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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.
Ibarra-González I, Fernández-Lainez C, Vela-Amieva M, Guillén-López S, Belmont-Martínez L, López-Mejía L, Carrillo-Nieto RI, Guillén-Zaragoza NA. Ibarra-González I, et al. Among authors: belmont martinez l. Int J Neonatal Screen. 2023 Oct 19;9(4):59. doi: 10.3390/ijns9040059. Int J Neonatal Screen. 2023. PMID: 37873850 Free PMC article.
[Characterization of inborn errors of intermediary metabolism in mexican patients].
Ibarra-González I, Fernández-Lainez C, Belmont-Martínez L, Guillén-López S, Monroy-Santoyo S, Vela-Amieva M. Ibarra-González I, et al. An Pediatr (Barc). 2014 May;80(5):310-6. doi: 10.1016/j.anpedi.2013.09.003. Epub 2013 Oct 17. An Pediatr (Barc). 2014. PMID: 24140120 Free article. Spanish.
Hepatorenal Tyrosinemia in Mexico: A Call to Action.
Ibarra-González I, Ridaura-Sanz C, Fernández-Lainez C, Guillén-López S, Belmont-Martínez L, Vela-Amieva M. Ibarra-González I, et al. Among authors: belmont martinez l. Adv Exp Med Biol. 2017;959:147-156. doi: 10.1007/978-3-319-55780-9_14. Adv Exp Med Biol. 2017. PMID: 28755193 Review.
Mutational spectrum of Mexican patients with tyrosinemia type 1: In silico modeling and predicted pathogenic effect of a novel missense FAH variant.
Ibarra-González I, Fernández-Lainez C, Alcántara-Ortigoza MA, González-Del Angel A, Fernández-Henández L, Guillén-López S, Belmont-Martínez L, López-Mejía L, Varela-Fascinetto G, Vela-Amieva M. Ibarra-González I, et al. Among authors: belmont martinez l. Mol Genet Genomic Med. 2019 Dec;7(12):e937. doi: 10.1002/mgg3.937. Epub 2019 Sep 30. Mol Genet Genomic Med. 2019. PMID: 31568711 Free PMC article.
Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screening.
Vela-Amieva M, Alcántara-Ortigoza MA, González-Del Angel A, Belmont-Martínez L, López-Candiani C, Ibarra-González I. Vela-Amieva M, et al. Among authors: belmont martinez l. Orphanet J Rare Dis. 2021 Feb 26;16(1):103. doi: 10.1186/s13023-021-01693-9. Orphanet J Rare Dis. 2021. PMID: 33637102 Free PMC article.
An Updated PAH Mutational Spectrum of Phenylketonuria in Mexican Patients Attending a Single Center: Biochemical, Clinical-Genotyping Correlations.
Vela-Amieva M, Alcántara-Ortigoza MA, Ibarra-González I, González-Del Angel A, Fernández-Hernández L, Guillén-López S, López-Mejía L, Carrillo-Nieto RI, Belmont-Martínez L, Fernández-Lainez C. Vela-Amieva M, et al. Among authors: belmont martinez l. Genes (Basel). 2021 Oct 23;12(11):1676. doi: 10.3390/genes12111676. Genes (Basel). 2021. PMID: 34828281 Free PMC article.
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