Results overview: Found 16 records in 0.02 seconds.
Articles, 11 records found
Contributions to meetings and congresses, 1 records found
Research literature, 3 records found
Graphic and multimedia documents, 1 records found
Articles 11 records found  1 - 10next  jump to record:
1.
10 p, 489.9 KB The Pyruvate Kinase Deficiency Global Longitudinal (Peak) Registry : rationale and study design / Grace, Rachael F. (Dana-Farber/Boston Children's Cancer and Blood Disorders Center) ; Van Beers, Eduard J. (University of Utrecht) ; Vives Corrons, Joan Lluís (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Glader, Bertil (Stanford University School of Medicine) ; Glenthøj, Andreas (Copenhagen University Hospital - Rigshospitalet) ; Kanno, Hitoshi (Department of Transfusion Medicine and Cell Processing. Tokyo Women's Medical University) ; Kuo, Kevin H M (University of Toronto) ; Lander, Carl (Hammersmith Hospital (Londres)) ; Pospíšilová, Dagmar (Department of Pediatrics. Palacky University and University Hospital) ; Viprakasit, Vip (Mahidol University) ; Li, Junlong (Agios Pharmaceuticals) ; Yan, Yan (Agios Pharmaceuticals (Estats Units d'Amèrica)) ; Boscoe, Audra N. (Agios Pharmaceuticals (Estats Units d'Amèrica)) ; Bianchi, P. (Fondazione Irccs Ca' Granda Ospedale Maggiore Policlinico (Itàlia))
Introduction Pyruvate kinase (PK) deficiency is a rare, under-recognised, hereditary condition that leads to chronic haemolytic anaemia and potentially serious secondary complications, such as iron overload, cholecystitis, pulmonary hypertension and extramedullary haematopoiesis. [...]
2023 - 10.1136/bmjopen-2022-063605
BMJ open, Vol. 13 Núm. 3 (23 2023) , p. e063605  
2.
8 p, 936.1 KB Concomitant Hereditary Spherocytosis and Pyruvate Kinase Deficiency in a Spanish Family with Chronic Hemolytic Anemia : Contribution of Laser Ektacytometry to Clinical Diagnosis / Vives Corrons, Juan Luís (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Krishnevskaya, Elena (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Montllor, Laura (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Leguizamon, Valentina (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Garcia Bernal, Marta (Hospital Universitari MútuaTerrassa (Terrassa, Catalunya)) ; Universitat Autònoma de Barcelona
Background: Hereditary spherocytosis (HS) and pyruvate kinase deficiency (PKD) are the most common causes of hereditary chronic hemolytic anemia. Here, we describe clinical and genetic characteristics of a Spanish family with concomitant β-spectrin (SPTB) c. [...]
2022 - 10.3390/cells11071133
Cells, Vol. 11 Núm. 7 (4-1 2022) , art. 1133  
3.
13 p, 1.9 MB Blood Rheological Characterization of β-Thalassemia Trait and Iron Deficiency Anemia Using Front Microrheometry / Méndez-Mora, Lourdes (Universitat de Barcelona. Departament de Física de la Matèria Condensada) ; Cabello-Fusarés, Maria (Centre de Recerca Matemàtica) ; Ferré-Torres, Josep (Universitat de Barcelona. Departament de Física de la Matèria Condensada) ; Riera-Llobet, Carla (Universitat de Barcelona. Departament de Física de la Matèria Condensada) ; Krishnevskaya, Elena (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Trejo-Soto, Claudia (Instituto de Física. Pontificia Universidad Católica de Valparaiso) ; Payán-Pernía, Salvador (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Hernandez-Rodriguez, Inés (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Morales-Indiano, Cristian (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Alarcón Cor, Tomás (Universitat Autònoma de Barcelona. Departament de Matemàtiques) ; Vives-Corrons, Joan-Lluís (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Hernández-Machado, Aurora (Universitat de Barcelona. Institut de Nanociència i Nanotecnologia)
The purpose of this work is to develop a hematocrit-independent method for the detection of beta-thalassemia trait (β-TT) and iron deficiency anemia (IDA), through the rheological characterization of whole blood samples from different donors. [...]
