-
1
-
-
0028017540
-
A quantitative magnetic resonance imaging study of changes in brain morphology from infancy to late adulthood
-
Pfefferbaum A., Mathalon D.H., Sullivan E.V., et al. A quantitative magnetic resonance imaging study of changes in brain morphology from infancy to late adulthood. Arch Neurol 51 9 (1994) 874-887
-
(1994)
Arch Neurol
, vol.51
, Issue.9
, pp. 874-887
-
-
Pfefferbaum, A.1
Mathalon, D.H.2
Sullivan, E.V.3
-
2
-
-
0033305929
-
Brain development during childhood and adolescence: a longitudinal MRI study
-
Giedd J.N., Blumenthal J., Jeffries N.O., et al. Brain development during childhood and adolescence: a longitudinal MRI study. Nat Neurosci 2 10 (1999) 861-863
-
(1999)
Nat Neurosci
, vol.2
, Issue.10
, pp. 861-863
-
-
Giedd, J.N.1
Blumenthal, J.2
Jeffries, N.O.3
-
5
-
-
33645453807
-
Intellectual ability and cortical development in children and adolescents
-
Shaw P., Greenstein D., Lerch J., et al. Intellectual ability and cortical development in children and adolescents. Nature 440 7084 (2006) 676-679
-
(2006)
Nature
, vol.440
, Issue.7084
, pp. 676-679
-
-
Shaw, P.1
Greenstein, D.2
Lerch, J.3
-
6
-
-
0033839568
-
Brain imaging in neurogenetic conditions: realizing the potential of behavioral neurogenetics research
-
Reiss A.L., Eliez S., Schmitt J.E., et al. Brain imaging in neurogenetic conditions: realizing the potential of behavioral neurogenetics research. Ment Retard Dev Disabil Res Rev 6 3 (2000) 186-197
-
(2000)
Ment Retard Dev Disabil Res Rev
, vol.6
, Issue.3
, pp. 186-197
-
-
Reiss, A.L.1
Eliez, S.2
Schmitt, J.E.3
-
7
-
-
0028223951
-
A behavioral neurogenetics approach to developmental disabilities: gene-brain-behavior associations
-
Baumgardner T.L., Green K.E., and Reiss A.L. A behavioral neurogenetics approach to developmental disabilities: gene-brain-behavior associations. Curr Opin Neurol 7 2 (1994) 172-178
-
(1994)
Curr Opin Neurol
, vol.7
, Issue.2
, pp. 172-178
-
-
Baumgardner, T.L.1
Green, K.E.2
Reiss, A.L.3
-
8
-
-
0023889961
-
The pathological association between Down syndrome and Alzheimer disease
-
Mann D.M. The pathological association between Down syndrome and Alzheimer disease. Mech Ageing Dev 43 2 (1988) 99-136
-
(1988)
Mech Ageing Dev
, vol.43
, Issue.2
, pp. 99-136
-
-
Mann, D.M.1
-
9
-
-
0035183495
-
Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia
-
Murphy K.C., and Owen M.J. Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia. Br J Psychiatry 179 (2001) 397-402
-
(2001)
Br J Psychiatry
, vol.179
, pp. 397-402
-
-
Murphy, K.C.1
Owen, M.J.2
-
10
-
-
23944490213
-
Recent advances in fragile X: a model for autism and neurodegeneration
-
Hagerman R.J., Ono M.Y., and Hagerman P.J. Recent advances in fragile X: a model for autism and neurodegeneration. Curr Opin Psychiatry 18 5 (2005) 490-496
-
(2005)
Curr Opin Psychiatry
, vol.18
, Issue.5
, pp. 490-496
-
-
Hagerman, R.J.1
Ono, M.Y.2
Hagerman, P.J.3
-
11
-
-
0025260871
-
Anomalous brain morphology on magnetic resonance images in Williams syndrome and Down syndrome
-
Jernigan T.L., and Bellugi U. Anomalous brain morphology on magnetic resonance images in Williams syndrome and Down syndrome. Arch Neurol 47 5 (1990) 529-533
-
(1990)
Arch Neurol
, vol.47
, Issue.5
, pp. 529-533
-
-
Jernigan, T.L.1
Bellugi, U.2
-
12
-
-
0027475963
-
Cerebral morphologic distinctions between Williams and Down syndromes
-
Jernigan T.L., Bellugi U., Sowell E., et al. Cerebral morphologic distinctions between Williams and Down syndromes. Arch Neurol 50 2 (1993) 186-191
-
(1993)
Arch Neurol
, vol.50
, Issue.2
, pp. 186-191
-
-
Jernigan, T.L.1
Bellugi, U.2
Sowell, E.3
-
13
-
-
0036570142
-
Cerebral growth in fragile X syndrome: review and comparison with Down syndrome
-
Kates W.R., Folley B.S., Lanham D.C., et al. Cerebral growth in fragile X syndrome: review and comparison with Down syndrome. Microsc Res Tech 57 3 (2002) 159-167
-
(2002)
Microsc Res Tech
, vol.57
, Issue.3
, pp. 159-167
-
-
Kates, W.R.1
Folley, B.S.2
Lanham, D.C.3
-
14
-
-
0026594076
-
Callosal morphology concurs with neurobehavioral and neuropathological findings in two neurodevelopmental disorders
-
Wang P.P., Doherty S., Hesselink J.R., et al. Callosal morphology concurs with neurobehavioral and neuropathological findings in two neurodevelopmental disorders. Arch Neurol 49 4 (1992) 407-411
-
(1992)
Arch Neurol
, vol.49
, Issue.4
, pp. 407-411
-
-
Wang, P.P.1
Doherty, S.2
Hesselink, J.R.3
-
15
-
-
0028898302
-
Neurodevelopmental effects of the FMR-1 full mutation in humans
-
Reiss A.L., Abrams M.T., Greenlaw R., et al. Neurodevelopmental effects of the FMR-1 full mutation in humans. Nat Med 1 2 (1995) 159-167
-
(1995)
Nat Med
, vol.1
, Issue.2
, pp. 159-167
-
-
Reiss, A.L.1
Abrams, M.T.2
Greenlaw, R.3
-
16
-
-
0032882849
-
High rates of schizophrenia in adults with velo-cardio-facial syndrome
-
Murphy K.C., Jones L.A., and Owen M.J. High rates of schizophrenia in adults with velo-cardio-facial syndrome. Arch Gen Psychiatry 56 10 (1999) 940-945
-
(1999)
Arch Gen Psychiatry
, vol.56
, Issue.10
, pp. 940-945
-
-
Murphy, K.C.1
Jones, L.A.2
Owen, M.J.3
-
17
-
-
0036846189
-
Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction
-
Brunberg J.A., Jacquemont S., Hagerman R.J., et al. Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction. AJNR Am J Neuroradiol 23 10 (2002) 1757-1766
-
(2002)
AJNR Am J Neuroradiol
, vol.23
, Issue.10
, pp. 1757-1766
-
-
Brunberg, J.A.1
Jacquemont, S.2
Hagerman, R.J.3
-
18
-
-
0037384643
-
Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates
-
Jacquemont S., Hagerman R.J., Leehey M., et al. Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates. Am J Hum Genet 72 4 (2003) 869-878
