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Dislexia
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1021por Pan, Ning, Guo, Yangfeng, Ma, Jingwen, Fan, Xiaoxuan, Yin, Zhixin, Xu, Xiaoyu, Cai, Lei, Zhang, Yue, Li, Xiuhong“…Chinese written vocabulary size, cognitive, emotional, and behavioral factors were assessed by the Chinese written vocabulary size assessment scale, the dyslexia checklist for Chinese children (DCCC) and the Strengths and Difficulties Questionnaire (SDQ), respectively. …”
Publicado 2021
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1022por Vishne, Gal, Jacoby, Nori, Malinovitch, Tamar, Epstein, Tamir, Frenkel, Or, Ahissar, Merav“…To assess the specificity of tapping characteristics to autism, we compare performance to both neurotypical individuals and individuals with dyslexia. Only the autism group shows poor sensorimotor synchronization. …”
Publicado 2021
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1023por de la Fuente-Munoz, Eduardo, Van Den Rym, Ana, García-Solis, Blanca, Ochoa Grullón, Juliana, Guevara-Hoyer, Kissy, Fernández-Arquero, Miguel, Galán Dávila, Lucía, Matías-Guiú, Jorge, Sánchez-Ramón, Silvia, Pérez de Diego, Rebeca“…Gain-of-function (GOF) mutations in STIM1 are responsible for tubular aggregate myopathy and Stormorken syndrome (TAM/STRMK), a clinically overlapping multisystemic disease characterised by muscle weakness, miosis, thrombocytopaenia, hyposplenism, ichthyosis, dyslexia, and short stature. Several mutations have been reported as responsible for the disease. …”
Publicado 2022
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1024
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1025Novel IRF2BPL gene mutation manifesting as a broad spectrum of neurological disorders: a case report“…Pathogenic variants lead to neurodegeneration and present with phenotypic features of a neurological disorder, including dyslexia, dyscalculia, epilepsy, dystonia, neurodevelopmental regression, loss of motor skills and cerebellar ataxia. …”
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1026“…Interestingly, a positive LOD score of 1.69 was shown at 18q, a region previously linked to dyslexia (DYX6) using combined music test scores. CONCLUSION: Our results show that there is a genetic contribution to musical aptitude that is likely to be regulated by several predisposing genes or variants.…”
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1027por Scerri, Tom S., Morris, Andrew P., Buckingham, Lyn-Louise, Newbury, Dianne F., Miller, Laura L., Monaco, Anthony P., Bishop, Dorothy V.M., Paracchini, Silvia“…BACKGROUND: Several susceptibility genes have been proposed for dyslexia (reading disability; RD) and specific language impairment (SLI). …”
Publicado 2011
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1028por Ivliev, Alexander E., 't Hoen, Peter A. C., van Roon-Mom, Willeke M. C., Peters, Dorien J. M., Sergeeva, Marina G.“…The novel findings included a set of genes (DCDC2, DYX1C1, KIAA0319) related to a neurological disease dyslexia suggesting their potential involvement in ciliary functions. …”
Publicado 2012
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1029“…In particular, a method for assessing neural entrainment and cross-modal phase resetting would be useful for exploring developmental learning difficulties thought to involve temporal sampling, such as dyslexia.…”
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1030por Roux, Franck-Emmanuel, Durand, Jean-Baptiste, Jucla, Mélanie, Réhault, Emilie, Reddy, Marion, Démonet, Jean-François“…These data are in line with many brain activation studies that showed that left superior temporal and inferior parietal regions had a crucial role respectively in word and pseudoword reading and were core regions for dyslexia.…”
Publicado 2012
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1031“…The cerebellum regulates complex movements and is also implicated in cognitive tasks, and cerebellar dysfunction is consequently associated not only with movement disorders, but also with conditions like autism and dyslexia. How information is encoded by specific cerebellar firing patterns remains debated, however. …”