2021 - 10.3389/fphys.2021.761411
Frontiers in physiology, Vol. 12 (21 2021) , p. 761411  
4.
11 p, 1.2 MB Rare anemias in adolescents / Vives Corrons, Juan Luís (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Krishnevskaya, Elena (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras)
Anemia can be the consequence of a single disease or an expression of external factors mainly nutritional deficiencies. Genetic issues are important in the primary care of adolescents because a genetic diagnosis may not be made until adolescence, when the teenager presents with the first signs or symptoms of the condition. [...]
2021 - 10.23750/abm.v92i1.11345
Acta Biomedica, Vol. 92 Núm. 1 (may 2021) , p. 1-11  
5.
11 p, 2.4 MB Immigration and screening programs for hemoglobinopathies in Italy, Spain and Turkey / Canatan, Duran (Thalassemia Diagnosis Center of Mediterranean Blood Diseases Foundation) ; Vives Corrons, Juan Luís (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Piacentini, Giorgio (Private Accredited Quisisana Hospital) ; Kara, Fatih (General Directory of Public Health of MOH of Turkey) ; Keskinkılıç, Bekir (General Directory of Public Health of MOH of Turkey) ; Tezel, Başak (General Directory of Public Health of MOH of Turkey) ; Uğur, Aslıhan Külekçi (General Directory of Public Health of MOH of Turkey) ; Babayiğit, Meliha (General Directory of Public Health of MOH of Turkey) ; Krishnevskaya, Elena (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Millimaggi, Giuseppe (Private Accredited Quisisana Hospital) ; Erinekçi, Ozlem (Thalassemia Diagnosis Center of Mediterranean Blood Diseases Foundation) ; Özdemir, Zekiye (Thalassemia Diagnosis Center of Mediterranean Blood Diseases Foundation) ; De Sanctis, Vincenzo (Private Accredited Quisisana Hospital) ; Universitat Autònoma de Barcelona
Sickle cell disease (SCD) and thalassemias are the most common monogenic diseases in the world. The number of migrants and refugees in Europe and Turkey, in the past decade, has increased dramatically due to war, violence or prosecutions in their homeland. [...]
2021 - 10.23750/abm.v92i4.11965
Acta Biomedica, Vol. 92 Núm. 4 (february 2021) , p. e2021410  
6.
14 p, 1.2 MB The limits of the foreign language effect on decision-making : The case of the outcome bias and the representativeness heuristic / Vives, Marc-Lluís (Universitat Pompeu Fabra. Centre de Cognició i Cervell) ; Aparici Aznar, Melina (Universitat Autònoma de Barcelona. Departament de Psicologia Bàsica, Evolutiva i de l'Educació) ; Costa, Albert (Institució Catalana de Recerca i Estudis Avançats)
Language context (native vs. foreign) affects people's choices and preferences in a wide variety of situations. However, emotional reactions are a key component driving people's choices in those situations. [...]
2018 - 10.1371/journal.pone.0203528
PloS one, Vol. 13 Núm. 9 (2018)  
7.
