Estudio de caso de dislexia de una estudiante universitaria

Referencias bibliográficas

• Asociación Americana de Psiquiatría (2013). Manual diagnóstico y estadístico de los trastornos mentales. DSM-5. Barcelona: Masson.
• Astrom, R. L., Wadsworth, S. J., Olson, R. K., Willcutt, E. G., & DeFries, J. C. (2012). Genetic and enviromental etiologies of reading difficulties: DeFries-fulker analysis of reading performance data from twin pairs and their non-twins siblings. Learning and Individual Differences, 22, 365-369.
• http://dx.doi.org/10.1016/j.lindif.2012.01.011
• PMid:22927712 PMCid:PMC3423974
• Auzias, M. (1977). Pruebas de Lateralidad. Recuperado de http://psicologia-psicopedagogia.es.tl/prueba-de-lateralidad--usual.htm
• Bowers, P. G., & Wolf, M. (1993). Theoretical links among naming speed, precise timing mechanisms, and orthographic skill in dislexia. Reading and Writing: An Interdisciplinary Journal, 5, 69-85.
• http://dx.doi.org/10.1007/BF01026919
• Cardon, L. E., Smith, S. D., Fulker, D. W., Kimberling, W. J., Pennington, B. F., & DeFries, J. C. (1994). Quantitative trait locus for reading disability chromosome 6. Science, 266, 276-279.
• http://dx.doi.org/10.1126/science.7939663
• PMid:7939663
• Cardon, L. E., Smith, S. D., Fulker, D. W., Kimberling, W. J., Pennington, B. F., & DeFries, J. C. (1995). Quantitative trait locus for reading disability: Correction. Science, 268, 1553.
• http://dx.doi.org/10.1126/science.7777847
• Costa, P.T., & McCrae, R.R. (1999). Inventario de Personalidad NEO Revisado (NEO PI-R) e InventarioNEO Reducido de Cinco Factores (NEO FFI). Madrid: TEA Ediciones.
• Cuetos, F., Rodríguez, B., Ruano, E. y Arribas, D. (2007). Prolec-R, Batería de evaluación de los procesos lectores, Revisada. Madrid: TEA.
• Derogatis, L. R. (1983). SCL-90-R: Administration, scoring and procedures: Manual II Towson, MD Clinical Psychometric Research.
• Eden, G.F., Vanmeter, J.W., Rumsey, J.W., & Zeffiro T.A. (1996). The visual déficit theory of developmental dyslexia. NeuroImage, 4, S108-S117.
• http://dx.doi.org/10.1006/nimg.1996.0061
• PMid:9345535
• Evans, C. E., Mellor-Clark, J., Margison, F., Barkham, M., Audin, K., Connell, J., & McGrath, G. (2000). CORE: Clinical outcomer in routine evaluation. Journal of Mental Health, 9, 247–255.
• http://dx.doi.org/10.1080/jmh.9.3.247.255
• http://dx.doi.org/10.1080/713680250
• Fawcett, A.J., Nicolson, R. I., & Dean, P. (1996). Impaired performance of children with dyslexia on a range of cerebellar tasks. Annals of Dyslexia, 46, 259-283.
• http://dx.doi.org/10.1007/BF02648179
• PMid:24234275
• Fisher, S. E., Marlow, A. J., Lamb, J., Mestrini, E., Williams, D. F., & Richardson, A. J. (1999). A quantitative-trait locus on chromosome 6p influencies different aspects of developmental dyslexia. American Journal of Human Genetics, 64, 146-156.
• http://dx.doi.org/10.1086/302190
• PMid:9915953 PMCid:PMC1377712
• Fletcher, J. M. (2009). The evolution of a scientific concept. Journal of the International Neuropsychological Society, 15, 501-508.
• http://dx.doi.org/10.1017/S1355617709090900
• PMid:19573267 PMCid:PMC3079378
• Francks, C., Fisher, S. E., Olson, R. K., Pennington, B. F., Smith, S. D., DeFries, J. C., Monaco, A. (2002). Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: Quantitative association analysisand positional candidate genes SEMA4F and OTX1. Phychiatrics Genetics, 12, 35-41.
• http://dx.doi.org/10.1097/00041444-200203000-00005
• Frith, U. (1997). Brain, mind and behaviour in dyslexia. En C. Hulme & M. Snowling (Eds.) Dyslexia, Biology, Cognition and Intervention. London: Whurr Publishers Ltd.
• Frith, U. (1999). Paradoxes in the definition of dyslexia. Dyslexia, 5, 192-214.
• http://dx.doi.org/10.1002/(SICI)1099-0909(199912)5:4<192::AID-DYS144>3.3.CO;2-E
• http://dx.doi.org/10.1002/(SICI)1099-0909(199912)5:4<192::AID-DYS144>3.0.CO;2-N
• Galaburda, A.M, & Livingstone, M. (1993). Evidence for a magnocellular defect in developmental dislexia. Annals of the New York Academy of Science, 682, 70-82.
