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Mexican consensus on lysosomal acid lipase deficiency diagnosis.
Rev Gastroenterol Mex (Engl Ed). 2018 Jan-Mar;83(1):51-61. doi: 10.1016/j.rgmx.2017.08.001. Epub 2017 Dec 27.
Rev Gastroenterol Mex (Engl Ed). 2018.
PMID: 29287906
Free article.
English, Spanish.
[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.
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Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing.
Carnevale A, Rosas-Madrigal S, Rosendo-Gutiérrez R, López-Mora E, Romero-Hidalgo S, Avila-Vazzini N, Jacobo-Albavera L, Domínguez-Pérez M, Vargas-Alarcón G, Pérez-Villatoro F, Navarrete-Martínez JI, Villarreal-Molina MT.
Carnevale A, et al. Among authors: navarrete martinez ji.
Mol Genet Genomic Med. 2020 Nov;8(11):e1504. doi: 10.1002/mgg3.1504. Epub 2020 Sep 24.
Mol Genet Genomic Med. 2020.
PMID: 32969603
Free PMC article.
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Wide allelic heterogeneity with predominance of large IDS gene complex rearrangements in a sample of Mexican patients with Hunter syndrome.
Alcántara-Ortigoza MA, García-de Teresa B, González-Del Angel A, Berumen J, Guardado-Estrada M, Fernández-Hernández L, Navarrete-Martínez JI, Maza-Morales M, Rius-Domínguez R.
Alcántara-Ortigoza MA, et al. Among authors: navarrete martinez ji.
Clin Genet. 2016 May;89(5):574-83. doi: 10.1111/cge.12738. Epub 2016 Feb 9.
Clin Genet. 2016.
PMID: 26762690
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Newborn screening for six lysosomal storage disorders in a cohort of Mexican patients: Three-year findings from a screening program in a closed Mexican health system.
Navarrete-Martínez JI, Limón-Rojas AE, Gaytán-García MJ, Reyna-Figueroa J, Wakida-Kusunoki G, Delgado-Calvillo MDR, Cantú-Reyna C, Cruz-Camino H, Cervantes-Barragán DE.
Navarrete-Martínez JI, et al.
Mol Genet Metab. 2017 May;121(1):16-21. doi: 10.1016/j.ymgme.2017.03.001. Epub 2017 Mar 9.
Mol Genet Metab. 2017.
PMID: 28302345
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