Search Results - "Rioja Villodres, J."

Higher insulin resistance is associated with reduced cerebral glucose metabolism in the temporal lobe with f-18 fluorodeoxyglucose positron emission tomography by García-Casares, N, García-Arnes, J.A, Cardo, A. Gutiérrez, Rioja-Villodres, J, Ariza-Corbo, M.J, Nabrozidis, A, González-Santos, P

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Higher insulin resistance is associated with cerebral atrophy in temporal lobe by García-Casares, N, Rioja-Villodres, J, García-Arnes, J.A, Ariza-Corbo, M.J, Nabrozidis, A, Alfaro-Rubio, F, Cardo, A. Gutiérrez, González-Santos, P

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Early detection of a patient with family hypertriglyceridemia by telemedicine laboratory program by Velilla, T. Arrobas, Moreno, R. Gonzalez, Corbo, M.J. Ariza, Corral, M.A. Rico, Villodres, J. Rioja, Felices, P. Valdivielso

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Clinical laboratory implication in the early detection of genetic duslipemias in primary care by Alguacil, B. Gallardo, Velilla, T. Arrobas, Corral, M.A. Rico, Villodres, J. Rioja, Corbo, M.J. Ariza, Felices, P. Valdivielso

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Molecular basis of the familial chylomicronemia syndrome in patients from the National Dyslipidemia Registry of the Spanish Atherosclerosis Society by Ariza, María José, Rioja, José, Ibarretxe, Daiana, Camacho, Ana, Díaz-Díaz, José Luis, Mangas, Alipio, Carbayo-Herencia, Julio A., Ruiz-Ocaña, Pablo, Lamíquiz-Moneo, Itziar, Mosquera, Daniel, Sáenz, Pedro, Masana, Luis, Muñiz-Grijalvo, Ovidio, Pérez-Calahorra, Sofía, Valdivielso, Pedro, Suárez Tembra, M., Iglesias, Gonzalo Pías, Carbayo Herencia, J.A., Guerrero Buitrago, C., Vila, L., Morales Coca, C., Llargués Rocabruna, E., Perea Castillo, V., Pedro-Botet, J., Climent, E., Mauri Pont, M., Pinto, X., Ortega Martínez de la Victoria, E., Amor, J., Zambón Rados, D., Blanco Vaca, F., Ramiro Lozano, J.M., Fuentes Jiménez, F.J., Soler, I., Ferrer, C., Zamora Cervantes, A., Vila Belmonte, A., Novoa Mogollón, F.J., Sanchez-Hernández, R.M., Expósito Montesdeoca, A.B., Romero Jiménez, M.J., González García, M.P., Bueno Díez, M., Brea Hernando, A., Lahoz, C., Mostaza Prieto, J., Millán Núñez-Cortés, J., Reinares García, L., Blanco Echevarría, A., Ariza Corbo, María José, Rioja Villodres, J., Sánchez-Chaparro, M.A., Jansen Chaparro, S., Sáenz Aranzubía, P., Martorell Mateu, E., Almagro Múgica, F., Muñiz Grijalvo, O., Masana Martín, L., Plana Gil, N., Ibarretxe Gerediaga, D., Rodríguez Borjabad, C., Zabala López, S., Hernández Mijares, A., Ascaso Gimilio, J.F., Pérez García, L., Civeira Murillo, F., Pérez-Calahorra, S., Lamiquiz-Moneo, I., Mateo Gallego, R., Marco Benedí, V., Ferrando Vela, J.

“…Familial chylomicronemia syndrome (FCS) is an extremely rare lipoprotein disorder caused by mutations in at least 5 genes of the lipoprotein lipase (LPL)…”
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