-
(2003)
Am J Hum Genet
, vol.72
, Issue.4
, pp. 869-878
-
-
Jacquemont, S.1
Hagerman, R.J.2
Leehey, M.3
-
19
-
-
0030046748
-
Automatic atlas-based volume estimation of human brain regions from MR images
-
Andreasen N.C., Rajarethinam R., Cizadlo T., et al. Automatic atlas-based volume estimation of human brain regions from MR images. J Comput Assist Tomogr 20 1 (1996) 98-106
-
(1996)
J Comput Assist Tomogr
, vol.20
, Issue.1
, pp. 98-106
-
-
Andreasen, N.C.1
Rajarethinam, R.2
Cizadlo, T.3
-
20
-
-
0037082876
-
A new rapid landmark-based regional MRI segmentation method of the brain
-
Bokde A.L., Teipel S.J., Zebuhr Y., et al. A new rapid landmark-based regional MRI segmentation method of the brain. J Neurol Sci 194 1 (2002) 35-40
-
(2002)
J Neurol Sci
, vol.194
, Issue.1
, pp. 35-40
-
-
Bokde, A.L.1
Teipel, S.J.2
Zebuhr, Y.3
-
21
-
-
0030752751
-
Reliability and validity of MRI measurement of the amygdala and hippocampus in children with fragile X syndrome
-
Kates W.R., Abrams M.T., Kaufmann W.E., et al. Reliability and validity of MRI measurement of the amygdala and hippocampus in children with fragile X syndrome. Psychiatry Res 75 1 (1997) 31-48
-
(1997)
Psychiatry Res
, vol.75
, Issue.1
, pp. 31-48
-
-
Kates, W.R.1
Abrams, M.T.2
Kaufmann, W.E.3
-
22
-
-
0033933649
-
Voxel-based morphometry: the methods
-
Ashburner J., and Friston K.J. Voxel-based morphometry: the methods. Neuroimage 11 6 Pt 1 (2000) 805-821
-
(2000)
Neuroimage
, vol.11
, Issue.6 PART 1
, pp. 805-821
-
-
Ashburner, J.1
Friston, K.J.2
-
23
-
-
7044253600
-
Mapping cortical change in Alzheimer's disease, brain development, and schizophrenia
-
Thompson P.M., Hayashi K.M., Sowell E.R., et al. Mapping cortical change in Alzheimer's disease, brain development, and schizophrenia. Neuroimage 23 Suppl 1 (2004) S2-S18
-
(2004)
Neuroimage
, vol.23
, Issue.SUPPL. 1
-
-
Thompson, P.M.1
Hayashi, K.M.2
Sowell, E.R.3
-
24
-
-
0034718613
-
Measuring the thickness of the human cerebral cortex from magnetic resonance images
-
Fischl B., and Dale A.M. Measuring the thickness of the human cerebral cortex from magnetic resonance images. Proc Natl Acad Sci USA 97 20 (2000) 11050-11055
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, Issue.20
, pp. 11050-11055
-
-
Fischl, B.1
Dale, A.M.2
-
25
-
-
0032741345
-
High-resolution intersubject averaging and a coordinate system for the cortical surface
-
Fischl B., Sereno M.I., Tootell R.B., et al. High-resolution intersubject averaging and a coordinate system for the cortical surface. Hum Brain Mapp 8 4 (1999) 272-284
-
(1999)
Hum Brain Mapp
, vol.8
, Issue.4
, pp. 272-284
-
-
Fischl, B.1
Sereno, M.I.2
Tootell, R.B.3
-
26
-
-
0037319171
-
Dynamics of gray matter loss in Alzheimer's disease
-
Thompson P.M., Hayashi K.M., de Zubicaray G., et al. Dynamics of gray matter loss in Alzheimer's disease. J Neurosci 23 3 (2003) 994-1005
-
(2003)
J Neurosci
, vol.23
, Issue.3
, pp. 994-1005
-
-
Thompson, P.M.1
Hayashi, K.M.2
de Zubicaray, G.3
-
27
-
-
0024274659
-
The human pattern of gyrification in the cerebral cortex
-
Zilles K., Armstrong E., Schleicher A., et al. The human pattern of gyrification in the cerebral cortex. Anat Embryol (Berl) 179 2 (1988) 173-179
-
(1988)
Anat Embryol (Berl)
, vol.179
, Issue.2
, pp. 173-179
-
-
Zilles, K.1
Armstrong, E.2
Schleicher, A.3
-
28
-
-
7044226476
-
A framework to study the cortical folding patterns
-
Mangin J.F., Riviere D., Cachia A., et al. A framework to study the cortical folding patterns. Neuroimage 23 Suppl 1 (2004) S129-S138
-
(2004)
Neuroimage
, vol.23
, Issue.SUPPL. 1
-
-
Mangin, J.F.1
Riviere, D.2
Cachia, A.3
-
29
-
-
0036265360
-
Brain volumes and surface morphology in monozygotic twins
-
White T., Andreasen N.C., and Nopoulos P. Brain volumes and surface morphology in monozygotic twins. Cereb Cortex 12 5 (2002) 486-493
-
(2002)
Cereb Cortex
, vol.12
, Issue.5
, pp. 486-493
-
-
White, T.1
Andreasen, N.C.2
Nopoulos, P.3
-
30
-
-
31844442345
-
A curvature-based approach to estimate local gyrification on the cortical surface
-
Luders E., Thompson P.M., Narr K.L., et al. A curvature-based approach to estimate local gyrification on the cortical surface. Neuroimage 29 4 (2006) 1224-1230
-
(2006)
Neuroimage
, vol.29
, Issue.4
, pp. 1224-1230
-
-
Luders, E.1
Thompson, P.M.2
Narr, K.L.3
-
31
-
-
0029828575
-
Diffusion tensor MR imaging of the human brain
-
Pierpaoli C., Jezzard P., Basser P.J., et al. Diffusion tensor MR imaging of the human brain. Radiology 201 3 (1996) 637-648
-
(1996)
Radiology
, vol.201
, Issue.3
, pp. 637-648
-
-
Pierpaoli, C.1
Jezzard, P.2
Basser, P.J.3
-
32
-
-
0036795140
-
Diffusion-tensor MR imaging of gray and white matter development during normal human brain maturation
-
Mukherjee P., Miller J.H., Shimony J.S., et al. Diffusion-tensor MR imaging of gray and white matter development during normal human brain maturation. AJNR Am J Neuroradiol 23 9 (2002) 1445-1456
-
(2002)
AJNR Am J Neuroradiol
, vol.23
, Issue.9
, pp. 1445-1456
-
-
Mukherjee, P.1
Miller, J.H.2
Shimony, J.S.3
-
33
-
-
0038417101
-
White matter tract alterations in fragile X syndrome: preliminary evidence from diffusion tensor imaging
-
Barnea-Goraly N., Eliez S., Hedeus M., et al. White matter tract alterations in fragile X syndrome: preliminary evidence from diffusion tensor imaging. Am J Med Genet B Neuropsychiatr Genet 118 1 (2003) 81-88
-
(2003)
Am J Med Genet B Neuropsychiatr Genet
, vol.118
, Issue.1
, pp. 81-88
-
-
Barnea-Goraly, N.1
Eliez, S.2
Hedeus, M.3
-
34
-
-
0642371334
-
Investigation of white matter structure in velocardiofacial syndrome: a diffusion tensor imaging study
