Professional Documents
Culture Documents
To cite this article: Luis Bravo (2014) Neuroscience and education: current state of research on
dyslexia / Neurociencias y educacin: estado actual de la investigacin en dislexias, Estudios de
Psicologa: Studies in Psychology, 35:1, 1-28, DOI: 10.1080/02109395.2014.893648
To link to this article: http://dx.doi.org/10.1080/02109395.2014.893648
Luis Bravo
Pontificia Universidad Catlica de Chile
(Received 17 December 2012; accepted 28 June 2013)
Abstract: In recent years, the contribution of research in Neuroscience to
Cognitive Psychology has broken new ground in Education, for the study,
diagnosis and treatment of dyslexia, and has confirmed previous research
studies. This article exposes some of the principal research conducted into
the areas of the brain that is involved in learning the written language, and the
effects of the application of psychopedagogical interventions in brain activity
of children with dyslexia.
Keywords: neurosciences; psycho pedagogy; dyslexia; brain areas; written
language
Resumen: El aporte de las investigaciones en Neurociencias en los ltimos
aos a la Psicologa Cognitiva ha abierto nuevos caminos en la Educacin
para el estudio, diagnstico y tratamiento de las dislexias y ha confirmado sus
investigaciones. En este artculo se presentan algunas de las principales
investigaciones recientes efectuadas en las reas cerebrales involucradas en
el aprendizaje del lenguaje escrito y los efectos de la aplicacin de las
intervenciones psicopedaggicas en la actividad cerebral de nios dislxicos.
Palabras clave: neurociencias; psicopedagoga; dislexias; reas cerebrales;
lenguaje escrito
Since the time of Luria, studies in neuropsychology have shown that all learning
happens in the brain (Luria, 1966, 1973). Research into the brain shows that
cognitive experiences in infancy are determinants of brain development, especially those that occur through language (Castro-Caldas, Peterson, Reis, StoneElander, & Ingvar, 1998; Dehaene, 2007; Shaywitz et al., 2004).
At the turn of the twenty-first century and due to the progress of neuroscience and
cognitive psychology, there was a change in the psychopedagogical approach to
English version: pp. 112 / Versin en espaol: pp. 1325
References / Referencias: pp. 2528
Translation / Traduccin: Liza DArcy
Authors Address / Correspondencia con el autor: Escuela de Psicologa, Pontificia
Universidad Catlica de Chile, Av. Vicua Mackenna 4860, Santiago, Chile. E-mail:
abravov@uc.cl
2014 Fundacion Infancia y Aprendizaje
L. Bravo
learning written languages and of the explanations on the origins of dyslexia (Bravo,
1985, 2011). This change of perspective was associated with the development of
cognitive neuropsychology (Dehaene, 2007; Fletcher, 2009; Fletcher, Lyon, Fuchs,
& Barnes, 2007; Goswami, 2008; Rumsey, 1996; Shaywitz & Shaywitz, 2008; Simos
et al., 2002; Vellutino, Fletcher, Snowling, & Scanlon, 2004).
A key finding of this research has been the interaction between brain development, of biological and genetic origin, with verbal and social stimuli caused by
the school and family environments, an interaction that is most clearly seen when
children learn to read. In the Journal of Child Psychology and Psychiatry
editorial, Leckman and March (2011) state that Last decade it became very
clear that in addition to the cascade of genetic, molecule and cell events that
result in the formation of billions of neurons that lead to the formation of human
neocortex in the utero, the postnatal environment and the close relationships
between children and their caregivers in the early years of life can have direct
and permanent effects on the childs brain development and behaviour
(pp. 333338).
On the contribution of Neuroscience to Education, Fawcett and Nicolson
(2007) also stated that The explosion in neuroscientific knowledge has profound
implications for Education, and we propose to establish a new discipline of
pedagogical neuroscience to combine psychological, medical, and educational
perspectives (p. 306). They believe that this approach is especially valid for
dyslexia research.
Moreover, Szcs and Goswami (2007) describe Educational Neuroscience as
a new discipline of the mental representations regarding neural activity in the
brain (p. 114). Accordingly, they define provisionally, educational neuroscience
as the combination of cognitive neuroscience and psychological methods for
research into the development of mental representations (2007, p. 114). They
cite Bruer (1997), who believes that this new discipline involves the integration of
three sciences: education, neuroscience and cognitive psychology. Cognitive
Psychology would be an intermediary between neuroscience and education.
