Zobrazeno 1 - 10
of 138
pro vyhledávání: '"Itziar, Astigarraga"'
MYC-rearranged mature B-cell lymphomas in children and young adults are molecularly Burkitt Lymphoma
Autor:
Sara Mato, Natalia Castrejón-de-Anta, Ariadna Colmenero, Lorenzo Carità, Julia Salmerón-Villalobos, Joan Enric Ramis-Zaldivar, Ferran Nadeu, Noelia Garcia, Luojun Wang, Jaime Verdú-Amorós, Mara Andrés, Nuria Conde, Verónica Celis, Maria José Ortega, Ana Galera, Itziar Astigarraga, Vanesa Perez-Alonso, Eduardo Quiroga, Aixiang Jiang, David W. Scott, Elias Campo, Olga Balagué, Itziar Salaverria
Publikováno v:
Blood Cancer Journal, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Aggressive B-cell non-Hodgkin lymphomas (NHL) in children, adolescents, and young adults (CAYA) include Burkitt lymphoma (BL), diffuse large B-cell lymphoma (DLBCL), and a subset of high-grade tumors with features intermediate between these
Externí odkaz:
https://doaj.org/article/b5511b21c2894e89b35f88764713ba8c
Autor:
Piedad Alba-Pavón, Lide Alaña, Miriam Gutierrez-Jimeno, Susana García-Obregón, Teresa Imízcoz, Elena Panizo, Paula González-Urdiales, Aizpea Echebarria-Barona, Ricardo Lopez Almaraz, Laura Zaldumbide, Itziar Astigarraga, Ana Patiño-García, Olatz Villate
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Genetic predisposition is an important risk factor for cancer in children and adolescents but detailed associations of individual genetic mutations to childhood cancer are still under intense investigation. Among pediatric cancers, sarcomas
Externí odkaz:
https://doaj.org/article/7606fb96c3924139bf9bc42a708d0fc4
Autor:
Angela Gutierrez-Camino, Maxime Caron, Chantal Richer, Claire Fuchs, Unai Illarregi, Lucas Poncelet, Pascal St-Onge, Alain R. Bataille, Pascal Tremblay-Dauphinais, Elixabet Lopez-Lopez, Mireia Camos, Manuel Ramirez-Orellana, Itziar Astigarraga, Éric Lécuyer, Guillaume Bourque, Idoia Martin-Guerrero, Daniel Sinnett
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 3, p 1477 (2024)
Childhood B-cell acute lymphoblastic leukemia (B-ALL) is a heterogeneous disease comprising multiple molecular subgroups with subtype-specific expression profiles. Recently, a new type of ncRNA, termed circular RNA (circRNA), has emerged as a promisi
Externí odkaz:
https://doaj.org/article/e3bdca681b954271a19f7a92bf315bde
Autor:
Patricia Reparaz, Idoya Serrano, Rosa Adan-Pedroso, Itziar Astigarraga, Jimena de Pedro Olabarri, Aizpea Echebarria-Barona, Miguel Garcia-Ariza, Ricardo Lopez-Almaraz, Rafael Andrés del Orbe-Barreto, Miriam Vara-Pampliega, Paula Gonzalez-Urdiales
Publikováno v:
Anales de Pediatría, Vol 97, Iss 1, Pp 4-11 (2022)
Resumen: Introducción: La drepanocitosis es una anemia emergente en Europa que condiciona una elevada morbilidad con complicaciones agudas y crónicas. El manejo de estos pacientes es complejo y requiere atención interdisciplinar. El objetivo del e
Externí odkaz:
https://doaj.org/article/795552aded8940b294f21743164edce1
Autor:
Patricia Reparaz, Idoya Serrano, Rosa Adan-Pedroso, Itziar Astigarraga, Jimena de Pedro Olabarri, Aizpea Echebarria-Barona, Miguel Garcia-Ariza, Ricardo Lopez-Almaraz, Rafael A. del Orbe-Barreto, Miriam Vara-Pampliega, Paula Gonzalez-Urdiales
Publikováno v:
Anales de Pediatría (English Edition), Vol 97, Iss 1, Pp 4-11 (2022)