-
Barnea-Goraly N., Menon V., Krasnow B., et al. Investigation of white matter structure in velocardiofacial syndrome: a diffusion tensor imaging study. Am J Psychiatry 160 10 (2003) 1863-1869
-
(2003)
Am J Psychiatry
, vol.160
, Issue.10
, pp. 1863-1869
-
-
Barnea-Goraly, N.1
Menon, V.2
Krasnow, B.3
-
35
-
-
0036158378
-
Imaging cortical association tracts in the human brain using diffusion-tensor-based axonal tracking
-
Mori S., Kaufmann W.E., Davatzikos C., et al. Imaging cortical association tracts in the human brain using diffusion-tensor-based axonal tracking. Magn Reson Med 47 2 (2002) 215-223
-
(2002)
Magn Reson Med
, vol.47
, Issue.2
, pp. 215-223
-
-
Mori, S.1
Kaufmann, W.E.2
Davatzikos, C.3
-
36
-
-
0042671350
-
DTI mapping of human brain connectivity: statistical fibre tracking and virtual dissection
-
Hagmann P., Thiran J.P., Jonasson L., et al. DTI mapping of human brain connectivity: statistical fibre tracking and virtual dissection. Neuroimage 19 3 (2003) 545-554
-
(2003)
Neuroimage
, vol.19
, Issue.3
, pp. 545-554
-
-
Hagmann, P.1
Thiran, J.P.2
Jonasson, L.3
-
37
-
-
0037092473
-
Visualizing the neural bases of a disconnection syndrome with diffusion tensor imaging
-
Molko N., Cohen L., Mangin J.F., et al. Visualizing the neural bases of a disconnection syndrome with diffusion tensor imaging. J Cogn Neurosci 14 4 (2002) 629-636
-
(2002)
J Cogn Neurosci
, vol.14
, Issue.4
, pp. 629-636
-
-
Molko, N.1
Cohen, L.2
Mangin, J.F.3
-
38
-
-
0019942204
-
Longevity and mortality in Down's syndrome
-
Thase M.E. Longevity and mortality in Down's syndrome. J Ment Defic Res 26 Pt 3 (1982) 177-192
-
(1982)
J Ment Defic Res
, vol.26
, Issue.PART 3
, pp. 177-192
-
-
Thase, M.E.1
-
39
-
-
0025071591
-
Brain growth in Down syndrome subjects 15 to 22 weeks of gestational age and birth to 60 months
-
Schmidt-Sidor B., Wisniewski K.E., Shepard T.H., et al. Brain growth in Down syndrome subjects 15 to 22 weeks of gestational age and birth to 60 months. Clin Neuropathol 9 4 (1990) 181-190
-
(1990)
Clin Neuropathol
, vol.9
, Issue.4
, pp. 181-190
-
-
Schmidt-Sidor, B.1
Wisniewski, K.E.2
Shepard, T.H.3
-
40
-
-
0034809935
-
Neuroanatomy of Down's syndrome: a high-resolution MRI study
-
Pinter J.D., Eliez S., Schmitt J.E., et al. Neuroanatomy of Down's syndrome: a high-resolution MRI study. Am J Psychiatry 158 10 (2001) 1659-1665
-
(2001)
Am J Psychiatry
, vol.158
, Issue.10
, pp. 1659-1665
-
-
Pinter, J.D.1
Eliez, S.2
Schmitt, J.E.3
-
41
-
-
0028306111
-
Magnetic resonance imaging analysis of age-related changes in the brains of individuals with Down's syndrome
-
Kesslak J.P., Nagata S.F., Lott I., et al. Magnetic resonance imaging analysis of age-related changes in the brains of individuals with Down's syndrome. Neurology 44 6 (1994) 1039-1045
-
(1994)
Neurology
, vol.44
, Issue.6
, pp. 1039-1045
-
-
Kesslak, J.P.1
Nagata, S.F.2
Lott, I.3
-
42
-
-
0028878675
-
Selective neuroanatomic abnormalities in Down's syndrome and their cognitive correlates: evidence from MRI morphometry
-
Raz N., Torres I.J., Briggs S.D., et al. Selective neuroanatomic abnormalities in Down's syndrome and their cognitive correlates: evidence from MRI morphometry. Neurology 45 2 (1995) 356-366
-
(1995)
Neurology
, vol.45
, Issue.2
, pp. 356-366
-
-
Raz, N.1
Torres, I.J.2
Briggs, S.D.3
-
43
-
-
0021749584
-
A morphometric CT study of Down's syndrome showing small posterior fossa and calcification of basal ganglia
-
Ieshima A., Kisa T., Yoshino K., et al. A morphometric CT study of Down's syndrome showing small posterior fossa and calcification of basal ganglia. Neuroradiology 26 6 (1984) 493-498
-
(1984)
Neuroradiology
, vol.26
, Issue.6
, pp. 493-498
-
-
Ieshima, A.1
Kisa, T.2
Yoshino, K.3
-
44
-
-
0021601145
-
Evidence of arrest of neurogenesis and synaptogenesis in brains of patients with Down's syndrome
-
Wisniewski K.E., Laure-Kamionowska M., and Wisniewski H.M. Evidence of arrest of neurogenesis and synaptogenesis in brains of patients with Down's syndrome. N Engl J Med 311 18 (1984) 1187-1188
-
(1984)
N Engl J Med
, vol.311
, Issue.18
, pp. 1187-1188
-
-
Wisniewski, K.E.1
Laure-Kamionowska, M.2
Wisniewski, H.M.3
-
45
-
-
0024411610
-
Postnatal delay of myelin formation in brains from Down syndrome infants and children
-
Wisniewski K.E., and Schmidt-Sidor B. Postnatal delay of myelin formation in brains from Down syndrome infants and children. Clin Neuropathol 8 2 (1989) 55-62
-
(1989)
Clin Neuropathol
, vol.8
, Issue.2
, pp. 55-62
-
-
Wisniewski, K.E.1
Schmidt-Sidor, B.2
-
46
-
-
0042025827
-
Down's syndrome: a genetic disorder in biobehavioral perspective
-
Nadel L. Down's syndrome: a genetic disorder in biobehavioral perspective. Genes Brain Behav 2 3 (2003) 156-166
-
(2003)
Genes Brain Behav
, vol.2
, Issue.3
, pp. 156-166
-
-
Nadel, L.1
-
47
-
-
0025887234
-
Conditioning and long-term memory in three-month-old infants with Down syndrome
-
Ohr P.S., and Fagen J.W. Conditioning and long-term memory in three-month-old infants with Down syndrome. Am J Ment Retard 96 2 (1991) 151-162
-
(1991)
Am J Ment Retard
, vol.96
, Issue.2
, pp. 151-162
-
-
Ohr, P.S.1
Fagen, J.W.2
-
48
-
-
0028276612
-
Contingency learning in 9-month-old infants with Down syndrome
-
Ohr P.S., and Fagen J.W. Contingency learning in 9-month-old infants with Down syndrome. Am J Ment Retard 99 1 (1994) 74-84
-
(1994)
Am J Ment Retard
, vol.99
, Issue.1
, pp. 74-84
-
-
Ohr, P.S.1
Fagen, J.W.2
-
49
-
-
0025340975
-
Myelination as a parameter of normal and retarded brain maturation
-
Dambska M., and Laure-Kamionowska M. Myelination as a parameter of normal and retarded brain maturation. Brain Dev 12 2 (1990) 214-220
