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Journal articles on the topic 'Fundació la Caixa'

Author: Grafiati

Published: 4 June 2021

Last updated: 30 July 2024

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1

Vives Chillida, Julio. "El Espai corbat de la Fundació Caixa Vinaròs. Un centro de divulgación del mueble curvado." Diferents. Revista de museus, no. 6 (November 23, 2021): 112–29. http://dx.doi.org/10.6035/diferents.5665.

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El artículo presenta una experiencia cultural impulsada desde la Fundació Caixa Vinaròs sobre la exposición de una colección de mueble curvado valenciano, en particular mecedoras, pero también de mueble curvado vienés: el Espai corbat. En el texto se explican e ilustran los orígenes, las características -también desde la perspectiva del patrimonio cultural- y el contenido de este espacio, incluidos sus aspectos didácticos. El Espai corbat ha contribuido a lo largo de sus diez años de funcionamiento a la difusión del patrimonio cultural constituido por el mueble curvado, especialmente del valen

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Hernández, Salvador, and Sergio Macario. "Invariance of compactness for the Bohr topology☆☆Research partially supported by Spanish DGES, grant number PB96-1075, and Fundació Caixa Castelló, grant number P1B98-24." Topology and its Applications 111, no. 1-2 (2001): 161–73. http://dx.doi.org/10.1016/s0166-8641(99)00196-0.

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3

Pazos, Antón M. "Joan BONET I BALTÀ - Casimir MARTÍ I MARTÍ, L'integrisme a Catalunya. Les Grans Polémiques: 1881-1888, III Premi Internacional Jaume Vicens Vives de Ciències Socials, Editorial Vicens-Vives, Fundació Caixa Barcelona, Barcelona 1990, 645 pp." Anuario de Historia de la Iglesia 1 (May 15, 2018): 392–93. http://dx.doi.org/10.15581/007.1.25189.

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Pazos, Antón M. "Joan BONET I BALTÀ - Casimir MARTÍ I MARTÍ, L'integrisme a Catalunya. Les grans polémiques: 1881-1888, IIIer Premi Internacional Jaume Vicens Vives de Ciències Socials, Editorial Vicens-Vives, Fundació Caixa Barcelona, Barcelona 1990, 645 pp." Anuario de Historia de la Iglesia 2 (May 15, 2018): 347–49. http://dx.doi.org/10.15581/007.2.25120.

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5

Marcos, Mari Carmen. "La Mediateca de la Fundación la Caixa." El Profesional de la Informacion 12, no. 6 (2003): 489–94. http://dx.doi.org/10.1076/epri.12.6.489.19784.

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Puiggros, Anna, Gonzalo Blanco, Aura Muntasell, et al. "Reduced Expression of the CD94/NKG2C NK Cell Receptor in Chronic Lymphocytic Leukemia (CLL) and CLL-like Monoclonal B-Cell Lymphocytosis (MBL)." Blood 134, Supplement_1 (2019): 5457. http://dx.doi.org/10.1182/blood-2019-128055.

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Background. Dysregulated NK-cell responses have been reported in chronic lymphocytic leukemia (CLL) patients, but little is known about the NK cell compartment in CLL-like monoclonal B cell lymphocytosis (MBL). Human cytomegalovirus (HCMV) infection induces an adaptive reconfiguration of the NK cell compartment characterized by the differentiation and persistent expansion of a subset displaying the CD94/NKG2C NK receptor (NKR). Moreover, a deletion of the NKG2C (KLRC2) gene has been reported to modulate the magnitude of the NK cell repertoire redistribution. Little is known about the expressio

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7

Cusso Parcerisas, Irene, Jordi Longás Mayayo, and Jordi Riera Romaní. "Acción socioeducativa en red con la infancia y adolescencia en situación de pobreza: análisis del programa CaixaProinfancia en Barcelona." Aloma: Revista de Psicologia, Ciències de l'Educació i de l'Esport 33, no. 2 (2015): 95–105. http://dx.doi.org/10.51698/aloma.2015.33.2.95-105.

