Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Rita Gómez"'
Autor:
Ma. de Lourdes Basurto, Miguel Abdo-Francis, Carlos A. Aguilar-Salinas, Lourdes J. Balcázar-Hernández, Gabriela Borrayo-Sánchez, Graciela E. Castro-Narro, Adolfo Chávez-Negrete, Alejo Díaz-Aragón, José M. Enciso-Muñoz, Carlos Fernández-Barros, Aldo Ferreira-Hermosillo, Antonio González-Chávez, Arturo Guerra-López, Rita Gómez-Díaz, Mario Molina-Ayala, César Rodríguez-Gilabert, Juan C. Tomás-López, Héctor R. Vargas-Sánchez, Edith Ruiz-Gastelum
Publikováno v:
Gaceta Médica de México, Vol 160, Iss 4 (2024)
La enfermedad cardiovascular es la principal causa de mortalidad en México y en el mundo; la dislipidemia constituye uno de los principales factores de riesgo. Pese a la importancia de su impacto epidemiológico, entre los médicos de primer contact
Externí odkaz:
https://doaj.org/article/79a257c862184a95a3f73cd64b36069e
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 2, Iss 4, Pp 292-296 (2014)
Abstract Inactivating mutations of the 5α‐steroid reductase type‐2 (SRD5A2) gene result in a broad spectrum of masculinization defects, ranging from a male phenotype with hypospadias to a female phenotype with Wolffian structures. Molecular stud
Externí odkaz:
https://doaj.org/article/f70d5067d37843be938c4a884e0de9a2
Publikováno v:
miradas (Pereira). 17:31-42
El presente artículo muestra la implementación de la ruta de la innovación social, metodología creada por el parque científico de innovación social PCIS, ruta que, aborda problemáticas, que intentan solucionarse, mediante la participación de
Publikováno v:
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme. 54(1)
Several studies have supported the usefulness of the triglycerides and glucose (TyG) index as a surrogate measure of insulin resistance; however, it has not been evaluated in insulin secretion. The aim of this study was to assess the association betw
Publikováno v:
Molecular Genetics & Genomic Medicine
Inactivating mutations of the 5α-steroid reductase type-2 (SRD5A2) gene result in a broad spectrum of masculinization defects, ranging from a male phenotype with hypospadias to a female phenotype with Wolffian structures. Molecular studies of the SR
Autor:
Lance, Betty Rita Gómez
Publikováno v:
Letras Femeninas, 1982 Jan 01. 8(2), 80-80.
Externí odkaz:
https://www.jstor.org/stable/23020908
Autor:
Lance, Betty Rita Gómez
Publikováno v:
Letras Femeninas, 1982 Jan 01. 8(2), 81-81.
Externí odkaz:
https://www.jstor.org/stable/23020909
Publikováno v:
Journal of Human Genetics. 53:401-406
Dihydrotestosterone is crucial for normal development of external genitalia and prostate in the male embryo. Autosomal recessive mutations in the 5 alpha-reductase type 2 (SRD5A2) gene disrupt the synthesis of dihydrotestosterone in the urogenital tr
Autor:
Elvia, Canalizo-Miranda, Eddie Alberto, Favela-Pérez, Javier Alejandro, Salas-Anaya, Rita, Gómez-Díaz, Ricardo, Jara-Espino, Laura, Del Pilar Torres-Arreola, Arturo, Viniegra-Osorio
Publikováno v:
Revista medica del Instituto Mexicano del Seguro Social. 51(6)
Non-communicable diseases are a public health problem in México. Coronary heart disease and diabetes mellitus are the first and second cause of death in the country, followed by thrombotic cerebrovascular events. Cardiovascular diseases are the lead
Publikováno v:
Investigacion clinica. 51(2)
Familial combined hyperlipidemia (FCHL) is the most frequent primary dyslipidemia. Its manifestations include hypercholesterolemia, hypertriglyceridemia or the combination of both abnormalities. In spite of its high frequency, the proper diagnosis is