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pro vyhledávání: '"M. T Ferrando-Lucas"'
Autor:
María-Luisa Martín-Ruiz, M. T. Ferrando Lucas, M. Penafiel Puerto, I. Pau de la Cruz, M. A. Valero Duboy
Publikováno v:
Proceedings of the 2012 IEEE 12th International Conference on Bioinformatics & Bioengineering (BIBE), Larnaca, Cyprus, 11-13 November 2012 | IEEE 12th International Conference on BioInformatics and BioEngineering, November 11-13 | Larnaca, Cyprus | 11/11/2012-13/11/2012 | Larnaca, Cyprus
Archivo Digital UPM
instname
BIBE
Archivo Digital UPM
instname
BIBE
Monitoring of neuro-evolutive development from birth until the age of six is a decisive factor in a child's quality of life. Early detection of development disorders in early childhood can facilitate necessary diagnosis and/or treatment. Primary-care
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2429cd9a921ef4241c6c2a8d665a688
https://oa.upm.es/20994/
https://oa.upm.es/20994/
Autor:
M T, Ferrando-Lucas
Publikováno v:
Revista de neurologia. 42
Attention deficit hyperactivity disorder (ADHD) is one of the most frequent reasons for patients' visits in everyday practice. The academic and social distortion it produces in those affected by this condition have turned it into a subject that is re
Publikováno v:
Revista de neurologia. 40
Following the diagnosis of intellectual disability, a prognosis can be offered concerning the degree of autonomy the child will be able to achieve based on prior experience, but which depends on the aetiology of the disability. It is still difficult
Publikováno v:
Revista de neurologia. 38
Fragile X syndrome (FXS) is the first cause of intellective dysfunction due to hereditary reasons, but above all it is a multisystemic pathology, in which the cognitive behavioural phenotype is going to mark the child's entire school and social life.
Publikováno v:
Revista de neurologia. 36
Fragile X syndrome, which is produced by mutation of a gene in the X chromosome, is the most frequent cause of hereditary mental retardation. The multisystemic alterations of the disorder are due to the inhibition of the expression of the FMR1 gene a
Autor:
M T, Ferrando-Lucas, J, Martos-Pérez, M, Llorente-Comí, S, Freire-Prudencio, R, Ayuda-Pascual, C, Martínez Díez-Jorge, A, González-Navarro
Publikováno v:
Revista de neurologia. 34
Although the concept of autistic spectrum may be useful to explain and describe the heterogeneity of the syndrome, its aetiology is still unknown. Different disorders have been reported as the biological basis of autism. Early diagnosis and a multi d
Autor:
M T, Angulo Carrere, J, Campos Castelló, M T, Ferrando Lucas, S, Angulo Gómez de Cadiñanos, F, López García
Publikováno v:
Archivos de neurobiologia. 53(1)
Seventy children with Down Syndrome (22 boys and 48 girls), ages ranging between five and seventeen years, were evaluated for instability of the upper cervical-spine. X-ray study of this region in lateral projection was did, in neutral position and f
Autor:
María Llorente-Comí, A González-Navarro, Raquel Ayuda-Pascual, S Freire-Prudencio, Juan Martos-Pérez, C Martínez Díez-Jorge, M. T Ferrando-Lucas
Publikováno v:
Revista de Neurología. 34:49