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El artículo presenta como estudio de caso la aplicación del programa CaixaProinfancia en Barcelona impulsado por la Obra Social de la Fundación Bancaria Caixa d’Estalvis i Pensions de Barcelona, “la Caixa”. Se presenta el marco teórico del programa y se analiza su incidencia y evolución en la ciudad. De los resultados de la investigación, cabe destacar las razones que han justificado el progresivo cambio hacia un planteamiento exigente de trabajo socioeducativo en red. A su vez, a partir de las nuevas experiencias, se presentan los aciertos, las expectativas y las limitaciones encontradas hast

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Cabezón, Marta, Yulia Medvedeva, Joan Bargay, et al. "Methylation Patterns in Patients with High-Risk Myelodysplatic Syndromes and Secondary Acute Myeloid Leukemia Treated with Azacitidine (high-risk MDS 2009 protocol from CETLAM Group)." Blood 126, no. 23 (2015): 1682. http://dx.doi.org/10.1182/blood.v126.23.1682.1682.

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Abstract INTRODUCTION: The myelodysplastic syndromes (MDS) are a group of hematologic disorders characterized by ineffective hematopoiesis and increased risk of transformation to acute myeloid leukemia (AML). Aberrant DNA methylation is the dominant and most well-studied epigenetic alteration in MDS. Various genes, including cell cycle regulators, apoptotic genes, and DNA repair genes, are epigenetically silenced and play a role in pathogenesis and transformation to leukemia. The clinical response of MDS and AML to drugs that revert the aberrant hypermethylation, such as 5-aza-2x-deoxicitidine

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Adema, Vera, Larrayoz Maria Jose, Calasanz Maria Jose, et al. "Myelodysplastic Syndromes with I(17)(q10) and Prognostic Implications of Mutations of TP53 and SETBP1." Blood 124, no. 21 (2014): 1910. http://dx.doi.org/10.1182/blood.v124.21.1910.1910.

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Abstract INTRODUCTION Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal myeloid stem cell disorders highly prevalent in elderly populations. MDS are characterized by inefficient hematopoiesis, peripheral blood (PB) cytopenias, and increased risk of transformation to acute myeloid leukemia (AML; 20–30%). Around 50% of MDS patients carry at least one karyotoypic aberration, the most common being 5q-, -7/7q-, +8, 20q-, and isochromosome 17(q10) [i(17q)]. Isochromosome 17(q10) according to cytogenetic risk stratification is of intermediate prognostic significance when is observed

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Soto, Ángel Pascual Martínez. "Joan Carles Maixé (dir). El ahorro de los gallegos. Orígenes e historia de Caixa Galicia (1876–2002). La Coruña: Fundación Caixa Galicia, 2003. Pp. 371." Revista de Historia Económica / Journal of Iberian and Latin American Economic History 22, no. 1 (2004): 236–38. http://dx.doi.org/10.1017/s0212610900010983.

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Smandia, Cristina. "CosmoExplainers. Explicando la ciencia en CosmoCaixa, el Museo de la Ciencia de la Fundación “la Caixa”, Barcelona (España)." Journal of Science Communication América Latina 03, no. 02 (2020): A07. http://dx.doi.org/10.22323/3.03020207.

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¿Cómo podemos vincular a los adolescentes a nuestros museos? El programa Explainer, insignia del Exploratorium de San Francisco, ha conseguido motivar a los más jóvenes al museo implicándolos en la mediación de sus contenidos. Desde 2013 en CosmoCaixa, el museo de la Ciencia de la Fundación “la Caixa”, hemos implementado el programa. En este artículo explicamos nuestra experiencia, sus características y diferencias con el programa de San Francisco, así como las dificultades que nos hemos encontrado, el estado actual del programa y su proyección de futuro.

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Pérez, Antonio M. "David Moscoso y Eduardo Moyano (Coords.). Deporte, salud y calidad de vida. Fundación la Caixa, 2009." Empiria. Revista de metodología de ciencias sociales, no. 23 (September 28, 2012): 223. http://dx.doi.org/10.5944/empiria.23.2012.835.

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13

Cabezon, Marta, Joan Bargay, Blanca Xicoy, et al. "Mutational Studies Using Next Generation Sequencing in High Risk Myelodysplastic Syndromes and Secondary Acute Myeloid Leukemia Patients Treated with Azacitidine (High risk MDS 2009 protocol from CETLAM Group)." Blood 126, no. 23 (2015): 2905. http://dx.doi.org/10.1182/blood.v126.23.2905.2905.

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Abstract INTRODUCTION: Myelodysplastic syndromes (MDS) are a group of myeloid neoplasms originated in hematopoietic stem cells, characterized by citopenias, dysplasia in one or more cell lines, ineffective hematopoiesis and an increased risk of progression to acute myeloid leukemia (AML). Treatment of MDS depends on subtype and prognostic category. DNA methyltranferase inhibitors are approved for high risk MDS. Over the past decade, the application of new high-throughput technologies to the study of MDS has led to the identification of several recurrently mutated genes. These include genes pro

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Ibarrondo, Paloma, Andres Insunza, Sonia González de Villambrosia, et al. "Prognostic Value of Chromosome 1 Abnormalities in Myelodysplastic Syndrome." Blood 124, no. 21 (2014): 3240. http://dx.doi.org/10.1182/blood.v124.21.3240.3240.