The aim of this article is to review current studies into Educational
Neuroscience research and its contributions to learning difficulties in the written
language and dyslexia.
normally are anatomical and operational and in many cases their relationship with
genetic factors have been established (Dansilio, 2009; Galaburda, 1989;
Galaburda, Lo Turco, Ramus, Fitch, & Rosen, 2006; Grigorenko, 2001;
Shaywitz, 2003; Shaywitz & Shaywitz, 2008).
Consequently, dyslexia has become a key issue for research into the relationship between brain development and activity with learning how to read.
According to Fletcher (2009) the greatest contribution of this research has been
the discovery that the phonological structure of speaking establishes a causal
relationship between spoken and written language. It states that neuropsychology
has been at the forefront of the evolution of the concept of dyslexia from a
scientific point of view (p. 506).
L. Bravo
L. Bravo
conducted into subjects with reading delay showed that their main difficulty was
using short term phonological memory inefficiently. Even when they could apply
and memorize phonological stimuli as well as normal readers, their problem
resided in the inefficient way they performed this process. According to this
research, the basis of the phonological memory problem of dyslexia does not
only concern connections, but also elicitation.
Van Atteveldt, Formisano, Goebel, and Blomert (2004) also researched into
the integration of perception of letters and the sound of language using functional
magnetic resonance imaging (fMRI). Their images showed that letters and phonemes are integrated in the superior temporal cortex. They found that responses to
phonemes in a specific region of the primary auditory cortex were modified when
letters were shown simultaneously. Both processes influenced each other.
Heim et al. (2010) used fMRI to research interaction between phonological
awareness and magnocellular processing in dyslexic and normal readers. They
state that some researchers attribute dyslexia to a low level of visual processing
due to deficiencies in the magnocellular system or direct communication in the
brain. The two studies showed that there really is an interaction between the
magnocellular processing and phonological awareness in reading. Phonological
awareness appears to be correlated with visual attention, but dyslexic persons
have reduced activity in the visual and auditory cortex as well as in all magnocellular tasks, whose function is the direct visual transmission of information.
This process affects the speed and quality of the visual perceptual transmission.
Kronschnabel, Schmid, Maurer, and Brandeis (2013) studied the rapid visual
recognition of letters, independent of their phonemes, in 13 dyslexic adolescents
and one control group, using magnetic resonance imaging in an experiment where
they showed true and false letters without exposure to phonemes. They found that
the dyslexic adolescents lacked sensitivity and were slower when shown the
printed stimuli, regardless of phonological processing. They concluded that dyslexic persons lacked the speed to recognize graphic representation when phonological or semantic stimuli were minimized. This research confirmed that dyslexic
persons also have shortcomings in speed when visually recognising graphic
representations, regardless of their phonological deficiencies.
Taken together these studies show that there is an interaction between phonological and visual orthographic awareness in the normal learning of written
language that allows children to quickly access the meaning of words, however,
dyslexic persons have shortcomings in both, especially in phonological
deficiencies.
the processes of learning, the brain selectively activates certain regions, which
determine the right connections in order to more efficiently assimilate the information required in the training of written language. Brain development is a
genetic programme, which promotes learning potential, but is flexible enough to
also be open to educational experiences. It follows that a dialogue between
neuroscience and educational research is essential (2006, p. 32).
Regarding the persistence of brain changes that occur because of learning,
Castro-Caldas et al. (1998) compared the reading of words and pseudo words in
60-year-old adult readers and recent ex-illiterate readers. They found that having
learnt written language in early years of development had produced stable changes
in brain structures. These differences were maintained until that age. The researchers mentioned concluded that learning to read and write during childhood
influences the functional organization of the adult brain, especially in the areas
underlying the processing of written language.
These research studies found that a fundamental element in the deficiency of
most dyslexic people is insufficient development of phonological awareness,
caused by reduced activity of the left parietal temporo-parietal junction, and
more delay when they have to associate the sound of letters with orthographic
visual stimuli (Simos et al., 2007; Shaywitz, 2003; Shaywitz & Shaywitz, 2008).
Consequently, the treatment of dyslexia involves intensive psychopedagogical
work on recognition, retention and association of the written words with their
meanings through their respective phonemes. Pronunciation of a new word is key
to understanding it.
L. Bravo
temporo-parietal areas and the inferior frontal areas, which perform phonological
processes (p. 283). They consider that this hypothesis is applicable to dyslexia in
languages that have either transparent or opaque orthography.