-
(1990)
Brain Dev
, vol.12
, Issue.2
, pp. 214-220
-
-
Dambska, M.1
Laure-Kamionowska, M.2
-
50
-
-
0035836647
-
Amygdala and hippocampal volumes in children with Down syndrome: a high-resolution MRI study
-
Pinter J.D., Brown W.E., Eliez S., et al. Amygdala and hippocampal volumes in children with Down syndrome: a high-resolution MRI study. Neurology 56 7 (2001) 972-974
-
(2001)
Neurology
, vol.56
, Issue.7
, pp. 972-974
-
-
Pinter, J.D.1
Brown, W.E.2
Eliez, S.3
-
51
-
-
0031041335
-
Cerebellar volume in adults with Down syndrome
-
Aylward E.H., Habbak R., Warren A.C., et al. Cerebellar volume in adults with Down syndrome. Arch Neurol 54 2 (1997) 209-212
-
(1997)
Arch Neurol
, vol.54
, Issue.2
, pp. 209-212
-
-
Aylward, E.H.1
Habbak, R.2
Warren, A.C.3
-
52
-
-
0022594340
-
Volumetric development of the fetal telencephalon, cerebral cortex, diencephalon, and rhombencephalon, including the cerebellum in man
-
Koop M., Rilling G., Herrmann A., et al. Volumetric development of the fetal telencephalon, cerebral cortex, diencephalon, and rhombencephalon, including the cerebellum in man. Bibl Anat 28 (1986) 53-78
-
(1986)
Bibl Anat
, Issue.28
, pp. 53-78
-
-
Koop, M.1
Rilling, G.2
Herrmann, A.3
-
53
-
-
0035232533
-
Developmental instability of the cerebellum and its relevance to Down syndrome
-
Shapiro B.L. Developmental instability of the cerebellum and its relevance to Down syndrome. J Neural Transm Suppl 61 (2001) 11-34
-
(2001)
J Neural Transm Suppl
, Issue.61
, pp. 11-34
-
-
Shapiro, B.L.1
-
54
-
-
0642340719
-
Relation of corpus callosum and hippocampal size to age in nondemented adults with Down's syndrome
-
Teipel S.J., Schapiro M.B., Alexander G.E., et al. Relation of corpus callosum and hippocampal size to age in nondemented adults with Down's syndrome. Am J Psychiatry 160 10 (2003) 1870-1878
-
(2003)
Am J Psychiatry
, vol.160
, Issue.10
, pp. 1870-1878
-
-
Teipel, S.J.1
Schapiro, M.B.2
Alexander, G.E.3
-
55
-
-
0024370171
-
A prospective study of Alzheimer disease in Down syndrome
-
Lai F., and Williams R.S. A prospective study of Alzheimer disease in Down syndrome. Arch Neurol 46 8 (1989) 849-853
-
(1989)
Arch Neurol
, vol.46
, Issue.8
, pp. 849-853
-
-
Lai, F.1
Williams, R.S.2
-
56
-
-
0024503377
-
The pattern of acquisition of plaques and tangles in the brains of patients under 50 years of age with Down's syndrome
-
Mann D.M., and Esiri M.M. The pattern of acquisition of plaques and tangles in the brains of patients under 50 years of age with Down's syndrome. J Neurol Sci 89 2-3 (1989) 169-179
-
(1989)
J Neurol Sci
, vol.89
, Issue.2-3
, pp. 169-179
-
-
Mann, D.M.1
Esiri, M.M.2
-
57
-
-
0023771356
-
Mapping of the gene encoding the beta-amyloid precursor protein and its relationship to the Down syndrome region of chromosome 21
-
Patterson D., Gardiner K., Kao F.T., et al. Mapping of the gene encoding the beta-amyloid precursor protein and its relationship to the Down syndrome region of chromosome 21. Proc Natl Acad Sci USA 85 21 (1988) 8266-8270
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, Issue.21
, pp. 8266-8270
-
-
Patterson, D.1
Gardiner, K.2
Kao, F.T.3
-
58
-
-
0036368653
-
Relation of medial temporal lobe volumes to age and memory function in nondemented adults with Down's syndrome: implications for the prodromal phase of Alzheimer's disease
-
Krasuski J.S., Alexander G.E., Horwitz B., et al. Relation of medial temporal lobe volumes to age and memory function in nondemented adults with Down's syndrome: implications for the prodromal phase of Alzheimer's disease. Am J Psychiatry 159 1 (2002) 74-81
-
(2002)
Am J Psychiatry
, vol.159
, Issue.1
, pp. 74-81
-
-
Krasuski, J.S.1
Alexander, G.E.2
Horwitz, B.3
-
59
-
-
33745028432
-
Neuroanatomy of Down syndrome in vivo: a model of preclinical Alzheimer's disease
-
Teipel S.J., and Hampel H. Neuroanatomy of Down syndrome in vivo: a model of preclinical Alzheimer's disease. Behav Genet 36 3 (2006) 405-415
-
(2006)
Behav Genet
, vol.36
, Issue.3
, pp. 405-415
-
-
Teipel, S.J.1
Hampel, H.2
-
60
-
-
0020331755
-
Basal ganglia calcification (BGC) in Down's syndrome (DS): another manifestation of premature aging
-
Wisniewski K.E., French J.H., Rosen J.F., et al. Basal ganglia calcification (BGC) in Down's syndrome (DS): another manifestation of premature aging. Ann N Y Acad Sci 396 (1982) 179-189
-
(1982)
Ann N Y Acad Sci
, vol.396
, pp. 179-189
-
-
Wisniewski, K.E.1
French, J.H.2
Rosen, J.F.3
-
61
-
-
0021875804
-
Basal ganglia calcification in Down's syndrome
-
Takashima S., and Becker L.E. Basal ganglia calcification in Down's syndrome. J Neurol Neurosurg Psychiatr 48 1 (1985) 61-64
-
(1985)
J Neurol Neurosurg Psychiatr
, vol.48
, Issue.1
, pp. 61-64
-
-
Takashima, S.1
Becker, L.E.2
-
62
-
-
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 A.J., Pieretti M., Sutcliffe J.S., 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 65 5 (1991) 905-914
-
(1991)
Cell
, vol.65
, Issue.5
, pp. 905-914
-
-
Verkerk, A.J.1
Pieretti, M.2
Sutcliffe, J.S.3
-
63
-
-
0030857615
-
Autistic behaviors among girls with fragile X syndrome
-
Mazzocco M.M., Kates W.R., Baumgardner T.L., et al. Autistic behaviors among girls with fragile X syndrome. J Autism Dev Disord 27 4 (1997) 415-435
-
(1997)
J Autism Dev Disord
, vol.27
, Issue.4
, pp. 415-435
-
-
Mazzocco, M.M.1
Kates, W.R.2
Baumgardner, T.L.3
-
65
-
-
0029896929
-
A controlled study of longitudinal IQ changes in females and males with fragile X syndrome
-
Wright-Talamante C., Cheema A., Riddle J.E., et al. A controlled study of longitudinal IQ changes in females and males with fragile X syndrome. Am J Med Genet 64 2 (1996) 350-355