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Abstract INTRODUCTION AND AIMS: Abnormalities of chromosome 1 (chr 1) are frequently found in hematopoietic stem cell disorders, but their impact and prognosis in Myelodysplastic Syndrome (MDS) remains unclear. For this reason, we retrospectively analyzed a large series of patients. MATERIALS AND METHODS: A series of 90 patients with MDS and abnormalities of chr 1 were retrospectively evaluated, coming from the Spanish Registry of MDS (68), Marqués de Valdecilla Universitary Hospital (16) and Azienda Careggi Universitary Hospital (Florence) (6). We compared this group to a control group of 992

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Adema, Vera, Laura Palomo, María Díez-Campelo, et al. "Whole-Exome Sequencing in Myelodysplastic Syndromes with 5q Deletion." Blood 124, no. 21 (2014): 4635. http://dx.doi.org/10.1182/blood.v124.21.4635.4635.

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Abstract INTRODUCTION Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal myeloid stem cell disorders that are highly prevalent in elderly populations. MDS are characterized by inefficient hematopoiesis, peripheral blood (PB) cytopenias, and increased risk of transformation to acute myeloid leukemia (AML; 20–30% of patients with MDS). Around 50% of MDS patients carry at least one karyotypic aberration. The interstitial deletion of the long arm of chromosome 5 ([del(5q)] is the most common aberration, accounting for almost 30% of abnormal MDS karyotype. Various studies supports

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16

Blanco, Gonzalo, Anna Puiggros, Barbara Sherry, et al. "Deciphering the CXCL9-CXCL10-CXCL11/CXCR3 Axis in CLL-like Monoclonal B-Cell Lymphocytosis and Chronic Lymphocytic Leukemia: A New Target for Immune Activation?" Blood 134, Supplement_1 (2019): 3029. http://dx.doi.org/10.1182/blood-2019-122061.

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INTRODUCTION: CXCL9, CXCL10 and CXCL11 (CXCL9-10-11) are closely related cytokines that specifically bind to their receptor CXCR3. They act inducing chemotaxis, proliferation and/or cytotoxicity of CD4+ Th1 and cytotoxic T cells, which express CXCR3. Although the CXCL9-10-11/CXCR3 axis promotes immune activation, their pro- or anti-tumor effects in chronic lymphocytic leukemia (CLL) remain controversial. The aims of this study are: 1. To investigate serum levels of CXCL9-10-11 and the protein expression of their receptor CXCR3, as well as Th1 and cytotoxic gene expression signatures and protei

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Palomo, Laura, Blanca Xicoy, Montse Arnan, et al. "Molecular Genetic Profiling in Chronic Myelomonocytic Leukemia with Low Risk Cytogenetic Features." Blood 126, no. 23 (2015): 2883. http://dx.doi.org/10.1182/blood.v126.23.2883.2883.

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Abstract Background: Chronic myelomonocytic leukemia (CMML) is a heterogeneous disease that can vary from a myelodysplastic (MD) predominant profile to a myeloproliferative (MP) one. CMML has a variable course, with a median overall survival of 20 months and 15-30% of progression to acute myeloid leukemia (AML). Cytogenetic abnormalities are present in 20-40% of cases and recurrent gene mutations have been reported in several genes. Patients with low risk cytogenetic features (normal karyotype and isolated -Y) account for approximately 80% of CMML patients and often fall into the low risk cate

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Mallo, Mar, Heinz Tuechler, Lee-Yung Shih, et al. "Genomic Microarray Alterations Add Prognostic Power to the IPSS-R in MDS with Normal Karyotype." Blood 124, no. 21 (2014): 3262. http://dx.doi.org/10.1182/blood.v124.21.3262.3262.

