-
1
-
-
0028000657
-
The place of neuronal migration abnormalities in child neurology
-
Aicardi J. The place of neuronal migration abnormalities in child neurology. J. Can. Sci. Neurol. 21 (1994) 185-193
-
(1994)
J. Can. Sci. Neurol.
, vol.21
, pp. 185-193
-
-
Aicardi, J.1
-
2
-
-
0344395644
-
RNAi reveals doublecortin is required for redial migration in rat neocortex
-
Bai J., Ramos R., Ackman J., Thomas A., Lee R., and LoTurco J. RNAi reveals doublecortin is required for redial migration in rat neocortex. Nat. Neurosci. 6 (2003) 1277-1283
-
(2003)
Nat. Neurosci.
, vol.6
, pp. 1277-1283
-
-
Bai, J.1
Ramos, R.2
Ackman, J.3
Thomas, A.4
Lee, R.5
LoTurco, J.6
-
3
-
-
0023122493
-
Disorders of neuronal migration
-
Barth P. Disorders of neuronal migration. Can. J. Neurol. Sci. 14 1 (1987) 1-16
-
(1987)
Can. J. Neurol. Sci.
, vol.14
, Issue.1
, pp. 1-16
-
-
Barth, P.1
-
4
-
-
27644480838
-
No evidence for association between dyslexia and Dyx1c1 functional variants in a group of children and adolescents from Sothern Italy
-
Bellini G., Gravaccio C., Calamoneri F., Donatella Cocuzza M., Fiorillo P., Gagliano A., Mazzone D., del Giudice M., Scuccimarra G., Militerni R., and Pascotto A. No evidence for association between dyslexia and Dyx1c1 functional variants in a group of children and adolescents from Sothern Italy. J. Mol. Neurosci. 27 (2005) 311-314
-
(2005)
J. Mol. Neurosci.
, vol.27
, pp. 311-314
-
-
Bellini, G.1
Gravaccio, C.2
Calamoneri, F.3
Donatella Cocuzza, M.4
Fiorillo, P.5
Gagliano, A.6
Mazzone, D.7
del Giudice, M.8
Scuccimarra, G.9
Militerni, R.10
Pascotto, A.11
-
5
-
-
0037126164
-
Infant discrimination of rapid auditory cues predicts later language impairment
-
Benasich A., and Tallal P. Infant discrimination of rapid auditory cues predicts later language impairment. Behav. Brain Res. 136 (2002) 31-49
-
(2002)
Behav. Brain Res.
, vol.136
, pp. 31-49
-
-
Benasich, A.1
Tallal, P.2
-
6
-
-
0036382753
-
Executive functioning in adults and children with developmental dyslexia
-
Brosnan M., Demetre J., Hamill S., Robson K., Shepherd H., and Cody G. Executive functioning in adults and children with developmental dyslexia. Neuropsychologia 40 (2002) 2144-2155
-
(2002)
Neuropsychologia
, vol.40
, pp. 2144-2155
-
-
Brosnan, M.1
Demetre, J.2
Hamill, S.3
Robson, K.4
Shepherd, H.5
Cody, G.6
-
7
-
-
0032544085
-
Neuronal migration disorders: heterotopic neocortical neurons in CA1 provide a bridge between the hippocampus and the neocortex
-
Chevassus-au-Louis N., Congar P., Represa A., Ben-Ari Y., and Gaiarsa J.-L. Neuronal migration disorders: heterotopic neocortical neurons in CA1 provide a bridge between the hippocampus and the neocortex. Proc. Natl. Acad. Sci. U.S.A. 95 (1998) 10263-10268
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, pp. 10263-10268
-
-
Chevassus-au-Louis, N.1
Congar, P.2
Represa, A.3
Ben-Ari, Y.4
Gaiarsa, J.-L.5
-
8
-
-
0033809495
-
Impaired processing of complex auditory stimuli in rats with induced cerebrocortical microgyria: an animal model of developmental language disabilities
-
Clark M., Rosen G., Tallal P., and Fitch R. Impaired processing of complex auditory stimuli in rats with induced cerebrocortical microgyria: an animal model of developmental language disabilities. J. Cogn. Neurosci. 12 (2000) 828-839
-
(2000)