-
(1996)
Am J Med Genet
, vol.64
, Issue.2
, pp. 350-355
-
-
Wright-Talamante, C.1
Cheema, A.2
Riddle, J.E.3
-
66
-
-
0031882461
-
Decreased cerebellar posterior vermis size in fragile X syndrome: correlation with neurocognitive performance
-
Mostofsky S.H., Mazzocco M.M., Aakalu G., et al. Decreased cerebellar posterior vermis size in fragile X syndrome: correlation with neurocognitive performance. Neurology 50 1 (1998) 121-130
-
(1998)
Neurology
, vol.50
, Issue.1
, pp. 121-130
-
-
Mostofsky, S.H.1
Mazzocco, M.M.2
Aakalu, G.3
-
67
-
-
0028070159
-
Neuroanatomy of fragile X syndrome: the temporal lobe
-
Reiss A.L., Lee J., and Freund L. Neuroanatomy of fragile X syndrome: the temporal lobe. Neurology 44 7 (1994) 1317-1324
-
(1994)
Neurology
, vol.44
, Issue.7
, pp. 1317-1324
-
-
Reiss, A.L.1
Lee, J.2
Freund, L.3
-
68
-
-
1842407859
-
Fragile-X: neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes
-
Jakala P., Hanninen T., Ryynanen M., et al. Fragile-X: neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes. J Clin Invest 100 2 (1997) 331-338
-
(1997)
J Clin Invest
, vol.100
, Issue.2
, pp. 331-338
-
-
Jakala, P.1
Hanninen, T.2
Ryynanen, M.3
-
69
-
-
0030053242
-
Quantitative MRI of the temporal lobe, amygdala, and hippocampus in normal human development: ages 4-18 years
-
Giedd J.N., Vaituzis A.C., Hamburger S.D., et al. Quantitative MRI of the temporal lobe, amygdala, and hippocampus in normal human development: ages 4-18 years. J Comp Neurol 366 2 (1996) 223-230
-
(1996)
J Comp Neurol
, vol.366
, Issue.2
, pp. 223-230
-
-
Giedd, J.N.1
Vaituzis, A.C.2
Hamburger, S.D.3
-
70
-
-
0034896495
-
Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome
-
Eliez S., Blasey C.M., Freund L.S., et al. Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome. Brain 124 Pt 8 (2001) 1610-1618
-
(2001)
Brain
, vol.124
, Issue.PART 8
, pp. 1610-1618
-
-
Eliez, S.1
Blasey, C.M.2
Freund, L.S.3
-
71
-
-
16044366721
-
Quantitative magnetic resonance imaging of human brain development: ages 4-18
-
Giedd J.N., Snell J.W., Lange N., et al. Quantitative magnetic resonance imaging of human brain development: ages 4-18. Cereb Cortex 6 4 (1996) 551-560
-
(1996)
Cereb Cortex
, vol.6
, Issue.4
, pp. 551-560
-
-
Giedd, J.N.1
Snell, J.W.2
Lange, N.3
-
72
-
-
0033797832
-
Dendritic spine structural anomalies in fragile-X mental retardation syndrome
-
Irwin S.A., Galvez R., and Greenough W.T. Dendritic spine structural anomalies in fragile-X mental retardation syndrome. Cereb Cortex 10 10 (2000) 1038-1044
-
(2000)
Cereb Cortex
, vol.10
, Issue.10
, pp. 1038-1044
-
-
Irwin, S.A.1
Galvez, R.2
Greenough, W.T.3
-
73
-
-
0026026911
-
The Fra(X) syndrome: neurological, electrophysiological, and neuropathological abnormalities
-
Wisniewski K.E., Segan S.M., Miezejeski C.M., et al. The Fra(X) syndrome: neurological, electrophysiological, and neuropathological abnormalities. Am J Med Genet 38 2-3 (1991) 476-480
-
(1991)
Am J Med Genet
, vol.38
, Issue.2-3
, pp. 476-480
-
-
Wisniewski, K.E.1
Segan, S.M.2
Miezejeski, C.M.3
-
74
-
-
0035912771
-
Synaptic regulation of protein synthesis and the fragile X protein
-
Greenough W.T., Klintsova A.Y., Irwin S.A., et al. Synaptic regulation of protein synthesis and the fragile X protein. Proc Natl Acad Sci USA 98 13 (2001) 7101-7106
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, Issue.13
, pp. 7101-7106
-
-
Greenough, W.T.1
Klintsova, A.Y.2
Irwin, S.A.3
-
75
-
-
0025969057
-
Neuroanatomy of fragile X syndrome: the posterior fossa
-
Reiss A.L., Aylward E., Freund L.S., et al. Neuroanatomy of fragile X syndrome: the posterior fossa. Ann Neurol 29 1 (1991) 26-32
-
(1991)
Ann Neurol
, vol.29
, Issue.1
, pp. 26-32
-
-
Reiss, A.L.1
Aylward, E.2
Freund, L.S.3
-
76
-
-
0028140045
-
Abnormality of cerebellar vermian lobules VI and VII in patients with infantile autism: identification of hypoplastic and hyperplastic subgroups with MR imaging
-
Courchesne E., Saitoh O., Yeung-Courchesne R., et al. Abnormality of cerebellar vermian lobules VI and VII in patients with infantile autism: identification of hypoplastic and hyperplastic subgroups with MR imaging. AJR Am J Roentgenol 162 1 (1994) 123-130
-
(1994)
AJR Am J Roentgenol
, vol.162
, Issue.1
, pp. 123-130
-
-
Courchesne, E.1
Saitoh, O.2
Yeung-Courchesne, R.3
-
77
-
-
0035943033
-
Unusual brain growth patterns in early life in patients with autistic disorder: an MRI study
-
Courchesne E., Karns C.M., Davis H.R., et al. Unusual brain growth patterns in early life in patients with autistic disorder: an MRI study. Neurology 57 2 (2001) 245-254
-
(2001)
Neurology
, vol.57
, Issue.2
, pp. 245-254
-
-
Courchesne, E.1
Karns, C.M.2
Davis, H.R.3
-
79
-
-
0026345716
-
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox
-
Fu Y.H., Kuhl D.P., Pizzuti A., et al. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox. Cell 67 6 (1991) 1047-1058
-
(1991)
Cell
, vol.67
, Issue.6
, pp. 1047-1058
-
-
Fu, Y.H.1
Kuhl, D.P.2
Pizzuti, A.3
-
80
-
-
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 M.L., 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 57 5 (1995) 1006-1018
-
(1995)
Am J Hum Genet
, vol.57
, Issue.5
, pp. 1006-1018
-
-
Rousseau, F.1
Rouillard, P.2
Morel, M.L.3
-
81
-
-
0031809893
-
Fragile X premutation screening in women with premature ovarian failure
-
Conway G.S., Payne N.N., Webb J., et al. Fragile X premutation screening in women with premature ovarian failure. Hum Reprod 13 5 (1998) 1184-1187
-
(1998)
Hum Reprod
, vol.13
, Issue.5
, pp. 1184-1187
-
-
Conway, G.S.1
Payne, N.N.2
Webb, J.3
-
82
-
-
0035838379
-
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X