Introduction: Sickle cell disease is an emerging anemia in Europe leading to high morbidity with severe acute complications requiring hospital admission and chronic consequences. The management of these patients is complex and needs interdisciplinary
Externí odkaz:
https://doaj.org/article/ca5c98152a9e4368a10f3654bab71c27
Autor:
Jose Pardos-Gea, Laura Martin-Fernandez, Laia Closa, Ainara Ferrero, Cristina Marzo, Manuel Rubio-Rivas, Francesca Mitjavila, José Ramón González-Porras, José María Bastida, José Mateo, Marina Carrasco, Ángel Bernardo, Itziar Astigarraga, Reyes Aguinaco, Irene Corrales, Iris Garcia-Martínez, Francisco Vidal
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 22, p 16372 (2023)
Acquired hemophilia A (AHA) is a rare bleeding disorder caused by the presence of autoantibodies against factor VIII (FVIII). As with other autoimmune diseases, its etiology is complex and its genetic basis is unknown. The aim of this study was to id
Externí odkaz:
https://doaj.org/article/cb9f3c25263847018638d24f035e1d69
Autor:
Idoya Serrano‐Pejenaute, Anabel Carmona‐Nunez, Ainhoa Zorrilla‐Sarriegui, Garazi Martin‐Irazabal, Julio Lopez‐Bayon, Jesus Sanchez‐Echaniz, Itziar Astigarraga
Publikováno v:
Journal of Paediatrics and Child Health. 59:625-630
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c31d43e90fe337bb4f7c625b745d69cb
https://doi.org/10.1111/jpc.16354
https://doi.org/10.1111/jpc.16354
Autor:
Susana Garcia-Obregon, Mikel Azkargorta, Iratxe Seijas, Javier Pilar-Orive, Francisco Borrego, Felix Elortza, Maria Dolores Boyano, Itziar Astigarraga
Publikováno v:
Journal of Microbiology, Immunology and Infection, Vol 51, Iss 4, Pp 465-472 (2018)
Background: Sepsis is a life-threatening illness with a challenging diagnosis. Current serum biomarkers are not sensitive enough for diagnosis. With the aim of finding proteins associated with sepsis, serum protein profile was compared between patien
Externí odkaz:
https://doaj.org/article/34c2dca66a2d44a4b75a8e61f5fda519
Autor:
Javier de las Heras, Ainara Cano, Ana Vinuesa, Marta Montes, María Unceta Suarez, Arantza Arza, Saioa Jiménez, Elena Vera, Marta del Hoyo, Miriam Gendive, Lizar Aguirre, Gisela Muñoz, Javier Fernández, Cynthia Ruiz-Espinoza, María Ángeles Fernández, José Miguel Galdeano, Irene Rodríguez, Lourdes Román, Amaya Rodríguez-Serna, Begoña Loureiro, Itziar Astigarraga
Publikováno v:
Children, Vol 8, Iss 11, p 1026 (2021)
Classic infantile Pompe disease (IPD) is a rare lysosomal storage disorder characterized by severe hypertrophic cardiomyopathy and profound muscle weakness. Without treatment, death occurs within the first 2 years of life. Although enzyme replacement
Externí odkaz:
https://doaj.org/article/05147c9eb1a64757918d5361ca6ff5e4
Autor:
Miriam Vara-Pampliega, Aizpea Echebarria-Barona, Miguel Garcia-Ariza, Jimena de Pedro Olabarri, Paula Gonzalez-Urdiales, Ricardo Lopez-Almaraz, Rosa Adan-Pedroso, Idoya Serrano, Rafael A. del Orbe-Barreto, Patricia Reparaz, Itziar Astigarraga
Publikováno v:
Anales de Pediatría. 97:4-11
Resumen Introduccion La drepanocitosis es una anemia emergente en Europa que condiciona una elevada morbilidad con complicaciones agudas y cronicas. El manejo de estos pacientes es complejo y requiere atencion interdisciplinar. El objetivo del estudi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::818aba0615f45f1da3cb2d6dff9fa888
https://doi.org/10.1016/j.anpedi.2021.08.010
https://doi.org/10.1016/j.anpedi.2021.08.010