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Abstract Background Disease karyotype is the parameter with the strongest prognostic impact in the IPSS-R. Around 50% of MDS patients have a normal karyotype. Conventional G-banding cytogenetics has a resolution of 5-10 Mb. SNP microarrays is a genomic array with a higher resolution than cytogenetics and allows the detection of small copy number alterations (CNA) and absence of heterozygosity (AOH). Our hypothesis is that in MDS patients with normal karyotype small cryptic alterations might exist, undetectable by conventional karyotyping, but with an impact on patient's outcome. Our aim is to

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Palomo, Laura, Blanca Xicoy, Olga Garcia, et al. "Utility of SNP Arrays in Chronic Myelomonocytic Leukemia with Low Risk Cytogenetic Features or No Metaphases." Blood 124, no. 21 (2014): 4659. http://dx.doi.org/10.1182/blood.v124.21.4659.4659.

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Abstract Background: Clinical, morphological and genetic characteristics of chronic myelomonocytic leukemia (CMML) are heterogeneous and vary from a myelodysplastic predominant profile to a myeloproliferative one. CMML has a highly variable course, with a median overall survival (OS) of 20 months and 15-30% of progression to acute myeloid leukemia (AML). Cytogenetic abnormalities are present in only 20-40% of cases. CMML-specific cytogenetic risk classification stratifies karyotypes into three groups: low risk (normal karyotype and isolated loss of Y chromosome, -Y), poor risk (trisomy 8, mono

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Blanco, Gonzalo, Anna Puiggros, Barbara Sherry, et al. "Gene Expression and Cytokine Analyses Identify Markers of Progression from CLL-like Monoclonal B-Cell Lymphocytosis to Chronic Lymphocytic Leukemia." Blood 134, Supplement_1 (2019): 3027. http://dx.doi.org/10.1182/blood-2019-122038.

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INTRODUCTION: Chronic lymphocytic leukemia (CLL)-like monoclonal B cell lymphocytosis (MBL) is considered a precursor of CLL. It is found in 5-10% of elderly healthy individuals and shows a progression rate to CLL requiring therapy of 1.1% per year. A balance between microenvironmental factors and intrinsic properties of the emerging B cell clone may be decisive for the transition from MBL to CLL, although biomarkers of progression remain unknown. The objective is to describe biological markers (B cell gene expression profiles and serum cytokine levels) that predict progression from MBL to CLL

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Bardolet, Ariadna, and Marta Solsona. "Work4Progress: plataformas de innovación para la creación de empleo." LAS ALIANZAS MULTIACTOR Y PLATAFORMAS DE INNOVACIÓN ABIERTA: NUEVAS INFRAESTRUCTURAS PARA ABORDAR PROBLEMAS COMPLEJOS 02, MAYO 2020 (2020): 69–84. http://dx.doi.org/10.36852/2695-4427_2020_02.05.

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Los paradigmas de la cooperación internacional están cambiando y Work4Progress es un ejemplo de ello. El origen y objetivo de este programa, lanzado en 2017 por la Fundación "la Caixa" tras más de 20 años de experiencia en cooperación internacional, permite poner las herramientas de innovación social más avanzadas a disposición de los programas de cooperación internacional mediante plataformas de innovación abierta. Todo ello con el objetivo de crear empleo para mujeres y los jóvenes en situación de vulnerabilidad en India, Mozambique y Perú. La principal novedad de Work4Progress es la incorpo

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Blanco, Gonzalo, Anna Puiggros, María Rodríguez-Rivera, et al. "Chromosome 8 Abnormalities (8p Losses and 8q Gains) in Patients with Chronic Lymphocytic Leukemia (CLL) and Del(17p)." Blood 124, no. 21 (2014): 5638. http://dx.doi.org/10.1182/blood.v124.21.5638.5638.

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Abstract Basis. Abnormalities in chromosome 8 (8p-/8q+) are observed in 2-5% of CLL patients. Microarray studies have revealed up to 30-40% of 8 alterations in del(17p) patients and an independent association with poor outcome. Large series assessing CLL patients with 8p-/8q+ are scarce. Aims. 1. To describe the frequency of 8q gains (8q+) and 8p losses (8p-) in CLL patients with del(17p); 2. To compare cytogenetic and clinical characteristics between patients with 8p-/8q+ (Alt-chr8) and those with normal chromosome 8 (N-chr8); 3. To assess their prognostic value. Patients and methods. From 2,

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Mudarra, Fernando, and Jaime Diaz. "Plataformas Multiactor en la nueva agenda de desarrollo. Un análisis desde la experiencia de Ayuda en Acción." LAS ALIANZAS MULTIACTOR Y PLATAFORMAS DE INNOVACIÓN ABIERTA: NUEVAS INFRAESTRUCTURAS PARA ABORDAR PROBLEMAS COMPLEJOS 02, MAYO 2020 (2020): 85–104. http://dx.doi.org/10.36852/2695-4427_2020_02.06.