-
Hagerman R.J., Leehey M., Heinrichs W., et al. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology 57 1 (2001) 127-130
-
(2001)
Neurology
, vol.57
, Issue.1
, pp. 127-130
-
-
Hagerman, R.J.1
Leehey, M.2
Heinrichs, W.3
-
83
-
-
23244441878
-
Magnetic resonance imaging study in older fragile X premutation male carriers
-
Loesch D.Z., Litewka L., Brotchie P., et al. Magnetic resonance imaging study in older fragile X premutation male carriers. Ann Neurol 58 2 (2005) 326-330
-
(2005)
Ann Neurol
, vol.58
, Issue.2
, pp. 326-330
-
-
Loesch, D.Z.1
Litewka, L.2
Brotchie, P.3
-
84
-
-
30344473617
-
Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS)
-
Greco C.M., Berman R.F., Martin R.M., et al. Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS). Brain 129 Pt 1 (2006) 243-255
-
(2006)
Brain
, vol.129
, Issue.PART 1
, pp. 243-255
-
-
Greco, C.M.1
Berman, R.F.2
Martin, R.M.3
-
85
-
-
33750335320
-
Molecular and imaging correlates of the fragile X-associated tremor/ataxia syndrome
-
Cohen S., Masyn K., Adams J., et al. Molecular and imaging correlates of the fragile X-associated tremor/ataxia syndrome. Neurology 67 8 (2006) 1426-1431
-
(2006)
Neurology
, vol.67
, Issue.8
, pp. 1426-1431
-
-
Cohen, S.1
Masyn, K.2
Adams, J.3
-
87
-
-
0017821181
-
A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome
-
Shprintzen R.J., Goldberg R.B., Lewin M.L., et al. A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome. Cleft Palate J 15 1 (1978) 56-62
-
(1978)
Cleft Palate J
, vol.15
, Issue.1
, pp. 56-62
-
-
Shprintzen, R.J.1
Goldberg, R.B.2
Lewin, M.L.3
-
88
-
-
12144290440
-
Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome
-
Gothelf D., Presburger G., Levy D., et al. Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome. Am J Med Genet B Neuropsychiatr Genet 126 1 (2004) 116-121
-
(2004)
Am J Med Genet B Neuropsychiatr Genet
, vol.126
, Issue.1
, pp. 116-121
-
-
Gothelf, D.1
Presburger, G.2
Levy, D.3
-
89
-
-
0031009068
-
Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS
-
Swillen A., Devriendt K., Legius E., et al. Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS. J Med Genet 34 6 (1997) 453-458
-
(1997)
J Med Genet
, vol.34
, Issue.6
, pp. 453-458
-
-
Swillen, A.1
Devriendt, K.2
Legius, E.3
-
90
-
-
33748109768
-
The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence
-
Swillen A., Devriendt K., Legius E., et al. The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence. Genet Couns 10 1 (1999) 79-88
-
(1999)
Genet Couns
, vol.10
, Issue.1
, pp. 79-88
-
-
Swillen, A.1
Devriendt, K.2
Legius, E.3
-
91
-
-
0037084412
-
Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: usefulness as phenotypic indicators of schizophrenia risk
-
Feinstein C., Eliez S., Blasey C., et al. Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: usefulness as phenotypic indicators of schizophrenia risk. Biol Psychiatry 51 4 (2002) 312-318
-
(2002)
Biol Psychiatry
, vol.51
, Issue.4
, pp. 312-318
-
-
Feinstein, C.1
Eliez, S.2
Blasey, C.3
-
92
-
-
13244261075
-
Adolescents and young adults with 22q11 deletion syndrome: psychopathology in an at-risk group
-
Baker K.D., and Skuse D.H. Adolescents and young adults with 22q11 deletion syndrome: psychopathology in an at-risk group. Br J Psychiatry 186 (2005) 115-120
-
(2005)
Br J Psychiatry
, vol.186
, pp. 115-120
-
-
Baker, K.D.1
Skuse, D.H.2
-
93
-
-
0032754790
-
Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia
-
Chow E.W., Mikulis D.J., Zipursky R.B., et al. Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia. Biol Psychiatry 46 10 (1999) 1436-1442
-
(1999)
Biol Psychiatry
, vol.46
, Issue.10
, pp. 1436-1442
-
-
Chow, E.W.1
Mikulis, D.J.2
Zipursky, R.B.3
-
94
-
-
0028239052
-
Brain anomalies in velo-cardio-facial syndrome
-
Mitnick R.J., Bello J.A., and Shprintzen R.J. Brain anomalies in velo-cardio-facial syndrome. Am J Med Genet 54 2 (1994) 100-106
-
(1994)
Am J Med Genet
, vol.54
, Issue.2
, pp. 100-106
-
-
Mitnick, R.J.1
Bello, J.A.2
Shprintzen, R.J.3
-
95
-
-
0035010976
-
Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome
-
van Amelsvoort T., Daly E., Robertson D., et al. Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome. Br J Psychiatry 178 (2001) 412-419
-
(2001)
Br J Psychiatry
, vol.178
, pp. 412-419
-
-
van Amelsvoort, T.1
Daly, E.2
Robertson, D.3
-
96
-
-
1842587656
-
Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome
-
Shashi V., Muddasani S., Santos C.C., et al. Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome. Neuroimage 21 4 (2004) 1399-1406
-
(2004)
Neuroimage
, vol.21
, Issue.4
, pp. 1399-1406
-
-
Shashi, V.1
Muddasani, S.2
Santos, C.C.3
-
97
-
-
0033753819
-
The 22q11 deletion syndromes
-
Scambler P.J. The 22q11 deletion syndromes. Hum Mol Genet 9 16 (2000) 2421-2426
-
(2000)
Hum Mol Genet
, vol.9
, Issue.16
, pp. 2421-2426
-
-
Scambler, P.J.1
-
98
-
-
33750580533
-
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation
-
Robin N.H., Taylor C.J., McDonald-McGinn D.M., et al. Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation. Am J Med Genet A 140 22 (2006) 2416-2425
-
(2006)
Am J Med Genet A
, vol.140
, Issue.22
, pp. 2416-2425
-
-
Robin, N.H.1
Taylor, C.J.2
McDonald-McGinn, D.M.3
-
99
-
-
0028968605
-
Correlation of prenatal events with the development of polymicrogyria
-
Barkovich A.J., Rowley H., and Bollen A. Correlation of prenatal events with the development of polymicrogyria. AJNR Am J Neuroradiol 16 4 Suppl (1995) 822-827
-
(1995)
AJNR Am J Neuroradiol
, vol.16
, Issue.4 SUPPL
, pp. 822-827
-
-
Barkovich, A.J.1
Rowley, H.2
Bollen, A.3
-
100
-
-
0034064651
-
Children and adolescents with velocardiofacial syndrome: a volumetric MRI study
