Zobrazeno 1 - 10
of 11
pro vyhledávání: '"César Zavala-Hernández"'
Autor:
Marion Echenagucía-Echenagucía, Rocío Trueba-Gómez, Fany Rosenfeld-Mann, César Zavala-Hernández, Carlos Martínez-Murillo, Aurora de la Peña-Díaz
Publikováno v:
Gaceta Médica de México, Vol 157, Iss 93 (2021)
Externí odkaz:
https://doaj.org/article/a00f375a84ad4781994aeea859723c52
Autor:
Marion Echenagucía-Echenagucía, Rocío Trueba-Gómez, Fany Rosenfeld-Mann, César Zavala-Hernández, Carlos Martínez-Murillo, Aurora de la Peña-Díaz
Publikováno v:
Gaceta Médica de México. 157
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2535c103df37f584619c07b284216ed8
https://doi.org/10.24875/gmm.m21000489
https://doi.org/10.24875/gmm.m21000489
Autor:
Elba Reyes-Maldonado, Jaime García-Chávez, César Zavala-Hernández, Abraham Majluf-Cruz, Edgar Hernández-Zamora, Carlos Martínez-Murillo, Jorge Vela-Ojeda
Publikováno v:
Annals of Vascular Surgery. 29:1625-1632
Background To identify inherited factors: Protein C (PC), protein S (PS), antithrombin (AT), plasminogen (Plg), the activated PC resistance (APCR), prothrombin (PT) mutation G20210 A (PTG20210 A) and methylenetetrahydrofolate reductase C677 T polymor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fa66a7bbf846f10a7a7d7b333485ffc
https://doi.org/10.1016/j.avsg.2015.05.035
https://doi.org/10.1016/j.avsg.2015.05.035
Autor:
Elba Reyes-Maldonado, César Zavala-Hernández, Luis Antonio Meillón-García, Gabriela Cesarman-Maus, Edgar Hernández-Zamora, Guadalupe Montiel-Manzano, Eduardo Ramírez-San Juan
Publikováno v:
Annals of Vascular Surgery. 29:222-226
Background To determine the activity of antithrombin (AT), protein C (PC), and protein S (PS), as well as the frequency of deficiencies of these proteins in a population of healthy Mexican mestizo blood donors. Methods AT, PC, and PS were determined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6ff93e960ceb9e5b5a534f8a2131b10
https://doi.org/10.1016/j.avsg.2014.09.023
https://doi.org/10.1016/j.avsg.2014.09.023
Autor:
Elba Reyes-Maldonado, Sandra Quintana-González, Edgar Hernández-Zamora, César Zavala-Hernández
Publikováno v:
Instituto Politécnico Nacional
IPN
Redalyc-IPN
Cirugía y Cirujanos (México) Num.3 Vol.83
IPN
Redalyc-IPN
Cirugía y Cirujanos (México) Num.3 Vol.83
ResumenAntecedentesLa enfermedad de von Willebrand es el trastorno hereditario más frecuente de las proteínas de la coagulación en los seres humanos. Existen 3 tipos: 1, 2A, 2B, 2N, 2M, y 3. Está asociada a mutaciones en el cromosoma 12, en la re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bfacbc13368cd0d2ad02c873018dbf2
https://www.redalyc.org/articulo.oa?id=66242705015
https://www.redalyc.org/articulo.oa?id=66242705015
Autor:
Edgar Hernández-Zamora PhD, Armando Odiseo Rodríguez-Olivas PhD, Erika Rosales-Cruz MSc, Marlene Alejandra Galicia-Alvarado MSc, Cesar Zavala-Hernández PhD, Elba Reyes-Maldonado PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 29 (2023)
Background Legg–Calvé–Perthes disease (LCPD) is a pediatric disorder that occurs due to the avascular necrosis of the femoral head and affects the range of motion of the hip in various degrees. Its etiology is still unknown, although it has been
Externí odkaz:
https://doaj.org/article/a82f85366ef34f618f08d2907c8869e4
Autor:
Edgar Hernández-Zamora, César Zavala-Hernández, Martha Eva Viveros-Sandoval, Ángeles Ochoa-Rico, Carlos Martínez-Murillo, Elba Reyes-Maldonado
Publikováno v:
Universidad Michoacana de San Nicolás de Hidalgo
UMICH
Redalyc-UMICH
Instituto Politécnico Nacional
IPN
Redalyc-IPN
Cirugía y Cirujanos (México) Num.6 Vol.82
UMICH
Redalyc-UMICH
Instituto Politécnico Nacional
IPN
Redalyc-IPN
Cirugía y Cirujanos (México) Num.6 Vol.82
"Antecedentes: la enfermedad de von Willebrand es un padecimiento hereditario en el que la estructura, función y concentración del factor de von Willebrand están alteradas y, en consecuencia, también la interacción plaqueta-factor de von Willebr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::05379f7435ccfbec8a419e9c868da59b
http://www.redalyc.org/articulo.oa?id=66232466003
http://www.redalyc.org/articulo.oa?id=66232466003
Autor:
Edgar Hernández-Zamora, César Zavala-Hernández, Elba Reyes-Maldonado, Sandra Quintana-González
Publikováno v:
Cirugia y cirujanos. 83(3)
Background von Willebrand disease is the most common inherited disorder of the coagulation proteins in humans. There are three types: 1, 2A, 2B, 2N, 2M and 3. It is associated with mutations on chromosome 12 in the region p13.2, encoding the von Will
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74bb646d00cc152a7cbf9367fde90f10
https://pubmed.ncbi.nlm.nih.gov/26055290
https://pubmed.ncbi.nlm.nih.gov/26055290
Autor:
César Zavala-Hernández, Elba Reyes-Maldonado, Martha G. Del Valle-Cabrera, Camilo Ríos, César Casiano-Rosas, Jesús K. Yamamoto-Furusho, María de la Luz Arenas-Sordo, Edgar Hernández-Zamora
Publikováno v:
Genetic testing and molecular biomarkers. 16(8)
Cerebral palsy (CP) is a persistent motor disorder that appears before the patient is 3 years old due to a nonprogressive interference in the brain's development which takes place before the central nervous system growth is complete. Causes of this h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::291073ff44e0bb8decd8b9e7ec129e66
https://pubmed.ncbi.nlm.nih.gov/22587599
https://pubmed.ncbi.nlm.nih.gov/22587599
Autor:
César, Zavala Hernández, Edgar, Hernández Zamora, Carlos, Martínez Murillo, María de la Luz, Arenas Sordo, Ana Elena, González Orozco, Elba, Reyes Maldonado
Publikováno v:
Cirugia y cirujanos. 78(2)
Leiden and Cambridge factor V coagulation mutations and activated protein C resistance (RaPC) are alterations related with vein and artery thrombosis. In this study we aimed to determine whether RaPC is associated with the presence of Leiden and Camb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::630ad2326d1a7410e490a77f8f63479e
https://pubmed.ncbi.nlm.nih.gov/20478113
https://pubmed.ncbi.nlm.nih.gov/20478113