J. Cogn. Neurosci.
, vol.12
, pp. 828-839
-
-
Clark, M.1
Rosen, G.2
Tallal, P.3
Fitch, R.4
-
9
-
-
0032894903
-
Prenatal methylazoxymethanol treatment in rats produces brain abnormalities with morphological similarities to human developmental brain dysgeneses
-
Colaciti C., Sancini G., DeBiasi S., Franceschetti S., Caputi A., Frassoni C., Cattabeni F., Avanzini G., Spreafico R., Di Luca M., and Battablia G. Prenatal methylazoxymethanol treatment in rats produces brain abnormalities with morphological similarities to human developmental brain dysgeneses. Neuropathol. Exp. Neurol. 58 (1999) 92-102
-
(1999)
Neuropathol. Exp. Neurol.
, vol.58
, pp. 92-102
-
-
Colaciti, C.1
Sancini, G.2
DeBiasi, S.3
Franceschetti, S.4
Caputi, A.5
Frassoni, C.6
Cattabeni, F.7
Avanzini, G.8
Spreafico, R.9
Di Luca, M.10
Battablia, G.11
-
11
-
-
15944372645
-
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia
-
Cope N., Harold D., Hill G., Moskvina V., Stevenson J., Holmans P., Owen M., O'Donovan M., and Williams J. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am. J. Hum. Genet. 76 (2005) 581-591
-
(2005)
Am. J. Hum. Genet.
, vol.76
, pp. 581-591
-
-
Cope, N.1
Harold, D.2
Hill, G.3
Moskvina, V.4
Stevenson, J.5
Holmans, P.6
Owen, M.7
O'Donovan, M.8
Williams, J.9
-
13
-
-
0034888287
-
Application of the Morris water maze in the study of learning and memory
-
D'Hooge R., and De Deyn P.P. Application of the Morris water maze in the study of learning and memory. Brain Res. Brain Res. Rev. 36 (2001) 60-90
-
(2001)
Brain Res. Brain Res. Rev.
, vol.36
, pp. 60-90
-
-
D'Hooge, R.1
De Deyn, P.P.2
-
14
-
-
0034130379
-
The importance of acclimation in acoustic startle amplitude and pre-pulse inhibition testing of male and female rats
-
Faraday M., and Grunberg N. The importance of acclimation in acoustic startle amplitude and pre-pulse inhibition testing of male and female rats. Pharmacol. Biochem. Behav. 66 (2000) 375-381
-
(2000)
Pharmacol. Biochem. Behav.
, vol.66
, pp. 375-381
-
-
Faraday, M.1
Grunberg, N.2
-
15
-
-
0038844105
-
The evidence for a temporal processing deficit linked to dyslexia: a review
-
Farmer M., and Klein R. The evidence for a temporal processing deficit linked to dyslexia: a review. Psychon. Bull. Rev. 2 (1995) 460-493
-
(1995)
Psychon. Bull. Rev.
, vol.2
, pp. 460-493
-
-
Farmer, M.1
Klein, R.2
-
16
-
-
3442893300
-
Neural mechanisms of language-based learning impairments: insights from human populations and animal models
-
Fitch R.H., and Tallal P. Neural mechanisms of language-based learning impairments: insights from human populations and animal models. Behav. Cogn. Neurosci. Rev. 2 (2003) 155-178
-
(2003)
Behav. Cogn. Neurosci. Rev.
, vol.2
, pp. 155-178
-
-
Fitch, R.H.1
Tallal, P.2
-
17
-
-
0030890591
-
Effects of sex and MK-801 on auditory-processing deficits associated with developmental microgyric lesions in rats
-
Fitch R.H., Brown C., Tallal P., and Rosen G. Effects of sex and MK-801 on auditory-processing deficits associated with developmental microgyric lesions in rats. Behav. Neurol. 111 (1997) 404-412
-
(1997)
Behav. Neurol.