Bolger, Minas, Burman, and Booth (2008) investigated differences in brain
activity with fMRI in two groups of 15-year-old children one group that read
consistent and inconsistent words in English slowly and one that read at a normal
pace in orthographic and phonological recognition. The comparison between
the two groups showed that the orthographic consistency of words have greater
effect in normal readers in certain areas in the brain. The group of children who
read slower showed more difficulty in efficiently integrating orthographic and
phonological features of words. They stated that normal readers committed the left
frontal area more effectively to the activity of phonological decoding and the left
temporal occipital cortex for words that were orthographically consistent. The
research was original in that it studied the effect of the degree of consistency of
the written word, in the context of a language that is particularly inconsistent, such
as English. This result does not contradict that stated by Wimmer and Schurz
(2010) in their German language research study, which concluded that the core of
dyslexia is the deficiency in orthographic-phonological connection, which can be
manifested in transparent and opaque orthographies. The main difference
observed between them would manifest in the rate children learn, recognize and
pronounce the words.
Another comparative research was conducted in the United Sates between
Spanish speaking children aged 36 years with English-speaking children, on the
development and intervention of Phonological Awareness (Anthony et al., 2011).
Their results show that in both languages phonological awareness precedes
learning how to read. However, this learning process occurs differently in both
languages. The difference is that learning to read in English begins with the
process of onset-rime of words, whereas in Spanish with pronunciation and
memorization of syllables. In both languages the initial recognition process of
the written word requires connecting orthographic visual stimuli with recognition
and phonological memory, which coincides with the conclusions put forward by
Wimmer and Schurz (2010) for German. The main difference in learning how to
read between orthographic systems is reading fluency, German children recognized words faster than English-speaking children.
Jimnez, Rodrguez, and Ramrez (2009) researched 35 Spanish (transparent)
speaking, eight-year-old, dyslexic children and compared them with a control
group, in high-frequency words and pseudo words. They found 12 phonological
dyslexic children and five surface dyslexic children. Both groups showed deficits
in phonological awareness, but the group who had surface dyslexia also showed
deficiencies in orthographic visual processing. However, this latter deficiency has
been associated with poor literacy experiences at home. This information confirms
that some learning difficulties in reading among children from lower sociocultural levels are influenced by previous educational and cultural gaps, especially
in language. The phonological deficiencies in these children induced them to
focus their efforts on the recognition and visual memory of words.
A consequence of the differences between orthographic systems is that learning in transparent languages starts with using the phonological route to recognize
words, whereas learning in opaque language requires greater involvement of the
orthographic visual pathway, due to the disparity between graphemes and their
pronunciation.
After an extensive review of dyslexia in Spanish, Gonzlez and Jimnez
(2012) stated that the results of the different research studies seem to suggest
that there would be differences in neurofunctional anomalies according to the
orthographic system, but that in order to make this claim a larger number of
studies need to be conducted into both transparent and opaque languages, that
have the same criteria and methodologies (p. 94).
10
L. Bravo
In addition, neuroimaging studies conducted by Temple et al. (2003) confirmed that there is a deficiency in the neural mechanisms of phonological
processing in children and adults with dyslexia. They conducted an fMRI study
with 20 children with dyslexia, who were eight to 12 years old during a phonological task, the images were taken before and after an auditory processing and
oral language training intervention programme. Subsequent to this intervention,
the children with dyslexia showed an increase in neural activity in the left
temporo-parietal region and in the left inferior frontal gyrus, similar to that
observed in children who read normally. This increased brain activity was also
observed in the frontal and temporal right regions. In addition, children with
dyslexia showed a correlation between activation in the left temporo-parietal
cortex and their oral language. These results showed that they had a repercussion
on the deficiency of oral and written language in brain regions associated with
phonological processing, confirming the favourable effect of psychopedagogical
intervention and confirming that neuronal recycling (Dehaene, 2007, p. 200)
would occur in those areas.
The effect of phonological intervention in reading on brain organization and
reading fluency in 77 dyslexic children and children from control groups, aged six
to nine years was also confirmed in a study by Shaywitz et al. (2004). They used
magnetic resonance imaging to examine the types of brain activation during letter
identification tasks. After one year of intervention, children who had experimental
stimulation showed significant improvement in left hemisphere regions. A year
later, those children were still activating the bilateral frontal region and the upper
left, temporal and occipital-temporal regions to read and had improved reading
fluency.
