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Showing results 86 to 98 of 98 < previous 
Issue DateTitleAuthor(s)
19-Nov-2021Role of MUC1 rs4072037 polymorphism and serum KL-6 levels in patients with antisynthetase syndromeRemuzgo Martínez, Sara; Atienza Mateo, Belén; Ocejo Vinyals, J. Gonzalo; Genre, Fernanda; Pulito Cueto, Verónica; Mora Cuesta, Víctor M.; Iturbe Fernández, David; Lera Gómez, Leticia; Pérez Fernández, Raquel; Prieto Peña, Diana; Irure, Juan; Romero Bueno, Fredeswinda; Sanchez Pernaute, Olga; Alonso Moralejo, Rodrigo; Nuño, Laura; Bonilla, Gema; Vicente Rabaneda, Esther F.; Grafia, Ignacio; Prieto González, Sergio; Narváez, Javier; Trallero Araguas, Ernesto; Selva O’Callaghan, Albert; Ortego Centeno, Norberto; Pérez Gómez, Nair; Mera, Antonio; Martínez Barrio, Julia; Moriano, Clara; Díez, Elvira; Calvo Alén, Jaime; Balsa, Alejandro; Ussetti, María Piedad; Laporta, Rosalía; Berastegui, Cristina; Solé, Amparo; Gualillo, Oreste; Cavagna, Lorenzo; Cifrián, José M.; Renzoni, Elisabetta A.; Castañeda, Santos; López Mejías, Raquel; González Gay, Miguel A.; Spanish Biomarkers Of Antisynthetase Syndrome Consortium; Spanish Biomarkers Of Interstitial Lung Disease Consortium
9-Aug-2021Role of the IL33 and IL1RL1 pathway in the pathogenesis of Immunoglobulin A vasculitisPrieto Peña, Diana; Remuzgo Martínez, Sara; Genre, Fernanda; Pulito Cueto, Verónica; Atienza Mateo, Belén; Llorca Ballester, Jaime; Sevilla Pérez, Belén; Ortego Centeno, Norberto; Marquez, Ana; Lera Gómez, Leticia; Leonardo, María Teresa; Peñalba, Ana; Narváez García, Francisco Javier; Martín Penagos, Luis; Rodrigo, Emilio; Miranda Filloy, José A.; Caminal Montero, Luis; Collado, Paz; Sánchez Pérez, Javier; Argila, Diego de; Rubio, Esteban; León Luque, Manuel; Blanco Madrigal, Juan María; Galíndez Agirregoikoa, Eva; Gualillo, Oreste; Martín, Javier; Castañeda, Santos; Blanco, Ricardo; González Gay, Miguel A.; López Mejías, Raquel
12-Mar-2021Role of Wnt pathway genes in complex and monogenic phenotypes of low and high bone massMartínez-Gil, Núria
Nov-2013Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic and functional studiesCarreño, Oriel; Corominas Castiñeira, Roser; Serra, Selma Angèlica; Sintas Vives, Cèlia; Fernàndez Castillo, Noèlia; Vila Pueyo, Marta; Toma, Claudio; González Gené, Gemma; Pons, Roser; Llaneza, Miguel; Sobrido, María Jesús; Grinberg Vaisman, Daniel Raúl; Valverde, Miguel Ángel; Fernández-Fernández, José Manuel; Macaya Ruiz, Alfons; Cormand Rifà, Bru
24-Jan-2015Segmental neurofibromatosis type 2: discriminating two hit from four hit in a patient presenting multiple schwannomas confined to one limbCastellanos, Elisabeth; Bielsa, Isabel; Carrato, Cristina; Rosas, Inma; Solanes, Ares; Hostalot, Cristina; Amilibia, Emilio; Prades, José; Roca Ribas, Francesc; Lázaro García, Conxi; Blanco Guillermo, Ignacio; Serra Arenas, Eduard; NF2 Multidisciplinary Clinics HUGTiP-ICO-IMPPC