, vol.111
, pp. 404-412
-
-
Fitch, R.H.1
Brown, C.2
Tallal, P.3
Rosen, G.4
-
18
-
-
0028365946
-
Induced microgyria and auditory temporal processing in rats: a model for language impairment?
-
Fitch R., Tallal P., Brown C., Galaburda A., and Rosen G. Induced microgyria and auditory temporal processing in rats: a model for language impairment?. Cereb. Cortex 4 (1994) 260-270
-
(1994)
Cereb. Cortex
, vol.4
, pp. 260-270
-
-
Fitch, R.1
Tallal, P.2
Brown, C.3
Galaburda, A.4
Rosen, G.5
-
19
-
-
4444296770
-
Age and experience-related improvements in gap detection in the rat
-
Friedman J., Peiffer A., Clark M., Benasich A., and Fitch R.H. Age and experience-related improvements in gap detection in the rat. Dev. Brain Res. 152 (2004) 83-91
-
(2004)
Dev. Brain Res.
, vol.152
, pp. 83-91
-
-
Friedman, J.1
Peiffer, A.2
Clark, M.3
Benasich, A.4
Fitch, R.H.5
-
20
-
-
0027965056
-
Evidence for aberrant auditory anatomy in developmental dyslexia
-
Galaburda A., Menard M., and Rosen G. Evidence for aberrant auditory anatomy in developmental dyslexia. Proc. Natl. Acad. Sci. U.S.A. 91 (1994) 8010-8013
-
(1994)
Proc. Natl. Acad. Sci. U.S.A.
, vol.91
, pp. 8010-8013
-
-
Galaburda, A.1
Menard, M.2
Rosen, G.3
-
22
-
-
0033667152
-
Mechanisms and disturbances of neural migration
-
Gressens P. Mechanisms and disturbances of neural migration. Pediatr. Res. 48 (2000) 725-730
-
(2000)
Pediatr. Res.
, vol.48
, pp. 725-730
-
-
Gressens, P.1
-
23
-
-
33745343959
-
The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia
-
Hannula-Jouppi K., Kaminen-Ahola N., Taipale M., Eklund R., Nolpola-Hemmi J., Kaariainen H., and Kere J. The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS Genet. 1 (2005) e50
-
(2005)
PLoS Genet.
, vol.1
-
-
Hannula-Jouppi, K.1
Kaminen-Ahola, N.2
Taipale, M.3
Eklund, R.4
Nolpola-Hemmi, J.5
Kaariainen, H.6
Kere, J.7
-
24
-
-
0030852085
-
Cerebral microgyria thalamic cell size and auditory temporal processing in male and female rats
-
Herman A., Galaburda A., Fitch R.H., Carder A., Rosen G., Carder A.R., and Rosen G.D. Cerebral microgyria thalamic cell size and auditory temporal processing in male and female rats. Cereb. Cortex 7 (1997) 453-464
-
(1997)
Cereb. Cortex
, vol.7
, pp. 453-464
-
-
Herman, A.1
Galaburda, A.2
Fitch, R.H.3
Carder, A.4
Rosen, G.5
Carder, A.R.6
Rosen, G.D.7
-
25
-
-
20244377078
-
A family-based association study does not support dyx1c1 on 15q21.3 as a candidate gene in developmental dyslexia
-
Marino C., Giorda R., Luisa Lorusso M., Vanzin L., Salandi N., Novile M., Citterio A., Beri S., Crespi V., Battaglia M., and Molteni M. A family-based association study does not support dyx1c1 on 15q21.3 as a candidate gene in developmental dyslexia. Eur. J. Hum. Genet. 4 (2005) 491-499
-
(2005)
Eur. J. Hum. Genet.