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Desde la entrada en vigor de los Objetivos de Desarrollo Sostenible, el sector de la cooperación al desarrollo está evolucionando. Todos los actores del mundo involucrados en estos objetivos, no solo las ONGs, tratan de buscar formas para tener mayor impacto y conseguir los objetivos comunes. El hecho de reconocer la existencia de estos retos de desarrollo globales ha provocado que más actores se interesen por ser parte de la solución. El papel de los gobiernos continúa siendo muy importante, pero la acción de la empresa, la universidad o los fondos financieros internacionales está progresivam

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Bas Peña, Encarnación, and Victoria Pérez-de-Guzmán. "Educación, salud y pobreza. Programa CaixaProInfancia en Murcia: Estudio de casos." Health and Addictions/Salud y Drogas 17, no. 2 (2017): 179–88. http://dx.doi.org/10.21134/haaj.v17i2.328.

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Introducción: Los informes sobre pobreza en España muestran la situación en la Comunidad Autónoma de la Región de Murcia y su incidencia en la infancia, en sus condiciones de vida, en su salud física, mental y social (UNICEF, 2012; FOESSA y Cáritas, 2014; Save the Children, 2015; EAPN-ES, 2012, 2016; Observatorio de Sostenibilidad, 2016). En España, la Obra Social de la Fundación “la Caixa” puso en marcha el programa CaixaProinfancia (CPI) para dar apoyo socioeducativo la infancia y sus familias, en situación de vulnerabilidad por causa de la pobreza. Este estudio forma parte de un proyecto má

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Freire López, Ana María. "literatura de Emilia Pardo Bazán (2009): José Manuel González Herrán, Cristina Patiño Eirín, Ermitas Penas Varela (editores), A Coruña, Fundación Caixa Galicia, Casa-Museo Emilia Pardo Bazán." La Tribuna: Cadernos de Estudos da Casa-Museo Emilia Pardo Bazán, no. 7 (February 21, 2010): 463–65. http://dx.doi.org/10.32766/tribuna.7.162.

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Costas, Miquel, and Lawrence Que, Jr. "Ligand Topology Tuning of Iron-Catalyzed Hydrocarbon Oxidations We thank the National Institutes of Health for financial support (GM33162 to L.Q.) and Fundacio La Caixa for a postdoctoral fellowship (M.C.)." Angewandte Chemie 114, no. 12 (2002): 2283. http://dx.doi.org/10.1002/1521-3757(20020617)114:12<2283::aid-ange2283>3.0.co;2-6.

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Costas, Miquel, and Lawrence Que, Jr. "Ligand Topology Tuning of Iron-Catalyzed Hydrocarbon Oxidations We thank the National Institutes of Health for financial support (GM33162 to L.Q.) and Fundacio La Caixa for a postdoctoral fellowship (M.C.)." Angewandte Chemie International Edition 41, no. 12 (2002): 2179. http://dx.doi.org/10.1002/1521-3773(20020617)41:12<2179::aid-anie2179>3.0.co;2-f.

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Paba, Tonina. "Emilia Pardo Bazán: el periodismo, III Simposio. Edición de José Manuel González Herrán, Cristina Patiño Eirín y Ermitas Penas Varela. A Coruña, Fundacion Caixa Galicia-Real Academia Galega, 2007, 383 págs." BOLETÍN DE LA BIBLIOTECA DE MENÉNDEZ PELAYO 83, Único (2022): 514–15. http://dx.doi.org/10.55422/bbmp.447.

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Con motivo de la celebración del III simposio de Emilia Pardo Bazán: el periodismo, se congregaron en A Coruña muchos investigadores para hablar sobre distintos temas relacionados con la escritora gallega. No solamente se trataron sus textos periodísticos, sino también algunos literarios que aparecieron publicados en revistas y periódicos de su época. Otros investigadores decidieron hablar del contexto político-social que le tocó vivir a Pardo Bazán, y también de sus abundantes colaboraciones en periódicos. En general, las Actas de este simposio ayudan a profundizar en su persona y obra y a en

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Almeida, Milton Luiz de, Luís Sangoi, Paulo Sérgio Trentin, and Jonatan Gálio. "Cultivares de trigo respondem diferentemente à qualidade da luz quanto à emissão de afilhos e acumulação de massa seca." Ciência Rural 32, no. 3 (2002): 377–83. http://dx.doi.org/10.1590/s0103-84782002000300003.

