Browsing by Author Lucas, Miguel

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 7 of 7
PreviewTitleAuthor(s)Issue Date
A PRKAR1A Mutation Associated with Primary Pigmented Nodular Adrenocortical Disease in 12 KindredsGroussin, Lionel; Horvath, Anelia; Jullian, Eric; Boikos, Sosipatros; Rene-Corail, Fernande; Lefebvre, Herve; Cephise-Velayoudom, Fritz-Line; Vantyghem, Marie-Cristine; Chanson, Philippe; Conte-Devolx, Bernard; Lucas, Miguel; Gentil, Alfonso; Malchoff, Carl D; Tissier, Frédérique; Carney, J Aidan; Bertagna, Xavier; Stratakis, Constantine A; Bertherat, JérômeMay-2006
Fine mapping and functional analysis of the multiple sclerosis risk gene CD6.Swaminathan, Bhairavi; Cuapio, Angélica; Alloza, Iraide; Matesanz, Fuencisla; Alcina, Antonio; García-Barcina, Maria; Fedetz, Maria; Fernández, Oscar; Lucas, Miguel; Orpez, Teresa; Pinto-Medel, M Jesus; Otaegui, David; Olascoaga, Javier; Urcelay, Elena; Ortiz, Miguel A; Arroyo, Rafael; Oksenberg, Jorge R; Antigüedad, Alfredo; Tolosa, Eva; Vandenbroeck, Koen24-Apr-2013
Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1.Matesanz, Fuencisla; González-Pérez, Antonio; Lucas, Miguel; Sanna, Serena; Gayán, Javier; Urcelay, Elena; Zara, Ilenia; Pitzalis, Maristella; Cavanillas, María L; Arroyo, Rafael; Zoledziewska, Magdalena; Marrosu, Marisa; Fernández, Oscar; Leyva, Laura; Alcina, Antonio; Fedetz, Maria; Moreno-Rey, Concha; Velasco, Juan; Real, Luis M; Ruiz-Peña, Juan Luis; Cucca, Francesco; Ruiz, Agustín; Izquierdo, Guillermo3-May-2012
HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV.García-Montojo, Marta; Hera, Belén de la; Varadé, Jezabel; Encarnación, Ana de la; Camacho, Iris; Domínguez-Mozo, María; Árias-Leal, Ana; García-Martínez, Angel; Casanova, Ignacio; Izquierdo, Guillermo; Lucas, Miguel; Fedetz, Maria; Alcina, Antonio; Arroyo, Rafael; Matesanz, Fuencisla; Urcelay, Elena; Alvarez-Lafuente, Roberto9-Jan-2014
IL2RA/CD25 gene polymorphisms: uneven association with multiple sclerosis (MS) and type 1 diabetes (T1D).Alcina, Antonio; Fedetz, María; Ndagire, Dorothy; Fernández, Oscar; Leyva, Laura; Guerrero, Miguel; Abad-Grau, María M; Arnal, Carmen; Delgado, Concepción; Lucas, Miguel; Izquierdo, Guillermo; Matesanz, Fuencisla6-Jan-2009
Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations.Alcina, Antonio; Fedetz, María; Izquierdo, Guillermo; Lucas, Miguel; Fernández, Oscar; Ndagire, Dorothy; Catalá-Rabasa, Antonio; Ruiz, Agustín; Gayán, Javier; Delgado, Concepción; Arnal, Carmen; Matesanz, Fuencisla13-Jan-2012
Mutation prevalence of cerebral cavernous malformation genes in Spanish patients.Mondéjar, Rufino; Solano, Francisca; Rubio, Rocío; Delgado, Mercedes; Pérez-Sempere, Angel; González-Meneses, Antonio; Vendrell, Teresa; Izquierdo, Guillermo; Martinez-Mir, Amalia; Lucas, Miguel23-Jan-2014