Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Susana Monroy-Santoyo"'
Autor:
Roberta Salinas-Marín, Yoshiko Murakami, Carlos Alberto González-Domínguez, Mario Ernesto Cruz-Muñoz, Héctor Manuel Mora-Montes, Eva Morava, Taroh Kinoshita, Susana Monroy-Santoyo, Iván Martínez-Duncker
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
A subgroup of congenital disorders of glycosylation (CDGs) includes inherited GPI-anchor deficiencies (IGDs) that affect the biosynthesis of glycosylphosphatidylinositol (GPI) anchors, including the first reaction catalyzed by the X-linked PIGA. Here
Externí odkaz:
https://doaj.org/article/ae958a3ab8354ab78668866d0b631d0e
Publikováno v:
Acta Pediátrica de México, Vol 33, Iss 6, Pp 331-334 (2014)
Hyperphenylalaninemia is caused by deficient enzyme activity of phenylalanine hydroxylase. It was one of the first genetic disorders susceptible to treatment with a natural protein restricted diet for life. While this treatment has proven effective i
Externí odkaz:
https://doaj.org/article/b02a356b478944db82458121b2058922
Autor:
Cynthia Fernández-Lainez, Isabel Ibarra-González, Leticia Belmont-Martínez, Susana Monroy-Santoyo, Sara Guillén-López, Marcela Vela-Amieva
Publikováno v:
Annals of Hepatology, Vol 13, Iss 2, Pp 265-272 (2014)
Introduction. Hepatorenal tyrosinemia (HT1) is a treatable, inherited, metabolic disease characterized by progressive liver failure with pronounced coagulopathy. The aim of this study is to describe the clinical, biochemical, and histopathological fi
Externí odkaz:
https://doaj.org/article/ff84bbe3c3fb4c91b84302715976c02e
Autor:
Miguel Angel Jimenez-Bravo-Luna, Carlos Jiménez-Gutiérrez, Susana Monroy-Santoyo, Fernando Villegas-Álvarez, Beatriz Pérez-Guillé, Arturo Carmona-Mancilla, Rosa Eugenia Soriano-Rosales, Susana Leticia Elizalde-Velázquez, José Francisco González-Zamora
Publikováno v:
Veterinary Record Open
The aim of this study was to describe the tracheal growth pattern and its zoometric relationship in related medium-sized mongrel puppies through adulthood. Fourteen puppies were studied. CT monitoring was performed monthly, starting in the 1st month
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fa734adbd72026969b85d82a87e4031
https://pubmed.ncbi.nlm.nih.gov/29632670
https://pubmed.ncbi.nlm.nih.gov/29632670
Autor:
Sara Guillén-López, Marcela Vela-Amieva, Miguel Angel Alcántara-Ortigoza, Rehotbevely Barrientos-Ríos, Susana Monroy-Santoyo, A. González-del Angel, Cynthia Fernández-Lainez, Isabel Ibarra-González, M. Abreu-González
Publikováno v:
Clinical Genetics. 88:62-67
The mutational spectrum of the phenylalanine hydroxylase gene (PAH) in Mexico is unknown, although it has been suggested that PKU variants could have a differential geographical distribution. Genotype-phenotype correlations and genotype-based predict
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f29ae45fb903986e24ef924e5b46c94a
https://doi.org/10.1111/cge.12444
https://doi.org/10.1111/cge.12444
Autor:
Cynthia Fernández-Lainez, Isabel Ibarra-González, Leticia Belmont-Martínez, Marcela Vela-Amieva, Susana Monroy-Santoyo, Sara Guillén-López
Publikováno v:
Anales de Pediatría, Vol 80, Iss 5, Pp 310-316 (2014)
Resumen: Introducción: Los errores innatos del metabolismo intermediario (EIMi) son enfermedades genéticas heterogéneas que causan importante morbimortalidad y representan un reto diagnóstico. El objetivo de este trabajo es describir el número,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a644022a85214f8b57da52a7278fca4f
https://doi.org/10.1016/j.anpedi.2013.09.003
https://doi.org/10.1016/j.anpedi.2013.09.003
Autor:
Sara, Guillén-López, Marcela, Vela-Amieva, Merit Valeria, Juárez-Cruz, José Francisco, González-Zamora, Susana, Monroy-Santoyo, Leticia, Belmont-Martínez
Publikováno v:
Nutricion hospitalaria. 32(1)
the nutrition management of patients with inborn errors of metabolism (IEM) requires the permanent use of elemental medical formulas whose organoleptic characteristics sometimes impede oral acceptance. In addition, these patients may have gastrointes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3b6ef0998e27c17b8e8254fa2c3694f4
https://pubmed.ncbi.nlm.nih.gov/26262719
https://pubmed.ncbi.nlm.nih.gov/26262719
Autor:
C Vázquez-Cárdenas, M Ruíz-García, José Francisco González-Zamora, Susana Monroy-Santoyo, CG Palacios-López, O Sánchez-Guerrero, J De Rubens-Figueroa, AM Niembro-Zúñiga, J Flores-Pérez, J Priego y Romo, A Escamilla Villa, SR Greenawalt-Rodríguez
Publikováno v:
Acta Pediátrica de México, Vol 38, Iss 2, Pp 125-127 (2017)
Los informes de abusos cometidos durante la Segunda Guerra Mundial, en sujetos sometidos a experimentos biomédicos, son el punto de referencia para la formulación de las reglas básicas a fin de llevar a cabo investigación en seres humanos. Así,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::842b50c8ac23135c7bed0f49caf2e05c
https://doi.org/10.18233/apm38no2pp125-1271364
https://doi.org/10.18233/apm38no2pp125-1271364
Autor:
Susana Monroy-Santoyo, Leticia Belmont-Martínez, Cynthia Fernández-Lainez, Sara Guillén-López, Isabel Ibarra-González, Romina Rodríguez-Schmidt, Marcela Vela-Amieva
Publikováno v:
Universidad Nacional Autónoma de México
UNAM
Redalyc-UNAM
Acta Pediátrica de México (México) Num.6 Vol.33
UNAM
Redalyc-UNAM
Acta Pediátrica de México (México) Num.6 Vol.33
"La hiperfenilalaninemia es debida a la deficiente actividad enzimática de la fenilalanina hidroxilasa. Fue uno de los primeros desórdenes genéticos susceptibles de tratamiento, con una dieta restringida en proteína intacta de por vida. Si bien e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::871c3632df86d68a62af31ffc0f12f2c
https://www.redalyc.org/articulo.oa?id=423640339008
https://www.redalyc.org/articulo.oa?id=423640339008
Autor:
Sara Guillén-López, Leticia Belmont-Martínez, Cynthia Fernández-Laínez, Isabel Ibarra-González, Susana Monroy-Santoyo, Marcela Vela-Amieva
Publikováno v:
Universidad Nacional Autónoma de México
UNAM
Redalyc-UNAM
Acta Pediátrica de México (México) Num.6 Vol.33
UNAM
Redalyc-UNAM
Acta Pediátrica de México (México) Num.6 Vol.33
"Para realizar un adecuado diagnóstico nutricio y dar un tratamiento personalizado a pacientes con PKU, es necesario evaluar el estado nutricional. Entre los parámetros de la evaluación del estado nutricio se encuentran indicadores antropométrico
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::90ea24af6148d117234a69d7abcad493
https://www.redalyc.org/articulo.oa?id=423640339012
https://www.redalyc.org/articulo.oa?id=423640339012