15-Sep-2017Síndromes Miasténicos Congénitos en Población Española: Caracterización Clínica, Genética y de su Respuesta TerapéuticaNatera de Benito, Daniel
Mar-2015Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromesNakagawa, Kenji; Gonzalez Roca, Eva; Souto, Alejandro; Kawai, Toshinao; Umebayashi, Hiroaki; Campistol Plana, Jaume; Cañellas, Jeronima; Takei, Syuji; Kobayashi, Norimoto; Callejas Rubio, José Luis; Ortego Centeno, Norberto; Ruiz Ortiz, Estíbaliz; Rius, Fina; Antón López, Jordi; Iglesias Jiménez, Estíbaliz; Jiménez Treviño, Santiago; Vargas, Carmen; Fernandez Martin, Julian; Calvo, Inmaculada; Hernández Rodríguez, José; Méndez, María; Dordal, María Teresa; Basagaña, Maria; Buján Rivas, Segundo; Yashiro, Masato; Kubota, Tetsuo; Koike, Ryuji; Akuta, Naoko; Shimoyama, Kumiko; Iwata, Naomi; Saito, Megumu K.; Ohara, Osamu; Kambe, Naotomo; Yasumi, Takahiro; Izawa, Kazushi; Kawai, Tomoki; Heike, Toshio; Yagüe, Jordi; Nishikomori, Ryuta; Aróstegui Gorospe, Juan Ignacio
31-May-2016Targeted next generation sequencing in patients with inborn errors of metabolismYubero Siles, Dèlia; Brandi, Nuria; Ormazabal Herrero, Aida; Garcia-Cazorla, Àngels; Pérez Dueñas, Belén; Campistol Plana, Jaume; Ribes Rubió, Maria Antònia; Palau Martínez, Francesc; Artuch Iriberri, Rafael; Armstrong i Morón, Judith
28-Nov-2014The COPD Knowledge Base: enabling data analysis and computational simulation in translational COPD researchCano Franco, Isaac; Tényi, Ákos; Schueller, Christine; Wolff, Martin; Huertas Migueláñez, M. Mercedes; Gomez Cabrero, David; Antczak, Philipp; Roca Torrent, Josep; Cascante i Serratosa, Marta; Falciani, Francesco; Maier, Dieter
16-Nov-2011The influence of genetic and environmental factors among MDMA users in cognitive performanceCuyàs, Elisabet; Verdejo García, Antonio; Fagundo, Ana Beatriz; Khymenets, Olha; Rodriguez, Joan; Cuenca, Aida; Sola Llopis, Susana de; Langohr, Klaus; Peña-Casanova, Jordi; Torrens, Marta; Martín-Santos Laffon, Rocío; Farré Albaladejo, Magí; Torre Fornell, Rafael de la
13-Jul-2021Towards disentangling the genetic complexity and clinical heterogeneity of psychotic disorders: from family-based approaches to gene-environment studiesSoler Garcia, Jordi
31-Jan-2022Unravelling genetic predisposition to familial breast and ovarian cancer: new susceptibility genes and variant interpretation by in silico approachesMoles Fernández, Alejandro
8-Feb-2013Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility AllelesGracia Aznarez, Francisco Javier; Fernandez, Victoria; Pita, Guillermo; Peterlongo, Paolo; Dominguez, Orlando; Hoya, Miguel de la; Durán, Mercedes; Osorio, Ana; Moreno, Leticia; González Neira, Anna; Rosa Rosa, Juan Manuel; Sinilnikova, Olga M.; Mazoyer, Sylvie; Hopper, John L.; Lázaro García, Conxi; Southey, Melissa C.; Odefrey, Fabrice; Manoukian, Siranoush; Catucci, Irene; Caldes, Trinidad; Lynch, Henry T.; Hilbers, Florentine S. M.; van Asperen, Christi J.; Vasen, Hans; Goldgar, David E.; Radice, Paolo; Devilee, Peter; Benitez, Javier