Zobrazeno 1 - 6
of 6
pro vyhledávání: '"María Emilia Arteaga-Espinosa"'
Autor:
Yazmina Lascano-Vaca, Esteban Ortiz-Prado, Lenin Gomez-Barreno, Katherine Simbaña-Rivera, Eduardo Vasconez, Alexander Lister, María Emilia Arteaga-Espinosa, Geovanny F. Perez
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-15 (2020)
Abstract Background To carry out a complete clinical, pathological, genetic and microbiological characterization of pediatric patients with molecular confirmed cystic fibrosis (CF) attending the Carlos Andrade Marín Hospital (HCAM) within the study
Externí odkaz:
https://doaj.org/article/ee57ede000d94263a8a564e24dcbdff1
Autor:
Esteban Ortiz-Prado, Ana Lucía Iturralde, Katherine Simbaña-Rivera, Lenin Gómez-Barreno, Iván Hidalgo, Mario Rubio-Neira, Nicolás Espinosa, Juan Izquierdo-Condoy, María Emilia Arteaga-Espinosa, Alex Lister, Andrés López-Cortés, Alejandro Cabrera-Andrade
Publikováno v:
Case Reports in Medicine, Vol 2021 (2021)
Background. The 15q11.1-13.1 duplication, also known as Dup15q syndrome, is a rare congenital disease affecting 1 in 30,000 to 1 in 60,000 children worldwide. This condition is characterized by the presence of at least one extra copy of genetical mat
Externí odkaz:
https://doaj.org/article/a3aad1774df84274a0e446d22906ec17
Publikováno v:
Revista Ecuatoriana de Pediatría. 22
Introducción: El síndrome de Noonan es un trastorno genético de herencia autosómica dominante con una expresión fenotípica variable. Se encuentra dentro de las enfermedades conocidas como rasopatías, producidas por las mutaciones en los genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09772d993f92252c0789442a703693bc
https://doi.org/10.52011/93
https://doi.org/10.52011/93
Autor:
Katherine Simbaña-Rivera, Nicolás Espinosa, Andrés López-Cortés, Lenin Gómez-Barreno, Alejandro Cabrera-Andrade, María Emilia Arteaga-Espinosa, Ana Lucia Iturralde, Alex Lister, Esteban Ortiz-Prado, Juan S. Izquierdo-Condoy, Iván Hidalgo, Mario Rubio-Neira
Publikováno v:
Case Reports in Medicine
Case Reports in Medicine, Vol 2021 (2021)
Case Reports in Medicine, Vol 2021 (2021)
Background. The 15q11.1-13.1 duplication, also known as Dup15q syndrome, is a rare congenital disease affecting 1 in 30,000 to 1 in 60,000 children worldwide. This condition is characterized by the presence of at least one extra copy of genetical mat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbc6258a26a1a1eb46cd4dd84a9fc9bd
http://europepmc.org/articles/PMC8110389
http://europepmc.org/articles/PMC8110389
Autor:
Eduardo Vasconez, Katherine Simbaña-Rivera, Alex Lister, Geovanny F. Perez, María Emilia Arteaga-Espinosa, Lenin Gómez-Barreno, Esteban Ortiz-Prado, Yazmina Lascano-Vaca
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-15 (2020)
BMC Pediatrics
BMC Pediatrics
BackgroundTo carry out a complete clinical, pathological, genetic and microbiological characterization of pediatric patients with molecular confirmed cystic fibrosis (CF) attending the Carlos Andrade Marín Hospital (HCAM) within the study period.Met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b31bc46e056d1fa7d9586f6521183d5
https://doi.org/10.21203/rs.2.12767/v2
https://doi.org/10.21203/rs.2.12767/v2
Autor:
Esteban Ortiz-Prado, Katherine Simbaña-Rivera, Eduardo Vasconez, Yazmina Lascano-Vaca, Geovanny F. Perez, Lenin Gómez-Barreno, María Emilia Arteaga-Espinosa, Alex Lister
Summary Objective To characterize the epidemiology and the clinical, pathological, microbiological and genetical profile of children with cystic fibrosis treated in Ecuador. Methods We conducted a cross-sectional analysis of the pediatric population
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e577f101f17ce241af0c1a3f4f8167f9
https://doi.org/10.21203/rs.2.12767/v1
https://doi.org/10.21203/rs.2.12767/v1