Eden et al. (2004) also studied the differences that occur in the brain in
dyslexic adults after treatment with phonological strategies. The evaluation was
conducted by comparing brain activity before and after the intervention, and
showed an increase in the activity in certain regions of the left hemisphere. The
result of their intervention confirmed what Simos et al. (2002) stated, that progress
in learning the written language and overcoming dyslexia is associated with a
regularization of activation in the left hemisphere.
In summary, all the above evidence shows that intensive interventions in
phonological processes and recognition of words that encourage learning how to
read also modify brain connections. They could identify a psychopedagogical
model of action to work with children who have severe reading difficulties.
11
letters were produced. They also showed that without mastering pronunciation,
learning and incorporating new words in semantic networks does not occur. These
changes result in increased oxygenation of the blood (increased blood oxygenation level dependent, BOLD) in the left temporal occipital cortex and in evoked
potentials, in the lower left posterior area, after perceiving graphic stimuli. They
also note that educational experiences induce changes in brain processes during
perception of letters in young children. These research studies conducted through
fMRI and Evoked Potentials concord with Brem et al. (2010) who showed that
changes in brain activity are produced in children at kindergarten while they
address different educational activities. Learning to read has proven to be a key
topic for these interdisciplinary studies between neuroscience and education.
Moreover, research shows that there might be a genetic component to the early
origins of dyslexia. (Dansilio, 2009; Galaburda et al., 2006; Grigorenko, 2001).
Lyytinen et al. (2001) did a comparative longitudinal study on 200 children from
birth to age five. Half of them had a parent diagnosed with dyslexia, an IQ over 80
and at least 10 years of schooling (they were considered children at risk). The
images, from birth to the age of five years showed differences with the control
group who did not have a family history of dyslexia. In evoked potentials (ERP)
the children at risk showed slower responses in the left hemisphere. The major
differences between them appeared after 3.5 years, in auditory discrimination, in
naming speed and verbal memory. This research shows an early association
between phonological development, verbal memory and processing speed, with
a family history of dyslexia.
Raschle, Zuk, and Gaab (2012) showed that children at risk of dyslexia show
differences in brain activity early, captured by magnetic resonance, before starting
to learn how to read. Researchers assessed 36 pre-schoolers while they performed
tasks where they had to decide whether two words started with the same sound.
During the phonological tasks, children with a family history of dyslexia showed
less metabolic activity in the junctions between the occipital and temporal lobes
and in the temporal and parietal lobes, in the posterior part of the brain, in
comparison with the control subjects. They also investigated the performance of
neural networks in pre-readers with a risk of dyslexia because of family history
compared with a control group. The functional neuroimaging showed reduced
activation in preschool readers who had a family history of dyslexia, compared
with those who had no history of dyslexia in the family, in the bilateral occipital
temporal and the left temporo-parietal brain regions. They coincided with research
by Leppanen et al. (2010) in new-borns from families at risk of dyslexia who had
an atypical auditory processing in the pre-reading stage, which may subsequently
alter phonological recognition in learning to read.
Together, this evidence suggests that some children with a family history of
dyslexia show an impaired phonological processing from an early age. These
deficiencies would be present before formal learning of the written language
begins and confirm that there could be a genetic component to the early origins
of dyslexia.
12
L. Bravo
13
14
L. Bravo
15
16
L. Bravo
17
18
L. Bravo
19
20
L. Bravo
fonolgicos (p. 283). Ellos consideran que esta hiptesis es aplicable a las
dislexias, tanto en idiomas de ortografa transparente como de ortografa opaca.
Por su parte, Bolger, Minas, Burman, y Booth (2008) investigaron mediante
fMRI las diferencias en la actividad cerebral en dos grupos de nios, con y sin
retardo lector, de 15 aos, cuando deban leer en idioma ingls palabras consistentes e inconsistentes, en el reconocimiento ortogrfico y fonolgico.
La comparacin entre ambos grupos mostr que la consistencia ortogrfica de
las palabras tiene mayor efecto en los lectores normales en algunas reas cerebrales. El grupo de los nios con retardo lector mostraron dificultad para integrar
eficientemente las caractersticas ortogrficas y fonolgicas de las palabras.
Expresan que los lectores normales comprometen ms efectivamente la actividad
del rea frontal izquierda para la decodificacin fonolgica y de la corteza
occipital temporal izquierda para las palabras ortogrficamente consistentes.
