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[Beginnings, evolution and current situation of the Newborn Screening Programs in Spain.].
Rev Esp Salud Publica. 2021 Feb 23;95:e202102041.
Rev Esp Salud Publica. 2021.
PMID: 33619242
Free article.
Spanish.
[False positive on neonatal screening: C5-carnitin increase in newborns due to pre-labour treatment with cefditoren pivoxil].
Fernández Ruano ML, Besga García B, Montero Plata A, Dulín Íñiguez E.
Fernández Ruano ML, et al.
Rev Esp Salud Publica. 2018 Jun 4;92:e201806025.
Rev Esp Salud Publica. 2018.
PMID: 29863107
Free article.
Spanish.
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Biochemical analysis in congenital neuroblastoma.
Montero Domínguez C, Ortiz Temprado A, Martínez Figueras L, Guillamón Seoane A, Fernández Ruano M.
Montero Domínguez C, et al.
Adv Lab Med. 2022 Dec 16;4(1):120-127. doi: 10.1515/almed-2022-0112. eCollection 2023 Apr.
Adv Lab Med. 2022.
PMID: 37359903
Free PMC article.
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Four Years' Experience in the Diagnosis of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency in Infants Detected in Three Spanish Newborn Screening Centers.
Merinero B, Alcaide P, Martín-Hernández E, Morais A, García-Silva MT, Quijada-Fraile P, Pedrón-Giner C, Dulin E, Yahyaoui R, Egea JM, Belanger-Quintana A, Blasco-Alonso J, Fernandez Ruano ML, Besga B, Ferrer-López I, Leal F, Ugarte M, Ruiz-Sala P, Pérez B, Pérez-Cerdá C.
Merinero B, et al. Among authors: fernandez ruano ml.
JIMD Rep. 2018;39:63-74. doi: 10.1007/8904_2017_40. Epub 2017 Jul 29.
JIMD Rep. 2018.
PMID: 28755359
Free PMC article.
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[Hereditary hyperferritinemia cataracts syndrome in a Spanish family caused by the A40G mutation (Paris) in the L-ferritin (FTL) gene associated with the mutation H63D in the HFE gene].
Del Castillo Rueda A, Fernández Ruano ML.
Del Castillo Rueda A, et al. Among authors: fernandez ruano ml.
Med Clin (Barc). 2007 Sep 29;129(11):414-7. doi: 10.1016/s0025-7753(07)72873-7.
Med Clin (Barc). 2007.
PMID: 17927936
Spanish.
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