Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Stanislaw Sadowinski Pine"'
Autor:
Alejandro Azamar, Carlos De la Torre-González, Luis Juárez-Villegas, Stanislaw Sadowinski-Pine, Hiram Álvarez-Neri
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 78, Iss 5 (2021)
Background: A relatively frequent clinical finding in children is an asymmetric tonsil, which can have multiple etiological possibilities, including a malignant disease. The clinical finding of tonsillar asymmetry is found in approximately 2% of the
Externí odkaz:
https://doaj.org/article/98b45b1f9cc64e10afb49f9e980665c1
Autor:
Jesús Aguirre-Hernández, Stanislaw Sadowinski-Pine, Ernesto Alarcón-Cabrera, Edwin Manolo Alarcón-De la Luz, Eduardo Javier Barragán-Pérez, Verónica Joomayra Quintana-Vega
Publikováno v:
Acta Pediátrica de México. 43:353-357
INTRODUCCIÓN: Durante las dos últimas décadas, el avance de técnicas de análisis molecular, así como de la terapia génica, han generado cambios en la manera de abordar las enfermedades neuromusculares. Las miopatías congénitas (MC) son un gr
Autor:
Fabiola Jimena Pérez-Linares, Mario Pérezpeña-Diazconti, Jorge García-Quintana, Guillermina Baay-Guzmán, Lourdes Cabrera-Muñoz, Stanislaw Sadowinski-Pine, Carlos Serrano-Bello, Marco Murillo-Maldonado, Alejandra Contreras-Ramos, Pilar Eguía-Aguilar
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Wilms tumor (WT) is the most frequently diagnosed malignant renal tumor in children. With current treatments, ~90% of children diagnosed with WT survive and generally present with tumors characterized by favorable histology (FHWT), whereas prognosis
Externí odkaz:
https://doaj.org/article/efa1d6fba8ea4406887a2752a3b59e95
Autor:
Blanca Elena Castro-Magdonel, Manuela Orjuela, Diana E Alvarez-Suarez, Javier Camacho, Lourdes Cabrera-Muñoz, Stanislaw Sadowinski-Pine, Aurora Medina-Sanson, Citlali Lara-Molina, Daphne García-Vega, Yolanda Vázquez, Noé Durán-Figueroa, María de Jesús Orozco-Romero, Adriana Hernández-Ángeles, M Verónica Ponce-Castañeda
Publikováno v:
PLoS ONE, Vol 15, Iss 4, p e0231394 (2020)
miRNAs regulate post-transcriptional gene expression in metazoans, and thus are involved in many fundamental cellular biological processes. Extracellular miRNAs are also found in most human biofluids including plasma. These circulating miRNAs constit
Externí odkaz:
https://doaj.org/article/5a4f5e4c97e1481b8a7d488201703f3b
Autor:
Blanca Elena Castro-Magdonel, Manuela Orjuela, Javier Camacho, Adda Jeanette García-Chéquer, Lourdes Cabrera-Muñoz, Stanislaw Sadowinski-Pine, Noé Durán-Figueroa, María de Jesús Orozco-Romero, Ana Claudia Velázquez-Wong, Adriana Hernández-Ángeles, Claudia Hernández-Galván, Citlali Lara-Molina, M. Verónica Ponce-Castañeda
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-12 (2017)
Abstract Background miRNAs exert their effect through a negative regulatory mechanism silencing expression upon hybridizing to their target mRNA, and have a prominent position in the control of many cellular processes including carcinogenesis. Previo
Externí odkaz:
https://doaj.org/article/46c3dbf14b774bcea40db8fdf217d4bc
Autor:
Salvador Villalpando Carrión, Mariana Xail Espriu Ramírez, Bertha Lilia Romero Baizabal, Stanislaw Sadowinski-Pine
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 73, Iss 2, Pp 129-138 (2016)
Externí odkaz:
https://doaj.org/article/751a8e73af57467a93a5e4ba1d2142d1
Autor:
Antonio Zamora-Chávez, Stanislaw Sadowinski-Pine, Carlos Serrano-Bello, Luis Velázquez-Jones, Omar Josué Saucedo-Ramírez, Jonathan Palafox-Flores, Erandi Josefina Mata-Vázquez
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 73, Iss 2, Pp 117-128 (2016)
Introducción: La sarcoidosis es una enfermedad sistémica de etiología desconocida que raramente se presenta en la infancia. Generalmente afecta los pulmones; sin embargo, puede involucrar diversos órganos. Ocasionalmente afecta el estado general,
Externí odkaz:
https://doaj.org/article/f0169dbb7c094af8b4fa778c419269b6
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:
Sigifredo Pedraza-Sánchez, Jose Luis Lezana-Fernández, Yolanda Gonzalez, Luis Martínez-Robles, María Laura Ventura-Ayala, Stanislaw Sadowinski-Pine, Margarita Nava-Frías, Sarbelio Moreno-Espinosa, Jean-Laurent Casanova, Anne Puel, Stephanie Boisson-Dupuis, Martha Torres
Publikováno v:
Frontiers in Immunology, Vol 8 (2017)
In humans, recessive loss-of-function mutations in STAT1 are associated with mycobacterial and viral infections, whereas gain-of-function (GOF) mutations in STAT1 are associated with a type of primary immunodeficiency related mainly, but not exclusiv
Externí odkaz:
https://doaj.org/article/84abefc6d80f44b3bdbeca633d2699ab
Autor:
Miguel Ángel Palomo-Colli, Stanislaw Sadowinski-Pine, Luis E. Juárez-Villegas, Alfonso Pérez-Bañuelos, José Félix Gaytán-Morales, Mónica Mier-Cabrera
Publikováno v:
Gaceta Mexicana de Oncolog�a. 19