-
1
-
-
0020641096
-
Classification of the hereditary ataxias and paraplegias
-
A.E. Harding Classification of the hereditary ataxias and paraplegias Lancet 1 8334 1983 1151 1155
-
(1983)
Lancet
, vol.1
, Issue.8334
, pp. 1151-1155
-
-
Harding, A.E.1
-
2
-
-
0036844683
-
Is the transportation highway the right road for hereditary spastic paraplegia?
-
A.H. Crosby, and C. Proukakis Is the transportation highway the right road for hereditary spastic paraplegia? Am J Hum Genet 71 5 2002 1009 1016
-
(2002)
Am J Hum Genet
, vol.71
, Issue.5
, pp. 1009-1016
-
-
Crosby, A.H.1
Proukakis, C.2
-
3
-
-
10344241450
-
Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2
-
A. Durr, C.S. Davoine, C. Paternotte, J. von Fellenberg, S. Cogilinicean, and P. Coutinho Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2 Brain 119 Pt 5 1996 1487 1496
-
(1996)
Brain
, vol.119
, Issue.5 PART
, pp. 1487-1496
-
-
Durr, A.1
Davoine, C.S.2
Paternotte, C.3
Von Fellenberg, J.4
Cogilinicean, S.5
Coutinho, P.6
-
4
-
-
0032721512
-
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
-
J. Hazan, N. Fonknechten, D. Mavel, C. Paternotte, D. Samson, and F. Artiguenave Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia Nat Genet 23 3 1999 296 303
-
(1999)
Nat Genet
, vol.23
, Issue.3
, pp. 296-303
-
-
Hazan, J.1
Fonknechten, N.2
Mavel, D.3
Paternotte, C.4
Samson, D.5
Artiguenave, F.6
-
5
-
-
0037081740
-
Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics
-
A. Errico, A. Ballabio, and E.I. Rugarli Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics Hum Mol Genet 11 2 2002 153 163
-
(2002)
Hum Mol Genet
, vol.11
, Issue.2
, pp. 153-163
-
-
Errico, A.1
Ballabio, A.2
Rugarli, E.I.3
-
6
-
-
0015945194
-
Strumpell's familial spastic paraplegia: Genetics and neuropathology
-
W.M. Behan, and M. Maia Strumpell's familial spastic paraplegia: genetics and neuropathology J Neurol Neurosurg Psychiatry 37 1 1974 8 20
-
(1974)
J Neurol Neurosurg Psychiatry
, vol.37
, Issue.1
, pp. 8-20
-
-
Behan, W.M.1
Maia, M.2
-
7
-
-
0037231374
-
Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus
-
D. Charvin, C. Cifuentes-Diaz, N. Fonknechten, V. Joshi, J. Hazan, and J. Melki Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus Hum Mol Genet 12 1 2003 71 78
-
(2003)
Hum Mol Genet
, vol.12
, Issue.1
, pp. 71-78
-
-
Charvin, D.1
Cifuentes-Diaz, C.2
Fonknechten, N.3
Joshi, V.4
Hazan, J.5
Melki, J.6
-
8
-
-
0034641262
-
Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation
-
K.D. White, P.G. Ince, M. Lusher, J. Lindsey, M. Cookson, and R. Bashir Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation Neurology 55 1 2000 89 94
-
(2000)
Neurology
, vol.55
, Issue.1
, pp. 89-94
-
-
White, K.D.1
Ince, P.G.2
Lusher, M.3
Lindsey, J.4
Cookson, M.5
Bashir, R.6
-
9
-
-
0242693281
-
The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin gene
-
S.B. Wharton, C.J. McDermott, A.J. Grierson, J.D. Wood, C. Gelsthorpe, and P.G. Ince The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin gene J Neuropathol Exp Neurol 62 11 2003 1166 1177
