@techreport{lawson_public_2019,
title = {Public Good or Private Wealth?},
author = {Max Lawson and Man-Kwun Chan and Francesca Rhodes and Anam Parvez Butt and Anna Marriott and Ellen Ehmke and Didier Jacobs and Julie Seghers and Jaime Atienza and Rebecca Gowland},
url = {http://hdl.handle.net/10546/620599},
doi = {10.21201/2019.3651},
year = {2019},
date = {2019-01-01},
keywords = {Informes},
pubstate = {published},
tppubtype = {techreport}
}
@techreport{world_inequality_lab_world_2018,
title = {World inequality report 2018},
author = {World Inequality Lab},
url = {https://wir2018.wid.world/files/download/wir2018-summary-english.pdf},
year = {2018},
date = {2018-01-01},
pages = {296},
address = {Paris},
institution = {World Inequality Lab},
abstract = {Cardiomyopathies are a heterogeneous group of heart muscle disorders, being defined as "a myocardial disorder in which the heart muscle is structurally and/or functionally abnormal in the absence of coronary artery disease, hypertension, valvular disease and congenital heart disease sufficient to cause the observed mitochondriale myocardial abnormality". Four major types are recognised, namely the dilated, the hypertrophic and the restrictive variants, and arrhythmogenic right ventricular cardiomyopathy. A more recent approach divides the cardiomyopathies into a primary (only heart involvement) and a secondary group (systemic/ multi-organ involvement). Hypertrophic and dilated cardiomyopathy are the most frequent types in childhood. The diagnosis and work-up in patients with cardiomyopathy is complex and extensive. Familial and non-familial forms need to be differentiated. A broad family history (more than three generations) is necessary; a clinical screening of first-degree relatives is recommended. Gene mutations, inborn errors of metabolism, malformative syndromes and neuromuscular disease are well-known causes of cardiomyopathy. Still, a large part remains idiopathic. The diagnosis of cardiomyopathy in children requires a thorough anamnesis and clinical examination. A multidisciplinary approach is requested due to the large differential diagnosis. This is not only in the interest of the child, but even more given the possible involvement of other family members.},
keywords = {Desigualtats Socials, Informes, Mundial},
pubstate = {published},
tppubtype = {techreport}
}
Cardiomyopathies are a heterogeneous group of heart muscle disorders, being defined as "a myocardial disorder in which the heart muscle is structurally and/or functionally abnormal in the absence of coronary artery disease, hypertension, valvular disease and congenital heart disease sufficient to cause the observed mitochondriale myocardial abnormality". Four major types are recognised, namely the dilated, the hypertrophic and the restrictive variants, and arrhythmogenic right ventricular cardiomyopathy. A more recent approach divides the cardiomyopathies into a primary (only heart involvement) and a secondary group (systemic/ multi-organ involvement). Hypertrophic and dilated cardiomyopathy are the most frequent types in childhood. The diagnosis and work-up in patients with cardiomyopathy is complex and extensive. Familial and non-familial forms need to be differentiated. A broad family history (more than three generations) is necessary; a clinical screening of first-degree relatives is recommended. Gene mutations, inborn errors of metabolism, malformative syndromes and neuromuscular disease are well-known causes of cardiomyopathy. Still, a large part remains idiopathic. The diagnosis of cardiomyopathy in children requires a thorough anamnesis and clinical examination. A multidisciplinary approach is requested due to the large differential diagnosis. This is not only in the interest of the child, but even more given the possible involvement of other family members.
@techreport{sindic_de_greuges_de_catalunya_informe_2017,
title = {Informe alternatiu al cinquè i sisè informe d'aplicació de la convenció de drets de l'infant a Espanya (2010-2016). Catalunya},
author = {{Síndic de Greuges de Catalunya}},
url = {http://www.sindic.cat/site/unitFiles/4328/UN Convention on children rights_catala_def.pdf},
year = {2017},
date = {2017-01-01},
pages = {62},
address = {Barcelona},
institution = {Síndic de Greuges de Catalunya},
keywords = {Infants, Informes},
pubstate = {published},
tppubtype = {techreport}
}
@book{banco_de_espana_encuesta_2017,
title = {Encuesta Financiera de las Familias (EFF) 2014: métodos, resultados y cambios desde 2011},
author = {Banco de España},
url = {http://www.bde.es/f/webbde/SES/Secciones/Publicaciones/InformesBoletinesRevistas/ArticulosAnaliticos/2017/T1/fich/beaa1701-art2.pdf},
year = {2017},
date = {2017-01-01},
abstract = {En este artículo se presentan los resultados principales de la Encuesta Financiera de las Familias 2014, que muestran la situación financiera de los hogares españoles a finales de ese año. Asimismo, se describen los cambios más relevantes ocurridos en el período comprendido entre finales de 2011 y finales de 2014.},
keywords = {Afers Socials, Crisi Econòmica, Espanya, Informes},
pubstate = {published},
tppubtype = {book}
}
En este artículo se presentan los resultados principales de la Encuesta Financiera de las Familias 2014, que muestran la situación financiera de los hogares españoles a finales de ese año. Asimismo, se describen los cambios más relevantes ocurridos en el período comprendido entre finales de 2011 y finales de 2014.
@techreport{sindic_de_greuges_de_catalunya_sindic_2016b,
title = {El Síndic de Greuges davant els reptes de la llei d'igualtat efectiva de dones i homes},
author = {Síndic de Greuges de Catalunya},
url = {http://www.sindic.cat/site/unitFiles/4277/Informe sobre igualtat%7B_%7Dcat%7B_%7Dok.pdf},
year = {2016},
date = {2016-01-01},
pages = {20},
address = {Barcelona},
institution = {Síndic de Greuges de Catalunya},
keywords = {Desigualtats de Génere, Informes},
pubstate = {published},
tppubtype = {techreport}
}
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