Literature DB >> 757073

Auditory cytoarchitectonic abnormalities in a case of familial developmental dyslexia.

A M Galaburda, T L Kemper.   

Abstract

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Year:  1978        PMID： 757073

Source DB:  PubMed          Journal:  Trans Am Neurol Assoc        ISSN： 0065-9479


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  4 in total

1.  Strong motion deficits in dyslexia associated with DCDC2 gene alteration.

Authors:  Guido Marco Cicchini; Cecilia Marino; Sara Mascheretti; Daniela Perani; Maria Concetta Morrone
Journal:  J Neurosci       Date:  2015-05-27       Impact factor: 6.167

2.  Overconnectivity of the right Heschl's and inferior temporal gyrus correlates with symptom severity in preschoolers with autism spectrum disorder.

Authors:  Daegyeom Kim; Joo Young Lee; Byeong Chang Jeong; Ja-Hye Ahn; Johanna Inhyang Kim; Eun Soo Lee; Hyuna Kim; Hyun Ju Lee; Cheol E Han
Journal:  Autism Res       Date:  2021-09-16       Impact factor: 4.633

3.  The genetics of reading disabilities: from phenotypes to candidate genes.

Authors:  Wendy H Raskind; Beate Peter; Todd Richards; Mark M Eckert; Virginia W Berninger
Journal:  Front Psychol       Date:  2013-01-07

4.  Position of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes.

Authors:  William T Adler; Maryann P Platt; Alison J Mehlhorn; Joshua L Haight; Timothy A Currier; Mikel A Etchegaray; Albert M Galaburda; Glenn D Rosen
Journal:  PLoS One       Date:  2013-05-28       Impact factor: 3.240
  4 in total

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