Montse Fernández Prieto
Montse Fernández Prieto
Fundación Pública Galega de Medicina Xenómica, Fundación Ramón Domínguez
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How executive functions are related to intelligence in Williams syndrome
A Osório, R Cruz, A Sampaio, E Garayzábal, R Martínez-Regueiro, ...
Research in developmental disabilities 33 (4), 1169-1175, 2012
382012
Cognitive functioning in children and adults with Smith-Magenis syndrome
A Osório, R Cruz, A Sampaio, E Garayzábal, Á Carracedo, ...
European Journal of Medical Genetics 55 (6-7), 394-399, 2012
192012
Alteraciones de la esfera emocional y el control de los impulsos en la enfermedad de Parkinson
M Fernández Prieto, M Lens, A López Real, A Puy, JJ Dias Silva, ...
Rev. neurol.(Ed. impr.), s41-s49, 2010
142010
Touch processing and social behavior in ASD
HO Miguel, A Sampaio, R Martínez-Regueiro, L Gómez-Guerrero, ...
Journal of autism and developmental disorders 47 (8), 2425-2433, 2017
82017
Interstitial microdeletions including the chromosome band 4q13.2 and the UBA6 gene as possible causes of intellectual disability and behavior disorder
I Quintela, F Barros, M Fernandez‐Prieto, R Martinez‐Regueiro, ...
American Journal of Medical Genetics Part A 167 (12), 3113-3120, 2015
82015
PET and MRI detection of early and progressive neurodegeneration in spinocerebellar ataxia type 36
P Aguiar, J Pardo, M Arias, B Quintáns, M Fernández‐Prieto, ...
Movement Disorders 32 (2), 264-273, 2017
72017
Female patient with autistic disorder, intellectual disability, and co‐morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13. 2–q13. 31 microdeletion
I Quintela, L Gomez‐Guerrero, M Fernandez‐Prieto, M Resches, F Barros, ...
American Journal of Medical Genetics Part A 167 (12), 3121-3129, 2015
52015
A 6q14. 1-q15 microdeletion in a male patient with severe autistic disorder, lack of oral language, and dysmorphic features with concomitant presence of a maternally inherited …
I Quintela, M Fernandez-Prieto, L Gomez-Guerrero, M Resches, J Eiris, ...
Clinical case reports 3 (6), 415, 2015
42015
A heterozygous splicing variant in NPC2 in a patient with PSP: 699
C Castro-Fernández, C García-Sancho, V Rodríguez-Sureda, ...
Movement Disorders 31, 2016
12016
Longitudinal assessment of narrative profile in a Williams syndrome patient
M Fernandez-Prieto, A Sampaio, M Lens, Á Carracedo, ÓF Gonçalves
The British Journal of Development Disabilities 57 (112), 91-99, 2011
12011
Disorders affecting the emotional sphere and impulse control in Parkinson's disease
M Fernández-Prieto, M Lens, A López-Real, A Puy, JJ Dias-Silva, ...
Revista de neurologia 50, S41-9, 2010
12010
Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36).
R Martínez-Regueiro, M Arias, R Cruz, B Quintáns, T Labella-Caballero, ...
Cerebellum (London, England), 2020
2020
Neuropsychological assessment in SCA36:'Costa da Morte'ataxia
R Martínez-Regueiro, MJ Sobrido, B Quintáns, M Arias, J Pardo, M Pardo, ...
European Journal of Neurology 21, 258-258, 2014
2014
Experiencia en el estudio genético de la enfermedad de Alzheimer en Galicia
M García Murias, A Robles Bayón, M Fernández Prieto, M Arias Gómez, ...
Alzheimer (Barcelona), 30-37, 2010
2010
Neuroplasticity in Williams Syndrome–Intervention on Attention Problems
M Férnandez-Prieto, A Sampaio, M Lens, E Garayzábal, O Gonçalves, ...
Front. Hum. Neurosci. Conference Abstract: 12th International Professional …, 2009
2009
Diferencias individuales en el perfil lingüístico-comunicativo de individuos con TEA de alto funcionamiento. Implicaciones de los problemas conductuales y emocionales asociados.
M Resches, R Martínez-Regueiro, L Gómez-Guerrero, S Gómez, ...
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