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Um experimento foi conduzido com o objetivo de avaliar os efeitos da qualidade da luz, através da suplementação com luz vermelha (V) e luz vermelha extrema (Ve), na emissão de afilhos, na acumulação de massa seca (MS) e na relação do tamanho das primeiras folhas do colmo principal (CP) com a emissão de afilhos em cultivares de trigo. Ele foi conduzido em Lages, SC, em caixas de madeira preenchidas com solo mineral, em ambiente com radiação solar natural. A suplementação com luz V e luz Ve foi feita entre a emissão da terceira e da quarta folha do CP. O experimento foi colhido no final do afilh

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Munoz, Sarah-Anne. "Residential strategies of the elderly. Mobility and the life course (estrategias residentiales de las personas de edad. Movilidad y curso de vida) by Maria Dolores Puga Gonzalez. Fundacion ?la Caixa?, Barcelona, 2004. No. of pages: 297." Population, Space and Place 11, no. 1 (2005): 65–67. http://dx.doi.org/10.1002/psp.352.

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Catelli, Laura. "José R. Olivier, editor. El caribe precolombino. Fray Ramón Pané y el universo taíno. Catalogue of the exhibit organized by the Museu Barbier-Mueller d'Art Precolombí (Barcelona), with the collaboration of The British Museum, Ministerio de Cultura, Museo de América, and Fundación Caixa Galicia 2008. Pp. 285." Americas 69, no. 04 (2013): 536–37. http://dx.doi.org/10.1017/s0003161500002674.

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Catelli, Laura. "José R. Olivier, editor. El caribe precolombino. Fray Ramón Pané y el universo taíno. Catalogue of the exhibit organized by the Museu Barbier-Mueller d'Art Precolombí (Barcelona), with the collaboration of The British Museum, Ministerio de Cultura, Museo de América, and Fundación Caixa Galicia 2008. Pp. 285." Americas 69, no. 4 (2013): 536–37. http://dx.doi.org/10.1353/tam.2013.0035.

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LOWENSTEIN, ARIELA. "Mariano Sánchez, Donna M. Butts, Alan Hatton-Yeo, Nancy A. Henkin, Shannon E. Jarrott, Matthew S. Kaplan, Antonio Martinez, Sally Newman, Sacramento Pinazo, Juan Sáez and Aaron P.C. Weintraub, Intergenerational Programmes: Towards a Society for All Ages, Social Studies Collection 23, Fundacion La Caixa, Barcelona, Spain, 2007, 232 pp., free. Available online at http://obrasocial.lacaixa.es/estudiossociales/vol23_es.html [Accessed 2 November 2008]." Ageing and Society 29, no. 3 (2009): 491–92. http://dx.doi.org/10.1017/s0144686x08008258.

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Administración, Revista Barataria. "Textos y glosas -Número 14- Barataria." Barataria. Revista Castellano-Manchega de Ciencias Sociales, no. 14 (April 10, 2016): 185–212. http://dx.doi.org/10.20932/barataria.v0i14.136.

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Reseñas del número 14 de Barataria. Para acceder a la reseña deseada, descargar el PDF completo. ÍNDICE de reseñas: D. Dueñas I Cid, p. 185 François DUBET La experiencia sociológica Barcelona: Gedisa. 2011. 141 pp.  Mª L. Gallardo García-Saavedra, pp. 186-187 Rafael SUMOZAS GARCÍA-PARDO Patrimonio monumental y minero de Almadén Biblioteca de Autores Manchegos, Ciudad Real: Diputación Provincial de Ciudad Real. 2012. 144 pp.  Mª I. Morán Morán, pp. 187-188 Luis GONZÁLEZ SEARA La metamorfosis de la ideologí

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Ribera, Jordi, Mireia Morgades, Isabel Granada, et al. "Role of Allogeneic Stem Cell Transplantation in Preventing Relapse in Adult BCR::ABL1-like Acute Lymphoblastic Leukemia." Blood 142, Supplement 1 (2023): 1461. http://dx.doi.org/10.1182/blood-2023-186265.