, vol.4
, pp. 491-499
-
-
Marino, C.1
Giorda, R.2
Luisa Lorusso, M.3
Vanzin, L.4
Salandi, N.5
Novile, M.6
Citterio, A.7
Beri, S.8
Crespi, V.9
Battaglia, M.10
Molteni, M.11
-
26
-
-
23744486231
-
Speech and non-speech processing in people with specific language impairment: a behavioral and electrophysiological study
-
Mcarthur G.M., and Bishop D.V.M. Speech and non-speech processing in people with specific language impairment: a behavioral and electrophysiological study. Brain Lang. 94 (2005) 260-273
-
(2005)
Brain Lang.
, vol.94
, pp. 260-273
-
-
Mcarthur, G.M.1
Bishop, D.V.M.2
-
27
-
-
20344383233
-
Auditory processing deficits in rats with neonatal hypoxic-ischemic injury
-
McClure M., Peiffer A., Rosen G., and Fitch R.H. Auditory processing deficits in rats with neonatal hypoxic-ischemic injury. Int. J. Dev. Neurosci. 23 (2005) 351-362
-
(2005)
Int. J. Dev. Neurosci.
, vol.23
, pp. 351-362
-
-
McClure, M.1
Peiffer, A.2
Rosen, G.3
Fitch, R.H.4
-
28
-
-
24044553030
-
Auditory processing deficits in unilaterally and bilaterally injured hypoxic-ischemic rats
-
McClure M.M., Threlkeld S.W., Rosen G.D., and Fitch R.H. Auditory processing deficits in unilaterally and bilaterally injured hypoxic-ischemic rats. Neuroreport 16 (2005) 1309-1312
-
(2005)
Neuroreport
, vol.16
, pp. 1309-1312
-
-
McClure, M.M.1
Threlkeld, S.W.2
Rosen, G.D.3
Fitch, R.H.4
-
29
-
-
28044465597
-
DCDC2 is associated with reading disability and modulates neuronal development in the brain
-
Meng H., Smith S., Hager K., Held M., Liu J., Olson R., Pennington B., DeFries J., Gelernter J., O'Reilly-Pol T., Somlo S., Skudlarski P., Shaywitz S., Shaywitz B., Marchione K., Wang Y., Paramasivam M., LoTurco J., Page G., and Gruen J. DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc. Natl. Acad. Sci. U.S.A. 102 (2005) 17053-17058
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 17053-17058
-
-
Meng, H.1
Smith, S.2
Hager, K.3
Held, M.4
Liu, J.5
Olson, R.6
Pennington, B.7
DeFries, J.8
Gelernter, J.9
O'Reilly-Pol, T.10
Somlo, S.11
Skudlarski, P.12
Shaywitz, S.13
Shaywitz, B.14
Marchione, K.15
Wang, Y.16
Paramasivam, M.17
LoTurco, J.18
Page, G.19
Gruen, J.20
more..
-
30
-
-
27644539693
-
Neuroscience. Genes that guide brain development linked to dyslexia
-
Miller G. Neuroscience. Genes that guide brain development linked to dyslexia. Science 310 (2005) 759
-
(2005)
Science
, vol.310
, pp. 759
-
-
Miller, G.1
-
31
-
-
27544444173
-
Genetic influences on language impairment and phonological short-term memory
-
Newbury D.F., Bishop D.V.M., and Manaco A.P. Genetic influences on language impairment and phonological short-term memory. Trends Cogn. Sci. 9 (2005) 528-534
-
(2005)
Trends Cogn. Sci.
, vol.9
, pp. 528-534
-
-
Newbury, D.F.1
Bishop, D.V.M.2
Manaco, A.P.3
-
32
-
-
0347355593
-
Mechanisms of verbal memory impairment in four neurodevelopmental disorders
-
Nichols S., Jones W., Roman M., Wulfeck B., Delis D., Reilly J., and Bellugi U. Mechanisms of verbal memory impairment in four neurodevelopmental disorders. Brain Lang. 88 (2004) 180-189
-
(2004)
Brain Lang.
