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Peña Quintana, Luis

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Title Issue Date
Quantification of urinary derivatives of Phenylbutyric and Benzoic acids by LC-MS/MS as treatment compliance biomarkers in Urea Cycle disorders Andrade, Fernando; Vitoria, Isidro; Martín Hernández, Elena; Pintos-Morell, Guillem; Correcher, Patricia, et al Issued date: 2019 DOI: 10.1016/j.jpba.2019.112798 Source: Journal of Pharmaceutical and Biomedical Analysis [ISSN 0731-7085], v. 176 SJR: 0,795 - Q1 JCR: 3,209 - Q2 SCIE Artículo
Decreased plasma L-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment Molema, Femke; Gleich, Florian; Burgard, Peter; van der Ploeg, Ans T.; Summar, Marshall L., et al Issued date: 2019 DOI: 10.1016/j.ymgme.2019.02.003 Source: Molecular Genetics and Metabolism [ISSN 1096-7192], v. 126 (4), p. 397-405 (Abril 2019) SJR: 1,404 - Q1 JCR: 4,17 - Q1 SCIE Artículo
Growth and nutrition Medina, Yeray Nóvoa; Peña Quintana, Luis Issued date: 2019 Source: Encyclopedia of Food Security and Sustainability / Pasquale Ferranti, Elliot M. Berr, Jock R. Anderson (eds.), v. 2, p. 353-363 itemlist.container.dc.description.spiq Q1 Capítulo de libro
Evolution of tyrosinemia type 1 disease in patients treated with nitisinone in Spain Luz Couce, Maria; Sanchez-Pintos, Paula; Aldamiz-Echevarria, Luis; Vitoria, Isidro; Navas, Victor, et al Issued date: 2019 DOI: 10.1097/MD.0000000000017303 Source: Medicine [ISSN 0025-7974], v. 98 (39), e17303 SJR: 0,639 - Q2 JCR: 1,552 - Q3 SCIE Artículo
Correction to: Age at disease onset and peak ammonium level rather than interventional variables predict the neurological outcome in urea cycle disorders (Journal of Inherited Metabolic Disease, (2016), 39, 5, (661-672), 10.1007/s10545-016-9938-9) Posset, Roland; Garcia-Cazorla, Angeles; Valayannopoulos, Vassili; Leão Teles, Elisa; Dionisi-Vici, Carlo, et al Issued date: 2018 DOI: 10.1007/s10545-017-0117-4 Source: Journal of Inherited Metabolic Disease[ISSN 0141-8955],v. 41 (4), p. 743-744 (Julio 2018) SJR: 1,56 - Q1 JCR: 4,287 - Q1 SCIE Comentario
Omega-3 LCPUFA supplementation improves neonatal and maternal bone turnover: A randomized controlled trial Kajarabille, Naroa; Peña, Manuela; Díaz-Castro, Javier; Hurtado, Jose A.; Peña Quintana, Luis , et al Issued date: 2018 DOI: 10.1016/j.jff.2018.04.065 Source: Journal of Functional Foods [ISSN 1756-4646], v. 46, p. 167-174 SJR: 1,107 - Q1 JCR: 3,197 - Q1 SCIE Artículo
Improving the diagnosis of cobalamin and related defects by genomic analysis, plus functional and structural assessment of novel variants Brasil, Sandra; Leal, Fátima; Vega, Ana; Navarrete, Rosa; Ecay, María Jesús, et al Issued date: 2018 DOI: 10.1186/s13023-018-0862-y Source: Orphanet Journal of Rare Diseases [ISSN 1750-1172], v. 13: 125 (Julio 2018) SJR: 1,589 - Q1 JCR: 3,687 - Q2 SCIE Artículo
Omega-3 LCPUFA supplement: a nutritional strategy to prevent maternal and neonatal oxidative stress Kajarabille, Naroa; Hurtado, Jose A.; Peña Quintana, Luis ; Peña, Manuela; Ruiz, Josefa, et al Issued date: 2017 DOI: 10.1111/mcn.12300 Source: Maternal and Child Nutrition [ISSN 1740-8695], v. 13 (2):e12300 (Abril 2017) SJR: 1,578 - Q1 JCR: 3,233 - Q1 SCIE Artículo
Excess weight in patients with cystic fibrosis: Is it always beneficial? González-Jiménez, David; Muñoz-Codoceo, Rosana; Garriga-García, María; Molina-Arias, Manuel; Álvarez-Beltrán, Marina, et al Issued date: 2017 DOI: 10.20960/nh.620 Source: Nutrición Hospitalaria [ISSN 0212-1611], v. 34(3), p. 578-583, (Junio 2015) SJR: 0,411 - Q3 JCR: 0,845 - Q4 SCIE Artículo
Fibrosis quística no clásica y la importancia del estudio genético Galan Henriquez, Gloria M.; Garcia Cruz,Loida Maria ; Reyes Suárez, Desiderio Zacarías ; González Azpeitia, Gloria ; Santana Rodríguez, Alfredo , et al Issued date: 2017 Source: 65º Congreso de la Sociedad Española de Pediatría / Asociación Española de Pediatría (AEP), Santiago de Compostela (1-3 de junio de 2017) Póster de congresos