-
(2003)
J Neuropathol Exp Neurol
, vol.62
, Issue.11
, pp. 1166-1177
-
-
Wharton, S.B.1
McDermott, C.J.2
Grierson, A.J.3
Wood, J.D.4
Gelsthorpe, C.5
Ince, P.G.6
-
10
-
-
0343238487
-
Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p
-
P.C. Byrne, P. McMonagle, S. Webb, B. Fitzgerald, N.A. Parfrey, and M. Hutchinson Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p Neurology 54 7 2000 1510 1517
-
(2000)
Neurology
, vol.54
, Issue.7
, pp. 1510-1517
-
-
Byrne, P.C.1
McMonagle, P.2
Webb, S.3
Fitzgerald, B.4
Parfrey, N.A.5
Hutchinson, M.6
-
11
-
-
0031971694
-
Autosomal dominant pure spastic paraplegia: A clinical, paraclinical, and genetic study
-
J.E. Nielsen, K. Krabbe, P. Jennum, P. Koefoed, L.N. Jensen, and K. Fenger Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study J Neurol Neurosurg Psychiatry 64 1 1998 61 66
-
(1998)
J Neurol Neurosurg Psychiatry
, vol.64
, Issue.1
, pp. 61-66
-
-
Nielsen, J.E.1
Krabbe, K.2
Jennum, P.3
Koefoed, P.4
Jensen, L.N.5
Fenger, K.6
-
12
-
-
0030807772
-
CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24
-
J.E. Nielsen, P. Koefoed, K. Abell, L. Hasholt, H. Eiberg, and K. Fenger CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24 Hum Mol Genet 6 11 1997 1811 1816
-
(1997)
Hum Mol Genet
, vol.6
, Issue.11
, pp. 1811-1816
-
-
Nielsen, J.E.1
Koefoed, P.2
Abell, K.3
Hasholt, L.4
Eiberg, H.5
Fenger, K.6
-
13
-
-
2642582687
-
Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG4) using direct mutation detection
-
J.E. Nielsen, P. Koefoed, S. Kjaergaard, L. Neerup Jensen, A. Nørremølle, and L. Hasholt Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG4) using direct mutation detection Prenat Diagn 24 2004 363 366
-
(2004)
Prenat Diagn
, vol.24
, pp. 363-366
-
-
Nielsen, J.E.1
Koefoed, P.2
Kjaergaard, S.3
Neerup Jensen, L.4
Nørremølle, A.5
Hasholt, L.6
-
14
-
-
10844278272
-
Hereditary spastic paraplegia with cerebellar ataxia: A complex phenotype associated with a new SPG4 gene mutation
-
J.E. Nielsen, B. Johnsen, P. Koefoed, K.H. Scheuer, M. Grønbech-Jensen, and I. Law Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation Eur J Neurol 11 2004 817 824
-
(2004)
Eur J Neurol
, vol.11
, pp. 817-824
-
-
Nielsen, J.E.1
Johnsen, B.2
Koefoed, P.3
Scheuer, K.H.4
Grønbech-Jensen, M.5
Law, I.6
-
15
-
-
0022519065
-
Hereditary ataxias. Occurrence and clinical features
-
L. Werdelin Hereditary ataxias. Occurrence and clinical features Acta Neurol Scand Suppl 106 1986 1 124
-
(1986)
Acta Neurol Scand Suppl
, vol.106
, pp. 1-124
-
-
Werdelin, L.1
-
16
-
-
0021035886
-
Rating neurologic impairment in multiple sclerosis: An expanded disability status scale (EDSS)
-
J.F. Kurtzke Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS) Neurology 33 11 1983 1444 1452
-
(1983)
Neurology
, vol.33
, Issue.11
, pp. 1444-1452
-
-
Kurtzke, J.F.1
-
17
-
-
0015021890
-
The assessment and analysis of handedness: The Edinburgh inventory
-
