Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Lucina Bobadilla‐Morales"'
Autor:
Carmina Angelica Perez-Romero, Lucero Mendoza-Maldonado, Alberto Tonda, Etienne Coz, Patrick Tabeling, Jessica Vanhomwegen, John MacSharry, Joanna Szafran, Lucina Bobadilla-Morales, Alfredo Corona-Rivera, Eric Claassen, Johan Garssen, Aletta D. Kraneveld, Alejandro Lopez-Rincon
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract As the COVID-19 pandemic winds down, it leaves behind the serious concern that future, even more disruptive pandemics may eventually surface. One of the crucial steps in handling the SARS-CoV-2 pandemic was being able to detect the presence
Externí odkaz:
https://doaj.org/article/d2bbaccce7d84463bda65db8ea3ef76d
Autor:
Elizabeth Acosta-Fernández, Jorge R. Corona-Rivera, Izabel M. Ríos-Flores, Elizabeth Torres-Anguiano, Alfredo Corona-Rivera, Christian Peña-Padilla, Lucina Bobadilla-Morales
Publikováno v:
Gaceta Médica de México, Vol 158, Iss 4 (2022)
Introducción: Las alteraciones epigenéticas y genómicas de la región improntada 11p15.5 producen crecimiento excesivo o deficiente, que se manifiesta como síndrome de Beckwith-Wiedemann o síndrome de Silver-Russell, respectivamente. Objetivo: E
Externí odkaz:
https://doaj.org/article/ea1a1616d60843078d577d510bd773fb
Autor:
Sinhue Alejandro Brukman-Jimenez, Lucina Bobadilla-Morales, Jorge Román Corona-Rivera, Pablo Alejandro Chávez-Panduro, Citlalli Ortega-de-la-Torre, Uriel Francisco Santana-Bejarano, Elizabeth Torres-Anguiano, Lucero Mendoza-Maldonado, Fernando Antonio Sánchez-Zubieta, Alfredo Corona-Rivera
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-7 (2020)
Abstract Background Acute leukemias represent the main malignancies occurring among children under the age of 15 years. Around 17% corresponds to acute myeloid leukemia (AML). The cytogenetic analysis of bone marrow complements the diagnosis of hemat
Externí odkaz:
https://doaj.org/article/5db998768ad84fdf806fc8ad66273a65
Autor:
Gerardo E. Fabián-Morales, Lucina Bobadilla-Morales, Christian Peña-Padilla, Rafael Nieto-García, Pascuala B. Rivera-Ramírez, Alfredo Corona-Rivera, Aurea Márquez-Mora, Graciela Macías-Salcedo, Idalid Cuero-Quezada, Jorge R. Corona-Rivera
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 79, Iss 6 (2022)
Background: Congenital heart defects (CHD) are among the most frequent manifestations of 22q11.2 deletion syndrome. Although we found relatively few studies aimed at specifically detecting 22q11.2 deletion in newborns (NB) with CHD, none of them has
Externí odkaz:
https://doaj.org/article/dfc31b69b4044c08b4a126ab9777b5ef
Autor:
Jorge R. Corona-Rivera, Topacio O. Andrade-Romo, Liuba M. Aguirre-Salas, Lucina Bobadilla-Morales, Cristian I. Aranda-Sánchez, Alfredo Corona-Rivera, René O. Pérez-Ramírez
Publikováno v:
Gaceta Médica de México, Vol 157, Iss 2 (2021)
Externí odkaz:
https://doaj.org/article/7c104778a97145038017b1388c151192
Akademický článek
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Autor:
Jorge Román Corona-Rivera, Juan Carlos Zenteno, Leopoldo Gildardo López-Pérez, Emiy Yokoyama-Rebollar, Camilo E. Villarroel, Tania Barragán-Arévalo, Luis Ángel Montes-Almanza, Luz Consuelo Zepeda-Romero, Guadalupe Elena Morales-Domínguez, Christian Peña-Padilla, Lucina Bobadilla-Morales, Alfredo Corona-Rivera
Publikováno v:
Molecular Syndromology. 14:143-151
Introduction: PACS1-related neurodevelopmental disorder (PACS1-related NDD) is caused by pathogenic variants in the PACS1 gene and is characterized by a distinctive facial appearance, intellectual disability, speech delay, seizures, feeding difficult
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2018172286f286a15a4d0c3e5434d33
https://doi.org/10.1159/000526975
https://doi.org/10.1159/000526975
Autor:
Jorge Román Corona‐Rivera, Felipe de Jesús Bustos Rodríguez, Laura Leticia Vega‐Silva, Fernando Hernández‐Camarena, Christian Peña‐Padilla, Katia Alejandra Castillo‐Reyes, Jessica Paola Cruz‐Cruz, Lucina Bobadilla‐Morales, Alfredo Corona‐Rivera
Publikováno v:
American Journal of Medical Genetics Part A. 191:1669-1671
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f66f21d3bdca3b12924123de8cb2c77
https://doi.org/10.1002/ajmg.a.63183
https://doi.org/10.1002/ajmg.a.63183
Autor:
Jehú, Rivera-Vargas, Andrea, Superti-Furga, Luisa, Bonafé, Christian, Peña-Padilla, Rocío Carolina, Cortés-Pastrana, Lucina, Bobadilla-Morales, Alfredo, Corona-Rivera, Jorge Román, Corona-Rivera
Publikováno v:
Clinical Dysmorphology. 32:14-17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::241b348c3942dea99f6ef5707187847a
https://doi.org/10.1097/mcd.0000000000000432
https://doi.org/10.1097/mcd.0000000000000432
Autor:
Alfredo Corona-Rivera, Lucina Bobadilla-Morales, Cristian Irela Aranda-Sánchez, Topacio O. Andrade-Romo, Rene O. Pérez-Ramírez, Jorge Román Corona-Rivera, Liuba M. Aguirre-Salas
Publikováno v:
Gaceta Médica de México. 157
Family history of thyroid disease (FHTD) constitutes a possible risk factor for congenital hypothyroidism (CH) in the general population; however, FHTD possible relationship with CH in subjects with Down syndrome (DS) has not yet been explored.To det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8866772de89844d07b3d98bde200f1e9
https://doi.org/10.24875/gmm.m21000538
https://doi.org/10.24875/gmm.m21000538