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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 1
2008 1
2010 1
2013 1
2014 1
2015 2
2016 2
2017 2
2018 2
2019 1
2021 2
2022 1
2023 1
2024 0

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18 results

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Page 1
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.
[Mexican consensus on Gaucher's disease].
Franco-Ornelas S; Grupo de Expertos en Enfermedad de Gaucher. Franco-Ornelas S, et al. Rev Med Inst Mex Seguro Soc. 2010 Mar-Apr;48(2):167-86. Rev Med Inst Mex Seguro Soc. 2010. PMID: 20929621 Spanish.
Case report of renal tubular acidosis and misdiagnosed.
Medeiros M, Enciso S, Hernández AM, García Hernández HR, Toussaint G, Pinto C, Navarrete Rodríguez EM, Del-Rio-Navarro BE, Saucedo-Ramírez OJ, Medina Bravo P, Miranda S, Worona L, Sosa G, Belmont Martinez L, Alcántara Ortigoza MÁ, Escobar L, Muñoz Arizpe R. Medeiros M, et al. Among authors: belmont martinez l. Nefrologia. 2016 May-Jun;36(3):323-5. doi: 10.1016/j.nefro.2015.10.012. Epub 2016 Feb 5. Nefrologia. 2016. PMID: 26857205 Free article. English, Spanish. No abstract available.
Functional characterization of the p.(Gln195His) or Tainan and novel p.(Ser184Cys) or Toluca glucose-6-phosphate dehydrogenase (G6PD) gene natural variants identified through Mexican newborn screening for glucose-6-phosphate dehydrogenase deficiency.
Alcántara-Ortigoza MA, Hernández-Ochoa B, González-Del Angel A, Ibarra-González I, Belmont-Martínez L, Gómez-Manzo S, Vela-Amieva M. Alcántara-Ortigoza MA, et al. Among authors: belmont martinez l. Clin Biochem. 2022 Nov-Dec;109-110:64-73. doi: 10.1016/j.clinbiochem.2022.08.012. Epub 2022 Sep 8. Clin Biochem. 2022. PMID: 36089067
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.
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.
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.
Kernicterus in a boy with ornithine transcarbamylase deficiency: A case report.
López-Corella E, Ibarra-González I, Fernández-Lainez C, Rodríguez-Weber MÁ, Guillén-Lopez S, Belmont-Martínez L, Agüero-Linares D, Vela-Amieva M. López-Corella E, et al. Among authors: belmont martinez l. Neuropathology. 2017 Dec;37(6):586-590. doi: 10.1111/neup.12404. Epub 2017 Aug 16. Neuropathology. 2017. PMID: 28815739
18 results