R.C. Oldfield The assessment and analysis of handedness: the Edinburgh inventory Neuropsychologia 9 1 1971 97 113
-
(1971)
Neuropsychologia
, vol.9
, Issue.1
, pp. 97-113
-
-
Oldfield, R.C.1
-
18
-
-
84981654260
-
Verbal and visuo-spatial memory
-
R. Andersen Verbal and visuo-spatial memory Scand J Psychol 17 1976 198 204
-
(1976)
Scand J Psychol
, vol.17
, pp. 198-204
-
-
Andersen, R.1
-
21
-
-
0001392453
-
The relation of the Trail Making Test to organic brain damage
-
R.M. Reitan The relation of the Trail Making Test to organic brain damage Consult Psychol 19 1955 393 394
-
(1955)
Consult Psychol
, vol.19
, pp. 393-394
-
-
Reitan, R.M.1
-
22
-
-
0018099766
-
Dementia: The estimation of premorbid intelligence levels using the New Adult Reading Test
-
H.E. Nelson, and A. O'Connell Dementia: the estimation of premorbid intelligence levels using the New Adult Reading Test Cortex 14 2 1978 234 244
-
(1978)
Cortex
, vol.14
, Issue.2
, pp. 234-244
-
-
Nelson, H.E.1
O'Connell, A.2
-
24
-
-
0015812367
-
Selective reminding for analysis of memory and learning
-
H. Buschke Selective reminding for analysis of memory and learning Verbal Learn Verbal Behav 12 1973 543 550
-
(1973)
Verbal Learn Verbal Behav
, vol.12
, pp. 543-550
-
-
Buschke, H.1
-
26
-
-
0343361650
-
Visual closure: Street completion test
-
A. Gade, H. Udesen, and E.L. Mortensen Visual closure: street completion test Nord Psyk 40 1988 194 201
-
(1988)
Nord Psyk
, vol.40
, pp. 194-201
-
-
Gade, A.1
Udesen, H.2
Mortensen, E.L.3
-
27
-
-
0017033821
-
A modified card sorting test sensitive to frontal lobe defects
-
H.E. Nelson A modified card sorting test sensitive to frontal lobe defects Cortex 12 4 1976 313 324
-
(1976)
Cortex
, vol.12
, Issue.4
, pp. 313-324
-
-
Nelson, H.E.1
-
28
-
-
84983947871
-
On the relation between demographic variables and neuropsychological test performance
-
E.L. Mortensen, A. Gade, and A. Gade On the relation between demographic variables and neuropsychological test performance Scand J Psychol 34 1993 305 317
-
(1993)
Scand J Psychol
, vol.34
, pp. 305-317
-
-
Mortensen, E.L.1
Gade, A.2
Gade, A.3
-
29
-
-
0028068644
-
Performance characteristics of a whole-body PET scanner
-
T.R. DeGrado, T.G. Turkington, J.J. Williams, C.W. Stearns, J.M. Hoffman, and R.E. Coleman Performance characteristics of a whole-body PET scanner J Nucl Med 35 8 1994 1398 1406
-
(1994)
J Nucl Med
, vol.35
, Issue.8
, pp. 1398-1406
-
-
Degrado, T.R.1
Turkington, T.G.2
Williams, J.J.3
Stearns, C.W.4
Hoffman, J.M.5
Coleman, R.E.6
-
30
-
-
33444462088
-
-
Flaga Hf. Medical Devices Reykjavik (Iceland)
-
Flaga Somnologica user manual 1999 Flaga Hf. Medical Devices Reykjavik (Iceland) 133 134
-
(1999)
Somnologica User Manual
, pp. 133-134
-
-
Flaga1
-
32
-
-
0029197929
-
Spatial registration and normalization of images
-
K.J. Friston, C.D. Frith, J.B. Poline, J.D. Heather, and R.S. Frackowiak Spatial registration and normalization of images Hum Brain Mapp 3 1995 165 189
-
(1995)
Hum Brain Mapp
, vol.3
, pp. 165-189
-
-
