The mismatch negativity (MMN)–a unique window to disturbed central auditory processing in ageing and different clinical conditions
In this article, we review clinical research using the mismatch negativity (MMN), a change-
detection response of the brain elicited even in the absence of attention or behavioural task …
detection response of the brain elicited even in the absence of attention or behavioural task …
The protein family of glucose transport facilitators: It's not only about glucose after all
R Augustin - IUBMB life, 2010 - Wiley Online Library
The protein family of facilitative glucose transporters comprises 14 isoforms that share
common structural features such as 12 transmembrane domains, N‐and C‐termini facing …
common structural features such as 12 transmembrane domains, N‐and C‐termini facing …
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia
A Gialluisi, TFM Andlauer, N Mirza-Schreiber… - Molecular …, 2021 - nature.com
Developmental dyslexia (DD) is a learning disorder affecting the ability to read, with a
heritability of 40–60%. A notable part of this heritability remains unexplained, and large …
heritability of 40–60%. A notable part of this heritability remains unexplained, and large …
[图书][B] The dyslexia debate
JG Elliott, EL Grigorenko - 2014 - books.google.com
The Dyslexia Debate examines how we use the term" dyslexia" and questions its efficacy as
a diagnosis. While many believe that a diagnosis of dyslexia will shed light on a reader's …
a diagnosis. While many believe that a diagnosis of dyslexia will shed light on a reader's …
[图书][B] Learning disabilities: From identification to intervention
" Reviewing the state of the science of learning disabilities (LD) and describing effective
educational practices, this authoritative text has been significantly revised and expanded …
educational practices, this authoritative text has been significantly revised and expanded …
The left occipitotemporal system in reading: disruption of focal fMRI connectivity to left inferior frontal and inferior parietal language areas in children with dyslexia
Developmental dyslexia is a severe reading disorder, which is characterized by dysfluent
reading and impaired automaticity of visual word processing. Adults with dyslexia show …
reading and impaired automaticity of visual word processing. Adults with dyslexia show …
Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms
Developmental dyslexia (DD) is a complex neurodevelopmental deficit characterized by
impaired reading acquisition, in spite of adequate neurological and sensorial conditions …
impaired reading acquisition, in spite of adequate neurological and sensorial conditions …
Molecular genetics of dyslexia: an overview
Dyslexia is a highly heritable learning disorder with a complex underlying genetic
architecture. Over the past decade, researchers have pinpointed a number of candidate …
architecture. Over the past decade, researchers have pinpointed a number of candidate …
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
A Gialluisi, TFM Andlauer, N Mirza-Schreiber… - Translational …, 2019 - nature.com
Developmental dyslexia (DD) is one of the most prevalent learning disorders, with high
impact on school and psychosocial development and high comorbidity with conditions like …
impact on school and psychosocial development and high comorbidity with conditions like …
Differential diagnosis of dysgraphia, dyslexia, and OWL LD: Behavioral and neuroimaging evidence
VW Berninger, TL Richards, RD Abbott - Reading and Writing, 2015 - Springer
In Study 1, children in grades 4–9 (N= 88, 29 females and 59 males) with persisting reading
and/or writing disabilities, despite considerable prior specialized instruction in and out of …
and/or writing disabilities, despite considerable prior specialized instruction in and out of …