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Predominance of Dystrophinopathy Genotypes in Mexican Male Patients Presenting as Muscular Dystrophy with A Normal Multiplex Polymerase Chain Reaction DMD Gene Result: A Study Including Targeted Next-Generation Sequencing.
Alcántara-Ortigoza MA, Reyna-Fabián ME, González-Del Angel A, Estandia-Ortega B, Bermúdez-López C, Cruz-Miranda GM, Ruíz-García M. Alcántara-Ortigoza MA, et al. Among authors: bermudez lopez c. Genes (Basel). 2019 Oct 29;10(11):856. doi: 10.3390/genes10110856. Genes (Basel). 2019. PMID: 31671740 Free PMC article.
Molecular Analysis Confirms that FKRP-Related Disorders are Underdiagnosed in Mexican Patients with Neuromuscular Diseases.
Navarro-Cobos MJ, González-Del Angel A, Estandia-Ortega B, Ruiz-Herrera A, Becerra A, Vargas-Ramírez G, Bermúdez-López C, Alcántara-Ortigoza MA. Navarro-Cobos MJ, et al. Among authors: bermudez lopez c. Neuropediatrics. 2017 Dec;48(6):442-450. doi: 10.1055/s-0037-1607054. Epub 2017 Oct 24. Neuropediatrics. 2017. PMID: 29065428 No abstract available.
Thiopurine S-methyltransferase (TPMT) genetic polymorphisms in Mexican newborns.
González-Del Angel A, Bermúdez-López C, Alcántara-Ortigoza MA, Vela-Amieva M, Castillo-Cruz RA, Martínez V, Torres-Espíndola L. González-Del Angel A, et al. Among authors: bermudez lopez c. J Clin Pharm Ther. 2009 Dec;34(6):703-8. doi: 10.1111/j.1365-2710.2009.01058.x. J Clin Pharm Ther. 2009. PMID: 20175804
[Pellegrini-Stieda syndrome as a cause of knee pain].
Santos Sánchez JA, Ramos Pascua LR, García Casado D, Bermúdez López C. Santos Sánchez JA, et al. Among authors: bermudez lopez c. Semergen. 2012 Nov-Dec;38(8):543-7. doi: 10.1016/j.semerg.2011.10.015. Epub 2011 Dec 20. Semergen. 2012. PMID: 23146709 Spanish.