Friston, K.J.1
Frith, C.D.2
Poline, J.B.3
Heather, J.D.4
Frackowiak, R.S.5
-
33
-
-
0000063846
-
-
K.J. Friston, K.J. Worsley, R.S.J. Frackowiak, J.C. Mazziotta, and A.C. Evans Hum Brain Mapp 1 1994 214 220
-
(1994)
Hum Brain Mapp
, vol.1
, pp. 214-220
-
-
Friston, K.J.1
Worsley, K.J.2
Frackowiak, R.S.J.3
Mazziotta, J.C.4
Evans, A.C.5
-
34
-
-
0027339590
-
A semiquantitative rating scale for the assessment of signal hyperintensities on magnetic resonance imaging
-
P. Scheltens, F. Barkhof, D. Leys, J.P. Pruvo, J.J. Nauta, and P. Vermersch A semiquantitative rating scale for the assessment of signal hyperintensities on magnetic resonance imaging Neurol Sci 114 1 1993 7 12
-
(1993)
Neurol Sci
, vol.114
, Issue.1
, pp. 7-12
-
-
Scheltens, P.1
Barkhof, F.2
Leys, D.3
Pruvo, J.P.4
Nauta, J.J.5
Vermersch, P.6
-
35
-
-
0034963827
-
Increased intracortical facilitation in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p
-
J.E. Nielsen, P. Jennum, K. Fenger, S.A. Sorensen, and A. Fuglsang-Frederiksen Increased intracortical facilitation in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p Eur J Neurol 8 4 2001 335 339
-
(2001)
Eur J Neurol
, vol.8
, Issue.4
, pp. 335-339
-
-
Nielsen, J.E.1
Jennum, P.2
Fenger, K.3
Sorensen, S.A.4
Fuglsang-Frederiksen, A.5
-
36
-
-
0037963056
-
Transcranial magnetic stimulation study in hereditary spastic paraparesis
-
R. Nardone, and F. Tezzon Transcranial magnetic stimulation study in hereditary spastic paraparesis Eur Neurol 49 4 2003 234 237
-
(2003)
Eur Neurol
, vol.49
, Issue.4
, pp. 234-237
-
-
Nardone, R.1
Tezzon, F.2
-
37
-
-
0033845095
-
Neurological and neuroradiological progression in hereditary spastic paraplegia with a thin corpus callosum
-
S. Okubo, M. Ueda, T. Kamiya, S. Mizumura, A. Terashi, and Y. Katayama Neurological and neuroradiological progression in hereditary spastic paraplegia with a thin corpus callosum Acta Neurol Scand 102 3 2000 196 199
-
(2000)
Acta Neurol Scand
, vol.102
, Issue.3
, pp. 196-199
-
-
Okubo, S.1
Ueda, M.2
Kamiya, T.3
Mizumura, S.4
Terashi, A.5
Katayama, Y.6
-
38
-
-
0034840353
-
Neuroradiological findings in hereditary spastic paraplegia with a thin corpus callosum
-
J. Ohnishi, Y. Tomoda, and K. Yokoyama Neuroradiological findings in hereditary spastic paraplegia with a thin corpus callosum Acta Neurol Scand 104 3 2001 191 192
-
(2001)
Acta Neurol Scand
, vol.104
, Issue.3
, pp. 191-192
-
-
Ohnishi, J.1
Tomoda, Y.2
Yokoyama, K.3
-
39
-
-
2642598065
-
Diaschisis and neurobehavior
-
D.K. Nguyen, and M.I. Botez Diaschisis and neurobehavior Can J Neurol Sci 25 1 1998 Feb 5 12
-
(1998)
Can J Neurol Sci
, vol.25
, Issue.1
, pp. 5-12
-
-
Nguyen, D.K.1
Botez, M.I.2
-
40
-
-
0027396268
-
Hypoperfusion and vasoreactivity in the thalamus and cerebellum after stroke
-
Y. Sakashita, H. Matsuda, K. Kakuda, and M. Takamori Hypoperfusion and vasoreactivity in the thalamus and cerebellum after stroke Stroke 24 1 1993 Jan 84 87
-
(1993)
Stroke
, vol.24
, Issue.1
, pp. 84-87
-
-
Sakashita, Y.1
