Dental pulp of the third molar: a new source of pluripotent-like stem cells
Atari, Maher, Gil-Recio, Carlos, Fabregat, Marc, García-Fernández, Dani, Barajas, Miguel, Carrasco, Miguel A, Jung, Han-Sung, Alfaro, F Hernández, Casals, Nuria, Prosper, Felipe, Ferrés-Padró, Eduard, Giner, Luis
Published in Journal of cell science (15.07.2012)
Published in Journal of cell science (15.07.2012)
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Incidents related to critical patient safety during in-hospital transfer
Catalán-Ibars, R M, Martín-Delgado, M C, Puigoriol-Juvanteny, E, Zapater-Casanova, E, Lopez-Alabern, M, Lopera-Caballero, J L, González de Velasco, J P, Coll-Solà, M, Juanola-Codina, M, Roger-Casals, N
Published in Medicina intensiva (01.01.2022)
Published in Medicina intensiva (01.01.2022)
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Isolation of pluripotent stem cells from human third molar dental pulp
Atari, M, Barajas, M, Hernández-Alfaro, F, Gil, C, Fabregat, M, Ferrés Padró, E, Giner, L, Casals, N
Published in Histology and histopathology (01.08.2011)
Published in Histology and histopathology (01.08.2011)
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Incidents related to critical patient safety during in-hospital transfer
Catalán-Ibars, R.M., Martín-Delgado, M.C., Puigoriol-Juvanteny, E., Zapater-Casanova, E., Lopez-Alabern, M., Lopera-Caballero, J.L., González de Velasco, J.P., Coll-Solà, M., Juanola-Codina, M., Roger-Casals, N.
Published in Medicina intensiva (01.01.2022)
Published in Medicina intensiva (01.01.2022)
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Implementation of simplified diagnostic method Apnealink™Air® to diagnose sleep apnea by general practioners of primary care
Muñoz-Pindado, C, Muñoz-Herrera, E, Arribas-Peña, V, Roura-Poch, P, Ruiz-Mori, F, Sánchez-Belmonte, S, Mateu-Carralero, B, Callís-Privat, M, Darnés-Surroca, A, Casademunt-Codina, I, Serra-Batlle, J, Roger-Casals, N
Published in Semergen, medicina de familia (01.01.2022)
Published in Semergen, medicina de familia (01.01.2022)
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Refining the diagnosis of mitochondrial HMG‐CoA synthase deficiency
Aledo, R., Mir, C., Dalton, R. N., Turner, C., Pié, J., Hegardt, F. G., Casals, N., Champion, M. P.
Published in Journal of inherited metabolic disease (01.02.2006)
Published in Journal of inherited metabolic disease (01.02.2006)
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A single‐residue mutation, G203E, causes 3‐hydroxy‐3‐methylglutaric aciduria by occluding the substrate channel in the 3D structural model of HMG‐CoA lyase
Mir, C., Lopez‐Viñas, E., Aledo, R., Puisac, B., Rizzo, C., Dionisi‐Vici, C., Deodato, F., Pié, J., Gomez‐Puertas, P., Hegardt, F. G., Casals, N.
Published in Journal of inherited metabolic disease (01.02.2006)
Published in Journal of inherited metabolic disease (01.02.2006)
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Genetic basis of mitochondrial HMG-CoA synthase deficiency
Aledo, R, Zschocke, J, Pié, J, Mir, C, Fiesel, S, Mayatepek, E, Hoffmann, G F, Casals, N, Hegardt, F G
Published in Human genetics (01.07.2001)
Published in Human genetics (01.07.2001)
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Molecular basis of 3-hydroxy-3-methylglutaric aciduria
Pie, J, Casals, N, Puisac, B, Hegardt, F G
Published in Journal of physiology and biochemistry (01.12.2003)
Published in Journal of physiology and biochemistry (01.12.2003)
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Pomace Olive Oil Enriched In Oleanolic Acid Improves Diet-Induced Obesity And Exerts Protective Effects In Vascular Dysfunction And Metabolic Parameters
Cala, C.M. Claro, Quintela, J.C., Miñano, J., Pérez-Montero, M., Casals, N., Alvarez de Sotomayor, M., Herrera, M.D., Rodríguez-Rodríguez, R.
Published in Atherosclerosis (01.08.2019)
Published in Atherosclerosis (01.08.2019)
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Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia
Rinaldi, Carlo, Schmidt, Thomas, Situ, Alan J, Johnson, Janel O, Lee, Philip R, Chen, Ke-Lian, Bott, Laura C, Fadó, Rut, Harmison, George H, Parodi, Sara, Grunseich, Christopher, Renvoisé, Benoît, Biesecker, Leslie G, De Michele, Giuseppe, Santorelli, Filippo M, Filla, Alessandro, Stevanin, Giovanni, Dürr, Alexandra, Brice, Alexis, Casals, Núria, Traynor, Bryan J, Blackstone, Craig, Ulmer, Tobias S, Fischbeck, Kenneth H
Published in JAMA neurology (01.05.2015)
Published in JAMA neurology (01.05.2015)
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A two-base deletion in exon 6 of the 3-hydroxy-3-methylglutaryl coenzyme A lyase (HL) gene producing the skipping of exons 5 and 6 determines 3-hydroxy-3-methylglutaric aciduria
Casals, N, Pié, J, Casale, C H, Zapater, N, Ribes, A, Castro-Gago, M, Rodriguez-Segade, S, Wanders, R J, Hegardt, F G
Published in Journal of lipid research (01.11.1997)
Published in Journal of lipid research (01.11.1997)
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Aberrantly spliced mRNAs of the 3-hydroxy-3-methylglutaryl coenzyme A lyase (HL) gene with a donor splice-site point mutation produce hereditary HL deficiency
Buesa, C, Pié, J, Barceló, A, Casals, N, Mascaró, C, Casale, C H, Haro, D, Duran, M, Smeitink, J A, Hegardt, F G
Published in Journal of lipid research (01.11.1996)
Published in Journal of lipid research (01.11.1996)
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Buccal Fat Pad, an Oral Access Source of Human Adipose Stem Cells with Potential for Osteochondral Tissue Engineering: An In Vitro Study
Farré-Guasch, Elisabet, Martí-Pagès, Carles, Hernández-Alfaro, Federico, Klein-Nulend, Jenneke, Casals, Núria
Published in Tissue engineering. Part C, Methods (01.10.2010)
Published in Tissue engineering. Part C, Methods (01.10.2010)
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Ceramides and mitochondrial fatty acid oxidation in obesity
Fucho, Raquel, Casals, Núria, Serra, Dolors, Herrero, Laura
Published in The FASEB journal (01.04.2017)
Published in The FASEB journal (01.04.2017)
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