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

Year Number of Results
2002 1
2003 5
2004 1
2006 1
2007 1
2009 1
2010 2
2011 2
2012 4
2013 4
2014 5
2015 3
2016 4
2017 2
2018 1
2020 2
2021 3
2022 1
2023 2
2024 2

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42 results

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Page 1
Natural history of three late-diagnosed classic Galactosemia patients.
Quelhas D, Kingma SDK, Jonckheere AI, Smeets-Peels CS, Gomes DC, Duro J, Oliveira A, Matthijs G, Steinbusch LKM, Jaeken J, Rivera I, Rubio-Gozalbo E. Quelhas D, et al. Among authors: oliveira a. Mol Genet Metab Rep. 2024 Jan 23;38:101057. doi: 10.1016/j.ymgmr.2024.101057. eCollection 2024 Mar. Mol Genet Metab Rep. 2024. PMID: 38469096 Free PMC article.
From skin lesions to tyrosinemia type II diagnosis.
da Silva ISF, Sopa I, Gomes D, Peixoto L, Oliveira A. da Silva ISF, et al. Among authors: oliveira a. J Inherit Metab Dis. 2024 Feb 26. doi: 10.1002/jimd.12720. Online ahead of print. J Inherit Metab Dis. 2024. PMID: 38408363 No abstract available.
Follow-up of Patients with Hereditary Metabolic Diseases during the 3 Years of the Pandemic in the Reference Center for Hereditary Metabolism Diseases of the Centro Hospitalar Universitário Lisboa Norte.
Belo A, Gomes D, Nunes P, Oliveira A. Belo A, et al. Among authors: oliveira a. Endocr Metab Immune Disord Drug Targets. 2023 Dec 13. doi: 10.2174/0118715303279331231123050015. Online ahead of print. Endocr Metab Immune Disord Drug Targets. 2023. PMID: 38093446
Multispectral Optical Remote Sensing for Water-Leak Detection.
Krapez JC, Sanchis Muñoz J, Mazel C, Chatelard C, Déliot P, Frédéric YM, Barillot P, Hélias F, Barba Polo J, Olichon V, Serra G, Brignolles C, Carvalho A, Carreira D, Oliveira A, Alves E, Fortunato AB, Azevedo A, Benetazzo P, Bertoni A, Le Goff I. Krapez JC, et al. Among authors: oliveira a. Sensors (Basel). 2022 Jan 29;22(3):1057. doi: 10.3390/s22031057. Sensors (Basel). 2022. PMID: 35161803 Free PMC article.
Nursing Students' Perceptions on Healthcare-Associated Infection Control and Prevention Teaching and Learning Experience: Development and Validation of a Scale in Four European Countries.
Yurrebaso Macho A, Ward Mayens AL, Picado Valverde EM, Guzmán Ordaz R, Juanes Méndez JA, Pérez Iglesias JL, Mirón Canelo JA, Pinto MDR, Costa Reis AMDS, Simões JA, Torres AL, Silén-Lipponen M, Korhonen U, Koponen L, Myllymäki M, Jankowiak-Bernaciak A, Patrzała A, Bączyk G, Basa A, Costa PS, Serambeque B, Oliveira AS, Pardal J, Graveto JMGDN, Parreira P. Yurrebaso Macho A, et al. Among authors: oliveira as. Front Psychol. 2021 Oct 8;12:701208. doi: 10.3389/fpsyg.2021.701208. eCollection 2021. Front Psychol. 2021. PMID: 34690861 Free PMC article.
Congenital Disorders of Glycosylation in Portugal-Two Decades of Experience.
Quelhas D, Martins E, Azevedo L, Bandeira A, Diogo L, Garcia P, Sequeira S, Ferreira AC, Teles EL, Rodrigues E, Fortuna AM, Mendonça C, Fernandes HC, Medeira A, Gaspar A, Janeiro P, Oliveira A, Laranjeira F, Ribeiro I, Souche E, Race V, Keldermans L, Matthijs G, Jaeken J. Quelhas D, et al. Among authors: oliveira a. J Pediatr. 2021 Apr;231:148-156. doi: 10.1016/j.jpeds.2020.12.026. Epub 2020 Dec 17. J Pediatr. 2021. PMID: 33340551
Pyruvate dehydrogenase complex deficiency: updating the clinical, metabolic and mutational landscapes in a cohort of Portuguese patients.
Pavlu-Pereira H, Silva MJ, Florindo C, Sequeira S, Ferreira AC, Duarte S, Rodrigues AL, Janeiro P, Oliveira A, Gomes D, Bandeira A, Martins E, Gomes R, Soares S, Tavares de Almeida I, Vicente JB, Rivera I. Pavlu-Pereira H, et al. Among authors: oliveira a. Orphanet J Rare Dis. 2020 Oct 22;15(1):298. doi: 10.1186/s13023-020-01586-3. Orphanet J Rare Dis. 2020. PMID: 33092611 Free PMC article.
42 results