Matsuda, H.2
Kakuda, K.3
Takamori, M.4
-
41
-
-
0031014081
-
Influence of spinal cord injury on cerebral sensorimotor systems: A PET study
-
U. Roelcke, A. Curt, A. Otte, J. Missimer, R.P. Maguire, and V. Dietz Influence of spinal cord injury on cerebral sensorimotor systems: a PET study Neurol Neurosurg Psychiatry 62 1 1997 61 65
-
(1997)
Neurol Neurosurg Psychiatry
, vol.62
, Issue.1
, pp. 61-65
-
-
Roelcke, U.1
Curt, A.2
Otte, A.3
Missimer, J.4
Maguire, R.P.5
Dietz, V.6
-
42
-
-
0035833930
-
Face memory impairments in patients with frontal lobe damage
-
S.Z. Rapcsak, L. Nielsen, L.D. Littrell, E.L. Glisky, A.W. Kaszniak, and J.F. Laguna Face memory impairments in patients with frontal lobe damage Neurology 57 7 2001 1168 1175
-
(2001)
Neurology
, vol.57
, Issue.7
, pp. 1168-1175
-
-
Rapcsak, S.Z.1
Nielsen, L.2
Littrell, L.D.3
Glisky, E.L.4
Kaszniak, A.W.5
Laguna, J.F.6
-
43
-
-
0030061766
-
Face encoding and recognition in the human brain
-
J.V. Haxby, L.G. Ungerleider, B. Horwitz, J.M. Maisog, S.I. Rapoport, and C.L. Grady Face encoding and recognition in the human brain Proc Natl Acad Sci U S A 93 2 1996 922 927
-
(1996)
Proc Natl Acad Sci U S a
, vol.93
, Issue.2
, pp. 922-927
-
-
Haxby, J.V.1
Ungerleider, L.G.2
Horwitz, B.3
Maisog, J.M.4
Rapoport, S.I.5
Grady, C.L.6
-
44
-
-
0005094315
-
Novel vs. well-learned memory for faces: A positron emission tomography study
-
A.K. Wiser, N. Andreasen, D.S. O'Leary, B. Crespo-Facorro, L.L. Boles-Ponto, and G.L. Watkins Novel vs. well-learned memory for faces: a positron emission tomography study J Cogn Neurosci 12 2 2000 255 266
-
(2000)
J Cogn Neurosci
, vol.12
, Issue.2
, pp. 255-266
-
-
Wiser, A.K.1
Andreasen, N.2
O'Leary, D.S.3
Crespo-Facorro, B.4
Boles-Ponto, L.L.5
Watkins, G.L.6
-
45
-
-
0031845205
-
Linkage of AD HSP and cognitive impairment to chromosome 2p: Haplotype and phenotype analysis indicates variable expression and low or delayed penetrance
-
P.C. Byrne, S. Webb, F. McSweeney, T. Burke, M. Hutchinson, and N.A. Parfrey Linkage of AD HSP and cognitive impairment to chromosome 2p: haplotype and phenotype analysis indicates variable expression and low or delayed penetrance Eur J Hum Genet 6 3 1998 275 282
-
(1998)
Eur J Hum Genet
, vol.6
, Issue.3
, pp. 275-282
-
-
Byrne, P.C.1
Webb, S.2
McSweeney, F.3
Burke, T.4
Hutchinson, M.5
Parfrey, N.A.6
-
46
-
-
0031960716
-
Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p
-
O. Heinzlef, C. Paternotte, F. Mahieux, J.F. Prud'homme, J. Dien, and M. Madigand Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p J Med Genet 35 2 1998 89 93
-
(1998)
J Med Genet
, vol.35
, Issue.2
, pp. 89-93
-
-
Heinzlef, O.1
Paternotte, C.2
Mahieux, F.3
Prud'Homme, J.F.4
Dien, J.5
Madigand, M.6
-
47
-
-
0031976287
-
Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p
-
S. Webb, D. Coleman, and P. Byrne Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p Brain 121 Pt 4 1998 601 609
-
(1998)
Brain
, vol.121
, Issue.4 PART
, pp. 601-609
-
-
Webb, S.1
