Microvascular COX-2/mPGES-1/EP-4 axis in human abdominal aortic aneurysm von Camacho, Mercedes, Dilmé, Jaume, Solà-Villà, David, Rodríguez, Cristina, Bellmunt, Sergi, Siguero, Laura, Alcolea, Sonia, Romero, José-María, Escudero, José-Román, Martínez-González, José, Vila, Luis

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Tumor cells induce COX-2 and mPGES-1 expression in microvascular endothelial cells mainly by means of IL-1 receptor activation von Casós, Kelly, Siguero, Laura, Fernández-Figueras, María-Teresa, León, Xavier, Sardá, María-Pilar, Vila, Luis, Camacho, Mercedes

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Genetic determinants of 5-lipoxygenase pathway in a Spanish population and their relationship with cardiovascular risk von Camacho, Mercedes, Martinez-Perez, Angel, Buil, Alfonso, Siguero, Laura, Alcolea, Sonia, López, Sonia, Fontcuberta, Jordi, Souto, Juan-Carlos, Vila, Luis, Soria, José-Manuel

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Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy von Sarkozy, Anna, López Siguero, Juan P, Tartaglia, Marco, Ackerman, Michael J, Rossi, Cesare, Digilio, Maria C, Mundel, Peter, Torrente, Isabella, Tenconi, Romano, Mazzanti, Laura, Selicorni, Angelo, Landstrom, Andrew, Marino, Bruno, Bos, J Martijn, Pogna, Edgar A, Oishi, Kimihiko, Gelb, Bruce D, Martinelli, Simone, Schackwitz, Wendy, Pennacchio, Len A, Carta, Claudio, Pandit, Bhaswati, Ustaszewska, Anna, Zampino, Giuseppe, Ommen, Steve R, Dallapiccola, Bruno, Esposito, Giorgia, Lepri, Francesca, Faul, Christian

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Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR: Expanding the PORD Phenotype von Parween, Shaheena, Fernández-Cancio, Mónica, Benito-Sanz, Sara, Camats, Núria, Rojas Velazquez, Maria Natalia, López-Siguero, Juan-Pedro, Udhane, Sameer S, Kagawa, Norio, Flück, Christa E, Audí, Laura, Pandey, Amit V

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Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype von Camats, Núria, Fernández-Cancio, Mónica, Audí, Laura, Mullis, Primus E, Moreno, Francisca, González Casado, Isabel, López-Siguero, Juan Pedro, Corripio, Raquel, Bermúdez de la Vega, José Antonio, Blanco, José Antonio, Flück, Christa E

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Biochemical and Functional Characterization of a Novel Mutation in the NADPH Cytochrome P450 Oxidoreductase von Pandey, Amit V, Benito‐Sanz, Sara, Parween, Shaheena, López‐Siguero, Juan‐Pedro, Camats, Núria, Fernández‐Cancio, Mónica, Udhane, Sameer S, Kagawa, Norio, Flück, Christa E, Audí, Laura

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Current situation of adult women with Turner syndrome in Spain von Godoy-Molina, Elena, López-Castillo, María del Carmen, Galán-Bueno, Laura, Morejón-García, Estrella, López-Siguero, Juan Pedro

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Current situation of adult women with Turner syndrome in Spain von Godoy-Molina, Elena, López-Castillo, María del Carmen, Galán-Bueno, Laura, Morejón-García, Estrella, López-Siguero, Juan Pedro

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Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism Genotype Frequencies in Spanish Short Small-for-Gestational-Age (SGA) Children and Adolescents (n = 247) and in an A... von Audí, Laura, Esteban, Cristina, Carrascosa, Antonio, Espadero, Rosa, Pérez-Arroyo, Annalisa, Arjona, Rosa, Clemente, María, Wollmann, Hartmut, Fryklund, Linda, Parodi, Luis A.

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Obesity associated with melanocortin 4 receptor: Different phenotype expression in the same family von Trujillo Caballero, Laura, Martín Tejedor, Beatriz María, López-Siguero, Juan Pedro

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Obesidad asociada al receptor 4 de la melanocortina: diferente expresión fenotípica en la misma familia von Trujillo Caballero, Laura, Martín Tejedor, Beatriz María, López-Siguero, Juan Pedro

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The exon 3-deleted/full-length Growth Hormone Receptor Polymorphism Does Not Influence the Effect of Puberty or Growth Hormone Therapy on Glucose Homeostasis in Short Non-Growth Ho... von Audí, L., Carrascosa, A., Esteban, C., Fernández-Cancio, M., Andaluz, P., Yeste, D., Espadero, R., Granada, M. L., Wollmann, H., Fryklund, L.

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Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype: e0142831 von Camats, Nuria, Fernandez-Cancio, Monica, Audi, Laura, Mullis, Primus E, Moreno, Francisca, Casado, Isabel Gonzalez, Lopez-Siguero, Juan Pedro, Corripio, Raquel, Vega, Bermudez dela, Blanco, Jose Antonio

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Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype von Camats Tarruella, Núria, Fernández Cancio, Mónica, Audí, Laura, Mullis, Primus E, Moreno, Francisca, González Casado, Isabel, López-Siguero, Juan Pedro, Corripio, Raquel, Bermúdez de la Vega, José Antonio, Blanco, José Antonio, Flück, Christa E, Universitat Autònoma de Barcelona

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Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype von Camats Tarruella, Núria, Fernández Cancio, Mónica, Audí, Laura, Mullis, Primus E, Moreno, Francisca, González Casado, Isabel, López-Siguero, Juan Pedro, Corripio, Raquel, Bermúdez de la Vega, José Antonio, Blanco, José Antonio, Flück, Christa E, Universitat Autònoma de Barcelona

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Clinical practice guidelines for assessment and treatment of transsexualism. SEEN Identity and Sexual Differentiation Group (GIDSEEN) von Moreno-Pérez, Oscar, Esteva De Antonio, Isabel

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Obesity associated with melanocortin 4 receptor: Different phenotype expression in the same family von Trujillo Caballero, Laura, Martín Tejedor, Beatriz María, López-Siguero, Juan Pedro

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