Zobrazeno 1 - 10
of 237
pro vyhledávání: '"César Paz y Miño"'
Autor:
Edwin Dávila
Publikováno v:
Práctica Familiar Rural, Vol 4, Iss 3 (2019)
Para quienes estamos relacionados con el tratamiento y toma de decisiones en asuntos de ética médica y bioética, la recopilación de artículos que hace César Paz y Miño en este libro de su autoría, merece toda la atención posible. Desde algun
Externí odkaz:
https://doaj.org/article/bb38f9c5988448e4a8367fd65d3a9123
Autor:
César Paz-y-Miño, Ramón Miguel Vargas-Vera, Martha Verónica Placencia-Ibadango, Kalid Stefano Vargas-Silva, Juan Luis García-Hernández, Thalía Balarezo-Díaz, Paola E. Leone
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-9 (2024)
Abstract We present the case of a 7-year-old Ecuadorian mestizo girl with multiple orofacial malformations. The patient is the product of a first-degree relationship (father–daughter). A cytogenetic study revealed a normal karyotype. The genetic ma
Externí odkaz:
https://doaj.org/article/e5cb558d8c9a49de8358bb127227dc23
Autor:
Paola E. LEONE, César PAZ-Y-MIÑO
Publikováno v:
Chasqui, Vol 1, Iss 145, Pp 301-310 (2020)
Los pilares fundamentales de la ciencia son la investigación científica, la tecnología y la innovación (C+T+I). Sin el desarrollo de cada uno de estos aspectos, los resultados y aportes científicos de un país se ven limitados. En Ecuador la rea
Externí odkaz:
https://doaj.org/article/4bd79828531c450ca08e961a897ca976
Autor:
Paola E. Leone, Verónica Yumiceba, Ariana Jijón-Vergara, Andy Pérez-Villa, Isaac Armendáriz-Castillo, Jennyfer M. García-Cárdenas, Santiago Guerrero, Patricia Guevara-Ramírez, Andrés López-Cortés, Ana K. Zambrano, Jesús M. Hernández-Rivas, Juan Luis García, César Paz-y-Miño
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-9 (2020)
Abstract Background Turner syndrome is a genetic disorder that affects women. It is caused by an absent or incomplete X chromosome, which can be presented in mosaicism or not. There are 12 cases of Turner syndrome patients who present structural alte
Externí odkaz:
https://doaj.org/article/2c3597f4f75d4d4f90fb70e2316006d5
Autor:
José R. Sandoval, Daniela R. Lacerda, Marilza M. S. Jota, Paulo Robles-Ruiz, Pierina Danos, César Paz-y-Miño, Spencer Wells, Fabrício R. Santos, Ricardo Fujita
Publikováno v:
BMC Genomics, Vol 21, Iss S7, Pp 1-10 (2020)
Abstract Background According to history, in the pre-Hispanic period, during the conquest and Inka expansion in Ecuador, many Andean families of the Cañar region would have been displaced to several places of Tawantinsuyu, including Kañaris, a Quec
Externí odkaz:
https://doaj.org/article/802104e8b1cb40ddaf34b0168a9228ff
Autor:
Andrés López-Cortés, Ana Karina Zambrano, Patricia Guevara-Ramírez, Byron Albuja Echeverría, Santiago Guerrero, Eliana Cabascango, Andy Pérez-Villa, Isaac Armendáriz-Castillo, Jennyfer M. García-Cárdenas, Verónica Yumiceba, Gabriela Pérez-M, Paola E. Leone, César Paz-y-Miño
Publikováno v:
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-9 (2020)
Abstract Background Congenital insensitivity to pain with anhidrosis (CIPA) is an extremely rare autosomal recessive disorder characterized by insensitivity to pain, inability to sweat and intellectual disability. CIPA is caused by mutations in the n
Externí odkaz:
https://doaj.org/article/44654014f34642bfb39137e3cbfaf637
Autor:
Jennyfer M. García-Cárdenas, Ana Karina Zambrano, Patricia Guevara-Ramírez, Santiago Guerrero, Gabriel Runruil, Andrés López-Cortés, Jorge P. Torres-Yaguana, Isaac Armendáriz-Castillo, Andy Pérez-Villa, Verónica Yumiceba, Paola E. Leone, César Paz-y-Miño
Publikováno v:
Journal of Medical Case Reports, Vol 14, Iss 1, Pp 1-9 (2020)
Abstract Background Anaplastic astrocytoma is a rare disorder in children from 10 to 14 years of age, with an estimated 0.38 new cases per 100,000 people per year worldwide. Panel-based next-generation sequencing opens new possibilities for diagnosis
Externí odkaz:
https://doaj.org/article/884ad400612d4525b37218f182fd26d8
Autor:
César Paz-y-Miño, Ana Proaño, Stella D. Verdezoto, Juan Luis García, Jesús María Hernández-Rivas, Paola E. Leone
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-9 (2019)
Abstract Background Since 1969, 49 cases have been presented on ring chromosome 4. All of these cases have been characterized for the loss of genetic material. The genes located in these chromosomal regions are related to the phenotype. Case presenta
Externí odkaz:
https://doaj.org/article/353ade6327964c5486791893cb80a856
Autor:
Andrés López-Cortés, Patricia Guevara-Ramírez, Nikolaos C. Kyriakidis, Carlos Barba-Ostria, Ángela León Cáceres, Santiago Guerrero, Esteban Ortiz-Prado, Cristian R. Munteanu, Eduardo Tejera, Doménica Cevallos-Robalino, Ana María Gómez-Jaramillo, Katherine Simbaña-Rivera, Adriana Granizo-Martínez, Gabriela Pérez-M, Silvana Moreno, Jennyfer M. García-Cárdenas, Ana Karina Zambrano, Yunierkis Pérez-Castillo, Alejandro Cabrera-Andrade, Lourdes Puig San Andrés, Carolina Proaño-Castro, Jhommara Bautista, Andreina Quevedo, Nelson Varela, Luis Abel Quiñones, César Paz-y-Miño
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Background: There is pressing urgency to identify therapeutic targets and drugs that allow treating COVID-19 patients effectively.Methods: We performed in silico analyses of immune system protein interactome network, single-cell RNA sequencing of hum
Externí odkaz:
https://doaj.org/article/12ff2b56580a4125942a16060c739b52
Autor:
Verónica Yumiceba, Andrés López-Cortés, Andy Pérez-Villa, Iván Yumiseba, Santiago Guerrero, Jennyfer M. García-Cárdenas, Isaac Armendáriz-Castillo, Patricia Guevara-Ramírez, Paola E. Leone, Ana Karina Zambrano, César Paz-y-Miño
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Polycystic ovary syndrome (PCOS) is a heterogeneous endocrine disorder characterized by hyperandrogenism, ovulatory dysfunction, and polycystic ovaries. Epidemiological findings revealed that women with PCOS are prone to develop certain cancer types
Externí odkaz:
https://doaj.org/article/1fde78d31453495893dd95c3efec6705