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Protein misfolding diseases: Prospects of pharmacological treatment.
Gámez A, Yuste-Checa P, Brasil S, Briso-Montiano Á, Desviat LR, Ugarte M, Pérez-Cerdá C, Pérez B. Gámez A, et al. Among authors: desviat lr. Clin Genet. 2018 Mar;93(3):450-458. doi: 10.1111/cge.13088. Epub 2017 Dec 4. Clin Genet. 2018. PMID: 28671287 Review.
A new PKU mutation associated with haplotype 12.
Desviat LR, Pérez B, Ugarte M. Desviat LR, et al. Hum Mol Genet. 1992 Dec;1(9):765-6. doi: 10.1093/hmg/1.9.765. Hum Mol Genet. 1992. PMID: 1363838 No abstract available.
Spectrum and origin of phenylketonuria mutations in Spain.
Pérez B, Desviat LR, De Lucca M, Ugarte M. Pérez B, et al. Among authors: desviat lr. Acta Paediatr Suppl. 1994 Dec;407:34-6. doi: 10.1111/j.1651-2227.1994.tb13444.x. Acta Paediatr Suppl. 1994. PMID: 7766951
160 results