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Background Philadelphia-like acute lymphoblastic leukemia (Ph-like ALL) is characterized by the activation of several kinase pathways that promote treatment resistance leading to poor survival of patients at all ages. Despite the use of tyrosine kinase inhibitors in the Ph-like ABL-class subtype (15% Ph-like ALL), there is not a consensus approach for treatment of most patients (JAK-class especially), and the role of allogeneic stem cell transplantation (alloSCT) has scarcely been explored so far (i.e., mandatory vs. MRD-oriented). Objective To assess the outcome of Ph-like patients enrolled i

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Ribera, Josep-Maria, Olga García, Marta Cervera, et al. "Rituximab and Specific Therapy for Patients with Burkitt's Leukemia and Lymphoma. Results of the BURKIMAB14 Trial from the Spanish Pethema and Geltamo Groups in 80 Patients." Blood 134, Supplement_1 (2019): 2584. http://dx.doi.org/10.1182/blood-2019-125683.

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Background and objective. Specific immunochemotherapy is the standard treatment of patients with Burkitt leukemia or lymphoma (BL/L). The BURKIMAB08 trial showed 3-yr overall survival (OS) probability of 72% (Ribera JM et al, Cancer. 2013; 119:1660-8). However, the toxicity was high, and 11% of patients died in complete response (CR). In the BURKIMAB14 trial, dose-intensity of chemotherapy blocks was reduced in patients ≤55 years who achieved CR, with the aim to decrease the death rate without impact on efficacy. We present the results of this trial in 80 patients with BL/L and compare them wi

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Prestes, Emília Maria da Trindade, and Edineide Jezine. "Interface da violência com a evasão e exclusão na educação superior (Interface of violence with evasion and exclusion in higher education)." Revista Eletrônica de Educação 15 (February 28, 2021): e3828021. http://dx.doi.org/10.14244/198271993828.

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e3828021The text is an essay based on theoretical reflections on institutional and symbolic violence in higher education which seeks to analyze the interface as evasion in exclusion processes. This is an exploratory study with a qualitative approach, which uses theoretical and documentary sources in order to elicit different investigations. The debate focuses on the contradictory elements of the university institution in the context of expanding access, it is assumed that the logic of its function, organization, and functioning contribute to the multiplication of inequalities and evasion mecha

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Lalueza, Ferran. "'World-class PR'." COMeIN, no. 24 (July 15, 2013). http://dx.doi.org/10.7238/c.n24.1355.

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Con el patrocinio de la Obra Social "la Caixa" y con el apoyo de la Fundació Joan Miró, este mes de julio se ha celebrado la tercera edición del Barcelona PR Meeting, el congreso internacional de relaciones públicas que cada verano reúne en la capital catalana a los académicos de la disciplina más reconocidos a nivel mundial. "Representing PR: Images, Identities and Innovations" ha sido el lema empleado este año como hilo conductor del programa.

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Cavero Carbonell, C., S. Moreno Marro, L. Barrachina Bonet, L. Páramo Rodríguez, S. Guardiola Vilarroig, and O. Zurriaga. "Validity of sources of information used for the identification of Wilson’s disease in the Registries." European Journal of Public Health 29, Supplement_4 (2019). http://dx.doi.org/10.1093/eurpub/ckz186.625.

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Abstract Background Objective: to determine the sources of information used by the Regional Population-based Registries of Rare Diseases (RD) (RRD) for the identification of the Wilson’s Disease (WD) during the period 2010-2015, and to evaluate the validity of these sources. Methods A cross-sectional study was conducted involving 14 different Spanish Regions and the RD Research Institute. Possible cases with WD diagnosis included in RRD were identified with codes 275.1 in ICD9CM or E83.0 in ICD10 (unspecific codes referring to ’Disorders of copper metabolism’), and they were confirmed or not t

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Rodero Franganillo, Adolfo. ""El empresario inmigrante en España"." Revista de Fomento Social, September 30, 2007, 497. http://dx.doi.org/10.32418/rfs.2007.247.2154.

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Rodero Franganillo, Adolfo. ""El empresario inmigrante en España"." Revista de Fomento Social, June 30, 2007, 274. http://dx.doi.org/10.32418/rfs.2007.246.2174.

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Trechera Herreros, José Luis. ""Infancia y futuro. Nuevas realidades, nuevos retos"." Revista de Fomento Social, June 30, 2011, 353–54. http://dx.doi.org/10.32418/rfs.2011.262.1888.

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Ríos Moyano, Sonia. "Miró Litógrafo. Colección de Obra Gráfica de la Fundación "la Caixa"." Boletín de Arte, no. 23 (September 10, 2002). http://dx.doi.org/10.24310/bolarte.2002.v0i23.4794.

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De los Ríos Berjillos, Araceli. ""Fracaso y abandono escolar en España"." Revista de Fomento Social, March 31, 2011, 145. http://dx.doi.org/10.32418/rfs.2011.261.1910.