-
Eliez S., Schmitt J.E., White C.D., et al. Children and adolescents with velocardiofacial syndrome: a volumetric MRI study. Am J Psychiatry 157 3 (2000) 409-415
-
(2000)
Am J Psychiatry
, vol.157
, Issue.3
, pp. 409-415
-
-
Eliez, S.1
Schmitt, J.E.2
White, C.D.3
-
101
-
-
0035176185
-
Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: a preliminary study
-
Eliez S., Antonarakis S.E., Morris M.A., et al. Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: a preliminary study. Arch Gen Psychiatry 58 1 (2001) 64-68
-
(2001)
Arch Gen Psychiatry
, vol.58
, Issue.1
, pp. 64-68
-
-
Eliez, S.1
Antonarakis, S.E.2
Morris, M.A.3
-
102
-
-
0035871350
-
Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis
-
Kates W.R., Burnette C.P., Jabs E.W., et al. Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis. Biol Psychiatry 49 8 (2001) 677-684
-
(2001)
Biol Psychiatry
, vol.49
, Issue.8
, pp. 677-684
-
-
Kates, W.R.1
Burnette, C.P.2
Jabs, E.W.3
-
103
-
-
3042738235
-
Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2)
-
Kates W.R., Burnette C.P., Bessette B.A., et al. Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2). J Child Neurol 19 5 (2004) 337-342
-
(2004)
J Child Neurol
, vol.19
, Issue.5
, pp. 337-342
-
-
Kates, W.R.1
Burnette, C.P.2
Bessette, B.A.3
-
104
-
-
14244256353
-
Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study
-
Simon T.J., Ding L., Bish J.P., et al. Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study. Neuroimage 25 1 (2005) 169-180
-
(2005)
Neuroimage
, vol.25
, Issue.1
, pp. 169-180
-
-
Simon, T.J.1
Ding, L.2
Bish, J.P.3
-
105
-
-
0027308186
-
Neuroanatomy of Rett syndrome: a volumetric imaging study
-
Reiss A.L., Faruque F., Naidu S., et al. Neuroanatomy of Rett syndrome: a volumetric imaging study. Ann Neurol 34 2 (1993) 227-234
-
(1993)
Ann Neurol
, vol.34
, Issue.2
, pp. 227-234
-
-
Reiss, A.L.1
Faruque, F.2
Naidu, S.3
-
106
-
-
0034044878
-
Neuroanatomy of Williams syndrome: a high-resolution MRI study
-
Reiss A.L., Eliez S., Schmitt J.E., et al. Neuroanatomy of Williams syndrome: a high-resolution MRI study. J Cogn Neurosci 12 Suppl 1 (2000) 65-73
-
(2000)
J Cogn Neurosci
, vol.12
, Issue.SUPPL. 1
, pp. 65-73
-
-
Reiss, A.L.1
Eliez, S.2
Schmitt, J.E.3
-
107
-
-
33645921626
-
A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children
-
Simon T.J., Bish J.P., Bearden C.E., et al. A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children. Dev Psychopathol 17 3 (2005) 753-784
-
(2005)
Dev Psychopathol
, vol.17
, Issue.3
, pp. 753-784
-
-
Simon, T.J.1
Bish, J.P.2
Bearden, C.E.3
-
108
-
-
0035746371
-
Functional brain imaging study of mathematical reasoning abilities in velocardiofacial syndrome (del22q11.2)
-
Eliez S., Blasey C.M., Menon V., et al. Functional brain imaging study of mathematical reasoning abilities in velocardiofacial syndrome (del22q11.2). Genet Med 3 1 (2001) 49-55
-
(2001)
Genet Med
, vol.3
, Issue.1
, pp. 49-55
-
-
Eliez, S.1
Blasey, C.M.2
Menon, V.3
-
109
-
-
0028236367
-
Brain regions associated with acquisition and retrieval of verbal episodic memory
-
Shallice T., Fletcher P., Frith C.D., et al. Brain regions associated with acquisition and retrieval of verbal episodic memory. Nature 368 6472 (1994) 633-635
-
(1994)
Nature
, vol.368
, Issue.6472
, pp. 633-635
-
-
Shallice, T.1
Fletcher, P.2
Frith, C.D.3
-
110
-
-
0035095617
-
Velocardiofacial syndrome: are structural changes in the temporal and mesial temporal regions related to schizophrenia?
-
Eliez S., Blasey C.M., Schmitt E.J., et al. Velocardiofacial syndrome: are structural changes in the temporal and mesial temporal regions related to schizophrenia?. Am J Psychiatry 158 3 (2001) 447-453
-
(2001)
Am J Psychiatry
, vol.158
, Issue.3
, pp. 447-453
-
-
Eliez, S.1
Blasey, C.M.2
Schmitt, E.J.3
-
111
-
-
33646776794
-
Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome (22q11.2 deletion syndrome)
-
Kates W.R., Miller A.M., Abdulsabur N., et al. Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome (22q11.2 deletion syndrome). J Am Acad Child Adolesc Psychiatry 45 5 (2006) 587-595
-
(2006)
J Am Acad Child Adolesc Psychiatry
, vol.45
, Issue.5
, pp. 587-595
-
-
Kates, W.R.1
Miller, A.M.2
Abdulsabur, N.3
-
112
-
-
33746123033
-
Hippocampal volume reduction in 22q11.2 deletion syndrome
-
Debbane M., Schaer M., Farhoumand R., et al. Hippocampal volume reduction in 22q11.2 deletion syndrome. Neuropsychologia 44 12 (2006) 2360-2365
-
(2006)
Neuropsychologia
, vol.44
, Issue.12
, pp. 2360-2365
-
-
Debbane, M.1
Schaer, M.2
Farhoumand, R.3
-
113
-
-
33144456319
-
Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): an MRI study
-
Schaer M., Schmitt J.E., Glaser B., et al. Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): an MRI study. Psychiatry Res 146 1 (2006) 1-11
-
(2006)
Psychiatry Res
, vol.146
, Issue.1
, pp. 1-11
-
-
Schaer, M.1
Schmitt, J.E.2
Glaser, B.3
-
114
-
-
0031037505
-
A tension-based theory of morphogenesis and compact wiring in the central nervous system
-
Van Essen D.C. A tension-based theory of morphogenesis and compact wiring in the central nervous system. Nature 385 6614 (1997) 313-318
-
(1997)
Nature
, vol.385
, Issue.6614
, pp. 313-318
-
-
Van Essen, D.C.1
-
115
-
-
28844447409
-
Arithmetic ability and parietal alterations: a diffusion tensor imaging study in velocardiofacial syndrome
-
Barnea-Goraly N., Eliez S., Menon V., et al. Arithmetic ability and parietal alterations: a diffusion tensor imaging study in velocardiofacial syndrome. Brain Res Cogn Brain Res 25 3 (2005) 735-740
-
(2005)
Brain Res Cogn Brain Res
, vol.25
, Issue.3
, pp. 735-740
-
-
