Current review of genetics of human obesity: from molecular mechanisms to an evolutionary perspective von Albuquerque, David, Stice, Eric, Rodríguez-López, Raquel, Manco, Licíno, Nóbrega, Clévio

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Sputum cytokines associated with raised FeNO after anti‐IL5 biologic therapy in severe asthma von Hekking, Pieter‐Paul, Zhang, Kayla, Garrido, Carmen Paz Venegas, Lopez‐Rodriguez, Raquel, Kjarsgaard, Melanie, Mukherjee, Manali, Nair, Parameswaran

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Autoinflammatory gene mutations associated with eosinophilia and asthma von Alotaibi, Bashayr M, Lopez Rodriguez, Raquel, Garrido, Carmen Venegas, Gonzalez Bravo, Lucia, Khalidi, Nader, Nair, Parameswaran

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Prenatal genetic diagnosis of monogenic diseases von Prior-de Castro, Carmen, Gómez-González, Clara, Rodríguez-López, Raquel, Macher, Hada C.

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Association study of common polymorphisms in MSRA, TFAP2B, MC4R, NRXN3, PPARGC1A, TMEM18, SEC16B, HOXB5 and OLFM4 genes with obesity-related traits among Portuguese children von Albuquerque, David, Nóbrega, Clévio, Rodríguez-López, Raquel, Manco, Licínio

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Diagnostic and Prognostic Value of Angiogenic Status in Hereditary Hemorrhagic Telangiectasia von Jaimes-Díaz, Sherlyne, Juan-Samper, Gustavo, Torres-Martínez, Susana, Escorihuela-Alares, Eva, Calabuig-Fariñas, Silvia, Rodríguez-López, Raquel, Prieto-Colodrero, Nieves, Ramon-Capilla, Mercedes, Fernández-Fabrellas, Estrella

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Differences in Gene Expression of Endogenous Opioid Peptide Precursor, Cannabinoid 1 and 2 Receptors and Interleukin Beta in Peripheral Blood Mononuclear Cells of Patients With Ref... von De Andrés, Jose, Navarrete‐Rueda, Francisco, Fabregat, Gustavo, García‐Gutiérrez, Maria Salud, Monsalve‐Dolz, Vincente, Harutyunyan, Anushik, Mínguez‐Martí, Ana, Rodriguez‐Lopez, Raquel, Manzanares, Jorge

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The effect of copy number variations in chromosome 16p on body weight in patients with intellectual disability von Gimeno-Ferrer, Fátima, Albuquerque, David, Guzmán Luján, Carola, Marcaida Benito, Goitzane, Torreira Banzas, Cristina, Repáraz-Andrade, Alfredo, Ballesteros Cogollos, Virginia, Aleu Pérez-Gramunt, Montserrat, Galán Gómez, Enrique, Quintela, Inés, Rodríguez-López, Raquel

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Previously Undescribed Family Mutation in the JAG1 Gene as a Cause for Alagille Syndrome von Muñoz‐Aguilar, Gemma, Domingo‐Triadó, Ignacio, Maravall‐Llagaria, María, Alcón‐Sáez, José J., Rodríguez‐López, Raquel

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Dental Phenotype with Minor Ectodermal Symptoms Suggestive of WNT10A Deficiency von García-Martínez, Victoria-Eugenia, Galiana-Vallés, Ximo, Zomeño-Alcalá, Otilia, Rodríguez-López, Raquel, Llena, Carmen, Martínez-Romero, María Del Carmen, Guillén-Navarro, Encarna

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Influence of TFAP2B and KCTD15 genetic variability on personality dimensions in anorexia and bulimia nervosa von Gamero‐Villarroel, Carmen, González, Luz M., Rodríguez‐López, Raquel, Albuquerque, David, Carrillo, Juan A., García‐Herráiz, Angustias, Flores, Isalud, Gervasini, Guillermo

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Polymorphisms in the SNRPN gene are associated with obesity susceptibility in a Spanish population von Albuquerque, David, Manco, Licínio, González, Luz M., Gervasini, Guillermo, Benito, Goitzane Marcaida, González, Juan R., Rodríguez‐López, Raquel

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Silver: An underdiagnosed allergen? von Lopez Rodriguez, Raquel, Goday Bujan, Jaime

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The modifier effect of the BDNF gene in the phenotype of the WAGRO syndrome von Rodríguez-López, Raquel, Pérez, José M. Carbonell, Balsera, Aránzazu Margallo, Rodríguez, Guillermo Gervasini, Moreno, Trinidad Herrera, García de Cáceres, Mayte, Serrano, Marta González-Carpio, Freijo, Felipe Casanueva, Ruiz, Juan Ramón González, Angueira, Francisco Barros, Pérez, Pilar Méndez, Estévez, Manuela Núñez, Gómez, Enrique Galán

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Retrospective variant reclassification and resequencing in hypertrophic cardiomyopathy: a reference unit centre experience von Cuesta-Llavona, Elías, Lorca, Rebeca, Salgado, María, García-Lago, Claudia, Rodríguez-Reguero, Julián, Rodríguez-López, Raquel, Escribano-Hernández, Vanesa, Peña-Cabia, Ana, Vázquez-Coto, Daniel, Pascual, Isaac, Coto, Eliecer, Gómez, Juan

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Twelve-year follow up of a case of autosomal recessive bestrophinopathy with transient resolution of retinal edema in one eye von Remolí Sargues, Lidia, Monferrer Adsuara, Clara, Rodríguez López, Raquel, Gallego Pinazo, Roberto, Montero Hernández, Javier, Castro Navarro, Verónica, Cervera Taulet, Enrique

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Genetic screening for MC4R gene identifies three novel mutations associated with severe familiar obesity in a cohort of Spanish individuals von Gimeno-Ferrer, Fátima, Albuquerque, David, García Banacloy, Amor, Guzmán Luján, Carola, Vidal Garcia, Clara, Marcaida Benito, Goitzane, Sánchez Juan, Carlos, Bruna Esteban, Marcos, Rodríguez-López, Raquel

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Immune Deficiency in Jacobsen Syndrome: Molecular and Phenotypic Characterization von Rodríguez-López, Raquel, Gimeno-Ferrer, Fátima, Montesinos, Elena, Ferrer-Bolufer, Irene, Luján, Carola Guzmán, Albuquerque, David, Cataluña, Carolina Monzó, Ballesteros, Virginia, Pérez-Gramunt, Monserrat Aleu

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BDNF genetic variability modulates psychopathological symptoms in patients with eating disorders von Gamero-Villarroel, Carmen, Gordillo, Inmaculada, Carrillo, Juan Antonio, García-Herráiz, Angustias, Flores, Isalud, Jiménez, Mercedes, Monge, Melchora, Rodríguez-López, Raquel, Gervasini, Guillermo

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The variant E233G of the RAD51D gene could be a low‐penetrance allele in high‐risk breast cancer families without BRCA1/2 mutations von Rodríguez‐López, Raquel, Osorio, Ana, Ribas, Gloria, Pollán, Marina, Sánchez‐Pulido, Luis, de la Hoya, Miguel, Ruibal, Álvaro, Zamora, Pilar, Arias, Jose Ignacio, Salazar, Raquel, Vega, Ana, Martínez, Jose Ignacio, Esteban‐Cardeñosa, Eva, Alonso, Carmen, Letón, Rocío, Urioste Azcorra, Miguel, Miner, Cristina, Armengod, M. Eugenia, Carracedo, Angel, González‐Sarmiento, Rogelio, Caldés, Trinidad, Díez, Orland, Benítez, Javier

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