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Reseña de la obra de: FERNÁNDEZ ENGUITA, M., MENA MARTÍNEZ, L. Y RIVIERE GÓMEZ, J. (2010) Fracaso y abandono escolar en España, Barcelona, Fundación “La Caixa”, Colección de Estudios Sociales,núm. 29, pp. 217.

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Yuste Charques, Rafael. ""La regulación de la inmigración en Europa" (Recensión)." Revista de Fomento Social, June 30, 2005, 353–60. http://dx.doi.org/10.32418/rfs.2005.238.2264.

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Recensión de l aobra de: AJA, E. Y DÍEZ, L., Coord. (2005), La regulación de la inmigración en Europa, Barcelona, Colección de Estudios Sociales, núm. 17, Obra Social de la Fundación “la Caixa”, 313 págs.

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Rodero Franganillo, Antonio. ""El cuidado de las personas. Un reto para el siglo XXI"." Revista de Fomento Social, June 30, 2010, 388–89. http://dx.doi.org/10.32418/rfs.2010.258.1940.

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Reseña de la obra de: TOBIO, Constanza, AGULLO TOMÁS, María, GÓMEZ, María Victoria y MARTÍN PALOMO, Mª Teresa (2010) El cuidado de las personas. Un reto para el siglo XXI, Barcelona, Fundación “La Caixa”, 206 pp.

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Camacho Laraña, S.I., Ildefonso, José Juan Romero Rodríguez, S.I., Vicente Theotonio Cáceres, S.I., and Pedro Castón Boyer. "Reseñas." Revista de Fomento Social, March 30, 2002, 193–208. http://dx.doi.org/10.32418/rfs.2002.225.2430.

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Reseñas de las obras: ETXEBERRIA, X. (2002), Temas básicos de ética, Bilbao, Desclée de Brouwer, 207 págs. VIELVA, J. (2002). Ética profesional de la enfermería, Bilbao, Desclée de Brouwer, 258 págs. BERMEJO, F. J. (2002), La ética del trabajo social, Bilbao, Desclée de Brouwer, 253 págs. GUTIÉRREZ GARCÍA, J. L (2001), Introducción a la doctrina social de la Iglesia, Barcelona, Ariel, 520 págs. IBÁÑEZ, H. (2002), De la integración a la exclusión. Los avatares del trabajo productivo a finales del siglo XX, Santander, Sal Terrae, Colección Presencia Social, nº 30, 2

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"Fernando Gil." Mosaic, no. 22 (December 19, 2003). http://dx.doi.org/10.7238/m.n22.0314.

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Raquel Herrera ha entrevistado a Fernando Gil (Madrid, 1951), director de la empresa Intermedia, especializada en gestionar la comunicación visual de empresas (Endesa, Iberia, Mahou)) e instituciones culturales como exposiciones, centros de interpretación, museos (Ministerio de Cultura, Museo Reina Sofía, Fundación La Caixa, etc).

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Ortega Carpio, María Luz, and José Juan Romero Rodríguez. "Formación de Recursos Humanos y Cooperación al Desarrollo. II Jornadas de ACADE en ETEA." Revista de Fomento Social, June 30, 2004, 351–57. http://dx.doi.org/10.32418/rfs.2004.234.2307.

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Más de 200 profesionales del mundo de la cooperación se dieron cita en ETEA (Córdoba) el día 14 de mayo de 2004 para asistir a las Jornadas Formación en Recursos Humanos y Cooperación al Desarrollo organizada por la Fundación La Caixa y ACADE (Asociación de profesionales por la calidad de la Cooperación para el desarrollo) con la colaboración del Ayuntamiento de Córdoba3 . Dado su posible interés para los lectores de la Revista de Fomento Social, presentamos una breve crónica de este evento.

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"Pilar Mateu." Mosaic, no. 30 (September 7, 2004). http://dx.doi.org/10.7238/m.n30.0420.

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Pilar Mateu (Barcelona, 1959) posee un doble perfil profesional en magisterio y diseño gráfico que la ha llevado, desde 1998, a participar a través de la empresa GEC en la gestión del proyecto Educalia, portal lúdico-educativo de la Fundación La Caixa. Educalia ofrece un portal de recursos para la comunidad educativa con talleres, juegos y programas de formación diversos, centrado en la difusión de los mejores recursos tecnológicos para el aprendizaje. Esta entrevista nos permitirá conocer más a fondo Educalia y las posibilidades de desarrollo del multimedia en campos didácticos.

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