Zobrazeno 1 - 10
of 50
pro vyhledávání: '"María del Carmen Castro-Mujica"'
Autor:
María del Carmen Castro-Mujica, Juan C. Gómez de la Torre, Jorge E. La Serna-Infantes, Daniella Arenas Siles
Publikováno v:
Revista de la Facultad de Medicina Humana, Vol 22, Iss 4, Pp 841-856 (2022)
Heart disease is the cause of sudden death in more than 80% of cases. Ischemic heart disease is the cause for 90% of all sudden cardiac deaths, while in the remaining 10% of cases, heart diseases have a hereditary origin and comprise a wide spectrum
Externí odkaz:
https://doaj.org/article/483ed3a4c833416cb8bbc3aa927f109c
Publikováno v:
Revista de la Facultad de Medicina Humana, Vol 22, Iss 3, Pp 589-605 (2022)
To understand the term genomic heterogeneity in prostate cancer, we must understand the clonal genomic evolution of cancer, as well as knowing that it is a dynamic and evolutionary phenomenon. Knowing the genome of prostate cancer not only allows us
Externí odkaz:
https://doaj.org/article/1a4167a0ac3f408b93a3851361ef69d7
Publikováno v:
Revista de la Facultad de Medicina Humana, Vol 21, Iss 2, Pp 399-416 (2021)
Today, the number of genetic diseases is around 10000 conditions, affecting to 6%-8% of all populations. This review shows us how the discovery of genetic variants in our genome, this facilitated to know with precision about the mechanisms physiopath
Externí odkaz:
https://doaj.org/article/7928e03455b04186a646e4032a3ead66
Autor:
Juan Carlos Lizarzaburu-Robles, Juan Carlos Gomez-de-la-Torre, María del Carmen Castro-Mujica, Flor Vento, Sofia Villanes, Elizabeth Salsavilca, Chris Guerin
Publikováno v:
Clinical Diabetes and Endocrinology, Vol 6, Iss 1, Pp 1-5 (2020)
Abstract Background Prevalence of maturity-onset diabetes of the young (MODY) is estimated between 1 and 2% of all diabetes cases. In Latin-America little information has been described about the frequency of the disease, perhaps due to limited acces
Externí odkaz:
https://doaj.org/article/93a5d47a713542c3a0266834e9ac992f
Publikováno v:
Revista de la Facultad de Ciencias Médicas de Córdoba, Vol 79, Iss 1 (2022)
Introduction: Cancer is the second leading cause of death worldwide, with 70% of cancer deaths occurring in low- or middle- income countries. To mitigate the mortality of this disease, it is recommended the evaluation of multiple high-penetrance gene
Externí odkaz:
https://doaj.org/article/14b0ebc7a8d0458f8a5fd4f08fcf417e
Autor:
Claudia Fiorella Barletta Carrillo, Julio Antonio Poterico Rojas, Carlos Barrionuevo Cornejo, Sandro Casavilca Zambrano, Alcides Pinedo Cárdenas, Isela Quispe Santibañez, María del Carmen Castro Mujica
Publikováno v:
Revista de la Facultad de Ciencias Médicas de Córdoba, Vol 75, Iss 4, Pp 303-309 (2018)
El cáncer medular de tiroides (CMT) es un tumor maligno de las células C parafoliculares secretoras de calcitonina. Se estima que el 25% de los casos de CMT se asocian a variantes patogénicas a nivel de línea germinal en el protooncogen RET (locu
Externí odkaz:
https://doaj.org/article/c910c18e500c4629b145531517f588b2
Autor:
María del Carmen Castro-Mujica, Claudia Barletta-Carrillo, Julio A. Poterico, Marisa Acosta, Jesús Valer, Miguel De La Cruz
Publikováno v:
Revista Peruana de Medicina Experimental y Salud Pública, Vol 34, Iss 4, Pp 744-50 (2017)
El síndrome Gorlin (SG) es una condición genética, con patrón de herencia autosómico dominante, con penetrancia completa y expresividad variable, debida a mutaciones germinales en los genes PTCH1 o SUFU, los cuales son componentes de la vía mol
Externí odkaz:
https://doaj.org/article/8f5fce7abd6143eb97f473aacbd56de3
Publikováno v:
Revista de la Facultad de Ciencias Médicas de Córdoba, Vol 77, Iss 4, Pp 385-386 (2020)
Sr. Editor, La Red Nacional Integral del Cáncer (NCCN) ha determinado que ante la sospecha de un síndrome de predisposición al cáncer, es necesario referir al paciente a evaluación genética debido a las implicancias en el diagnóstico y manejo,
Externí odkaz:
https://doaj.org/article/3b7b215aec084ae4af948c2198c0be3c
Autor:
Juan Carlos Lizarzaburu-Robles, Juan Carlos Gomez-de-la-Torre, María del Carmen Castro-Mujica, Flor Vento, Sofia Villanes, Elizabeth Salsavilca, Chris Guerin
Publikováno v:
Clinical Diabetes and Endocrinology, Vol 6, Iss 1, Pp 1-1 (2020)
It was highlighted that the original article [1] contained an error regarding the nomenclature in the gene described.
Externí odkaz:
https://doaj.org/article/28a26ce3e06146a7b2db549c6093b400
Autor:
Yasser Sullcahuaman-Allende, María del Carmen Castro-Mujica, Roberto Mejía Farro, Carlos A. Castañeda, Miluska Castillo, Ketty Dolores-Cerna, Ebert Poquioma
Publikováno v:
Revista Peruana de Medicina Experimental y Salud Pública, Vol 32, Iss 3, Pp 509-514 (2015)
In order to determine the sociodemographic characteristics of human papillomavirus (HPV) in patients referred to the National Institute of Neoplastic Diseases (INEN) between 2012-2014, the detection of HPV in cervical cells was performed by polymeras
Externí odkaz:
https://doaj.org/article/2a5720c7b0b143fb94d08531e4da67a1