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A new metabolic disorder in human cationic amino acid transporter-2 that mimics arginase 1 deficiency in newborn screening.
J Inherit Metab Dis. 2019 May;42(3):407-413. doi: 10.1002/jimd.12063. Epub 2019 Feb 21.
J Inherit Metab Dis. 2019.
PMID: 30671984
In Vivo 1H Magnetic Resonance Spectroscopy.
Muñoz-Hernández MC, García-Martín ML.
Muñoz-Hernández MC, et al.
Methods Mol Biol. 2018;1718:151-167. doi: 10.1007/978-1-4939-7531-0_10.
Methods Mol Biol. 2018.
PMID: 29341008
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A Distinct Metabolite Profile Correlates with Neurodegenerative Conditions and the Severity of Congenital Hydrocephalus.
García-Bonilla M, García-Martín ML, Muñoz-Hernández MC, Domínguez-Pinos D, Martínez-León MI, Peñalver A, Castilla L, Alonso FJ, Márquez J, Shumilov K, Hidalgo-Sánchez R, Gutiérrez A, Páez-González P, Jiménez AJ.
García-Bonilla M, et al. Among authors: munoz hernandez mc.
J Neuropathol Exp Neurol. 2018 Dec 1;77(12):1122-1136. doi: 10.1093/jnen/nly097.
J Neuropathol Exp Neurol. 2018.
PMID: 30364991
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Neocortical tissue recovery in severe congenital obstructive hydrocephalus after intraventricular administration of bone marrow-derived mesenchymal stem cells.
García-Bonilla M, Ojeda-Pérez B, García-Martín ML, Muñoz-Hernández MC, Vitorica J, Jiménez S, Cifuentes M, Santos-Ruíz L, Shumilov K, Claros S, Gutiérrez A, Páez-González P, Jiménez AJ.
García-Bonilla M, et al. Among authors: munoz hernandez mc.
Stem Cell Res Ther. 2020 Mar 17;11(1):121. doi: 10.1186/s13287-020-01626-6.
Stem Cell Res Ther. 2020.
PMID: 32183876
Free PMC article.
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