A M Galaburda
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Explore the profile of A M Galaburda including associated specialties, affiliations and a list of published articles.
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116
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2814
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Recent Articles
1.
Truong D, Che A, Rendall A, Szalkowski C, LoTurco J, Galaburda A, et al.
Genes Brain Behav
. 2014 Aug;
13(8):802-11.
PMID: 25130614
Dyslexia is a complex neurodevelopmental disorder characterized by impaired reading ability despite normal intellect, and is associated with specific difficulties in phonological and rapid auditory processing (RAP), visual attention and...
2.
Galaburda A
Ann Dyslexia
. 2013 Nov;
35(1):19-33.
PMID: 24243407
The discovery of biological substrates underlying medical conditions is an important step for their better understanding and for the design of appropriate medical therapies. In the case of developmental dyslexia...
3.
Galaburda A
Ann Dyslexia
. 2013 Nov;
40(1):18-38.
PMID: 24233624
The Geschwind hypothesis proposes a causal interaction among non-right-handedness, immune disorders, and learning disabilities, including dyslexia, via the intrauterine action of the male hormone testosterone. Some epidemiologic studies have supported...
4.
Galaburda A
Ann Dyslexia
. 2013 Nov;
39(1):65-80.
PMID: 24233472
Eight brains, six male and two female, of reliably diagnosed cases of developmental dyslexia have been analyzed in this laboratory thus far. Common to all the specimens is the absence...
5.
Rademacher J, Galaburda A, Kennedy D, Filipek P, Caviness Jr V
J Cogn Neurosci
. 2013 Aug;
4(4):352-74.
PMID: 23968129
We describe a system of parcellation of the human brain that is based on the functional anatomy of the cerebral cortex and that is applied to the analysis of magnetic...
6.
Platt M, Adler W, Mehlhorn A, Johnson G, Wright K, Choi R, et al.
Neuroscience
. 2013 Jul;
248:585-93.
PMID: 23831424
Developmental dyslexia, the most common childhood learning disorder, is highly heritable, and recent studies have identified KIAA0319-Like (KIAA0319L) as a candidate dyslexia susceptibility gene at the 1p36-34 (DYX8) locus. In...
7.
Wang Y, Yin X, Rosen G, Gabel L, Guadiana S, Sarkisian M, et al.
Neuroscience
. 2011 Jun;
190:398-408.
PMID: 21689730
The dyslexia-associated gene DCDC2 is a member of the DCX family of genes known to play roles in neurogenesis, neuronal migration, and differentiation. Here we report the first phenotypic analysis...
8.
Currier T, Etchegaray M, Haight J, Galaburda A, Rosen G
Neuroscience
. 2010 Nov;
172:535-46.
PMID: 21070838
Developmental dyslexia is a language-based learning disability, and a number of candidate dyslexia susceptibility genes have been identified, including DYX1C1, KIAA0319, and DCDC2. Knockdown of function by embryonic transfection of...
9.
Higgins N, Escabi M, Rosen G, Galaburda A, Read H
Neuroscience
. 2008 Apr;
153(2):535-49.
PMID: 18384966
Induced or genetically based cortical laminar malformations in somatosensory cortex have been associated with perceptual and acoustic processing deficits in mammals. Perinatal freeze-lesions of developing rat primary somatosensory (S1) cortex...
10.
Burbridge T, Wang Y, Volz A, Peschansky V, Lisann L, Galaburda A, et al.
Neuroscience
. 2008 Mar;
152(3):723-33.
PMID: 18313856
Embryonic knockdown of candidate dyslexia susceptibility gene (CDSG) homologs in cerebral cortical progenitor cells in the rat results in acute disturbances of neocortical migration. In the current report we investigated...