• http://dx.doi.org/10.1111/j.1749-6632.1993.tb22960.x
• Galaburda, A. M., LoTurco, J., Ramus, F., Fitch, R. H., & Rosen, G. D. (2006). From genes to behaviour in developmental dyslexia. Nature Neuroscience, 9, 1213-1217.
• http://dx.doi.org/10.1038/nn1772
• PMid:17001339
• Galaburda, A., Rosen, G., & Sherman, (1990). Individual variability in cortical organizations: Its reslationship to brain laterality and implications to function. Neuropsychologia, 28, 529-546.
• http://dx.doi.org/10.1016/0028-3932(90)90032-J
• Gayán, J., Smith, S. D., Cherny, S. S., Cardon, R. L., Fulker, D. W., Kimberling, W. J., Pennington, B. F. (1999). Quantitative-trait locus for specific language and reading deficits on chromosome 6p. American Journal of Human Genetics, (64), 157-164.
• http://dx.doi.org/10.1086/302191
• PMid:9915954 PMCid:PMC1377713
• Gayán, J., Smith, S. D., Cherny, S. S., Cardon, R. L., Fulker, D. W., Kimberling, W. J., DeFries, J. C. (1999). Quantitative-trait locus for specific languaje and reading deficits on chromosome 6p. American Journal of Human Genetics, 64, 157-164.
• http://dx.doi.org/10.1086/302191
• PMid:9915954 PMCid:PMC1377713
• González, D., Jiménez, J. E., García, E., Díaz, A., Rodríguez, C., & Crespo, P. (2010). Prevalencia de las dificultades específicas de aprendizaje en la ense-anza secundaria obligatoria. Europe’s Journal of Pychology, 3, 317-327.
• Grigorenko, E. L., Wood, F. B., Meyer, M. S., Hart, L. A., Speed, W. C., Shuster, A., & Pauls, D. L. (1997). Susceptibility loci for distinct components of developmental dyslexia on chromosome 6 and 15. American Journal of Human Genetics, 30, 27-39.
• Grigorenko, E. L., Wood, F. B., Meyer, M. S., Pauls, J. E., Hart, L. A., & Pauls, D. L. (2001). Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p. American Journal of Medical Genetics, 41, 43-49.
• http://dx.doi.org/10.1002/1096-8628(20010108)105:1<120::aid-ajmg1075>3.0.co;2-t
• http://dx.doi.org/10.1002/1096-8628(20010108)105:1<120::aid-ajmg1075>3.3.co;2-k
• Hoien, T. (1999). Theories of déficits in dislexia. En I. Lundberg, F.E. Tonnesen & I. Austad (Eds). Dyslexia: Advances in theory and practise. London: Kluwer Academic Publishers.
• Illingworth, S., & Bishop, D. V. (2009). Atypical cerebral lateralisation in adults with compensated developmental dyslexia demonstrated using functional transcranial doppler ultrasound. Brain Language, 111, 61-65.
• http://dx.doi.org/10.1016/j.bandl.2009.05.002
• PMid:19525003 PMCid:PMC2977530
• Jiménez, J. E., Gúzman, R., Rodríguez, C., & Artiles, C. (2009). Prevalencia de las dificultades específicas de aprendizaje: La dislexia en espa-ol. Annals of Psychology, 25, 78-85.
• Kaminen, N., Hannula- Jouppi, K., Kestilä, M., Lahermo, P., Muller, K., & Kaarenen, M. (2002). A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32. Journal of Medical Genetics, 40, 340-345.
• http://dx.doi.org/10.1136/jmg.40.5.340
• PMCid:PMC1735449
• Lehongre, K., Morillon, B., Giraud, A., & Ramus, F. (2013). Impaired auditory sapling in dyslexia: Futher evidence from cobinated fMRI and EEG. Frontiers in Human Neuroscience, 7, 454.
• http://dx.doi.org/10.3389/fnhum.2013.00454
• PMid:23950742 PMCid:PMC3738857
• Leiner, H.C., Leiner, A.L., & Dow, R.S. (1989). Reappraising the cerebellum; What does the hindbrain contribute to the forebrain? Behavioral Neuroscience, 103, 998-1008.
• http://dx.doi.org/10.1037/0735-7044.103.5.998
• PMid:2679667
• Matute, E.; Rosselli, M., Ardila, A., y Ostrosky, F. (2007b). Evaluación Neuropsicológica Infantil. ENI. México: Manual moderno.
• Mody, M. (2003). Phonological basis in Reading disability; A review and analysis of the evidence. Reading and Writing: An Interdisciplinart Journal, 16, 21-39.
• http://dx.doi.org/10.1023/A:1021741921815
• Nicolson, R.I., Fawcett, A.J., & Dean. P. (2001). Developmental dyslexia: the cerebellar déficit hypothesis. Trends in Neurosciences, 24 (9), 508-511.
