Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Ignacio Isola"'
Autor:
Anna deDaniel, Luis Gerardo Rodríguez‐Lobato, Natalia Tovar, M. Teresa Cibeira, David F. Moreno, Aina Oliver‐Caldés, Ignacio Isola, Ester Lozano, Joan Bladé, Laura Rosiñol, Carlos Fernández de Larrea
Publikováno v:
HemaSphere, Vol 8, Iss 5, Pp n/a-n/a (2024)
Abstract The 2/20/20 International Myeloma Working Group (IMWG) score is the most employed risk score in clinical practice to evaluate the risk of progression from smoldering multiple myeloma (SMM) to symptomatic multiple myeloma. However, it faces a
Externí odkaz:
https://doaj.org/article/1de8802a875642aa8d1b51cf74359b01
Autor:
Ignacio Isola, Fara Brasó-Maristany, David F. Moreno, Mari-Pau Mena, Aina Oliver-Calders, Laia Paré, Luis Gerardo Rodríguez-Lobato, Beatriz Martin-Antonio, María Teresa Cibeira, Joan Bladé, Laura Rosiñol, Aleix Prat, Ester Lozano, Carlos Fernández de Larrea
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundWe previously reported algorithms based on clinical parameters and plasma cell characteristics to identify patients with smoldering multiple myeloma (SMM) with higher risk of progressing who could benefit from early treatment. In this work,
Externí odkaz:
https://doaj.org/article/b9061fb81fbb4274961401c2b3964701
Autor:
Laura Rey-Barroso, Mónica Roldán, Francisco J. Burgos-Fernández, Susanna Gassiot, Anna Ruiz Llobet, Ignacio Isola, Meritxell Vilaseca
Publikováno v:
Sensors, Vol 20, Iss 14, p 4039 (2020)
Hemoglobinopathies represent the most common single-gene defects in the world and pose a major public health problem, particularly in tropical countries, where they occur with high frequency. Diagnosing hemoglobinopathies can sometimes be difficult d
Externí odkaz:
https://doaj.org/article/8ae797a7ea174c0db177ce2de02c11de
Autor:
Laura Rey-Barroso, Mónica Roldán, Francisco J Burgos-Fernández, Ignacio Isola, Anna Ruiz Llobet, Susanna Gassiot, Edurne Sarrate, Meritxell Vilaseca
Publikováno v:
Microscopy and Microanalysis. 29:777-785
In hereditary spherocytosis (HS), genetic mutations in the cell membrane and cytoskeleton proteins cause structural defects in red blood cells (RBCs). As a result, cells are rigid and misshapen, usually with a characteristic spherical form (spherocyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79daf7aded757a85f893dd988f709c35
https://doi.org/10.1093/micmic/ozac055
https://doi.org/10.1093/micmic/ozac055
Autor:
Emanuele Lodolo, José Ignacio Isola, Luca Baradello, Juan Pablo Ormazabal, Federico Damián Esteban, J. F. Vilas, Jorge Gabriel Lozano, Maria Elena Cerredo, Alejandro Alberto Tassone, Marco Menichetti, L. Onnis, Donaldo Mauricio Bran
Publikováno v:
International Journal of Earth Sciences. 109:971-994
The outer Fuegian fold and thrust belt is the deformed sector of the Austral-Magallanes Basin, which underwent a contractional phase since the Late Cretaceous and a strike-slip phase during the Neogene. The area hosts two Neogene basins (Yehuin and C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1bc7e49bef05057bcd3db61e5862098
https://doi.org/10.1007/s00531-020-01847-3
https://doi.org/10.1007/s00531-020-01847-3
Autor:
Ignacio Isola, Susanna Gassiot, Anna Ruiz Llobet, Monica Roldan, Laura Rey-Barroso, Francisco J. Burgos-Fernández, Meritxell Vilaseca
Publikováno v:
2021 Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC).
