Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Sergio Cuevas Covarrubias"'
Autor:
Jaime Toral López, Sandra Gómez Martinez, María del Refugio Rivera Vega, Edgar Hernández-Zamora, Sergio Cuevas Covarrubias, Belem Arely Ibarra Castrejón, Luz María González Huerta
Publikováno v:
Biology, Vol 13, Iss 3, p 173 (2024)
Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal dysplasia characterized by persistent open skull sutures with bulging calvaria, hypoplasia, or aplasia of clavicles permitting abnormal opposition of the shoulders; wide public symphysis
Externí odkaz:
https://doaj.org/article/c7952edb2e9a472cada4ff3df044f6ba
Autor:
Sergio Cuevas-Covarrubias
Publikováno v:
Revista Médica del Hospital General de México, Vol 86, Iss 2 (2023)
Externí odkaz:
https://doaj.org/article/7cba693013494d2f98226f8edd383024
Autor:
Flavia Morales-Vásquez, Rocío Castillo-Sánchez, María J. Gómora, Miguel Ángel Almaraz, Enrique Pedernera, Delia Pérez-Montiel, Elizabeth Rendón, Horacio Noé López-Basave, Edgar Román-Basaure, Sergio Cuevas-Covarrubias, Juan Maldonado-Cubas, Antonio Villa, Carmen Mendez
Publikováno v:
Journal of Ovarian Research, Vol 13, Iss 1, Pp 1-10 (2020)
Abstract Background The current study evaluated the metalloproteinases MMP-2 and MMP-9 expression in epithelial cells and the surrounding stroma in ovarian tumors and the association of MMPs with the histological subtypes, the clinical stage and the
Externí odkaz:
https://doaj.org/article/af4bcc4b28d24e92925c5c0999079769
Autor:
Dennise L. Smith-Pellegrin, María R. Rivera-Vega, Jorge R. Cazarín-Barrientos, Aralí Melgarejo-Gómez, Olga M. Messina-Baas, Sergio Cuevas-Covarrubias
Publikováno v:
Revista Médica del Hospital General de México, Vol 84, Iss 4 (2021)
Darier disease is a clinically variable rare disease with autosomal dominant inheritance caused by mutations in ATP2A2 gene. It affects skin, mucous membranes, and nails. The onset of symptoms is during adolescence and persists through adulthood, aff
Externí odkaz:
https://doaj.org/article/6a849eefe5874ac7934fb49b565407b3
Autor:
Eréndira Villanueva-Ortega, María José Garcés-Hernández, Arturo Herrera-Rosas, Juan Carlos López-Alvarenga, Estibalitz Laresgoiti-Servitje, Galileo Escobedo, Gloria Queipo, Sergio Cuevas-Covarrubias, Guadalupe Nayely Garibay-Nieto
Publikováno v:
Annals of Hepatology, Vol 18, Iss 5, Pp 693-700 (2019)
Introduction and Objectives: Non-alcoholic fatty liver disease (NAFLD) is the most common liver disease in children and it is more prevalent in Hispanic males. The gender differences can be explained by body fat distribution, lifestyle, or sex hormon
Externí odkaz:
https://doaj.org/article/8abe6ec0223545cc9b81395f0efda1b6
Autor:
Jaime Toral-López, Luz M. González-Huerta, Mirna Martínez-Saucedo, Olga M. Messina-Baas, Juan Manuel-Valdes, Sergio Cuevas-Covarrubias
Publikováno v:
Revista Médica del Hospital General de México, Vol 84, Iss 1 (2021)
Tetrasomy 18p is characterized by intellectual disability and systemic alterations. The aim of this study is to describe two patients with tetrasomy 18p, one of them with clinical data not previously reported. Genomic DNA was analyzed by multiplex li
Externí odkaz:
https://doaj.org/article/6b11398c258347d7b7208d61f8d3e523
Autor:
Sergio Cuevas-Covarrubias
Publikováno v:
Revista M�dica del Hospital General de M�xico. 83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6b70d716635b786ef8e2ecf988ef6b8
https://doi.org/10.24875/hgmx.m20000037
https://doi.org/10.24875/hgmx.m20000037
Autor:
Mirna, Martínez-Saucedo, Martínez-Saucedo, Mirna, María del Refugio, Rivera-Vega, Rivera-Vega, María Del Refugio, María, Gonzalez--Huerta Luz, Gonzalez-Huerta Luz, María, Héctor, Urueta-Cuellar, Urueta-Cuellar, Héctor, Jaime, Toral-López, Toral-López, Jaime, Pedro, Berruecos-Villalobos, Berruecos-Villalobos, Pedro, Sergio, Cuevas-Covarrubias, Cuevas-Covarrubias, Sergio
Publikováno v:
International journal of pediatric otorhinolaryngology. 79(12)
Background Sensorineural hearing loss (SNHL) is a genetically heterogeneous disease. GJB2 gene mutations seem to be the most frequent cause of hereditary hearing impairment in several populations. There is variability in the mutations in the GJB2 gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76f5a21077787a76fd5fa296858e7c6e
https://pubmed.ncbi.nlm.nih.gov/26553399
https://pubmed.ncbi.nlm.nih.gov/26553399
Autor:
Mirna Martínez-Saucedo, María del Refugio Rivera-Vega, Luz María Gonzalez-Huerta, Héctor Urueta-Cuellar, Jaime Toral-López, Pedro Berruecos-Villalobos, Sergio Cuevas-Covarrubias
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 83:93
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b0e1f9b334e191ab78e8fd997ceb2c1
https://doi.org/10.1016/j.ijporl.2016.02.001
https://doi.org/10.1016/j.ijporl.2016.02.001
Autor:
Martínez-Saucedo M, Rivera-Vega Mdel R, Gonzalez--Huerta Luz M, Urueta-Cuellar H, Toral-López J, Berruecos-Villalobos P, Cuevas-Covarrubias S; Servicio de Genética, Facultad de Medicina, Hospital General de Mexico, Universidad Nacional Autonoma de Mexico, Edo. México, Mexico. Electronic address: sergiocuevasunam@gmail.com.
Publikováno v:
International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2015 Dec; Vol. 79 (12), pp. 2295-9. Date of Electronic Publication: 2015 Oct 28.