Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Rocío Sánchez‐Urbina"'
Autor:
Mari Carmen Moran-Espinosa, Héctor Diaz-García, Rocío Sánchez-Urbina, Javier T. Granados-Riveron, Miriam Deyanira Rodriguez-Piña, Ángeles Leyda Avilés-García, Miguel Ángel Rubio-Leal, Karla Ariadna Martínez-Camacho, Hugo Mendieta-Zeron
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Background Pheochromocytoma is a rare disease, and its familial occurrence is quite uncommon. The aim of this paper is to report a three-generation phenotypical expression of a case familial occurrence of pheochromocytoma. Case presentation
Externí odkaz:
https://doaj.org/article/138b7df97c6e4f0798c6c7a33cae9d9c
Autor:
Maryangel Perea‐Cabrera, Javier T. Granados‐Riveron, Begoña Segura‐Stanford, Liliana M. Moreno‐Vargas, Diego Prada‐Gracia, Mari C. Moran‐Espinosa, Julio Erdmenger, Hector Diaz‐Garcia, Rocío Sánchez‐Urbina
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 9, Pp n/a-n/a (2023)
Abstract Background Opitz GBBB syndrome (GBBB) is an X‐linked disease characterized by midline defects, including congenital heart defects. We present our diagnostic approach to the identification of GBBB in a consanguineous family in which two mal
Externí odkaz:
https://doaj.org/article/ff3b89a49b444ee885443b6b405fec54
Autor:
Arodi Farrera, María Villanueva, Alfredo Vizcaíno, Patricia Medina-Bravo, Norma Balderrábano-Saucedo, Mariana Rives, David Cruz, Elizabeth Hernández-Carbajal, Javier Granados-Riveron, Rocío Sánchez-Urbina
Publikováno v:
Head & Face Medicine, Vol 15, Iss 1, Pp 1-12 (2019)
Abstract Background 22q11.2 deletion syndrome is a medical condition that results from genomic loss at chromosome 22. Affected patients exhibit large variability that ranges from a severe condition to mild symptoms. In addition, the spectrum of clini
Externí odkaz:
https://doaj.org/article/4befd271a73f4c04b2b2a8f0241efdfe
Autor:
Arturo Lopez-Yañez Blanco, Keyla M Díaz-López, Jenny Vilchis-Gil, Hector Diaz-Garcia, Jacqueline Gomez-Lopez, Patricia Medina-Bravo, Javier T Granados-Riveron, Juan M Gallardo, Miguel Klünder-Klünder, Rocío Sánchez-Urbina
Publikováno v:
Nutrients, Vol 14, Iss 4, p 746 (2022)
Overweight and obesity have become a world-health public problem, mainly for developing countries. Both health conditions have a higher prevalence among women of childbearing age. Physiopathology, overweight and obesity are characterized by a chronic
Externí odkaz:
https://doaj.org/article/b5cc14ea440449f39be4017695a7a943
Autor:
Rocío Sánchez-Urbina, Guillermo Aquino-Jarquin, Samara Téllez-Camacho, Mirna Martínez-Saucedo, Javier T. Granados-Riveron
Publikováno v:
Gaceta Médica de México. 156
Traditional peer review is undergoing increasing questioning, given the increase in scientific fraud detected and the replication crisis biomedical research is currently going through. Researchers, academic institutions, and research funding agencies
La revisión por pares pospublicación: otro control de calidad del registro científico en biomedicina
Autor:
Javier T. Granados-Riveron, Samara Téllez-Camacho, Guillermo Aquino-Jarquin, Rocío Sánchez-Urbina, Mirna Martínez-Saucedo
Publikováno v:
Gaceta Médica de México. 156
Autor:
Karla Sarahí Cano-Hernández, Adriana Sánchez-Boiso, Julio Erdmenger-Orellana, Begoña Segura-Stanford, Santiago Nava-Townsend, Rosario Becerra-Becerra, Tania Tamayo-Espinosa, Norma Balderrabano-Saucedo, Liborio Solano-Fiesco, Alejandra Contreras-Ramos, Rocío Sánchez-Urbina
Publikováno v:
Archivos de Cardiología de México. 88:268-276
Objective To determine the prevalence and spectrum of diseases that predispose to sudden cardiac death in Mexican children, and to identify the main early signs and symptoms that can enable the health personnel to suspect these diseases and to refer
Autor:
Carolina Ornelas-Fuentes, Mirna Martínez-Saucedo, Guillermo Aquino-Jarquin, Hector Diaz-Garcia, Mark Dedden, Rodrigo Moreno-Salgado, Rocío Sánchez-Urbina, Javier T. Granados-Riveron
Publikováno v:
The journal of gene medicineREFERENCES. 22(5)
Background Focal dermal hypoplasia (FDH) is rare X-linked dominant disease characterized by atrophy and linear pigmentation of the skin, split hand/foot deformities and ocular anomalies. FDH is caused by mutations of the Porcupine (PORCN) gene, which
Autor:
Javier T. Granados Riverón, Maryangel Perea-Cabrera, Leonardo J. Mejía-Marín, Begoña Segura-Stanford, Rocío Sánchez-Urbina, Julio R. Erdmenger-Orellana, Alejandra Contreras-Ramos, Evelyn G. Alvarado-Terrones, Arturo Lopez-Yañez Blanco, Miguel Klünder-Klünder, Norma Balderrabano-Saucedo, Elizabeth Hernández-Carbajal, G. Díaz-Rosas
Publikováno v:
Archives of Medical Research. 49:109-113
The incidence of total anomalous pulmonary venous connection (TAPVC) in the Caucasian population is 2.5/100,000 live births (LB), and the incidence in the Hispanic population is 19.8/100,000 LB. Without knowing the exact etiology for the development
Autor:
Norma Balderrabano-Saucedo, J A Botello-Flores, Alejandra Contreras-Ramos, G. Díaz-Rosas, Icela Palma-Lara, K A García-Mejía, Ma C Sánchez-Gómez, M Pérez-Díaz Conti, Rocío Sánchez-Urbina, Miguel Klünder-Klünder
Publikováno v:
Pediatric Cardiology. 38:991-1003
Complex congenital heart disease (CHD) affects cardiac blood flow, generating a pressure overload in the compromised ventricles and provoking hypertrophy that over time will induce myocardial dysfunction and cause a potential risk of imminent death.