Hemoglobinopathies represent the most common single-gene defects in the world and pose a major public health problem. These defects can affect the synthesis of hemoglobin, the molecule in charge of oxygen transportation, quantitatively (thalassemia)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9068ee11e880c1ed91530e10b395847
https://doi.org/10.1109/cleo/europe-eqec52157.2021.9542487
https://doi.org/10.1109/cleo/europe-eqec52157.2021.9542487
Autor:
Dolors Colomer, Joan Bladé, Natalia Tovar, Beatriz Martín-Antonio, Ignacio Isola, Arturo Pereira, Mari Pau Mena, Luis Gerardo Rodríguez-Lobato, Carlos Fernández de Larrea, Aina Oliver-Caldés, María Teresa Cibeira, Raquel Jiménez-Segura, María Rozman, Laura Magnano, David Moreno, Laura Rosiñol, Mónica López-Guerra
Publikováno v:
Cancers, Vol 13, Iss 2055, p 2055 (2021)
Cancers
Volume 13
Issue 9
Cancers
Volume 13
Issue 9
We analyzed 171 patients with asymptomatic IgM monoclonal gammopathies (64 with IgM monoclonal gammopathy of undetermined significance—MGUS and 107 with smoldering Waldenström macroglobulinemia - SWM) who had a bone marrow (BM) evaluation performe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d98f3a2911705a8b16d081a4668b1ddf
https://www.mdpi.com/2072-6694/13/9/2055
https://www.mdpi.com/2072-6694/13/9/2055
Autor:
Aina Oliver-Caldés, Luis Gerardo Rodríguez-Lobato, Jordi Yagüe, Natalia Tovar, Joan Bladé, Laura Rosiñol, M Carmen Salgado, Mari-Pau Mena, Fara Brasó-Maristany, Aleix Prat, Esther Moga, David Moreno, Carlos Fernández de Larrea, M. Teresa Cibeira, Ignacio Isola
Publikováno v:
ANNALS OF HEMATOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Smoldering multiple myeloma (SMM) is an asymptomatic and biologically heterogeneous plasma cell disorder, with a highly variable clinical course. Immunoparesis, defined by total immunoglobulin measurements, has been shown to be an independent risk fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10f8e4167e824f937f66cd20d87ead0a
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4413
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4413
Autor:
Ignacio Isola, Rubén Berrueco, Mercedes Serrano, Maribel Diaz-Ricart, Albert Català, Antonio Martinez-Monseny, Susanna Gassiot, Anna Ruiz-Llobet
Publikováno v:
Thrombosis and haemostasis. 120(3)
Introduction An underlying thrombocytopathy seems to be responsible for hemorrhagic symptoms in patients diagnosed with 22q11.2 deletion syndrome (22q11DS) or Noonan syndrome (NS). In 22q11DS, it is explained by a defect in the membrane glycoprotein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a3730808bbdf44bbdbae8ce527b2c9e
https://pubmed.ncbi.nlm.nih.gov/32135567
https://pubmed.ncbi.nlm.nih.gov/32135567
Autor:
Guillermo Suñe, Ignacio Isola, Beatriz Martín-Antonio, Marcos Calderón, Mari-Pau Mena, Ester Lozano, Xavier Calvo, Tania Díaz, Patricia Pérez-Galán, Lorena Perez-Amill, Carlos Fernández de Larrea, Gaël Roué, Luis Gerardo Rodríguez-Lobato, Laura Rosiñol, Joan Bladé, M. Teresa Cibeira, Vanina Rodriguez
Publikováno v:
Journal of Immunology
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Mechanisms of immune regulation may control proliferation of aberrant plasma cells (PCs) in patients with monoclonal gammopathy of undetermined significance (MGUS) preventing progression to active multiple myeloma (MM). We hypothesized that CD85j (LI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::249b196e7ed365aef36d7748fbba66df
https://doi.org/10.4049/jimmunol.1701622
https://doi.org/10.4049/jimmunol.1701622