Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Verónica F, Morán Barroso"'
Autor:
Carlos De la Torre-González, Dina Villanueva-García, Constanza García-Delgado, Salvador Castillo-Castillo, Marisol Huante-Guido, Josefina Chichitz-Madrigal, María E. Juárez-Torres, Ana L. Sánchez-Sandoval, Eira V. Barrón-Palma, Verónica F. Morán-Barroso
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 79, Iss 4 (2022)
Hearing loss is the most frequent sensory disorder, with an incidence of 1:1500 live newborns. In more than 50% of patients, it is associated with a genetic cause, while in up to 30% of cases, it is related to syndromic entities. We performed a liter
Externí odkaz:
https://doaj.org/article/0dabe409cafd42d4819f400ce49b8dad
Autor:
Constanza García-Delgado, Miguel Angel Noriega-Juárez, Alicia Cervantes, José D Abad-Flores, Mirna Toledo-Bahena, Adriana Valencia-Herrera, Carlos A Mena-Cedillos, América Villaseñor-Domínguez, Adriana Sánchez-Boiso, Yumiko Akaki-Carreño, Blanca Del Río-Navarro, Jesús Aguirre-Hernández, Marisol López-López, Marco Cerbón, Verónica F Morán-Barroso, Nancy Monroy-Jaramillo
Publikováno v:
Dermatologica Sinica, Vol 38, Iss 3, Pp 172-175 (2020)
X-linked hypohidrotic ectodermal dysplasia (XLHED) is caused by EDA pathogenic variants. Female carriers show several clinical manifestations in variable percentages. We studied 11 Mexican heterozygous females with an EDA variant. The most frequent s
Externí odkaz:
https://doaj.org/article/483a1ce9046445dbadc08803a0c8a538
Autor:
Silvia Martínez-Valverde, Guillermo Salinas-Escudero, Constanza García-Delgado, Juan Garduño-Espinosa, Verónica F Morán-Barroso, Víctor Granados-García, Ma Teresa Tiro-Sánchez, Filiberto Toledano-Toledano, Ma Vanessa Aldaz-Rodríguez
Publikováno v:
PLoS ONE, Vol 14, Iss 1, p e0208076 (2019)
AimTo examine the burden of out-of-pocket household expenditures and time spent on care by families responsible for children with Down Syndrome (DS).MethodsA cross-sectional analysis was performed after surveying families of children with DS. The chi
Externí odkaz:
https://doaj.org/article/50d698e8d90e4f4d87378ce5e640f5f1
Autor:
Miguel A, Noriega-Juárez, Constanza, García-Delgado, América, Villaseñor-Domínguez, Carlos A, Mena-Cedillos, Mirna, Toledo-Bahena, Adriana, Valencia-Herrera, Patricia, Baeza-Capetillo, Alicia, Cervantes, Verónica F, Morán-Barroso, Nancy, Monroy-Jaramillo
Publikováno v:
Boletin medico del Hospital Infantil de Mexico. 77(4)
Ectodermal dysplasias are a group of genodermatoses characterized by dystrophy of ectodermal derived structures. The most frequent presentation of the ectodermal dysplasias is the hypohidrotic type, which has an incidence of 7/100,000 newborns and ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e72f4b6327e0f7fb27db83fa0ba323c9
https://pubmed.ncbi.nlm.nih.gov/32713954
https://pubmed.ncbi.nlm.nih.gov/32713954
Autor:
Miguel Angel Noriega-Juárez, Alicia Cervantes, Marco Cerbón, Marisol López-López, América Villaseñor-Domínguez, Mirna Toledo-Bahena, Jesús Aguirre-Hernández, José D Abad-Flores, Adriana Sánchez-Boiso, Adriana Valencia-Herrera, Blanca Del Río-Navarro, Carlos Mena-Cedillos, Nancy Monroy-Jaramillo, Verónica F Morán-Barroso, Yumiko I. Akaki-Carreño, Constanza García-Delgado
Publikováno v:
Dermatologica Sinica, Vol 38, Iss 3, Pp 172-175 (2020)
X-linked hypohidrotic ectodermal dysplasia (XLHED) is caused by EDA pathogenic variants. Female carriers show several clinical manifestations in variable percentages. We studied 11 Mexican heterozygous females with an EDA variant. The most frequent s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21d5a16590d4b93d70c15eacfe04fcad
https://doi.org/10.4103/ds.ds_19_20
https://doi.org/10.4103/ds.ds_19_20
Autor:
Constanza García-Delgado, Carlos Serrano-Bello, Verónica F Morán Barroso, Alicia Cervantes, Nayla Y León-Carlos, Ariadna Berenice Morales-Jiménez
Publikováno v:
Archivos Argentinos de Pediatria. 116
In patients with malformations and delayed psychomotor development it is important to discard chromosomopathies. Balanced reciprocal translocations are the most frequent chromosomopathies present in 1:500 live newborns. In general, carriers have norm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ec6b075c32ce4e604978aa52eace88e
https://doi.org/10.5546/aap.2018.e603
https://doi.org/10.5546/aap.2018.e603
Autor:
Nayla Y, León-Carlos, Constanza, García-Delgado, Ariadna B, Morales-Jiménez, Carlos, Serrano-Bello, Alicia, Cervantes, Verónica F, Morán Barroso
Publikováno v:
Archivos argentinos de pediatria. 116(4)
In patients with malformations and delayed psychomotor development it is important to discard chromosomopathies. Balanced reciprocal translocations are the most frequent chromosomopathies present in 1:500 live newborns. In general, carriers have norm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ae3549043ec356817cbca0983bad8740
https://pubmed.ncbi.nlm.nih.gov/30016040
https://pubmed.ncbi.nlm.nih.gov/30016040
Autor:
Adriana, Sánchez-Boiso, Rosenda I, Peñaloza-Espinosa, Eduardo, Castro-Sierra, Ricardo M, Cerda-Flores, Leonora, Buentello-Malo, Rocío, Sánchez-Urbina, Rosa I, Ortiz-de-luna, Benjamín A, Rodríguez-Espino, Fabio A, Salamanca-Gómez, Martha P, Flores-Ayón, Teresita, Salamanca-Vargas, Jesús, Aguirre-Hernández, Elsa, Cerón-Vázquez, Juanita, López-Castillejos, Verónica F, Morán-Barroso
Publikováno v:
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 63(6)
The goals of this population genetics study were to describe mtDNA haplogroups and ABO and Rh blood group systems of 3 Native Mexican populations, to determine their genetic variability, and to compare their haplogroups with those of 13 Native Mexica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8e9e68896fdcb399f1b67cfbebd8384
https://pubmed.ncbi.nlm.nih.gov/23650674
https://pubmed.ncbi.nlm.nih.gov/23650674
Autor:
Martínez-Valverde, Silvia1, Salinas-Escudero, Guillermo1, García-Delgado, Constanza2, Garduño-Espinosa, Juan3, Morán-Barroso, Verónica F.2, Granados-García, Víctor4 vic.granados@gmail.com, Tiro-Sánchez, Ma. Teresa5, Toledano-Toledano, Filiberto6, Aldaz-Rodríguez, Ma. Vanessa7
Publikováno v:
PLoS ONE. 1/10/2019, Vol. 14 Issue 01, p1-13. 13p.
Publikováno v:
Genes; Feb2023, Vol. 14 Issue 2, p238, 51p