Esta investigacin tiene la originalidad de estudiar el efecto de la mayor o
menor consistencia de las palabras escritas, en el contexto de un idioma que es
especialmente inconsistente, como el ingls. Este resultado no es contradictorio
con lo expresado por Wimmer y Schurz (2010) en su investigacin en idioma
alemn, que concluyeron que el ncleo de las dislexias es la deficiencia en la
conexin ortogrfico-fonolgico, que puede manifestarse tanto en ortografas
transparentes como opacas. La principal diferencia observada entre ellas estara
en la velocidad de los nios para aprender, reconocer y pronunciar las palabras.
Otra investigacin comparativa fue efectuada en Estados Unidos entre nios
de habla castellana de tres a seis aos con otros de habla inglesa, sobre el
desarrollo e intervencin de la Conciencia Fonolgica (Anthony et al., 2011).
Sus resultados muestran que en ambos idiomas la conciencia fonolgica predice el
aprendizaje lector. Sin embargo este proceso de aprendizaje se da de diferentes
maneras en ambos idiomas. La diferencia pedaggica reside en que el aprendizaje
lector en ingls se inicia con el proceso de onset-rime de las palabras, en cambio
en castellano con la pronunciacin y memoria de las slabas. En ambos idiomas
este proceso de reconocimiento inicial de las palabras escritas requiere la conexin
de los estmulos visuales ortogrficos con el reconocimiento y memoria
fonolgica, lo cual coincide con el planteamiento de Wimmer y Schurz (2010)
para el idioma alemn. La principal diferencia en el aprendizaje lector entre ambos
sistemas ortogrficos sera la fluidez de la lectura, los nios alemanes reconocieron las palabras con ms velocidad que los de habla inglesa.
Por otra parte, Jimnez, Rodrguez, y Ramrez (2009) investigaron a 35 nios
dislxicos de habla hispana (transparente) de cuarto grado y los compararon con
un grupo control, en palabras de alta frecuencia y pseudo palabras. Encontraron
12 dislxicos fonolgicos y cinco dislxicos de superficie. Ambos grupos mostraron dficit en la conciencia fonolgica, pero el grupo con dislexia de superficie
adems, mostr deficiencias en el procesamiento visual ortogrfico. Sin embargo,
esta ltima deficiencia estuvo asociada con las experiencias alfabticas en el
hogar. Esta informacin confirma que algunas dificultades en el aprendizaje de
la lectura entre los nios de niveles socioculturales deficientes dependeran de
carencias culturales y educacionales previas, especialmente del lenguaje. En estos
21
22
L. Bravo
23
24
L. Bravo
Anlisis y conclusiones
Como consecuencia de estas investigaciones es posible concluir que un dficit
cognitivo en el aprendizaje escolar del lenguaje escrito puede tener causas neuronales que son identificables mediante los estudios de neurociencias (Goswami,
2004). La mayor parte de las investigaciones aqu descritas se refieren a su falla
ms comn: las dislexias.
En las dislexias se ha encontrado un componente psicolgico cognitivo, uno
pedaggico y uno neurolgico. Las investigaciones ms recientes en neurociencias tienden a confirmar las hiptesis psicolgicas e investigaciones experimentales efectuadas en dcadas anteriores respecto al papel que tienen los dficits de
la conciencia fonolgica y del procesamiento perceptivo visual-ortogrfico para el
reconocimiento de las palabras escritas y para adquirir la fluidez lectora.
Las imgenes de resonancia magntica funcional (fRMI) muestran que las
conexiones entre algunas reas cerebrales son claves para el aprendizaje del
lenguaje escrito, donde los estudios diferenciales entre dislxicos y sujetos de
lectura normal sealan deficiencias de los primeros en alguna zonas del hemisferio izquierdo, especialmente relacionadas con el procesamiento del lenguaje y
con la asociacin fonolgica-visual ortogrfica. En algunos casos los sujetos
dislxicos manifiestan una sobreactividad compensatoria en reas del hemisferio
derecho, que proviene, probablemente de una fuerte ejercitacin en el reconocimiento y memoria visual de las palabras.
Estas deficiencias aparecen en algunos nios desde la primera infancia, y en
especial en los que tienen antecedentes familiares dislxicos. Desde el punto de
vista cognitivo se manifiestan en las pruebas de conciencia fonolgica, de vocabulario, velocidad para nominar, y memoria verbal de corto alcance. El reconocimiento de estas diferencias implica que hay reas donde es necesaria la
intervencin psicopedaggica temprana para disminuir su impacto en el aprendizaje o para ayudarlos a superar sus dificultades. En consecuencia, algunos investigadores hablan que tendran un dficit de desconexin (Paulesu et al., 1996)
Otros hacen hincapi en la mayor lentitud en este proceso (Wolf y Bowers, 1999).