Coleman, D.2
Byrne, P.3
-
48
-
-
0033782943
-
Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis
-
J.C. Lindsey, M.E. Lusher, C.J. McDermott, K.D. White, E. Reid, and D.C. Rubinsztein Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis J Med Genet 37 10 2000 759 765
-
(2000)
J Med Genet
, vol.37
, Issue.10
, pp. 759-765
-
-
Lindsey, J.C.1
Lusher, M.E.2
McDermott, C.J.3
White, K.D.4
Reid, E.5
Rubinsztein, D.C.6
-
49
-
-
0041522717
-
Subtle cognitive impairment but no dementia in patients with spastin mutations
-
C.M. Tallaksen, E. Guichart-Gomez, P. Verpillat, V. Hahn-Barma, M. Ruberg, B. Fontaine, A. Brice, B. Dubois, and A. Durr Subtle cognitive impairment but no dementia in patients with spastin mutations Arch Neurol 60 8 2003 Aug 1113 1118
-
(2003)
Arch Neurol
, vol.60
, Issue.8
, pp. 1113-1118
-
-
Tallaksen, C.M.1
Guichart-Gomez, E.2
Verpillat, P.3
Hahn-Barma, V.4
Ruberg, M.5
Fontaine, B.6
Brice, A.7
Dubois, B.8
Durr, A.9
-
50
-
-
0036704933
-
Frontal-subcortical neuronal circuits and clinical neuropsychiatry: An update
-
S. Tekin, and J.L. Cummings Frontal-subcortical neuronal circuits and clinical neuropsychiatry: an update J Psychosom Res 53 2 2002 Aug 647 654
-
(2002)
J Psychosom Res
, vol.53
, Issue.2
, pp. 647-654
-
-
Tekin, S.1
Cummings, J.L.2
-
51
-
-
0030777273
-
MRI of autosomal dominant pure spastic paraplegia
-
K. Krabbe, J.E. Nielsen, E. Fallentin, K. Fenger, and M. Herning MRI of autosomal dominant pure spastic paraplegia Neuroradiology 39 10 1997 724 727
-
(1997)
Neuroradiology
, vol.39
, Issue.10
, pp. 724-727
-
-
Krabbe, K.1
Nielsen, J.E.2
Fallentin, E.3
Fenger, K.4
Herning, M.5
-
52
-
-
0033821055
-
Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation
-
F.M. Santorelli, C. Patrono, D. Fortini, A. Tessa, G. Comanducci, and E. Bertini Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation Neurology 55 5 2000 702 705
-
(2000)
Neurology
, vol.55
, Issue.5
, pp. 702-705
-
-
Santorelli, F.M.1
Patrono, C.2
Fortini, D.3
Tessa, A.4
Comanducci, G.5
Bertini, E.6
-
53
-
-
0035208727
-
A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: Association with multiple sclerosis in two affected siblings and epilepsy in other affected family members
-
S.H. Mead, C. Proukakis, N. Wood, A.H. Crosby, G.T. Plant, and T.T. Warner A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members J Neurol Neurosurg Psychiatry 71 6 2001 788 791
-
(2001)
J Neurol Neurosurg Psychiatry
, vol.71
, Issue.6
, pp. 788-791
-
-
Mead, S.H.1
Proukakis, C.2
Wood, N.3
Crosby, A.H.4
Plant, G.T.5
Warner, T.T.6
-
54
-
-
0034973141
-
A voxel-based morphometric study of ageing in 465 normal adult human brains
-
C.D. Good, I.S. Johnsrude, J. Ashburner, R.N. Henson, K.J. Friston, and R.S. Frackowiak A voxel-based morphometric study of ageing in 465 normal adult human brains Neuroimage 14 1 Pt 1 2001 Jul 21 36
-
(2001)
Neuroimage
, vol.14
, Issue.1 PART 1
, pp. 21-36
-
-
Good, C.D.1
Johnsrude, I.S.2
Ashburner, J.3
Henson, R.N.4
Friston, K.J.5
Frackowiak, R.S.6
|