9 p, 468.5 KB Preliminary data on COVID-19 in patients with hemoglobinopathies : A multicentre ICET-A study / De Sanctis, Vincenzo (Pediatric and Adolescent Outpatient Clinic. Quisisana Hospital) ; Canatan, Duran (Antalya Genetic Diseases Diagnostic Center) ; Vives Corrons, Juan Luís (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Karimi, M. (Hematology Research Center. Shiraz University of Medical Sciences) ; Daar, S. (Department of Haematology. College of Medicine and Health Sciences. Sultan Qaboos University) ; Kattamis, C. (First Department of Paediatrics. National Kapodistrian University of Athens) ; Soliman, A. T. (Department of Pediatrics. University of Alexandria) ; Wali, Y. (Department of Paediatrics. Faculty of Medicine. Alexandria University) ; Alkindi, S. (Department of Haematology. College of Medicine and Health Sciences. Sultan Qaboos University) ; Huseynov, V. (Center of Thalassemia) ; Nasibova, A. (Center of Thalassemia) ; Tiryaki, T. O. (İstanbul University. Faculty of Medicine. Department of Hematology) ; Evim, M. S. (Uludag University. Medical Faculty. Dept. of Pediatric Hematology) ; Gunes, A. M. (Uludag University. Medical Faculty. Dept. of Pediatric Hematology) ; Karakas, Z. (Istanbul University. Istanbul Faculty of Medicine. Pediatric Hematology / Oncology) ; Christou, S. (Archibishop Makarios III Hospital. Thalassaemia Clinic) ; Campisi, S. (UOSD Thalassemia. Umberto I° Hospital) ; Zarei, T. (Hematology Research Center. Shiraz University of Medical Sciences) ; Khater, D. (Department of Pediatrics. Sultan Qaboos University) ; Oymak, Y. (Dr. Behcet Uz Children's Hospital) ; Kaleva, V. (Expert Center for Coagulopathies and Rare Anemias) ; Stoyanova, D. (Pediatric Hematoncology. University Hospital "Tzaritza Giovanna - ISUL") ; Banchev, A. (Pediatric Hematoncology. University Hospital "Tzaritza Giovanna - ISUL") ; Galati, M. C. (Pediatric Haematoncology. Pugliese-Ciaccio Hospital) ; Yassin, M. A. (Hematology Section. National Center for Cancer Care and Research. Hamad Medical Corporation. (HMC)) ; Kakar, S. (Pediatric Hematology Oncology. Department of Pediatrics. Dayanand Medical College and Hospital) ; Skafida, M. (First Department of Paediatrics. National Kapodistrian University of Athens) ; Kilinc, Y. (Pediatric Hematology Department. Çukurova University) ; Alyaarubi, S. (Pediatric Endocrinology Unit. Child Health Department. College of Medicine and Health Sciences. Sultan Qaboos University) ; Verdiyevas, N. (Center of Thalassemia) ; Stoeva, I. ("Screening and Functional Endocrine Diagnostics". University Paediatric Hospital) ; Raiola, G. (Department of Paediatrics. Pugliese-Ciaccio Hospital) ; Mariannis, D. (Royal Lancaster Infirmary) ; Ruggiero, L. (Pediatrician) ; Di Maio, S. (Emeritus Director in Pediatrics. "Santobono-Pausilipon" Children's Hospital) ; Universitat Autònoma de Barcelona
Objectives: This study aims to investigate, retrospectively, the epidemiological and clinical characteristics, laboratory results, radiologic findings, and outcomes of COVID-19 in patients with transfusion-dependent β thalassemia major (TM), β-thalassemia intermedia (TI) and sickle cell disease (SCD). [...]
2020 - 10.4084/MJHID.2020.046
Mediterranean Journal of Hematology and Infectious Diseases, Vol. 12 Núm. 1 (2020) , p. e2020046  
8.
14 p, 572.6 KB European expert network on rare communicable diseases and other rare diseases linked to mobility and globalisation focused on health care provision (EURaDMoG) : a feasibility study / Requena-Méndez, Ana (Karolinska Institutet (Estocolm, Suècia). Department of Medicine) ; Bisoffi, Zeno (Università di Verona. Dipartimento di Diagnostica e Sanità Pubblica) ; Vives Corrons, Juan Luís (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Gascon, Joaquim (Barcelona Institute for Global Health (ISGlobal)) ; Plasència, A.. (Barcelona Institute for Global Health (ISGlobal)) ; Universitat Autònoma de Barcelona
Introduction: In the current mobility and globalization context, there is a growing need to identify potential changes on the pattern of diseases in the European Union (EU)/European Economic Area (EEA) and provide accurate diagnosis and treatment for the population. [...]
2020 - 10.1186/s13023-020-01534-1
Orphanet Journal of Rare Diseases, Vol. 15 Núm. 1 (january 2020) , p. 291  
9.