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1032por Seghier, Mohamed L., Neufeld, Nicholas H., Zeidman, Peter, Leff, Alex P., Mechelli, Andrea, Nagendran, Arjuna, Riddoch, Jane M., Humphreys, Glyn W., Price, Cathy J.“…Hypotheses were derived from a stroke patient who acquired dyslexia following extensive LvOT damage. The patient followed a reading trajectory typical of that associated with pure alexia, re-gaining the ability to read aloud many words with declining performance as the length of words increased. …”
Publicado 2012
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1033“…Abnormal functioning in these loops could eventually contribute to the pathogenesis of major brain pathologies including not just ataxia but also dyslexia, autism, schizophrenia, and depression.…”
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1034por Hillen, Rebekka, Günther, Thomas, Kohlen, Claudia, Eckers, Cornelia, van Ermingen-Marbach, Muna, Sass, Katharina, Scharke, Wolfgang, Vollmar, Josefine, Radach, Ralph, Heim, Stefan“…Consequently, the Landolt paradigm may provide novel insights into the contributions of linguistic and non-linguistic factors on reading failure e.g., in developmental dyslexia.…”
Publicado 2013
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1035por Brandler, William M., Morris, Andrew P., Evans, David M., Scerri, Thomas S., Kemp, John P., Timpson, Nicholas J., St Pourcain, Beate, Smith, George Davey, Ring, Susan M., Stein, John, Monaco, Anthony P., Talcott, Joel B., Fisher, Simon E., Webber, Caleb, Paracchini, Silvia“…We report a genome-wide association study meta-analysis for a quantitative measure of relative hand skill in individuals with dyslexia [reading disability (RD)] (n = 728). The most strongly associated variant, rs7182874 (P = 8.68×10(−9)), is located in PCSK6, further supporting an association we previously reported. …”
Publicado 2013
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1036por Yong, Keir X.X., Warren, Jason D., Warrington, Elizabeth K., Crutch, Sebastian J.“…The current data emphasise the need for much clearer evidence of causality when attempting to draw connections between specific aspects of visual processing and different types of acquired peripheral dyslexia.…”
Publicado 2013
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1037por Yong, Keir X.X., Shakespeare, Timothy J., Cash, Dave, Henley, Susie M.D., Warren, Jason D., Crutch, Sebastian J.“…These findings improve the characterisation of dyslexia in PCA, shed light on the causative and associative factors, and provide clear direction for the development of reading aids and strategies to maximise and sustain reading ability in the early stages of disease.…”
Publicado 2014
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1038por Wang, Rui, Chen, Chun-Chun, Hara, Erina, Rivas, Miriam V, Roulhac, Petra L, Howard, Jason T, Chakraborty, Mukta, Audet, Jean-Nicolas, Jarvis, Erich D“…These findings are consistent with SLIT and ROBO gene dysfunctions associated with autism, dyslexia, and speech sound language disorders and suggest that convergent evolution of vocal learning was associated with convergent changes in the SLIT–ROBO axon guidance pathway. …”
Publicado 2015
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1039“…Consequently, much printed reading material has the potential to elicit PRVS that may impair reading performance, and this problem appears to be common in individuals with reading difficulties including dyslexia. However, the manner in which PRVS affects reading ability is unknown. …”
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1040por Ojanen, Emma, Ronimus, Miia, Ahonen, Timo, Chansa-Kabali, Tamara, February, Pamela, Jere-Folotiya, Jacqueline, Kauppinen, Karri-Pekka, Ketonen, Ritva, Ngorosho, Damaris, Pitkänen, Mikko, Puhakka, Suzanne, Sampa, Francis, Walubita, Gabriel, Yalukanda, Christopher, Pugh, Ken, Richardson, Ulla, Serpell, Robert, Lyytinen, Heikki“…In this article we will describe how GG has been developed from a Finnish dyslexia prevention game to an intervention method that can be used not only to improve children’s reading performance but also to raise teachers’ and parents’ awareness of the development of reading skill and effective reading instruction methods. …”
Publicado 2015
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