Zobrazeno 1 - 10 of 313 pro vyhledávání: '"Lozano, ML"'
3
A decade of changes in management of immune thrombocytopenia, with special focus on elderly patients
Autor: Lozano ML, Mingot-Castellano ME, Perera MM, Jarque I, Campos-Alvarez RM, González-López TJ, Carreño-Tarragona G, Bermejo N, Lopez-Fernandez MF, de Andrés A, Valcarcel D, Casado-Montero LF, Alvarez-Roman MT, Orts MI, Novelli S, González-Porras JR, Bolaños E, López-Ansoar E, Orna-Montero E, Vicente V
Publikováno v: BLOOD CELLS MOLECULES AND DISEASES
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Ten years after their availability, thrombopoietin receptor agonists (TPO-RA) have heralded a paradigm shift in the treatment of immune thrombocytopenia (ITP). This study was aimed to analyze the implementation of current recommendations in the stand
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::ad741ef238978c2a61d19bd0a811bb48
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=13257
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6
Multirefractory primary immune thrombocytopenia; targeting the decreased sialic acid content
Autor: Revilla N, Corral J, Miñano A, Mingot-Castellano ME, Campos RM, Velasco F, Gonzalez N, Galvez E, Berrueco R, Fuentes I, Gonzalez-Lopez TJ, de la Morena-Barrio ME, Gonzalez-Porras JR, Vicente V, Lozano ML
Publikováno v: Platelets
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Patients with multirefractory immune thrombocytopenia (ITP) have limited treatment options. Recent data suggest that specific anti-platelet antibodies may cause destruction of platelets by favoring platelet loss of sialic acid. In this multicenter st
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::74496c0a93e85b1424d82226a1d39756
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=15221
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8
Bleeding risk of surgery and its prevention in patients with inherited platelet disorders
Autor: Orsini, S, Noris, P, Bury, L, Heller, PG, Santoro, C, Kadir, RA, Butta, NC, Falcinelli, E, Cid, AR, Fabris, F, Fouassier, M, Miyazaki, K, Lozano, ML, Zúñiga P, Flaujac, C, Podda, GM, Bermejo, N, Favier, R, Henskens, Y, De Maistre, E, De Candia, E, Mumford, AD, Ozdemir, GN, Eker, I, Nurden, P, Bayart, S, Lambert, MP, Bussel, J, Zieger, B, Tosetto, A, Melazzini, F, Glembotsky, AC, Pecci, A, Cattaneo, M, Schlegel, N, Gresele, P, European Hematology Association - Scientific Working Group (EHA-SWG) on thromboc
Publikováno v: HAEMATOLOGICA
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Excessive bleeding at surgery is a feared complication in patients with inherited platelet disorders. However, very few studies have evaluated the frequency of surgical bleeding in these hemorrhagic disorders. We performed a worldwide, multicentric,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::939a07c33a5cd1d93fc503d1b4128ae5
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=7033
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9
Novel mutations in RASGRP2, which encodes CalDAG-GEFI, abrogate Rap1 activation, causing platelet dysfunction
Autor: Lozano ML, Cook A, Bastida JM, Paul DS, Iruin G, Cid AR, Adan-Pedroso R, Ramon Gonzalez-Porras J, Hernandez-Rivas JM, Fletcher SJ, Johnson B, Morgan N, Ferrer-Marin F, Vicente V, Sondek J, Watson SP, Bergmeier W, Rivera J
Publikováno v: Blood
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
In addition to mutations in ITG2B or ITGB3 genes that cause defective alpha(IIb)beta(3) expression and/or function in Glanzmann's thrombasthenia patients, platelet dysfunction can be a result of genetic variability in proteins that mediate inside-out
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::7762c09744ef2350eaf69f41a596717e
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=9884
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10
Functional and molecular characterization of inherited platelet disorders in the Iberian Peninsula: results from a collaborative study
Autor: Sánchez-Guiu I, Antón AI, Padilla J, Velasco F, Lucia JF, Lozano M, Cid AR, Sevivas T, Lopez-Fernandez MF, Vicente V, González-Manchón C, Rivera J, Lozano ML
Publikováno v: ORPHANET JOURNAL OF RARE DISEASES
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Background: The diagnostic evaluation of inherited platelet disorders (IPDs) is complicated and time-consuming, resulting in a relevant number of undiagnosed and incorrectly classified patients. In order to evaluate the spectrum of IPDs in individual
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::2f1e2a405f27213bf34d338629e21534
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=2049
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