Search Results - "Jimenez, Víctor Martinez"

Hypouricemia in a patient with metabolic syndrome by Hernández González, Ana Noelia, Valda de Miguel, María Teresa, Ortuño López, Pedro Pablo, Albero Dolón, José Luis, Martínez Jiménez, Víctor, Cabezuelo Romero, Juan Bernardo

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Oral-facio-digital syndrome type I: In the differential diagnosis of autosomic dominant polycystic kidney disease, about three cases by Martínez Jiménez, Víctor, Ortuño López, Pedro Pablo, Roca Meroño, Susana, Rodríguez Peña, Lidia, Galán Carrillo, Isabel, Galbis Martínez, Liliana, Ramos Carrasco, Fernanda, Piñero Hernández, Juan Alberto, González Rodríguez, Juan David, Guillén Navarro, Encarnación

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Are Kidney Cysts More Frequent in Individuals With COL4A3-COL4A4 Pathogenic Variants?: PUB197 by Teran, Melissa Pilco, Furlano, Monica, Jimenez, Víctor Martinez, Pybus, Marc, vanessa Pérez gómez, María, Peris, Asunción Rius, de Arizón, Leonor Fayos, Berná, Gerson, Mancera, Jonathan Hernandez, Pérez, Hugo Vergara, Ars, Elisabet, Torra, Roser

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The importance of the number of antihypertensives in the progression of autosomal dominant polycystic kidney disease by Martínez Jiménez, Víctor, Hernández González, Ana Noelia, López Jiménez, Inmaculada, Rodríguez Peña, Lidya, Galbis Martínez, Liliana, Santa-Olalla González, Manuel, Ruiz Merino, Guadalupe, Guillén Navarro, Encarna

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An atlas of cells in the human tonsil by Massoni-Badosa, Ramon, Aguilar-Fernández, Sergio, Nieto, Juan C, Soler-Vila, Paula, Elosua-Bayes, Marc, Marchese, Domenica, Kulis, Marta, Vilas-Zornoza, Amaia, Bühler, Marco Matteo, Rashmi, Sonal, Alsinet, Clara, Caratù, Ginevra, Moutinho, Catia, Ruiz, Sara, Lorden, Patricia, Lunazzi, Giulia, Colomer, Dolors, Frigola, Gerard, Blevins, Will, Romero-Rivero, Lucia, Jiménez-Martínez, Víctor, Vidal, Anna, Mateos-Jaimez, Judith, Maiques-Diaz, Alba, Ovejero, Sara, Moreaux, Jérôme, Palomino, Sara, Gomez-Cabrero, David, Agirre, Xabier, Weniger, Marc A, King, Hamish W, Garner, Lucy C, Marini, Federico, Cervera-Paz, Francisco Javier, Baptista, Peter M, Vilaseca, Isabel, Rosales, Cecilia, Ruiz-Gaspà, Silvia, Talks, Benjamin, Sidhpura, Keval, Pascual-Reguant, Anna, Hauser, Anja E, Haniffa, Muzlifah, Prosper, Felipe, Küppers, Ralf, Gut, Ivo Glynne, Campo, Elias, Martin-Subero, José Ignacio, Heyn, Holger

“…Palatine tonsils are secondary lymphoid organs (SLOs) representing the first line of immunological defense against inhaled or ingested pathogens. We generated…”
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Lymphoma lurks within aged B cells by Pérez, Raúl F., Jiménez-Martínez, Víctor, Martín-Subero, José I.

“…Cancer and aging are inextricably linked conditions. However, whether cancer emerges as a byproduct of the aging process or whether aged cells themselves are…”
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Análisis de procedencia de la Formación Tena en el río Anzu, Puyo – Ecuador by Romero-Cóndor, Christian Wladimir, Cervantes-Gualuchico, Heidy Liliana, Oyague-Vergara, Emilio José, Heredia-Puente, Sofia Tatiana, Pazmiño-Aguiar, Paola Dominique, Proaño-Altamirano, Antonio Patricio, Ortiz-Mercado, María Angelica, Carranco-Andino, Fausto Rodolfo, Guerrero-Tamayo, Erick Javier, Martínez-Jimenez, Víctor Horacio

“…La mega secuencia sedimentaria del Cretácico Superior de la cuenca Oriente en Ecuador se compone por las formaciones Hollín, Napo y Tena, que ha sido…”
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Clinical and Genetic Features of Autosomal Dominant Alport Syndrome: PO1598 by Furlano, Monica, Jimenez, Vĭctor Martinez, Pybus, Marc, Gallego, Andrea Domingo, Ayasreh, Nadia, Garcĭa, Silvia Benito, Gallego, Rosa Arlandis, Ars, Elisabet, Torra, Roser

