Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Argelia Escobar-Sánchez"'
Autor:
Magdalena Cerón‐Rodríguez, Daniela Castillo‐García, Carlos‐Patricio Acosta‐Rodríguez‐Bueno, Jesús Aguirre‐Hernández, Juan‐Rafael Murillo‐Eliosa, Pedro Valencia‐Mayoral, Argelia Escobar‐Sánchez, Juan‐Luis Salgado‐Loza
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract Pompe disease (PD) is an autosomal recessive disorder by a deficiency of acid α‐glucosidase (GAA) with intralysosomal glycogen accumulation in multiple tissues. We present the case of a 5‐month‐old male with hypertrophic cardiomyopath
Externí odkaz:
https://doaj.org/article/1d4d719b65a24738b6cb1df1be263651
Autor:
Antonio Zamora-Chávez, Argelia Escobar-Sánchez, Stanislaw Sadowinski-Pine, Omar Josué Saucedo-Ramírez, Palmira Delgado-Barrera, Claudia G. Enríquez-Quiñones
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 72, Iss 5, Pp 325-332 (2015)
Introducción: La incontinencia pigmenti es una enfermedad genética rara ligada al cromosoma X, letal en el varón, que afecta a todos los tejidos derivados del ectodermo, como piel, faneras, ojos, dientes y sistema nervioso central, y presenta alte
Externí odkaz:
https://doaj.org/article/435a1dc2060348cbaae1911b79bca0bb
Autor:
Argelia Escobar-Sánchez, Alicia G. Aguilar-Navarro, Emina Torlakovic, Louise E. Purton, Vivienne I. Rebel, John E. Dick, Dita Gratzinger, Eugenia Flores-Figueroa, Fany G. Juárez-Aguilar, Elisa Dorantes-Acosta, Berenice Meza-León
Publikováno v:
Experimental hematology. 100
Bone marrow stromal cells (BMSCs) are a key part of the hematopoietic niche. Mouse and human BMSCs are recognized by different markers (LepR and NGFR/CD271, respectively). However, there has not been a detailed in situ comparison of both populations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::298467f99769163a0572efbc6cb15bac
https://pubmed.ncbi.nlm.nih.gov/34228982
https://pubmed.ncbi.nlm.nih.gov/34228982
Autor:
Arturo Ramírez-Pacheco, Luis E. Juárez-Villegas, María Argelia Escobar-Sánchez, Silvia Selene Moreno-Guerrero, Alfonso Reyes-López, Juan José Luis Sienra-Monge, Pilar Eguía-Aguilar, Gabriela Hernández-Pliego, Luz María Rocha-Ramírez
Publikováno v:
Cancers
Volume 13
Issue 3
Cancers, Vol 13, Iss 529, p 529 (2021)
Volume 13
Issue 3
Cancers, Vol 13, Iss 529, p 529 (2021)
Simple Summary Neuroblastoma (NB) presents diverse biological and clinical characteristics, from spontaneous regression to highly malignant and aggressive unfavorable tumors that condition the therapeutic failure of conventional treatments. The tumor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fce0f22171b265a3dc05421ad80fcb5
Autor:
Israel Parra-Ortega, Luis E. Juárez-Villegas, Argelia Escobar-Sánchez, Elisa Dorantes-Acosta, Alberto Saucedo-Campos, Sonia Ramírez-Pérez, Alejandro Islas-Pérez, Briceida López-Martínez
Publikováno v:
Boletin medico del Hospital Infantil de Mexico. 77(6)
Background"Rare subgroups of pediatric patients with acute myeloid leukemia (AML), such as t(16:21) (p11;q22), require international cooperation to establish a proper stratification system to assign clinical risk.Here, we report a 13-year-old female
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b85f0c2a413c6b27db277c28870ea8ad
https://pubmed.ncbi.nlm.nih.gov/33186348
https://pubmed.ncbi.nlm.nih.gov/33186348
Akademický článek
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Autor:
Omar Josué Saucedo-Ramírez, Palmira Delgado-Barrera, Antonio Zamora-Chávez, Stanislaw Sadowinski-Pine, Claudia G. Enríquez-Quiñones, Argelia Escobar-Sánchez
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 72, Iss 5, Pp 325-332 (2015)
ResumenIntroducciónLa incontinencia pigmenti es una enfermedad genética rara ligada al cromosoma X, letal en el varón, que afecta a todos los tejidos derivados del ectodermo, como piel, faneras, ojos, dientes y sistema nervioso central, y presenta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adbaa669687935b8e88df1131d48c14c
https://doi.org/10.1016/j.bmhimx.2015.08.003
https://doi.org/10.1016/j.bmhimx.2015.08.003
Autor:
Bertha Lilia Romero-Baizabal, Jaime Nieto-Zermeño, Ebenezer Viridiana Cruz-Romero, María Argelia Escobar-Sánchez
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 72, Iss 4, p 296 (2015)
En el articulo titulado ‘‘Malformacion congenita de la via aerea tipo I’’ publicado en el Boletin Medico del Hospital Infantil de Mexico, Bol Med Hosp Infant Mex. 2015;72(3):199-207, se ha detectado el siguiente error: En la pagina 206, donde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d77041aaec971601fa726751e199245
http://www.sciencedirect.com/science/article/pii/S166511461500194X
http://www.sciencedirect.com/science/article/pii/S166511461500194X
Autor:
Antonio, Zamora-Chávez, Argelia, Escobar-Sánchez, Stanislaw, Sadowinski-Pine, Omar Josué, Saucedo-Ramírez, Palmira, Delgado-Barrera, Claudia G, Enríquez-Quiñones
Publikováno v:
Boletin medico del Hospital Infantil de Mexico. 72(5)
Incontinentia pigmenti is a rare, X-linked genetic disease and affects all ectoderm-derived tissues such as skin, appendages, eyes, teeth and central nervous system as well as disorders of varying degree of cellular immunity characterized by decreasi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3a39dadcdc885f79c81c32c1929f3ad0
https://pubmed.ncbi.nlm.nih.gov/29421531
https://pubmed.ncbi.nlm.nih.gov/29421531
Autor:
Jaime, Nieto-Zermeño, Ebenezer Viridiana, Cruz-Romero, Bertha Lilia, Romero-Baizabal, María Argelia, Escobar-Sánchez
Publikováno v:
Boletin medico del Hospital Infantil de Mexico. 72(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1d26cd8895428d77338cc62a2fe0b16b
https://pubmed.ncbi.nlm.nih.gov/29421503
https://pubmed.ncbi.nlm.nih.gov/29421503