Search research articles
Contact Us
Filters
Showing results (1-10 of 34) with videos related to
Page
of 4
Sort By:
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 24, 2014
DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development
Fahimeh Darki, Myriam Peyrard-Janvid, Hans Matsson, et al.
Journal of Cognitive Neuroscience
|
September 5, 2013
Polymorphisms in the dopamine receptor 2 gene region influence improvements during working memory training in children and adolescents
Stina Söderqvist, Hans Matsson, Myriam Peyrard-Janvid, et al.
Biological Psychiatry
|
June 12, 2012
Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure
Fahimeh Darki, Myriam Peyrard-Janvid, Hans Matsson, et al.
Acta Orthopaedica
|
December 10, 2009
Multiple epiphyseal dysplasia
Johanna Dahlqvist, Hanna Orlén, Hans Matsson, et al.
Brain Structure & Function
|
June 1, 2016
Human ROBO1 regulates white matter structure in corpus callosum
Fahimeh Darki, Satu Massinen, Elina Salmela, et al.
Biological Psychiatry
|
October 19, 2010
The SNAP25 gene is linked to working memory capacity and maturation of the posterior cingulate cortex during childhood
Stina Söderqvist, Fiona McNab, Myriam Peyrard-Janvid, et al.
Biological Psychiatry
|
April 26, 2011
Influence of the COMT genotype on working memory and brain activity changes during development
Iroise Dumontheil, Chantal Roggeman, Tim Ziermans, et al.
Developmental Psychology
|
November 23, 2011
Dopamine, working memory, and training induced plasticity: implications for developmental research
Stina Söderqvist, Sissela Bergman Nutley, Myriam Peyrard-Janvid, et al.
Haematologica
|
March 15, 2015
High-throughput mutational screening adds clinically important information in myelodysplastic syndromes and secondary or therapy-related acute myeloid leukemia
Mohsen Karimi, Christer Nilsson, Marios Dimitriou, et al.
British Journal of Haematology
|
October 3, 2002
Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) gene
Peter Gustavsson, Joakim Klar, Hans Matsson, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 4
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 24, 2014
DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development
Fahimeh Darki, Myriam Peyrard-Janvid, Hans Matsson, et al.
Journal of Cognitive Neuroscience
|
September 5, 2013
Polymorphisms in the dopamine receptor 2 gene region influence improvements during working memory training in children and adolescents
Stina Söderqvist, Hans Matsson, Myriam Peyrard-Janvid, et al.
Biological Psychiatry
|
June 12, 2012
Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure
Fahimeh Darki, Myriam Peyrard-Janvid, Hans Matsson, et al.
Acta Orthopaedica
|
December 10, 2009
Multiple epiphyseal dysplasia
Johanna Dahlqvist, Hanna Orlén, Hans Matsson, et al.
Brain Structure & Function
|
June 1, 2016
Human ROBO1 regulates white matter structure in corpus callosum
Fahimeh Darki, Satu Massinen, Elina Salmela, et al.
Biological Psychiatry
|
October 19, 2010
The SNAP25 gene is linked to working memory capacity and maturation of the posterior cingulate cortex during childhood
Stina Söderqvist, Fiona McNab, Myriam Peyrard-Janvid, et al.
Biological Psychiatry
|
April 26, 2011
Influence of the COMT genotype on working memory and brain activity changes during development
Iroise Dumontheil, Chantal Roggeman, Tim Ziermans, et al.
Developmental Psychology
|
November 23, 2011
Dopamine, working memory, and training induced plasticity: implications for developmental research
Stina Söderqvist, Sissela Bergman Nutley, Myriam Peyrard-Janvid, et al.
Haematologica
|
March 15, 2015
High-throughput mutational screening adds clinically important information in myelodysplastic syndromes and secondary or therapy-related acute myeloid leukemia
Mohsen Karimi, Christer Nilsson, Marios Dimitriou, et al.
British Journal of Haematology
|
October 3, 2002
Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) gene
Peter Gustavsson, Joakim Klar, Hans Matsson, et al.
Page
of 4