Exp Psychol
, vol.58
, pp. 193-198
-
-
Peterson, L.R.1
Peterson, M.J.2
-
47
-
-
0018447661
-
The theory of learning by doing
-
Anzai Y, Simon H. The theory of learning by doing. Psychol Rev. 1979;86:124-180.
-
(1979)
Psychol Rev
, vol.86
, pp. 124-180
-
-
Anzai, Y.1
Simon, H.2
-
49
-
-
33646723545
-
Dementia with mood symptoms in a fragile X premutation carrier with the Fragile-X Associated Tremor/Ataxia Syndrome (FXTAS): Clinical intervention with donepezil and venlafaxine
-
Bourgeois JA, Farzin F, Brunberg JA, et al. Dementia with mood symptoms in a fragile X premutation carrier with the Fragile-X Associated Tremor/Ataxia Syndrome (FXTAS): clinical intervention with donepezil and venlafaxine. J Neuropsychiatry Clin Neurosci. 2006;18:171-177.
-
(2006)
J Neuropsychiatry Clin Neurosci
, vol.18
, pp. 171-177
-
-
Bourgeois, J.A.1
Farzin, F.2
Brunberg, J.A.3
-
50
-
-
0033910501
-
Which neuropsychiatric and behavioural features distinguish frontal and temporal variants of frontotemporal dementia from Alzheimer's disease?
-
Bozeat S, Gregory CA, Ralph MAL, et al. Which neuropsychiatric and behavioural features distinguish frontal and temporal variants of frontotemporal dementia from Alzheimer's disease? J Neurol Neurosurg Psychiatry. 2000;69:178-186.
-
(2000)
J Neurol Neurosurg Psychiatry
, vol.69
, pp. 178-186
-
-
Bozeat, S.1
Gregory, C.A.2
Ralph, M.A.L.3
-
51
-
-
0037062568
-
Utility of clinical criteria in differentiating frontotemporal lobar degeneration (FTLD) from AD
-
Rosen HJ, Hartikainen KM, Jagust W, et al. Utility of clinical criteria in differentiating frontotemporal lobar degeneration (FTLD) from AD. Neurology. 2002;58:1608-1615.
-
(2002)
Neurology
, vol.58
, pp. 1608-1615
-
-
Rosen, H.J.1
Hartikainen, K.M.2
Jagust, W.3
-
52
-
-
0023285704
-
Ideomotor apraxia in patients with dementia of the Alzheimer type
-
Della Sala S, Lucchelli F, Spinnler H. Ideomotor apraxia in patients with dementia of the Alzheimer type. Neurology. 1987;234:91-93.
-
(1987)
Neurology
, vol.234
, pp. 91-93
-
-
Della Sala, S.1
Lucchelli, F.2
Spinnler, H.3
-
53
-
-
23844442499
-
Longitudinal volumetric MRI change and rate of cognitive decline
-
Mungas D, Harvey D, Reed BR, et al. Longitudinal volumetric MRI change and rate of cognitive decline. Neurology. 2005;65:565-571.
-
(2005)
Neurology
, vol.65
, pp. 565-571
-
-
Mungas, D.1
Harvey, D.2
Reed, B.R.3
-
54
-
-
0343416812
-
Medial temporal atrophy on MRI in normal aging and very mild Alzheimer's disease
-
Jack CR Jr, Petersen RC, Xu YC, et al. Medial temporal atrophy on MRI in normal aging and very mild Alzheimer's disease. Neurology. 1997;49:786-794.
-
(1997)
Neurology
, vol.49
, pp. 786-794
-
-
Jack Jr., C.R.1
Petersen, R.C.2
Xu, Y.C.3
-
55
-
-
0026785906
-
Longitudinal changes in lateral ventricular volume in patients with dementia of the Alzheimer type
-
DeCarli C, Haxby JV, Gillette JA, et al. Longitudinal changes in lateral ventricular volume in patients with dementia of the Alzheimer type. Neurology. 1992;42:2029-2036.
