Galaviz-Hernandez C.
342
Coauthors
16
Documentos
Volumen de publicaciones por año
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Año de publicación | Num. Publicaciones |
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2012 | 1 |
2013 | 2 |
2014 | 1 |
2015 | 2 |
2016 | 3 |
2017 | 1 |
2018 | 2 |
2019 | 1 |
2020 | 2 |
2022 | 1 |
Publicaciones por áreas de conocimiento
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Área de conocimiento | Num. Publicaciones |
---|---|
Genética | 16 |
Farmacología | 9 |
Obstetricia | 3 |
Fisiología | 2 |
Pediatría | 1 |
Migración humana | 1 |
Bioquímica | 1 |
Salud pública | 1 |
Publicaciones por áreas temáticas
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Área temática | Num. Publicaciones |
---|---|
Farmacología y terapéutica | 12 |
Ginecología, obstetricia, pediatría, geriatría | 6 |
Enfermedades | 4 |
Bioquímica | 4 |
Medicina y salud | 3 |
Fisiología humana | 3 |
Salud y seguridad personal | 2 |
Genética y evolución | 1 |
Mammalia | 1 |
Cultura e instituciones | 1 |
Principales fuentes de datos
Origen | Num. Publicaciones |
---|---|
Scopus | 16 |
Google Scholar | 8 |
RRAAE | 1 |
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Coautores destacados por número de publicaciones
Coautor | Num. Publicaciones |
---|---|
Sosa-Macías M.G. | 17 |
Adrián LLerena | 11 |
Enrique Terán | 11 |
Tarazona-Santos E.M. | 9 |
Lazalde-Ramos B.P. | 7 |
Moya G.E. | 7 |
Penãs-Lledó E.M. | 7 |
Ramírez-Roa R. | 6 |
López-López M. | 6 |
Francisco J.López Hernández | 6 |
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Top Keywords
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Publicaciones del autor
Paternal determinants in preeclampsia
ReviewAbstract: Preeclampsia is a condition associated with high rates of maternal-fetal morbidity and mortality. ItPalabras claves:Genetics, Immunology, Paternal, PLACENTA, Preeclampsia, PrimipaternityAutores:Enrique Terán, Galaviz-Hernandez C., Garcia-Ortiz J.E., Lazalde-Ramos B.P., Sosa-Macías M.G.Fuentes:googlescopusCYP2D6 gene polymorphisms and pbkp_redicted phenotypes in eight indigenous groups from northwestern Mexico
ArticleAbstract: Aim: Polymorphisms in CYP2D6 impact the interindividual and interethnic variability of drug efficienPalabras claves:allele frequency, CYP2D6polymorphism, Mexican indigenous, pbkp_redicted phenotype, pharmacogeneticsAutores:Adrián LLerena, Galaviz-Hernandez C., Garza-Veloz I., Lazalde-Ramos B.P., Martínez-Fierro M.L., Naranjo M.E.G., Sosa-Macías M.G.Fuentes:scopusAssociation of ABCB1, ABCC5 and xanthine oxidase genetic polymorphisms with methotrexate adverse reactions in Mexican pediatric patients with ALL
ArticleAbstract: Background: Acute lymphoblastic leukemia (ALL) is one of the most frequent oncological disorders inPalabras claves:Atp-Binding Cassette Transporter Gene, drug therapy/genetics, Genetic Polymorphisms, methotrexate, pharmacovigilance, precursor cell lymphoblastic leukemia-lymphoma/, xanthine oxidase (XO)Autores:Almanza-Reyes H., Chairez-Hernández I., Fausto Zaruma-Torres, Galaviz-Hernandez C., Lares-Asseff I., Loera-Castañeda V., Reyes-Espinoza A., Sosa-Macías M.G.Fuentes:rraaescopusMitochondria and coenzyme Q10 in the pathogenesis of preeclampsia
ReviewAbstract: Hypertensive disorders during pregnancy constitute one of the main causes of maternal and perinatalPalabras claves:Coenzyme Q10, Mitochondria, PLACENTA, Preeclampsia, PregnancyAutores:Andrés Calle, Enrique Terán, Galaviz-Hernandez C., Gustavo Molina, Isabel Hernández, Leandro R. Tana, Santiago Terán, Sosa-Macías M.G.Fuentes:googlescopusGenetic polymorphisms associated to folate transport as pbkp_redictors of increased risk for acute lymphoblastic leukemia in Mexican children
ArticleAbstract: Acute lymphoblastic leukemia (ALL) is a frequent neoplasia occurring in children. The most commonlyPalabras claves:Acute lymphoblastic leukemia, Folate transporters, Genetic Polymorphisms, methotrexate, Molecular epidemiologyAutores:Fausto Zaruma-Torres, Galaviz-Hernandez C., Lares-Asseff I., Lima A., Loera-Castañeda V., María Cristina Arias-Peláez, Quiñones L.A., Reyes-Espinoza A., Reyes-López M., Sosa-Macías M.G.Fuentes:scopus