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Treatment and long-term outcome in primary nephrogenic diabetes insipidus by Lopez-Garcia, Sergio C, Downie, Mallory L, Kim, Ji Soo, Boyer, Olivia, Walsh, Stephen B, Nijenhuis, Tom, Papizh, Svetlana, Yadav, Pallavi, Reynolds, Ben C, Decramer, Stéphane, Besouw, Martine, Perelló Carrascosa, Manel, La Scola, Claudio, Trepiccione, Francesco, Ariceta, Gema, Hummel, Aurélie, Dossier, Claire, Sayer, John A, Konrad, Martin, Keijzer-Veen, Mandy G, Awan, Atif, Basu, Biswanath, Chauveau, Dominique, Madariaga, Leire, Koster-Kamphuis, Linda, Furlano, Mónica, Zacchia, Miriam, Marzuillo, Pierluigi, Tse, Yincent, Dursun, Ismail, Pinarbasi, Ayse Seda, Tramma, Despoina, Hoorn, Ewout J, Gokce, Ibrahim, Nicholls, Kathleen, Eid, Loai A, Sartz, Lisa, Riordan, Michael, Hooman, Nakysa, Printza, Nikoleta, Bonny, Olivier, Arango Sancho, Pedro, Schild, Raphael, Sinha, Rajiv, Guarino, Stefano, Martinez Jimenez, Victor, Rodríguez Peña, Lidia, Belge, Hendrica, Devuyst, Olivier, Wlodkowski, Tanja, Emma, Francesco, Levtchenko, Elena, Knoers, Nine V A M, Bichet, Daniel G, Schaefer, Franz, Kleta, Robert, Bockenhauer, Detlef

“…Abstract Background Primary nephrogenic diabetes insipidus (NDI) is a rare disorder and little is known about treatment practices and long-term outcome…”
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Hipouricemia en paciente con síndrome metabólico by Hernández González, Ana Noelia, Valda de Miguel, María Teresa, Ortuño López, Pedro Pablo, Albero Dolón, José Luis, Martínez Jiménez, Víctor, Cabezuelo Romero, Juan Bernardo

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Síndrome orofaciodigital tipo i: en el diagnóstico diferencial de la poliquistosis renal autosómica dominante, a próposito de 3 casos by Martínez Jiménez, Víctor, Ortuño López, Pedro Pablo, Roca Meroño, Susana, Rodríguez Peña, Lidia, Galán Carrillo, Isabel, Galbis Martínez, Liliana, Ramos Carrasco, Fernanda, Piñero Hernández, Juan Alberto, González Rodríguez, Juan David, Guillén Navarro, Encarnación

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Usefulness of an specific out patient clinic on hereditary kidney diseases: A different approach based on the family tree by Martínez Jiménez, Víctor, Ramos Carrasco, Fernanda, Alcázar Fajardo, Concepción, Cabezuelo Romero, Juan Bernardo

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La importancia del número de antihipertensivos en la progresión de la poliquistosis renal autosómica dominante by Martínez Jiménez, Víctor, Hernández González, Ana Noelia, López Jiménez, Inmaculada, Rodríguez Peña, Lidya, Galbis Martínez, Liliana, Santa-Olalla González, Manuel, Ruiz Merino, Guadalupe, Guillén Navarro, Encarna

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Utilidad de una consulta de enfermedades renales hereditarias: un enfoque diferente basado en el árbol genealógico by Martínez Jiménez, Víctor, Ramos Carrasco, Fernanda, Alcázar Fajardo, Concepción, Cabezuelo Romero, Juan B.

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3812 ARE KIDNEY CYSTS MORE COMMON IN PEOPLE WITH COL4A3/COL4A4 PATHOGENIC VARIANTS? by Teran, Melissa Pilco, Furlano, Monica, Pybus, Marc, Jiménez, Víctor Martínez, Peris, Asunción Rius, Gomez, Maria Vanessa Perez, Redondo, Gerson Berna, De Arizon, Leonor Fayos, Ars, Elisabet, Torra, Roser

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2068 Factors affecting disease progression in individuals with heterozygous COL4A3/COL4A4 pathogenic variants by Teran, Melissa Pilco, Furlano, Monica, Pybus, Marc, Jiménez, Víctor Martínez, Gomá-Garcés, Elena, Carrillo, Isabel Galan, Leon, Rafael, Romeo, Maria Jose Soler, de Arizón, Leonor Fayos, Perera, Alexandre, Ars, Elisabet, Torra, Roser

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MO039: Multidisciplinary approach improves genetic diagnosis of Alport syndrome in the next-generation sequencing ERA by Galan Carrillo, Isabel, Galbis, Liliana, Martínez Jiménez, Víctor, Pablo Ortuño, Pedro, Roca, Susana, David Castro, Juan, Ramos, Fernanda, Rodríguez, Lidia, Guillén, Encarnación

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MO044TARGETED NEXT GENERATION SEQUENCING AND MULTIDISCIPLINARY APPROACH IN AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE, ALPORT DISEASE AND FAMILIAL HAEMATURIA: GENETIC SPECTRUM AND CLINICAL UTILITY IN A SPANISH COHORT by Galan Carrillo, Isabel, Galbis, Liliana, Martínez Jiménez, Víctor, Castro, Juan David, Ramos, Fernanda, Roca, Susana, Rodríguez, Lidia, Piñero, Juan, Guillén, Encarnación

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SP016PARENTS WERE DIAGNOSED OF HEREDITARY NEPHROPATHY BY THE PEDIATRIC by Martínez Jiménez, Víctor, Alonso García, Andres, García Arnedo, Carlota, Vicente Calderon, Carmen, Piñero Fernández, Juan A

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Oral-facio-digital syndrome type I: In the differential diagnosis of autosomic dominant polycystic kidney disease, about three cases by Martínez Jiménez, Víctor, Ortuño López, Pedro Pablo, Roca Meroño, Susana, Rodríguez Peña, Lidia, Galán Carrillo, Isabel, Galbis Martínez, Liliana, Ramos Carrasco, Fernanda, Piñero Hernández, Juan Alberto, González Rodríguez, Juan David, Guillén Navarro, Encarnación

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