-
(1992)
Neurology
, vol.42
, pp. 2029-2036
-
-
DeCarli, C.1
Haxby, J.V.2
Gillette, J.A.3
-
56
-
-
2342494460
-
Cognitive and behavioral aspects of basal ganglia diseases
-
Jankovic JJ, Tolosa E, eds. Philadelphia: Lippincott Williams & Wilkins
-
Dubois B, Pillon B. Cognitive and behavioral aspects of basal ganglia diseases. In: Jankovic JJ, Tolosa E, eds. Parkinson's Disease and Movement Disorders. 4th ed. Philadelphia: Lippincott Williams & Wilkins; 2002:530-545.
-
(2002)
Parkinson's Disease and Movement Disorders. 4th Ed.
, pp. 530-545
-
-
Dubois, B.1
Pillon, B.2
-
57
-
-
12544250989
-
Cerebral atrophy and its relation to cognitive impairment in Parkinson disease
-
Nagano-Saito A, Washimi Y, Arahata Y, et al. Cerebral atrophy and its relation to cognitive impairment in Parkinson disease. Neurology. 2005;64:224-229.
-
(2005)
Neurology
, vol.64
, pp. 224-229
-
-
Nagano-Saito, A.1
Washimi, Y.2
Arahata, Y.3
-
58
-
-
0026547624
-
Cognitive performance in multiple system atrophy
-
Robbins TW, James M, Lange KW, et al. Cognitive performance in multiple system atrophy. Brain. 1992;115:271-291.
-
(1992)
Brain
, vol.115
, pp. 271-291
-
-
Robbins, T.W.1
James, M.2
Lange, K.W.3
-
59
-
-
0028922172
-
Neuropsychological pattern of striatonigral degeneration: Comparison with Parkinson's disease and progressive supranuclear palsy
-
Pillon B, Gouider-Khouja N, Deweer B, et al. Neuropsychological pattern of striatonigral degeneration: comparison with Parkinson's disease and progressive supranuclear palsy. J Neurol Neurosurg Psychiatry. 1995;58:174-179.
-
(1995)
J Neurol Neurosurg Psychiatry
, vol.58
, pp. 174-179
-
-
Pillon, B.1
Gouider-Khouja, N.2
Deweer, B.3
-
60
-
-
23844506635
-
Subcortical dementia revisited: Similarities and differences in cognitive function between progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) and multiple system atrophy (MSA)
-
Bak TH, Crawford LM, Hearn VC, et al. Subcortical dementia revisited: similarities and differences in cognitive function between progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) and multiple system atrophy (MSA). Neurocase. 2005;11:268-273.
-
(2005)
Neurocase
, vol.11
, pp. 268-273
-
-
Bak, T.H.1
Crawford, L.M.2
Hearn, V.C.3
-
61
-
-
0141993606
-
In vivo voxel-based morphometry in multiple system atrophy of the cerebellar type
-
Specht K, Minnerop M, Abele M, et al. In vivo voxel-based morphometry in multiple system atrophy of the cerebellar type. Arch Neurol. 2003;60:1431-1435.
-
(2003)
Arch Neurol
, vol.60
, pp. 1431-1435
-
-
Specht, K.1
Minnerop, M.2
Abele, M.3
-
62
-
-
23444442557
-
The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: Data from the EMSA Study Group
-
Kamm C, Healy DG, Quinn NP, et al. The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group. Brain. 2005;128:1855-1860.
-
(2005)
Brain
, vol.128
, pp. 1855-1860
-
-
Kamm, C.1
Healy, D.G.2
Quinn, N.P.3
-
63
-
-
0037320236
-
Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3
-
Bürk K, Globas C, Bösch S, et al. Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3. J Neurol. 2003;250:207-211.
-
(2003)
J Neurol
, vol.250
, pp. 207-211
-
-
Bürk, K.1
Globas, C.2
Bösch, S.3
-
64
-
-
17844365587
-
Clinical, psychological, and genetic characteristics of spinocerebellar ataxia type 19 (SCA19)
-
Schelhaas HJ, van de Warrenburg BPC. Clinical, psychological, and genetic characteristics of spinocerebellar ataxia type 19 (SCA19). Cerebellum. 2005;4:51-54.
-
(2005)
Cerebellum
, vol.4
, pp. 51-54
-
-
Schelhaas, H.J.1
Van De Warrenburg, B.P.C.2
-
65
-
-
0035852808
-
SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion
-
O'Hearn E, Holmes SE, Calvert PC, et al. SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion. Neurology. 2001;56:299-303.