25
Acknowledgements / Agradecimientos
I express my thanks to Professor Jess Alegra from lUniversit libre de Bruxelles for his
thoughtful suggestions and Professor Eugenia Orellana from the Pontificia Universidad
Catlica de Chile. / Expreso mis agradecimientos por sus atinadas sugerencias al
Profesor Jess Alegra de la Universidad Libre de Bruselas y a la Profesora Eugenia
Orellana de la Pontificia Universidad Catlica de Chile.
References / Referencias
Alegra, J. (2006). Por un enfoque psicolingstico del aprendizaje de la lectura y sus
dificultades 20 aos despus. Infancia y Aprendizaje, 29, 93111.
Anthony, J., Williams, J., Durn, L., Gillam, S. L., Liang, L., Aghara, R., Swank, P.,
Assel, M., & Landry, S. (2011). Spanish Phonological Awareness: Dimensionality and
Sequence of development during the Preschool and Kindergarten years. Journal of
Educational Psychology, 103, 857876.
Bolger, D., Minas, J., Burman, D., & Booth, J. (2008). Differential effects of orthographic
and phonological consistency in cortex for children with and without reading impairment. Neuropsychologia, 46, 32103224.
Bravo, L. (1985). Dislexia y Retraso Lector. Madrid: Santillana.
Bravo, L. (2011). Lenguaje escrito y dislexias. Enfoque cognitivo del retardo lector.
Santiago: Editorial Universidad Catlica.
Brem, S., Bach, S., Kucian, K., Guttorm, T., Martin, E., Lyytinen, H., Brandeis, D., &
Richardson, U. (2010). Brain sensitivity to print emerges when children learn letter
speech sound correspondences. Proceedings of the National Academy of Science,
10, 79397944.
Bruer, J. (1997). Education and the brain: A bridge too far. Educational Researcher,
26, 416.
Carrillo, M. & Alegra, J. (2009). Mecanismos de identificacin de palabras en Nios
dislxicos en espaol: existen subtipos? Ciencias Psicolgicas, 3, 125256.
Carrillo, M., & Domnguez, A. B. (2010). Dislexia y sordera: lneas actuales en el estudio
de la lengua escrita y sus dificultades. (Dyslexia and deafness: current lines of study in
written language and its difficulties). Archidona: Aljibe.
26
L. Bravo
Castro-Caldas, A., Peterson, A., Reis, A., Stone-Elander, S., & Ingvar M. (1998).
Learning to read and write during childhood influences the functional organization
of the adult brain. Brain, 121, 10531063
Cuadro, A. (2010). La lectura y sus dificultades: Dislexia Evolutiva. Montevideo: Grupo
magro Editores.
Dansilio, S. (2009). Cerebro y Dislexia: Una revisin. Ciencias Psicolgicas, 3, 225240.
Dehaene, S. (2007). Les neurones de la lectura. Paris: Editorial Odile Jacob.
Dehaene, S., & Cohen, L. (2007). Cultural recycling of cortical maps. Neuron, 56, 384
398.
Demonet, J., Taylor, M., & Chaix, Y. (2004). Developmental Dyslexia. Lancet, 363,
14511460.
Eden, G., Jones, K., Cappell, K., Gareau, L., Wood, F., Zeffiro, T., & Dietz, T. (2004).
Neural Changes following Clinical Study Remediation in Adult Developmental
Dislexia Neuron, 44, 411422.
Fawcett, A., & Nicolson, R. (2007). Dyslexia, learning, and pedagogical neuroscience.
Developmental Medicine and Child Neurology, 49, 306311.
Fletcher, J. (2009). Dyslexia: The evolution of a scientific concept. Journal of the
International Neuropsychological Society, 15, 501508.
Fletcher, J., Lyon, G., Fuchs, L., & Barnes, M. (2007). Learning Disabilities: From
Identification to intervention. New York: Guilford.
Galaburda, A. (1989). Ordinary and extra ordinary brain development anatomical variation in developmental dyslexia. Annals of Dyslexia, 39, 6780.
Galaburda, A., Lo Turco, J., Ramus, F., Fitch, H., & Rosen, G. (2006). La Dislexia del
Desarrollo: Gen, Cerebro y Cognicin. Psykh, 15, 311.
