Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Carlos Alberto Serrano-Juárez"'
Autor:
Marybeth Alejandra Téllez-Rodríguez, Adriana Amaya-Hernández, Mayaro Ortega-Luyando, Carlos Alberto Serrano-Juárez, Guillermina Yáñez-Téllez, Verónica Elsa López-Alonso, Juan Manuel Mancilla-Diaz, Rodrigo Erick Escartín-Pérez
Publikováno v:
Frontiers in Public Health, Vol 11 (2023)
IntroductionThe study of food addiction (FA) has become relevant due to its high prevalence, the negative impact on quality of life, and its association with neuropsychological and psychiatric symptoms. Several studies have provided scientific suppor
Externí odkaz:
https://doaj.org/article/d3ddaff951d348098a3b727a3a67c754
Publikováno v:
Cuadernos de Neuropsicologia, Vol 12, Iss 2, Pp 1-23 (2018)
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://doaj.org/article/e6b37cf299864b74ade63f73c5252ffa
Autor:
Ana Natalia Seubert-Ravelo, Carlos Alberto Serrano-Juárez, José-Ángel Cabañas-Tinajero, Fátima Aideé González-Gutiérrez, Julieta Moreno-Villagómez, Belén Prieto-Corona, Carolina Reyes-Méndez, Marybeth Téllez-Rodríguez, Ma Guillermina Yáñez-Téllez
Publikováno v:
Journal of Clinical and Experimental Neuropsychology. 45:12-30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec8313f7d5599c888832aee39014bc49
https://doi.org/10.1080/13803395.2023.2189229
https://doi.org/10.1080/13803395.2023.2189229
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
https://doi.org/10.1093/arclin/acac077
Autor:
Alejandra Estefanía Hernández‐Martínez, Carlos Alberto Serrano‐Juárez, Karen Grisel Barrera‐Medellín, Cecilia Inés Ramírez‐Quiroga, Alma Griselda Ramírez‐Reyes, Roberto Casarrubias Islas, Belén Prieto‐Corona
Publikováno v:
Journal of Neuropsychology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::038a8740a216ed84881904ad79d54c2d
https://doi.org/10.1111/jnp.12320
https://doi.org/10.1111/jnp.12320
Autor:
Cintia Michelle Domínguez-García, Carlos Alberto Serrano-Juárez, Mario Rodríguez-Camacho, Julieta Moreno-Villagómez, María Antonieta Araujo Solís, Belén Prieto-Corona
Publikováno v:
Applied neuropsychology. Child.
Williams Syndrome (WS) is a neurodevelopmental disorder with a distinctive physical, cognitive, and behavioral profile caused by a microdeletion in the q11.23 region of chromosome 7. The neuropsychological profile of WS is characterized by intellectu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6902fca89ff6786d8db3dde583e13cb
https://pubmed.ncbi.nlm.nih.gov/35476532
https://pubmed.ncbi.nlm.nih.gov/35476532
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
https://doi.org/10.1007/s10803-020-04656-4
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
https://pubmed.ncbi.nlm.nih.gov/36520254
Autor:
Karla Cristina, Razón-Hernández, Belén, Prieto-Corona, Guillermina, Yáñez-Téllez, Miguel Ángel, Mendoza-Meléndez, Diana Michelle, Cantallano-García, Carlos Alberto, Serrano-Juárez
Publikováno v:
Panamerican Journal of Neuropsychology / Cuadernos de Neuropsicología; sep-dic2022, Vol. 16 Issue 3, p121-128, 8p
Autor:
Juan Silva-Pereyra, Mario Rodríguez-Camacho, Hermelinda Salgado-Ceballos, Belén Prieto-Corona, Ma. Guillermina Yáñez-Téllez, Carlos Alberto Serrano-Juárez, Carlos A. Venegas-Vega
Publikováno v:
Journal of the International Neuropsychological Society : JINS. 24(9)
Williams syndrome (WS) is a neurodevelopmental disorder that results from a heterozygous microdeletion on chromosome 7q11.23. Most of the time, the affected region contains ~1.5 Mb of sequence encoding approximately 24 genes. Some 5–8% of patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad33adc78be9b7fac37f5f4ea8e5cfd8
https://pubmed.ncbi.nlm.nih.gov/30375319
https://pubmed.ncbi.nlm.nih.gov/30375319