-
(2001)
Neurology
, vol.56
, pp. 299-303
-
-
O'Hearn, E.1
Holmes, S.E.2
Calvert, P.C.3
-
66
-
-
0036830123
-
A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1
-
Vuillaume I, Devos D, Schraen-Maschke S, et al. A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1. Ann Neurol. 2002;52:666-670.
-
(2002)
Ann Neurol
, vol.52
, pp. 666-670
-
-
Vuillaume, I.1
Devos, D.2
Schraen-Maschke, S.3
-
67
-
-
0033910529
-
Mapping of spinocerebellar ataxia 13 to chromosome 19q13.1-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation
-
Herman-Bert A, Stevanin G, Netter JC, et al. Mapping of spinocerebellar ataxia 13 to chromosome 19q13.1-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation. Am J Hum Genet. 2000;67:229-235.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 229-235
-
-
Herman-Bert, A.1
Stevanin, G.2
Netter, J.C.3
-
68
-
-
0034649399
-
The corticobasal degeneration syndrome overlaps progressive aphasia and frontotemporal dementia
-
Kertesz A, Martinez-Lage P, Davidson W, et al. The corticobasal degeneration syndrome overlaps progressive aphasia and frontotemporal dementia. Neurology. 2000;55:1368-1375.
-
(2000)
Neurology
, vol.55
, pp. 1368-1375
-
-
Kertesz, A.1
Martinez-Lage, P.2
Davidson, W.3
-
69
-
-
0034764622
-
Clinical and pathological diagnosis of frontotemporal dementia
-
McKhann GM, Albert MS, Grossman M, et al. Clinical and pathological diagnosis of frontotemporal dementia. Arch Neurol. 2001;58:1803-1809.
-
(2001)
Arch Neurol
, vol.58
, pp. 1803-1809
-
-
McKhann, G.M.1
Albert, M.S.2
Grossman, M.3
-
70
-
-
0037154206
-
Patterns of brain atrophy in frontotemporal dementia and semantic dementia
-
Rosen HJ, Gorno-Tempini ML, Goldman WP, et al. Patterns of brain atrophy in frontotemporal dementia and semantic dementia. Neurology. 2002;58:198-208.
-
(2002)
Neurology
, vol.58
, pp. 198-208
-
-
Rosen, H.J.1
Gorno-Tempini, M.L.2
Goldman, W.P.3
-
71
-
-
24344457727
-
The evolution and pathology of frontotemporal dementia
-
Kertesz A, McMonagle P, Blair M. The evolution and pathology of frontotemporal dementia. Brain. 2005;128:1996-2005.
-
(2005)
Brain
, vol.128
, pp. 1996-2005
-
-
Kertesz, A.1
McMonagle, P.2
Blair, M.3
-
72
-
-
0034896957
-
Frontotemporal dementia with ubiquitinated cytoplasmic and intranuclear inclusions
-
Woulfe J, Kertesz A, Munoz DG. Frontotemporal dementia with ubiquitinated cytoplasmic and intranuclear inclusions. Acta Neuropathol. 2001;102:94-102.
-
(2001)
Acta Neuropathol
, vol.102
, pp. 94-102
-
-
Woulfe, J.1
Kertesz, A.2
Munoz, D.G.3
-
73
-
-
0032976201
-
From genotype to phenotype: A clinical, pathological, and biochemical investigation of frontotemporal dementia and Parkinsonism (FTDP-17) caused by the P301L tau mutation
-
Nasreddine ZS, Loginov M, Clark LN, et al. From genotype to phenotype: a clinical, pathological, and biochemical investigation of frontotemporal dementia and Parkinsonism (FTDP-17) caused by the P301L tau mutation. Ann Neurol. 1999;45:704-715.
-
(1999)
Ann Neurol
, vol.45
, pp. 704-715
-
-
Nasreddine, Z.S.1
Loginov, M.2
Clark, L.N.3
-
74
-
-
1542316174
-
Behavioral disorders in the frontal and temporal variants of frontotemporal dementia
-
Liu W, Miller BL, Kramer JH, et al. Behavioral disorders in the frontal and temporal variants of frontotemporal dementia. Neurology. 2004;62:742-748.
-
(2004)
Neurology
, vol.62
, pp. 742-748
-
-
Liu, W.1
Miller, B.L.2
Kramer, J.H.3
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