Barnea-Goraly, N.1
Eliez, S.2
Menon, V.3
-
116
-
-
0035869620
-
A quantitative MRI study of posterior fossa development in velocardiofacial syndrome
-
Eliez S., Schmitt J.E., White C.D., et al. A quantitative MRI study of posterior fossa development in velocardiofacial syndrome. Biol Psychiatry 49 6 (2001) 540-546
-
(2001)
Biol Psychiatry
, vol.49
, Issue.6
, pp. 540-546
-
-
Eliez, S.1
Schmitt, J.E.2
White, C.D.3
-
117
-
-
33646131176
-
Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome
-
Bish J.P., Pendyal A., Ding L., et al. Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome. Neurosci Lett 399 3 (2006) 245-248
-
(2006)
Neurosci Lett
, vol.399
, Issue.3
, pp. 245-248
-
-
Bish, J.P.1
Pendyal, A.2
Ding, L.3
-
118
-
-
0023808833
-
Social gaze, social avoidance, and repetitive behavior in fragile X males: a controlled study
-
Cohen I.L., Fisch G.S., Sudhalter V., et al. Social gaze, social avoidance, and repetitive behavior in fragile X males: a controlled study. Am J Ment Retard 92 5 (1988) 436-446
-
(1988)
Am J Ment Retard
, vol.92
, Issue.5
, pp. 436-446
-
-
Cohen, I.L.1
Fisch, G.S.2
Sudhalter, V.3
-
120
-
-
0034806183
-
Enlarged cerebellar vermis in Williams syndrome
-
Schmitt J.E., Eliez S., Warsofsky I.S., et al. Enlarged cerebellar vermis in Williams syndrome. J Psychiatr Res 35 4 (2001) 225-229
-
(2001)
J Psychiatr Res
, vol.35
, Issue.4
, pp. 225-229
-
-
Schmitt, J.E.1
Eliez, S.2
Warsofsky, I.S.3
-
121
-
-
33646263842
-
Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study
-
Campbell L.E., Daly E., Toal F., et al. Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study. Brain 129 Pt 5 (2006) 1218-1228
-
(2006)
Brain
, vol.129
, Issue.PART 5
, pp. 1218-1228
-
-
Campbell, L.E.1
Daly, E.2
Toal, F.3
-
122
-
-
0036468696
-
Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome
-
Chow E.W., Zipursky R.B., Mikulis D.J., et al. Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome. Biol Psychiatry 51 3 (2002) 208-215
-
(2002)
Biol Psychiatry
, vol.51
, Issue.3
, pp. 208-215
-
-
Chow, E.W.1
Zipursky, R.B.2
Mikulis, D.J.3
-
123
-
-
0035870757
-
A review of MRI findings in schizophrenia
-
Shenton M.E., Dickey C.C., Frumin M., et al. A review of MRI findings in schizophrenia. Schizophr Res 49 1-2 (2001) 1-52
-
(2001)
Schizophr Res
, vol.49
, Issue.1-2
, pp. 1-52
-
-
Shenton, M.E.1
Dickey, C.C.2
Frumin, M.3
-
124
-
-
7744229511
-
Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study
-
van Amelsvoort T., Daly E., Henry J., et al. Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study. Arch Gen Psychiatry 61 11 (2004) 1085-1096
-
(2004)
Arch Gen Psychiatry
, vol.61
, Issue.11
, pp. 1085-1096
-
-
van Amelsvoort, T.1
Daly, E.2
Henry, J.3
-
125
-
-
27644524899
-
COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome
-
Gothelf D., Eliez S., Thompson T., et al. COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome. Nat Neurosci 8 11 (2005) 1500-1502
-
(2005)
Nat Neurosci
, vol.8
, Issue.11
, pp. 1500-1502
-
-
Gothelf, D.1
Eliez, S.2
Thompson, T.3
-
126
-
-
0037947438
-
Catechol O-methyltransferase val158-met genotype and individual variation in the brain response to amphetamine
-
Mattay V.S., Goldberg T.E., Fera F., et al. Catechol O-methyltransferase val158-met genotype and individual variation in the brain response to amphetamine. Proc Natl Acad Sci USA 100 10 (2003) 6186-6191
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, Issue.10
, pp. 6186-6191
-
-
Mattay, V.S.1
Goldberg, T.E.2
Fera, F.3
-
127
-
-
0025876197
-
Down syndrome: MR quantification of brain structures and comparison with normal control subjects
-
Weis S., Weber G., Neuhold A., et al. Down syndrome: MR quantification of brain structures and comparison with normal control subjects. AJNR Am J Neuroradiol 12 6 (1991) 1207-1211
-
(1991)
AJNR Am J Neuroradiol
, vol.12
, Issue.6
, pp. 1207-1211
-
-
Weis, S.1
Weber, G.2
Neuhold, A.3
-
128
-
-
0030848690
-
Small planum temporale volume in Down's syndrome: a volumetric MRI study
-
Frangou S., Aylward E., Warren A., et al. Small planum temporale volume in Down's syndrome: a volumetric MRI study. Am J Psychiatry 154 10 (1997) 1424-1429
-
(1997)
Am J Psychiatry
, vol.154
, Issue.10
, pp. 1424-1429
-
-
Frangou, S.1
Aylward, E.2
Warren, A.3
-
129
-
-
0030747946
-
Basal ganglia volume in adults with Down syndrome
-
Aylward E.H., Li Q., Habbak Q.R., et al. Basal ganglia volume in adults with Down syndrome. Psychiatry Res 74 2 (1997) 73-82
-
(1997)
Psychiatry Res
, vol.74
, Issue.2
, pp. 73-82
-
-
Aylward, E.H.1
Li, Q.2
Habbak, Q.R.3
-
130
-
-
0036641248
-
Increased basal ganglia volumes in velo-cardio-facial syndrome (deletion 22q11.2)
-
Eliez S., Barnea-Goraly N., Schmitt J.E., et al. Increased basal ganglia volumes in velo-cardio-facial syndrome (deletion 22q11.2). Biol Psychiatry 52 1 (2002) 68-70
-
(2002)
Biol Psychiatry
, vol.52
, Issue.1
, pp. 68-70
-
-
Eliez, S.1
Barnea-Goraly, N.2
Schmitt, J.E.3
-
131
-
-
3142720255
-
Thalamic reductions in children with chromosome 22q11.2 deletion syndrome
-
Bish J.P., Nguyen V., Ding L., et al. Thalamic reductions in children with chromosome 22q11.2 deletion syndrome. Neuroreport 15 9 (2004) 1413-1415
-
(2004)
Neuroreport
, vol.15
, Issue.9
, pp. 1413-1415
-
-
Bish, J.P.1
Nguyen, V.2
Ding, L.3
-
132
-
-
18044377629
-
Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome)
-
Antshel K.M., Conchelos J., Lanzetta G., et al. Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome). Psychiatry Res 138 3 (2005) 235-245
-
(2005)
Psychiatry Res
, vol.138
, Issue.3
, pp. 235-245
-
-
Antshel, K.M.1
Conchelos, J.2
Lanzetta, G.3
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