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

Year Number of Results
2002 1
2003 1
2004 1
2005 1
2007 1
2010 2
2012 1
2013 2
2014 2
2015 3
2016 2
2017 1
2020 2
2021 4
2022 1
2023 2
2024 0

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24 results

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Page 1
Newborn screening-progress and challenges.
Hoffmann GF, Cornejo V, Pollitt RJ. Hoffmann GF, et al. Among authors: cornejo v. J Inherit Metab Dis. 2010 Oct;33(Suppl 2):S199-200. doi: 10.1007/s10545-010-9191-6. J Inherit Metab Dis. 2010. PMID: 20835763 No abstract available.
Cognitive functioning in mild hyperphenylalaninemia.
de la Parra A, García MI, Waisbren SE, Cornejo V, Raimann E. de la Parra A, et al. Among authors: cornejo v. Mol Genet Metab Rep. 2015 Oct 29;5:72-75. doi: 10.1016/j.ymgmr.2015.10.009. eCollection 2015 Dec. Mol Genet Metab Rep. 2015. PMID: 28649547 Free PMC article.
[What should the paediatrician know about hyperphenylalaninaemia?].
Bravo P, Raimann E, Cabello JF, Arias C, Peredo P, Castro G, Hamilton V, Campo K, Cornejo V. Bravo P, et al. Among authors: cornejo v. Rev Chil Pediatr. 2015 May-Jun;86(3):214-8. doi: 10.1016/j.rchipe.2015.06.006. Epub 2015 Jul 6. Rev Chil Pediatr. 2015. PMID: 26363863 Free article. Spanish.
Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria: A comparison between two genetic disorders affecting the same metabolic pathway.
van Vliet K, van Ginkel WG, Jahja R, Daly A, MacDonald A, Santra S, De Laet C, Goyens PJ, Vara R, Rahman Y, Cassiman D, Eyskens F, Timmer C, Mumford N, Gissen P, Bierau J, van Hasselt PM, Wilcox G, Morris AAM, Jameson EA, de la Parra A, Arias C, Garcia MI, Cornejo V, Bosch AM, Hollak CEM, Rubio-Gozalbo ME, Brouwers MCGJ, Hofstede FC, de Vries MC, Janssen MCH, van der Ploeg AT, Langendonk JG, Huijbregts SCJ, van Spronsen FJ. van Vliet K, et al. Among authors: cornejo v. J Inherit Metab Dis. 2022 Sep;45(5):952-962. doi: 10.1002/jimd.12528. Epub 2022 Jun 30. J Inherit Metab Dis. 2022. PMID: 35722880 Free PMC article.
Pathogenic variants of DNAJC12 and evaluation of the encoded cochaperone as a genetic modifier of hyperphenylalaninemia.
Gallego D, Leal F, Gámez A, Castro M, Navarrete R, Sanchez-Lijarcio O, Vitoria I, Bueno-Delgado M, Belanger-Quintana A, Morais A, Pedrón-Giner C, García I, Campistol J, Artuch R, Alcaide C, Cornejo V, Gil D, Yahyaoui R, Desviat LR, Ugarte M, Martínez A, Pérez B. Gallego D, et al. Among authors: cornejo v. Hum Mutat. 2020 Jul;41(7):1329-1338. doi: 10.1002/humu.24026. Epub 2020 Apr 30. Hum Mutat. 2020. PMID: 32333439 Free article.
Current Practices and Challenges in the Diagnosis and Management of PKU in Latin America: A Multicenter Survey.
Poloni S, Dos Santos BB, Chiesa A, Specola N, Pereyra M, Saborío-Rocafort M, Salazar MF, Leal-Witt MJ, Castro G, Peñaloza F, Wong SP, Porras RB, Paranza LO, Sanabria MC, Amieva MV, Morales M, Naranjo ARC, Mahfoud A, Colmenares AR, Lemes A, Sotillo-Lindo JF, Perez C, Rey LM, Torriente GMZ, Refosco LF, Schwartz IVD, Cornejo V. Poloni S, et al. Among authors: cornejo v. Nutrients. 2021 Jul 27;13(8):2566. doi: 10.3390/nu13082566. Nutrients. 2021. PMID: 34444728 Free PMC article.
24 results