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1
Test of a motor theory of long-term auditory memory.
In: Proc Natl Acad Sci U S A , 109 (18) 7121 - 7125. (2012) (2012)
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2
Role of cerebellum in fine speech control in childhood: Persistent dysarthria after surgical treatment for posterior fossa tumour
Morgan, AT; Liegeois, F; Liederkerke, C. - : ACADEMIC PRESS INC ELSEVIER SCIENCE, 2011
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3
Role of cerebellum in fine speech control in childhood: Persistent dysarthria after surgical treatment for posterior fossa tumour
In: BRAIN LANG , 117 (2) 69 - 76. (2011) (2011)
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4
Endophenotypes of FOXP2: Dysfunction within the human articulatory network
In: EUR J PAEDIATR NEURO , 15 (4) 283 - 288. (2011) (2011)
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5
Speech and oral motor profile after childhood hemispherectomy
Liegeois, F; Morgan, AT; Stewart, LH. - : ACADEMIC PRESS INC ELSEVIER SCIENCE, 2010
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6
Speech and oral motor profile after childhood hemispherectomy
Liegeois, F; Morgan, A; Stewart, L. - : Elsevier, 2010
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7
Is the hippocampus necessary for visual and verbal binding in working memory?
In: NEUROPSYCHOLOGIA , 48 (4) 1089 - 1095. (2010) (2010)
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8
Speech and oral motor profile after childhood hemispherectomy
In: BRAIN LANG , 114 (2) 126 - 134. (2010) (2010)
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9
Speaking with a single cerebral hemisphere: fMRI language organization after hemispherectomy in childhood
In: BRAIN LANG , 106 (3) 195 - 203. (2008) (2008)
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10
Cortical abnormalities and language function in young patients with basal ganglia stroke
In: NEUROIMAGE , 36 (2) 431 - 440. (2007) (2007)
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11
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2005)
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12
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
In: American Journal of Human Genetics , 76 (6) pp. 1074-1080. (2005) (2005)
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13
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
In: AM J HUM GENET , 76 (6) 1074 - 1080. (2005) (2005)
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14
Identification of FOXP2 Truncation as a novel cause of developmental speech and language deficits
In: American Journal of Human Genetics , 76 (6) pp.1074 - 1080. (2005) (2005)
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15
Language reorganization in children with early-onset lesions of the left hemisphere: an fMRI study
In: BRAIN , 127 1229 - 1236. (2004) (2004)
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16
Cortical lateralization during verb generation: a combined ERP and fMRI study
In: NEUROIMAGE , 22 (2) 665 - 675. (2004) (2004)
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17
Functional MRI abnormalities during covert speech associated with FOXP2 gene mutation
In: Nature Neuroscience , 6 (11 ) pp.1230 - 1237 . (2003) (2003)
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18
Language fMRI abnormalities associated with FOXP2 gene mutation
In: NAT NEUROSCI , 6 (11) 1230 - 1237. (2003) (2003)
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19
Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia
Dronkers, N. F.; Vargha-Khadem, F.; Watkins, K. E.. - : Oxford University Press, 2002
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20
Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2002)
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