Gonzlez, D., & Jimnez, J. (2012). Indicadores biolgicos de la dislexia. In J. Jimnez
(Coord.), Dislexia en Espaol (pp. 79100). Madrid: Pirmide.
Goswami, U. (2004). Neuroscience and Education. British Journal of Educational
Psychology, 74, 114.
Goswami, U. (2008). Reading, dyslexia and the brain. Educational Research, 50,
135148.
Grigorenko, E. L. (2001). Developmental dyslexia: An update on genes, brains, and
environments. Journal of Child Psychology and Psychiatry, 42, 91125.
Habib, M. (2005). La dislexia a libro abierto. Montevideo: Prensa Mdica.
Hasko, S., Bruder, J., Bartling, J., & Schulte-Krne, G. (2012). N300 indexes deficient
integration of orthographic and phonological representations in children with dyslexia.
Neuropsychologia, 50, 640654.
Heim, S., Grande, M., Pape-Neumannn, J., van Ermingen, M., Meffert, E., Grabowska,
A., Huber, W., & Amunts, K. (2010). Interaction of Phonological Awareness and
Magnocelular processing during normal and Dyslexic Reading: Behavioural and
fMRI investigations. Dyslexia, 16, 258282.
Henderson, V. (1986). Anatomy of posterior pathways in reading: A reassessment. Brain
and Language, 29, 119133.
Hoeft, F., McCandliss, B., Blackad, J., Gantmana, A., Zakerania, N., Hulmes, C.,
Lyytinen, H., Whitfield-Gabrielig, S., Gloverh, G., Reissa, A., & Gabrielih, J.
(2011). Neural systems predicting long-term outcome in dyslexia. Proceedings of
the National Academy of Sciences, 108, 361366.
James, K. H. (2010). Sensori-motor experience leads to changes in visual processing in
the developing brain. Development Science, 13, 279288.
Jimnez, J. E. (2012). Dislexia en Espaol. Madrid: Pirmide.
Jimnez, J. E., Rodrguez, C., & Ramrez, G. (2009). Spanish developmental dyslexia:
Prevalence, cognitive profile and home literacy experiences. Journal of Experimental
Child Psychology, 103, 167185.
27
Kronschnabel, J., Schmid, R., Maurer, U., & Brandeis, D. (2013). Visual print tuning
deficits in dyslexic adolescents under minimized phonological demands. NeuroImage,
74, 5869.
Leckman, J., & March, J. (2011). Editorial: Developmental neuroscience comes of age.
Journal of Child Psychology and Psychiatry, 52, 333338.
Leppanen, P., Hamalainen, J., Salminen, H., Eklund, K., Guttorm, T., Lohvansuu, K.,
Puolakanaho, A., & Lyytinen, H. (2010). Newborn brain event-related potentials
revealing atypical processing of sound frequency and the subsequent association
with later literacy skills in children with familial dyslexia. Cortex, 46, 13621376.
Luria, A. R. (1966). Human brain and psychological processes. New York: Harper and
Row.
Luria, A. R. (1973) The working brain. New York: Basic books.
Lyytinen, H., Ahonen, T., Eklund, K., Guttorm, T., Laakso, M., Leinonen, S., Leppnnen,
P., Lyytinen, P., Poikkeus, A., Puolakanaho, A., Richardson, U., & Viholainen, H.
(2001). Developmental pathways of children with and without familial risk for
dyslexia during the first years of life. Developmental Neuropsychology, 20, 535554.
McCandliss, B. (2010). Educational neuroscience: The early years. Proceedings of the
National Academy of Sciences, 107, 80498050.
McCandliss, B., & Wolmetz, M. (2004). Developmental Psychobiology of Reading
Disability. In B. J. Casey (Ed.), Developmental Psychobiology (Vol. 23, pp. 69
110). Washington, DC: American Psychiatric Publishing.
McCrory, E. J., Mechelli, A., Frith, U., & Price, C. J. (2005). More than words:
A common neural basis for reading and naming deficits in developmental dyslexia?
Brain, 128, 261267.
Orellana, E. (2010). Psicologa de la enseanza del lenguaje escrito. Santiago de Chile:
Editorial Lenguaje y Pensamiento.
Paulesu, E., Frith, U., Snowling, M., Gallgher, A., Morton, J., Frackwiak, R., & Frith, C.
