Search Results - "Rodríguez Borjabad, C."

Lipoprotein profile assessed by 1H NMR, BMI and blood pressure are associated with vascular alterations in children with familial hypercholesterolaemia by Llop, D., Feliu, A., Ibarretxe, D., Escribano, J., Plana, N., Borjabad-Rodríguez, C., Masana, L., Vallvé, J.C.

“…Children with familial hypercholesterolaemia (FH) have elevated low-density lipoprotein cholesterol (LDL-C) concentrations since birth, which increases the…”
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Significant Impact Of A Lifestyle Educational Program On Children With Genetically Driven Hypercholesterolemia by Rodríguez-Borjabad, C., Ibarretxe, D., Feliu, A., Ferré, R., Rosell, L., Gil, M., Masana, L., Plana, N.

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Plasma IDOL, soluble LDLR and PCSK9 levels as potential biomarkers of familial hypercholesterolemia in children by Girona, J., Rodríguez-Borjabad, C., Ibarretxe, D., Heras, M., Amigó, N., Feliu, A., Masana, L., Plana, N.

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Circulating Grp78/Bip Is Increased In Patients With Obesity And Related Metabolic Disorders And Is Associated With Atherosclerosis by Girona, J., Rodríguez-Borjabad, C., Ibarretxe, D., Vallvé, J.C., Ferré, R., Heras, M., Rodríguez-Calvo, R., Guaita-Esteruelas, S., Martínez-Micaelo, N., Plana, N., Masana, L.

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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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Cardiopatía isquémica con o sin signo de Frank by Ramírez, R., Perales, R., Carulla, M., Rodríguez-Borjabad, C.

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Ischemic heart disease with or without Frank's sign by Ramírez, R, Perales, R, Carulla, M, Rodríguez-Borjabad, C

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