• http://dx.doi.org/10.1016/S0166-2236(00)01896-8
• Nittrouer, S. (1999). Do temporal processing déficits cause phonological processing problems?. Journal of Speech, Language, and Hearing Research, 42, 925-942.
• http://dx.doi.org/10.1044/jslhr.4204.925
• Penninton, B. F. (1999). Toward an integrated understanding of dyslexia : Genic, neurological, and cognitive mechanisms. Development and Psychopathology, 11, 629-654.
• http://dx.doi.org/10.1017/S0954579499002242
• Peterson, R. L., & Penninton, B. F. (2007). Developmental dyslexia. Lancet, 379, 1997-2007.
• http://dx.doi.org/10.1016/S0140-6736(12)60198-6
• Petryshen, R., Kaplan, B. J., Hughes, M. L., Tzenova, J., & Field, L. L. (2002). Supportive evidence for the DYX3 dyslexia susceptibility gene in canadian families. Journal of Medical Genetics, 39, 125-126.
• http://dx.doi.org/10.1136/jmg.39.2.125
• PMid:11836362 PMCid:PMC1735047
• Rabin, M., Wen, X. L., Hepburn, M., Lubs, H. A., Feldman, E., & Duara, R. (1993). Suggestive linkage of developmental dyslexia to chromosome 1p34-p36. Lancet, 40, 751-758.
• http://dx.doi.org/10.1016/0140-6736(93)91384-x
• Ramus, F., Pidgeon, E., & Frith, U. (2003). The relationship between motor control and phonology in dyslexic childen. Journal of Child Psychology and Psychiatry, 44(5), 712-722.
• http://dx.doi.org/10.1111/1469-7610.00157
• PMid:12831115
• Serrano, F. (2005). Dislexicos en espa-ol. papel de la fonología y la ortografía (Universidad de Granada). Doi:84-338-3573-4.
• Serrano, F., & Defior, S. (2008). Dyslexia speed problems in a transparent orthography. Annals of Dyslexia, 58, 81-95.
• http://dx.doi.org/10.1007/s11881-008-0013-6
• PMid:18483868
• Skottum, B.C. (1997). The magnocellular déficit theory of dyslexia. Trends in Neuroscience, 20, 397-398.
• Skottum, B.C. (2000). The magnocellular déficit theory of dyslexia: the evidence from contrast sensitivity. Vision research, 40, 111-127.
• http://dx.doi.org/10.1016/S0042-6989(99)00170-4
• Soriano-Ferrer, M., & Piedra Martínez, E. (2014). Una revisión de las bases neurobiológicas de la dislexia en población adulta. El Servier, (662), 8/8/2014
• http://dx.doi.org/10.1016/j.nrl.2014.08.003
• Spielberger C.D., Gorsuch, R.L., & Lushene, R.E. (1982). Cuestionario de Ansiedad Estado/Rasgo. Madrid: TEA.
• Steinbrink, C., Groth, K., Lachmann, T., & Riecker, A. (2012). Neural correlates of temporal auditory processing in developmental dyslexia during german vowel length discrimination: An fMRI study. Brain Language, 121, 1-11.
• http://dx.doi.org/10.1016/j.bandl.2011.12.003
• PMid:22377262
• Tallal, P., Miller, S., Fitch, R. H. (1993). Neurobiological basis of speech: a case for the preeminence of temporal processing. Annals NY Academic Science, 682, 27-47.
• http://dx.doi.org/10.1111/j.1749-6632.1993.tb22957.x
• Van der Leij, A., & Van Daal, H. P. (1999). Automaticity, automatization and Dyslexia. En I. L. Kundberg, F. E. Tonnessen, & I. Austad (eds), Dyslexia: Advances in Theory and Practice (pp. 75-90). Dordrecht: Kluwer Academic Publishers.
• http://dx.doi.org/10.1007/978-94-011-4667-8_6
• Vidal-Abarca, E, (2007). TEC. Test de estrategias de comprensión. Madrid: Instituto Calasanz de ciencias de la educación.
• http://dx.doi.org/10.1021/es0706899
• Wadsworth, S. J., Olson, R. K., & DeFries, J. C. (2010). Differential genetic etiology of reading difficulties as a function of IQ: An update. Behavior Genetics, 40, 751-758.
• http://dx.doi.org/10.1007/s10519-010-9349-x
• PMid:20333543 PMCid:PMC2892633
• Wechsler, D. (1999). WAIS-III. Escala de inteligencia de Wechsler para adultos-III. Madrid, TEA (Edición original, 1997).
• Wolf, M. (1991). Naming speed and Reading: The contribution of the cognitive neurosciences. Reading Research Quarterly, 26(2), 123-141.
• http://dx.doi.org/10.2307/747978
• Wolf, M., & Bowers, P. G. (2000). Naming Speed Processes and Developmental Reading Disabilities: An Introduction to the Special Issue on the Double-Deficit Hypothesis. Journal of Learning disabilities, 33 (4), 322-324.
• http://dx.doi.org/10.1177/002221940003300404