, vol.88
, pp. 180-189
-
-
Nichols, S.1
Jones, W.2
Roman, M.3
Wulfeck, B.4
Delis, D.5
Reilly, J.6
Bellugi, U.7
-
33
-
-
32544461279
-
Embryonic and early postnatal abnormalities contributing to the development of hippocampal malformations in a rodent model of dysplasia
-
Paredes M., Pleasure S., and Baraban S. Embryonic and early postnatal abnormalities contributing to the development of hippocampal malformations in a rodent model of dysplasia. J. Comp. Neurol. 495 (2006) 133-148
-
(2006)
J. Comp. Neurol.
, vol.495
, pp. 133-148
-
-
Paredes, M.1
Pleasure, S.2
Baraban, S.3
-
34
-
-
0037016188
-
Sex differences in rapid auditory processing deficits in ectopic BXSB/MpJ mice
-
Peiffer A., Rosen G., and Fitch R.H. Sex differences in rapid auditory processing deficits in ectopic BXSB/MpJ mice. Neuroreport 13 (2002) 2277-2280
-
(2002)
Neuroreport
, vol.13
, pp. 2277-2280
-
-
Peiffer, A.1
Rosen, G.2
Fitch, R.H.3
-
35
-
-
0037145451
-
Rapid auditory processing and MGN morphology in microgyric rats reared in varied acoustic environments
-
Peiffer A., Rosen G., and Fitch R.H. Rapid auditory processing and MGN morphology in microgyric rats reared in varied acoustic environments. Brain Res. Dev. Brain Res. 138 (2002) 187-193
-
(2002)
Brain Res. Dev. Brain Res.
, vol.138
, pp. 187-193
-
-
Peiffer, A.1
Rosen, G.2
Fitch, R.H.3
-
36
-
-
0742324446
-
Sex differences in rapid auditory processing deficits in microgyric rats
-
Peiffer A., Rosen G., and Fitch R.H. Sex differences in rapid auditory processing deficits in microgyric rats. Dev. Brain Res. 148 (2004) 53-57
-
(2004)
Dev. Brain Res.
, vol.148
, pp. 53-57
-
-
Peiffer, A.1
Rosen, G.2
Fitch, R.H.3
-
38
-
-
0029047964
-
Behavioral consequences of neonatal injury of the neocortex
-
Rosen G., Waters N., Galaburda A., and Denenberg V. Behavioral consequences of neonatal injury of the neocortex. Brain Res. 681 (1995) 177-189
-
(1995)
Brain Res.
, vol.681
, pp. 177-189
-
-
Rosen, G.1
Waters, N.2
Galaburda, A.3
Denenberg, V.4
-
39
-
-
33846420050
-
-
G.D. Rosen, J. Bai, Y. Wang, S.W. Threlkeld, J.J. LoTurco, A.M. Galaburda, Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations (2006), submitted for publication.
-
-
-
-
40
-
-
8744255235
-
Putative functional alleles of dyx1c1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK
-
Scerri T., Fisher S., Francks C., MacPhie I., Paracchini S., Richardson A., Stein J., and Monaco A. Putative functional alleles of dyx1c1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. J. Med. Genet. 41 (2004) 853-857
-
(2004)
J. Med. Genet.
, vol.41
, pp. 853-857
-
-
Scerri, T.1
Fisher, S.2
Francks, C.3
MacPhie, I.4
Paracchini, S.5
Richardson, A.6
Stein, J.7
Monaco, A.8
-
41
-
-
29244468273
-
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
-
Shumacher J., Anthoni H., Dahdouh F., Konig I.R., Hillmer A.M., Kluck N., Manthey M., Plume E., Warnke A., Remschmidt H., Hulsmann J., Cichon S., Lindgren C.M., Propping P., Zucchelli M., Ziegler A., Peyrard-Janvid M., Schulte-Korne G., Nothen M.M., and Kere J. Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Am. J. Hum. Genet. 78 (2006) 52-62
-
(2006)
Am. J. Hum. Genet.
