Showing 1 - 11 results of 11 for search 'Sara Guillén‐López', query time: 0.04s
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Fórmulas metabólicas disponibles en México para pacientes con fenilcetonuria by Lizbeth López-Mejía, Sara Guillén-López, Marcela Vela-Amieva
Published 2021-01-01
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Nutritional evaluation of the patient with phenylketonuria (PKU) by Sara Guillén-López, Leticia Belmont-Martínez, Cynthia Fernández-Lainez
Published 2014-07-01
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Polyunsaturated long-chain fatty acids in hyperphenylalaninemias by Sara Guillén-López, Romina Rodríguez-Schmidt, Marcela Vela-Amieva
Published 2014-07-01
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Crisis neuropática por suspensión de nitisinona en una paciente con tirosinemia: informe de un caso by Isabel Ibarra-González, Leticia Belmont-Martínez, Roberto Cervantes-Bustamante, Flora Zárate-Mondragón, Sara Guillén-López, Cynthia Fernández-Lainez, Nuria Revilla-Estivil, Marcela Vela-Amieva
Published 2017-08-01
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A Review of Disparities and Unmet Newborn Screening Needs over 33 Years in a Cohort of Mexican Patients with Inborn Errors of Intermediary Metabolism by Isabel Ibarra-González, Cynthia Fernández-Lainez, Marcela Vela-Amieva, Sara Guillén-López, Leticia Belmont-Martínez, Lizbeth López-Mejía, Rosa Itzel Carrillo-Nieto, Nidia Alejandra Guillén-Zaragoza
Published 2023-10-01
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In Silico Structural Protein Evaluation of the Phenylalanine Hydroxylase p.(Tyr77His) Variant Associated with Benign Hyperphenylalaninemia as Identified through Mexican Newborn Scr... by Marcela Vela-Amieva, Miguel Angel Alcántara-Ortigoza, Ariadna González-del Angel, Isabel Ibarra-González, Liliana Fernández-Hernández, Sara Guillén-López, Lizbeth López-Mejía, Cynthia Fernández-Lainez
Published 2023-11-01
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Importance of genetic sequencing studies in managing chronic neonatal diarrhea: a case report of a novel variant in the glucose–galactose transporter SLC5A1 by Lizbeth López-Mejía, Sara Guillén-Lopez, Marcela Vela-Amieva, Rosalía Santillán-Martínez, Melania Abreu, Melania Abreu, María Dolores González-Herrra, Rubicel Díaz-Martínez, Juan Gaspar Reyes-Magaña
Published 2024-02-01
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Mutational spectrum of Mexican patients with tyrosinemia type 1: In silico modeling and predicted pathogenic effect of a novel missense FAH variant by Isabel Ibarra‐González, Cynthia Fernández‐Lainez, Miguel Angel Alcántara‐Ortigoza, Ariadna González‐Del Angel, Liliana Fernández‐Henández, Sara Guillén‐López, Leticia Belmont‐Martínez, Lizbeth López‐Mejía, Gustavo Varela‐Fascinetto, Marcela Vela‐Amieva
Published 2019-12-01
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An Updated <i>PAH</i> Mutational Spectrum of Phenylketonuria in Mexican Patients Attending a Single Center: Biochemical, Clinical-Genotyping Correlations by Marcela Vela-Amieva, Miguel Angel Alcántara-Ortigoza, Isabel Ibarra-González, Ariadna González-del Angel, Liliana Fernández-Hernández, Sara Guillén-López, Lizbeth López-Mejía, Rosa Itzel Carrillo-Nieto, Leticia Belmont-Martínez, Cynthia Fernández-Lainez
Published 2021-10-01
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