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IFITM5-related (type V) osteogenesis imperfecta with evidence of perinatal involvement: A case report.
Bone Rep. 2024 Apr 17;21:101766. doi: 10.1016/j.bonr.2024.101766. eCollection 2024 Jun.
Bone Rep. 2024.
PMID: 38681748
Free PMC article.
Infantile-onset Pompe disease in seven Mexican children.
Sánchez-Sánchez LM, Ávila-Rejón C, Díaz-Martínez R, Díaz-Murillo B, Kazakova E, López-Valdez J, Martínez-Montoya V, Olaiz-Urbina J, Radillo-Díaz P, Ricárdez-Marcial E, Sandoval-Pacheco R, Torres-Octavo B, Vergara-Sánchez I.
Sánchez-Sánchez LM, et al. Among authors: martinez montoya v.
Gac Med Mex. 2022;158(5):265-270. doi: 10.24875/GMM.M22000694.
Gac Med Mex. 2022.
PMID: 36572041
Free article.
English.
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[Late onset Pompe disease: an analysis of 19 patients from Mexico].
Sánchez-Sánchez LM, Martinez-Montoya V, Sandoval-Pacheco R, Torres-Octavo B, Anaya-Castro DM, Padilla-de la Torre O, Arellano-Valdez CA, Ávila-Rejón CA, Aguilar-Juárez PA, Espino-Pluma M, González-Santillanes Cruz A, Kazakova E, Martinez-Segovia RI, Olmos-Morfin D, Radillo-Díaz PF, Solís-Sánchez I, Vázquez Del Mercado-Espinosa M, Villarroel-Cortés CE, Velarde-Félix JS.
Sánchez-Sánchez LM, et al. Among authors: martinez montoya v.
Rev Neurol. 2022 Sep 1;75(5):103-108. doi: 10.33588/rn.7505.2022227.
Rev Neurol. 2022.
PMID: 35880963
Free PMC article.
Spanish.
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