, vol.78
, pp. 52-62
-
-
Shumacher, J.1
Anthoni, H.2
Dahdouh, F.3
Konig, I.R.4
Hillmer, A.M.5
Kluck, N.6
Manthey, M.7
Plume, E.8
Warnke, A.9
Remschmidt, H.10
Hulsmann, J.11
Cichon, S.12
Lindgren, C.M.13
Propping, P.14
Zucchelli, M.15
Ziegler, A.16
Peyrard-Janvid, M.17
Schulte-Korne, G.18
Nothen, M.M.19
Kere, J.20
more..
-
42
-
-
0141482054
-
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain
-
Taipale M., Kaminen N., Nopola-Hemmi J., Haltia T., Myllyluoma B., Lyytinen H., Muller K., Kaaranen M., Lindsberg P., Hannula-Jouppi K., and Kere J. A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proc. Natl. Acad. Sci. U.S.A. 100 (2003) 11553-11558
-
(2003)
Proc. Natl. Acad. Sci. U.S.A.
, vol.100
, pp. 11553-11558
-
-
Taipale, M.1
Kaminen, N.2
Nopola-Hemmi, J.3
Haltia, T.4
Myllyluoma, B.5
Lyytinen, H.6
Muller, K.7
Kaaranen, M.8
Lindsberg, P.9
Hannula-Jouppi, K.10
Kere, J.11
-
43
-
-
0036615222
-
Developmental language learning impairments
-
Tallal P., and Benasich A. Developmental language learning impairments. Dev. Psychopathol. 14 (2002) 559-579
-
(2002)
Dev. Psychopathol.
, vol.14
, pp. 559-579
-
-
Tallal, P.1
Benasich, A.2
-
44
-
-
0027279980
-
Neurobiological basis of speech: a case for the preeminence of temporal processing
-
Tallal P., Miller S., and Fitch R.H. Neurobiological basis of speech: a case for the preeminence of temporal processing. Ann. N.Y. Acad. Sci. 682 (1993) 27-47
-
(1993)
Ann. N.Y. Acad. Sci.
, vol.682
, pp. 27-47
-
-
Tallal, P.1
Miller, S.2
Fitch, R.H.3
-
45
-
-
33747808617
-
Developmental timeframes for induction of microgyria and rapid auditory processing deficits in the rat
-
Threlkeld S.W., McClure M.M., Rosen G.D., and Fitch R.H. Developmental timeframes for induction of microgyria and rapid auditory processing deficits in the rat. Brain Res. 1109 (2006) 22-31
-
(2006)
Brain Res.
, vol.1109
, pp. 22-31
-
-
Threlkeld, S.W.1
McClure, M.M.2
Rosen, G.D.3
Fitch, R.H.4
-
46
-
-
33751251057
-
-
Y. Wang, M. Paramasivam, A. Thomas, J. Bai, N. Kaminen-Ahola, J. Kere, J. Voskuil, G.D. Rosen, A.M. Galaburda, J.J. LoTurco, DYX1C1 functions in neuronal migration in developing neocortex, Neuroscience (2006) [Epub ahead of print].
-
-
-
-
47
-
-
19944428926
-
Support for EKN1 as the susceptibility locus for dyslexia on 15q21
-
Wigg K., Couto J., Feng Y., Anderson B., Cate-Carter T., Macciardi F., Tannock R., Lovett M., Humphries T., and Barr C. Support for EKN1 as the susceptibility locus for dyslexia on 15q21. Mol. Psychiatry 9 (2004) 1111-1121
-
(2004)
Mol. Psychiatry
, vol.9
, pp. 1111-1121
-
-
Wigg, K.1
Couto, J.2
Feng, Y.3
Anderson, B.4
Cate-Carter, T.5
Macciardi, F.6
Tannock, R.7
Lovett, M.8
Humphries, T.9
Barr, C.10
|