Comparative analysis of emotional facial expression recognition and empathy in children with prader-willi syndrome and autism spectrum disorder

Autor: Ane Perosanz, Oscar Martínez, Patricia Espinosa-Blanco, Irune García, Mohammad Al-Rashaida, Juan Francisco López-Paz

Publikováno v: BMC Psychology, Vol 12, Iss 1, Pp 1-14 (2024)

Abstract Background Prader-Willi Syndrome (PWS) is a rare neurodevelopmental disorder that is often comorbid with Autism Spectrum Disorder (ASD). Due to the close association between these two conditions, and recognizing that Theory of Mind (ToM) is

Externí odkaz: https://doaj.org/article/7c387c5856424942a45499af09bc0c2c

Effects of Teleassistance on the Quality of Life of People With Rare Neuromuscular Diseases According to Their Degree of Disability

Autor: Oscar Martínez, Imanol Amayra, Juan Francisco López-Paz, Esther Lázaro, Patricia Caballero, Irune García, Alicia Aurora Rodríguez, Maitane García, Paula María Luna, Paula Pérez-Núñez, Jaume Barrera, Nicole Passi, Sarah Berrocoso, Manuel Pérez, Mohammad Al-Rashaida

Publikováno v: Frontiers in Psychology, Vol 12 (2021)

Rare neuromuscular diseases (RNMDs) are a group of pathologies characterized by a progressive loss of muscular strength, atrophy, fatigue, and other muscle-related symptoms, which affect quality of life (QoL) levels. The low prevalence, high geograph

Externí odkaz: https://doaj.org/article/68588013866f4433baca0136c7d013a0

Anxiety and depression in Chiari malformation

Autor: Esther Lázaro, Maitane Garca, Imanol Amayra, Juan-Francisco López-Paz, Oscar Martnez, Manuel Pérez, Sarah Berrocoso, Mohammad Al Rashaida, Paula Fernández, Alicia Rodrguez, Amaia Jometón, Begoña Ruz

Publikováno v: Journal of Integrative Neuroscience, Vol 17, Iss 4, Pp 343-348 (2018)

There are few studies that explore the involvement of the cerebellum in the affective area. This study aims to evaluate the affective component and, specifically, the emotional states of depression and anxiety associated with the Chiari malformation,

Externí odkaz: https://doaj.org/article/1940e9487ac04a0fb42e765754c58b8f

Music therapy and Sanfilippo syndrome: an analysis of psychological and physiological variables of three case studies

Autor: Juan Francisco López-Paz, Imanol Amayra, Paula Pérez-Núñez, Sarah Berrocoso, Oscar Martínez, Patricia Caballero, Manuel Pérez, Maitane García, Paula María Luna, Esther Lázaro, Mohammad Al-Rashaida, Alicia Aurora Rodríguez

Publikováno v: Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-14 (2021)
Orphanet Journal of Rare Diseases

Introduction Mucopolysaccharidosis type III (MPS III) or Sanfilippo syndrome is a neurodegenerative disease caused by the accumulation of mucopolysaccharides in the body. As the symptoms are wide ranging, it is a challenge to provide a diagnosis and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1934edd611c4d2d85a9c1e7247fdaef3
https://doaj.org/article/0d7ac5a060b34b628be331fd8b46ad13

The role of associations in reducing the emotional and financial impact on parents caring for children with duchenne muscular dystrophy : a cross-cultural study

Autor: Alicia Aurora Rodríguez, Imanol Amayra, Juan Francisco López-Paz, Oscar Martínez, Maitane García, Mónika Salgueiro, Mohammad Al-Rashaida, Paula María Luna, Paula Pérez-Nuñez, Nicole Passi, Irune García, Javiera Ortega

Publikováno v: Int. J. Environ. Res. Public Health 2022, 19
Repositorio Institucional (UCA)
Pontificia Universidad Católica Argentina
instacron:UCA
International Journal of Environmental Research and Public Health; Volume 19; Issue 19; Pages: 12334

Fil: Rodríguez, Alicia Aurora. Universidad de Deusto. Facultad de Ciencias de la Salud. Equipo de Investigación Neuro-e-Motion; España Fil: Amayra Caro, Imanol. Universidad de Deusto. Facultad de Ciencias de la Salud. Equipo de Investigación Neur

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d7121d61ce40dd205601e55c8ff43ce
https://repositorio.uca.edu.ar/handle/123456789/15186