Tyrosinemia type II: Mutation update, 11 novel mutations and description of 5 independent subjects with a novel founder mutation Peña Quintana, Luis ; Scherer, G.; Curbelo-Estévez, M. L.; Jimenez Acosta, Francisco ; Hartmann, B., et al Issued date: 2017 DOI: 10.1111/cge.13003 Source: Clinical Genetics [ISSN 0009-9163], v. 92 (3), p. 306-317 SJR: 1,522 - Q2 JCR: 3,512 - Q2 SCIE Artículo
Homocigosis mutacional en una paciente canaria con tirosimenia tipo I Garcia Cruz,Loida Maria ; Boza Medina, Dara ; Rodriguez Hernández, C.; Reyes Suárez, Desiderio Zacarías ; Pintado Almeida, L., et al Issued date: 2017 Source: XII Congreso Nacional de Errores Congénitos del Metabolismo / AECOM (Las Palmas de Gran Canaria, 18-20 de octubre de 2017) Póster de congresos
Protocolo de diagnóstico y tratamiento de las deficiencias de la β-oxidación mitocondrial de los ácidos grasos Couce Pico, M.L.; García Villoria, J.; Martín Hernández, E.; Peña Quintana, Luis ; Rausell Félix, L., et al Issued date: 2017 Source: Protocolos de diagnóstico y tratamiento de los errores congénitos del metabolismo / David Gil Ortega (ed.), p. 43-66 itemlist.container.dc.description.spiq Q2 Capítulo de libro
Dietary flavonoids of Spanish youth: intakes, sources, and association with the mediterranean diet Bawaked, Rowaedh Ahmed; Schröder, Helmut; Ribas-Barba, Lourdes; Cárdenas, Gabriela; Peña-Quintana, Luis , et al Issued date: 2017 DOI: 10.7717/peerj.3304 Source: PeerJ [ISSN 2167-8359], v. 5 (e3304), (2017) SJR: 1,087 - Q1 JCR: 2,118 - Q2 SCIE Artículo
Cytokine distribution in mothers and breastfed children after omega-3 LCPUFAs supplementation during the last trimester of pregnancy and the lactation period: A randomized, controlled trial Rodriguez-Santana, Yessica; Ochoa, J. J.; Lara-Villoslada, F.; Kajarabille, N.; Saavedra-Santana, Pedro , et al Issued date: 2017 DOI: 10.1016/j.plefa.2017.09.006 Source: Prostaglandins Leukotrienes and Essential Fatty Acids [ISSN 1532-2823], v 126, p. 32-36 SJR: 1,131 - Q1 JCR: 2,437 - Q3 SCIE Artículo
Síndrome de Alagille; una patología que tener en cuenta Ortega Pérez, S. N.; González Santana, D. ; Ramos Varela, J. C.; Cañizo Fernández, D.; Peña Quintana, Luis Issued date: 2017 Source: Pediatria de Atencion Primaria [ISSN 1139-7632], v. 19 (75), p. 267-270 SJR: 0,122 - Q4 Artículo
Profile of sodium phenylbutyrate granules for the treatment of urea-cycle disorders: Patient perspectives Peña Quintana, Luis ; Llarena, M.; De los Reyes Rosales Medina, D. ; Reyes Súarez, D. ; Aldámiz-Echevarria, L. Issued date: 2017 DOI: 10.2147/PPA.S136754 Source: Patient Preference and Adherence [ISSN 1177-889X], v. 11, p. 1489-1496 SJR: 0,727 - Q1 JCR: 1,733 - Q2 SCIE Artículo
Nutrición en las enfermedades hepatobiliares Cabré, Eduard; Uria, Virgili; Peña Quintana, Luis Issued date: 2017 Source: Tratado de nutrición (3ª ed.) / Ángel Gil (dir.), v. V Capítulo de libro
Age at disease onset and peak ammonium level rather than interventional variables predict the neurological outcome in urea cycle disorders Posset, Roland; Garcia-Cazorla, Angeles; Valayannopoulos, Vassili; Leão Teles, Elisa; Dionisi-Vici, Carlo, et al Issued date: 2016 DOI: 10.1007/s10545-016-9938-9 Source: Journal of Inherited Metabolic Disease [ISSN 0141-8955], v. 39 (5), p. 661-672, (Septiembre 2016) SJR: 1,502 - Q2 JCR: 3,97 - Q1 SCIE Artículo
Molecular epidemiology, genotype-phenotype correlation and BH 4 responsiveness in Spanish patients with phenylketonuria Aldámiz-Echevarría, Luis; Llarena, Marta; Bueno, María A.; Dalmau, Jaime; Vitoria, Isidro, et al Issued date: 2016 DOI: 10.1038/jhg.2016.38 Source: Journal of Human Genetics[ISSN 1434-5161],v. 61(8), p. 731-744 (Abril 2016) SJR: 1,244 - Q2 JCR: 2,471 - Q3 SCIE Artículo