Social Cognition in Patients with Early-Onset Parkinson’s Disease

Autor: Ana Natalia Seubert-Ravelo, Ma Guillermina Yáñez-Téllez, María Lizbeth Lazo-Barriga, Alejandra Calderón Vallejo, Carlos Eduardo Martínez-Cortés, Adela Hernández-Galván

Publikováno v: Parkinson's Disease, Vol 2021 (2021)

Social cognition (SC) deficits have been linked to Parkinson’s disease (PD) but have been less well researched than general cognitive processes, especially in early-onset PD (EOPD), despite this population often having greater social and family dem

Externí odkaz: https://doaj.org/article/40437c1d839544e281f444a9711b85eb

A Systematic Review and a Latin American Clinical Model for Teleneuropsychological Assessment

Autor: Carlos Alberto Serrano-Juárez, Carolina Reyes-Méndez, Belén Prieto-Corona, Ana Natalia Seubert-Ravelo, Julieta Moreno-Villagómez, José-Ángel Cabañas-Tinajero, Ma Guillermina Yáñez-Téllez, Rocío Alejandra Quezada-Torres, Marybeth Téllez-Rodríguez, Bárbara Barrera-Rodríguez, Martha Paola Soto-Jiménez, Fátima Aideé González-Gutiérrez, Elena Castillo-Tejeda

Publikováno v: Archives of Clinical Neuropsychology. 38:283-300

Objective The objective of this study is to propose a TeleNP model for remote assessment and offer practical recommendations for clinical practice with patients in Mexico and Latin America, based on a systematic literature review and clinical experie

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a48e34862deba098d9107be684f4476
https://doi.org/10.1093/arclin/acac077

An Exploration of Social Cognition in Children with Different Degrees of Genetic Deletion in Williams Syndrome

Autor: Belén Prieto-Corona, Ma. Guillermina Yáñez-Téllez, Natalia Arias-Trejo, Juan Silva-Pereyra, Carlos Alberto Serrano-Juárez, Mario Rodríguez-Camacho, Hermelinda Salgado-Ceballos, Carlos A. Venegas-Vega, Miguel Angel De León Miranda

Publikováno v: Journal of Autism and Developmental Disorders. 51:1695-1704

An explanation for the social dysfunction observed in Williams syndrome may be deficits in social cognition. This study explored aspects of social cognition in children with Williams syndrome with different genotypes. The 12 participants included one

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d970447142e76be4db772de552a02a77
https://doi.org/10.1007/s10803-020-04656-4

Neuropsychological Genotype-Phenotype in Patients with Williams Syndrome with Atypical Deletions: A Systematic Review

Autor: Carlos Alberto Serrano-Juárez, Belén Prieto-Corona, Mario Rodríguez-Camacho, Lucero Sandoval-Lira, Ángel Fernando Villalva-Sánchez, Ma. Guillermina Yáñez-Téllez, María Fernanda Rangel López

Publikováno v: Neuropsychology review.

Williams syndrome (WS) is a neurodevelopmental disorder caused by a microdeletion in the q11.23 region of chromosome 7. Recent case series reports and clinical case studies have suggested that the cognitive, behavioral, emotional, and social profile

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f002394c44aa2abf4926834f78bc1f7
https://pubmed.ncbi.nlm.nih.gov/36520254

Intervención Neuropsicológica en un caso de una niña con Síndrome de Williams

Autor: Carlos Alberto Serrano-Juárez, Dulce María Belén Prieto-Corona, Ma. Guillermina Yáñez-Téllez

Publikováno v: Cuadernos de Neuropsicologia, Vol 12, Iss 2, Pp 1-23 (2018)
Universidad Nacional Autónoma de México
UNAM
Redalyc-UNAM
Cuadernos de Neuropsicología / Panamerican Journal of Neuropsychology (Chile) Num.2 Vol.12

"El Síndrome de Williams (SW) es un trastorno genético del neurodesarrollo poco común, que se caracteriza por un perfil neuropsicológico definido por la presencia de mejores habilidades verbales que visoespaciales. El objetivo de este trabajo fue

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5ebb5f612b24621d1df7bbd02fece61e
http://www.redalyc.org/articulo.oa?id=439655913005