10 p, 1.8 MB Density, heterogeneity and deformability of red cells as markers of clinical severity in hereditary spherocytosis / Huisjes, R. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Makhro, A. (Red Blood Cell Research Group. Institute of Veterinary Physiology. Vetsuisse Faculty. Zurich Center for Integrative Human Physiology (ZIHP). University of Zurich) ; Llaudet-Planas, Esther (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Hertz, L. (Theoretical Medicine and Biosciences. Medical Faculty. Saarland University) ; Petkova-Kirova, P. (Theoretical Medicine and Biosciences. Medical Faculty. Saarland University) ; Verhagen, L. P. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Pignatelli, S. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Rab, M. A. E. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Schiffelers, Raymond M. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Seiler, E. (Red Blood Cell Research Group. Institute of Veterinary Physiology. Vetsuisse Faculty. Zurich Center for Integrative Human Physiology (ZIHP). University of Zurich) ; Van Solinge, W. W. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Vives Corrons, Juan Luís (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Kaestner, L. (Experimental Physics. Saarland University) ; Mañú Pereira, María del Mar (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Bogdanov, A. (Red Blood Cell Research Group. Institute of Veterinary Physiology. Vetsuisse Faculty. Zurich Center for Integrative Human Physiology (ZIHP). University of Zurich) ; Van Wijk, R. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Universitat Autònoma de Barcelona
Hereditary spherocytosis (HS) originates from defective anchoring of the cytoskeletal network to the transmembrane protein complexes of the red blood cell (RBC). Red cells in HS are characterized by membrane instability and reduced deformability and there is marked heterogeneity in disease severity among patients. [...]
2020 - 10.3324/haematol.2018.188151
Haematologica, Vol. 105 Núm. 2 (31 2020) , p. 338-347  
10.
5 p, 788.2 KB Great ape genetic diversity and population history / Prado-Martinez, Javier (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Sudmant, Peter H. (Department of Genome Sciences. University of Washington) ; Kidd, Jeffrey (Department of Genetics. Stanford University) ; Li, Heng (Department of Genetics. Harvard Medical School, Boston) ; Kelley, Joanna (Department of Genetics. Stanford University) ; Lorente-Galdos, Belen (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Veeramah, Krishna (Arizona Research Laboratories. Division of Biotechnology. University of Arizona) ; Woerner, August (Arizona Research Laboratories. Division of Biotechnology. University of Arizona) ; O'Connor, Timothy (Department of Genome Sciences. University of Washington) ; Santpere, Gabriel (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Cagan, Alexander (Max Planck Institute for Evolutionary Anthropology. Department of Evolutionary Genetics) ; Theunert, Christoph (Max Planck Institute for Evolutionary Anthropology. Department of Evolutionary Genetics) ; Casals, Ferran (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Laayouni, Hafid (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Munch Terkelsen, Kasper (Aarhus University. Bioinformatics Research Centre) ; Hobolth, Asger (Aarhus University. Bioinformatics Research Centre) ; Halager, Anders E. (Aarhus University. Bioinformatics Research Centre) ; Malig, Maika (Department of Genome Sciences. University of Washington) ; Hernandez-Rodriguez, Jessica (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Hernando-Herraez, Irene (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Prüfer, Kay (Max Planck Institute for Evolutionary Anthropology. Department of Evolutionary Genetics) ; Pybus, Marc (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Johnstone, Laurel (Arizona Research Laboratories. Division of Biotechnology. University of Arizona) ; Lachmann, Michael (Max Planck Institute for Evolutionary Anthropology. Department of Evolutionary Genetics) ; Alkan, Can (Bilkent University. Faculty of Engineering) ; Twigg, Dorina (Department of Human Genetics. University of Michigan) ; Petit Marty, Natalia (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Baker, Carl (Department of Genome Sciences. University of Washington) ; Hormozdiari, Fereydoun (University of Washington. Department of Genome Sciences) ; Fernández, Marcos (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Dabad, Marc (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Wilson, Michael L. (Department of Anthropology. University of Minnesota) ; Stevison, Laurie (Institute for Human Genetics. University of California San Francisco) ; Camprubí Sánchez, Cristina (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia) ; Carvalho, Tiago (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Ruiz-Herrera Moreno, Aurora (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí") ; Vives, Laura T. (Department of Genome Sciences. University of Washington) ; Mele, Marta (Centre de Regulació Genòmica) ; Abelló, María Teresa. (Zoo de Barcelona) ; Kondova, Ivanela (Biomedical Primate Research Centre) ; Bontrop, Ronald (Biomedical Primate Research Centre) ; Pusey, Anne E (Duke University. Department of Evolutionary Anthropology) ; Lankester, Felix (Washington State University. Paul G. Allen School for Global Animal Health) ; Kiyang, John A. (Limbe Wildlife Centre) ; Bergl, Richard A. (North Carolina Zoological Park) ; Lonsdorf, E. (Franklin and Marshall College. Department of Psychology) ; Myers, S. (Oxford University. Department of Statistics) ; Ventura, M. (University of Bari. Department of Genetics and Microbiology) ; Gagneux, Pascal (University of California San Diego. Department of Cellular and Molecular Medicine) ; Comas, D. (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Siegismund, H. (University of Copenhagen Department of Biology, Bioinformatics) ; Blanc, Julie (Centro Nacional de Análisis Genómico (CNAG). PCB) ; Agueda Calpena, Lidia (Centro Nacional de Análisis Genómico (CNAG). PCB) ; Gut, Marta (Centro Nacional de Análisis Genómico (CNAG). PCB) ; Fulton, L. A (Washington University School of Medicine. Genome Sequencing Center) ; Tishkoff, S. A. (University of Pennsylvania. Department of Biology and Genetics) ; Mullikin, J. C. (National Institutes of Health Intramural Sequencing Center (Bethesda, Estats Units d'Amèrica)) ; Wilson, R. K. (Washington University School of Medicine. Genome Sequencing Center) ; Gut, I. G. (Centro Nacional de Análisis Genómico (CNAG). PCB) ; Gonder, M. K. (University at Albany) ; Ryder, O. A. (Genetics Division. San Diego Zoo's Institute for Conservation Research) ; Hahn, B. H. (University of Pennsylvania. Departments of Medicine and Microbiology) ; Navarro, Arcadi, 1969- (Institució Catalana de Recerca i Estudis Avançats) ; Akey, J. M. (University of Washington. Department of Genome Sciences) ; Bertranpetit, Jaume (Institut de Biologia Evolutiva (UPF-CSIC) (Barcelona)) ; Reich, D. (Harvard Medical School. Department of Genetics) ; Mailund, Thomas (Aarhus University. Bioinformatics Research Centre) ; Schierup, Mikkel Heide (Aarhus University. Department of Bioscience) ; Hvilsom, Christina (Copenhagen Zoo) ; Andrés, A. M. (Max Planck Institute for Evolutionary Anthropology. Department of Evolutionary Genetics) ; Wall, J. D. (University of California San Francisco. Institute for Human Genetics) ; Bustamante, Carlos D (Stanford University. Department of Genetics) ; Hammer, M. F. (University of Arizona. Arizona Research Laboratories. Division of Biotechnology) ; Eichler, Evan E (Howard Hughes Medical Institute) ; Marques-Bonet, Tomas 1975- (Institució Catalana de Recerca i Estudis Avançats)
Most great ape genetic variation remains uncharacterized; however, its study is critical for understanding population history, recombination, selection and susceptibility to disease. Here we sequence to high coverage a total of 79 wild- and captive-born individuals representing all six great ape species and seven subspecies and report 88. [...]
2013 - 10.1038/nature12228
Nature, Vol. 499, issue 7459 (July 2013) , p. 471-475  

Articles : 11 records found   1 - 10next  jump to record:
Contributions to meetings and congresses 1 records found  
1.