(1996). Is developmental dyslexia disconnection syndrome? Evidence from PET
scanning. Brain, 119, 143157.
Raschle, N. M., Zuk, J., & Gaab, N. (2012). Functional characteristics of developmental
dyslexia in left-hemispheric posterior brain regions predate reading onset. Proceedings
of the National Academy of Sciences, 109, 21562161.
Rumsey, J. M. (1996). Neuroimaging in Developmental Dyslexia. A review and conceptualization. In G. R. Lyon & J. Rumsey (Eds.), Neuroimaging. A window to the
neurological foundations of Learning and Behavior in Children (pp. 5777).
Baltimore: Paul Brookes.
Shaywitz, B., Shaywitz, S., Blachman, B., Pugh, K., Fulbright, R., Skudlarski, P., Mencl,
W., Constable, T., Holahan, J., Marchione, K., Fletcher, J., Lyon, R., & Gore, J.
(2004). Development of left occipito-temporal systems for skilled reading in children
after a phonologically-based intervention. Biological Psychiatry, 55, 926933.
Shaywitz, S. (2003). Overcoming dyslexia. New York: Alfred Knopf.
Shaywitz, S., & Shaywitz, B. (2008). Paying attention to reading: The neurobiology of
reading and dyslexia. Developmental Psychopathology, 20, 13291349.
Simos, P. G., Fletcher, J. M., Bergman, E., Breier, J., Foorman, B., Castillo, E., Davis, M.,
Fitzgerald, M., & Papanicolau, A. (2002). Dislexia-specific brain activation profile
becomes normal following successful remedial training. Neurology, 58, 12031213.
Simos, P. G., Fletcher, J., Sarkari, S., Billingsley, R., Francis, D., & Castillo D. (2005).
Early development of neurophysiological processes involved in normal reading and
reading disability: A magnetic source imaging study. Neuropsychology, 19, 787798.
Simos, P. G., Fletcher, J., Sarkari, S., Billingsted-Marshall, R., Denton, C., & Papanicolau,
A. (2007). Intensive instruction affects brain magnetic activity associated with oral
word reading in children with persistent reading disabilities. Journal of Learning
disabilities, 40, 3748.
28
L. Bravo
Steinbrink, C., & Klatte, M. (2008). Phonological working memory in German children
with poor reading and spelling abilities. Dyslexia, 14, 271290.
Stern, E., Grabner, R., Schumacher, R., Neuper, C., & Saalbach, H. (2006). Education
Reform Volume 13: Educational Research and Neurosciences Expectations,
Evidence, Research Prospects. (D. R. Grabner, & A. Kanape, Trans.) Berlin: Federal
Ministry of Education and Research (BMBF) - Public Relations Division.
Szcs, D., & Goswami, U. (2007). Educational Neuroscience: Defining a new discipline
for the study of mental representations. Mind, Brain and Education, 1, 114127.
Temple, E., Deutsch, G. K., Poldrack, R. A., Miller, S. L., Tallal, P., Merzenich, M. M., &
Gabrieli, J. D. (2003). Neural deficits in children with dyslexia ameliorated by
behavioral remediation: Evidence from functional MRI. Proceedings of the National
Academy of Sciences, 100, 28602865.
Van Atteveldt, N., Formisano, E., Goebel, R., & Blomert, L. (2004). Integration of letters
and speech sounds in the human brain. Neuron, 43, 271282.
Vandermosten, M., Boets, B., Poelmans, H., Sunaert, S., Wouters, J., & Ghesquire, P.
(2012). A tractography study in dyslexia: neuroanatomic correlates of orthographic,
phonological and speech processing. Brain, 135, 935948.
Vellutino, F. (1979). Dyslexia. Theory and Research. Cambridge: The M.I.T. Press.
Vellutino, F., Fletcher, J., Snowling, M., & Scanlon, D. (2004). Specific reading disability
(dyslexia): what have we learned in the past four decades? Journal of Child
Psychology and Psychiatry, 45, 240.
Wimmer, H., & Schurz, M. (2010). Dyslexia in regular orthographies: Dyslexia 16, 283
299.
Wimmer, H., Schurz, M., Sturm, D., Richlan, F., Klackl, J., & Kronbichler, M. (2010).
A dual-route perspective on poor reading in a regular orthography: An fMRI study.
Cortex, 46, 12841298.
Wolf, M., & Bowers, P. (1999). The double-deficit hypothesis for the developmental
dyslexias. Journal of Educational Psychology, 91, 415438.