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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 1 |
2021 | 6 |
2024 | 0 |
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6 results
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Page 1
Importance of Timely Treatment Initiation in Infantile-Onset Pompe Disease, a Single-Centre Experience.
Children (Basel). 2021 Nov 9;8(11):1026. doi: 10.3390/children8111026.
Children (Basel). 2021.
PMID: 34828739
Free PMC article.
The Genetic Landscape of Mitochondrial Diseases in Spain: A Nationwide Call.
Bellusci M, Paredes-Fuentes AJ, Ruiz-Pesini E, Gómez B; MITOSPAIN Working Group; Martín MA, Montoya J, Artuch R.
Bellusci M, et al.
Genes (Basel). 2021 Oct 9;12(10):1590. doi: 10.3390/genes12101590.
Genes (Basel). 2021.
PMID: 34680984
Free PMC article.
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Urine Phenylacetylglutamine Determination in Patients with Hyperphenylalaninemia.
Andrade F, Cano A, Unceta Suarez M, Arza A, Vinuesa A, Ceberio L, López-Oslé N, de Frutos G, López-Oceja R, Aznal E, González-Lamuño D, de Las Heras J.
Andrade F, et al. Among authors: unceta suarez m.
J Clin Med. 2021 Aug 19;10(16):3674. doi: 10.3390/jcm10163674.
J Clin Med. 2021.
PMID: 34441968
Free PMC article.
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Transferrin Isoforms, Old but New Biomarkers in Hereditary Fructose Intolerance.
Cano A, Alcalde C, Belanger-Quintana A, Cañedo-Villarroya E, Ceberio L, Chumillas-Calzada S, Correcher P, Couce ML, García-Arenas D, Gómez I, Hernández T, Izquierdo-García E, Martínez Chicano D, Morales M, Pedrón-Giner C, Petrina Jáuregui E, Peña-Quintana L, Sánchez-Pintos P, Serrano-Nieto J, Unceta Suarez M, Vitoria Miñana I, de Las Heras J.
Cano A, et al. Among authors: unceta suarez m.
J Clin Med. 2021 Jun 30;10(13):2932. doi: 10.3390/jcm10132932.
J Clin Med. 2021.
PMID: 34208868
Free PMC article.
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[The metabolic newborn screening as a healthcare model of the precision medicine. Perspective from the Spanish Association for the Study of Congenital Errors of Metabolism (AECOM).].
González-Lamuño Leguina D, Bóveda Fontán MD, Bueno Delgado M, Gort Mas L, Unceta Suárez M, Morales Conejo M.
González-Lamuño Leguina D, et al. Among authors: unceta suarez m.
Rev Esp Salud Publica. 2021 Jan 26;95:e202101021.
Rev Esp Salud Publica. 2021.
PMID: 33496277
Free article.
Spanish.
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Leigh syndrome associated with TRMU gene mutations.
Sala-Coromina J, Miguel LD, de Las Heras J, Lasa-Aranzasti A, Garcia-Arumi E, Carreño L, Arranz JA, Carnicer C, Unceta-Suárez M, Sanchez-Montañez A, Gort L, Tort F, Del Toro M.
Sala-Coromina J, et al. Among authors: unceta suarez m.
Mol Genet Metab Rep. 2020 Dec 15;26:100690. doi: 10.1016/j.ymgmr.2020.100690. eCollection 2021 Mar.
Mol Genet Metab Rep. 2020.
PMID: 33365252
Free PMC article.
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