16 p, 270.6 KB ¿La protección civil o penal de la intimidad? un diálogo entre ambas jurisdicciones como solución al actual problema legislativo / Heras Vives, Luis de las
2017
La Creación judicial del derecho y el diálogo entre jueces. Universitat Autònoma de Barcelona, Bellaterra, : 2017  

Research literature 3 records found  
1.
87 p, 1.4 MB Les peces del trencaclosques : Requisits per abordar integralment la prostitució, un reportatge feminista interseccional / Vives Bosch, Laia ; Muntané Rodríguez, Isabel, dir. (Universitat Autònoma de Barcelona. Departament de Mitjans, Comunicació i Cultura) ; Universitat Autònoma de Barcelona. Facultat de Ciències de la Comunicació
Les peces del trencaclosques és un reportatge audiovisual que exposa els diferents aspectes a tenir en compte a l'hora d'abordar la prostitució, aquests són: situación administrativa, la seguretat, l'habitatge, la salut i l'imaginari col·lectiu. [...]
Las piezas del rompecabezas es un reportaje audiovisual que expone los distintos aspectos que tener en cuenta a la hora de abordar la prostitución, estos son: la situación administrativa, la seguridad, la vivienda, la salud y el imaginario colectivo. [...]
The pieces of the puzzle is an audiovisual report that exposes the different aspects to consider when addressing prostitution, those are: administrative situation, security, housing, health and collective thinking. [...]

2023
Grau en Periodisme [1432]  
2.
720 p, 3.5 MB Protección penal de la intimidad : una revisión crítica a propósito del nuevo artículo 197.7 del código penal español / de las Heras Vives, Luis ; Morales Prats, Fermín, dir. ; Espanya. ; Universitat Autònoma de Barcelona. Departament de Ciència Política i de Dret Públic
La intimidad, como valor, exige que el Estado, a través de la Ley, le otorgue la oportuna tutela. Sin embargo, hallamos, en el ordenamiento jurídico español, una especial característica, y es que su protección penal ha transitado de la insuficiencia (presente a lo largo de toda la tradición codificadora) al horror vacui que preside el actual Capítulo del Código Penal, dedicado al descubrimiento y revelación de secretos, el cual, además, se encuentra en continua desnaturalización por la inclusión de nuevos tipos que, desde una perspectiva sistemática, mal se compadecen con el bien jurídico intimidad. [...]
In order to guarantee the right of privacy, the State must use the tools provided by the legal framework to ensure that this fundamental value is granted the commensurate level of legal protection. However, in the case of Spanish legislation, it would appear that said protection has evolved from an essentially inadequate system (throughout the entire legislative tradition) to the horror vacui of the current Chapter of the Penal Code that deals with the discovery and revelation of secrets, which, furthermore, undergoes continual distortion through the inclusion of new crimes that, from a systematic perspective, are inconsistent with the legal right of privacy. [...]

[Barcelona] : Universitat Autònoma de Barcelona, 2018.  
3.
57 p, 324.3 KB Informes pericials de les necròpsies / Rafel Celada, Marta ; Torrentà, Maria ; Vives, Laia ; Villaverde, Cecilia
1999 (Treballs de l'assignatura Deontologia Veterinària)  

Graphic and multimedia documents 1 records found  
1.
453x394, 25.4 KB Columnes de l'Autònoma / Alfaro, Andreu arquitecte ; Solà i Ferrando, Carles 1945- (Universitat Autònoma de Barcelona. Departament d'Enginyeria Química, Biològica i Ambiental) ; Universitat Autònoma de Barcelona. Servei de Publicacions ; Institut Joan Lluís Vives
El campus de la UAB compta des de l'any 1999 amb una obra d'art emblemàtica que ja s'ha convertit en un signe d'identitat de la Universitat. Es tracta de les quatre columnes de granit vermellós que es recargolen i s'estiren alhora, buscant el cel. [...]
1999
4 documents

See also: similar author names
1 Vives, Laia
1 Vives, Laura T.
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