Mostrando ítems 61-80 de 102

    DNA methylome in HER2-positive resistant breast cancer 

    Palomeras, Sònia (Fecha de defensa: 2019-02-27)

    The major clinical problem for HER2+ breast cancer target therapies is the acquisition of resistance. The DNA methylation status of the promoter gene region has been described as a common epigenetic alteration for ...

    Influencia de la grasa epicárdica en la arritmia: fibrilación auricular, la cardioversión eléctrica, la recurrencia y el tratamiento 

    Valenzuela Leal, Helen (Fecha de defensa: 2019-04-09)

    The thickness of epicartic fat can be directly measured by transthoracic echocardiography. Epicartic fat has recently been associated with the onset of atrial fibrillation (AF). In this work we will analyze the relationship ...

    Therapeutic potential of pituitary adenylate cyclase-activating polypeptide and epigallocatechin gallate in motor and cognitive deficits of Huntington's disease models 

    Cabezas Llobet, Núria (Fecha de defensa: 2019-02-28)

    Huntington's disease (MH) is a progressive neurodegenerative disorder characterized by a motor dysfunction, cognitive impairment, and psychiatric symptoms. At neuropathological level, it has been described that cognitive ...

    Muerte súbita natural inexplicada: valor de la investigación genética post mortem 

    Sánchez-Molero Núñez, Olallo-Efrén (Fecha de defensa: 2017-12-15)

    Natural death defines the death primarily attributed to an illness or an internal malfunction of the body, and not directly influenced by external forces. Most causes can be identified directly with macroscopic forensic ...

    Regulome-seq: a novel approach for the identification of non-coding variants associated with human disease. Assessment of its applicability in 89 Brugada syndrome individuals 

    Pinsach Abuin, Mel·lina (Fecha de defensa: 2019-01-30)

    Brugada syndrome (BrS) is a cardiac electrical disease with high susceptibility to sudden cardiac death. Approximately 25-30% of BrS patients are explained by pathogenic variants in coding sequences of cardiac ion channels, ...

    Factors associated with arterial stiffness in a general Mediterranean population and in a Mediterranean intermediate cardiovascular risk population 

    Camós Llovet, Lourdes (Fecha de defensa: 2019-02-26)

    The objectives of the thesis are to estimate the prevalence of pathological arterial stiffness (measured with the Cardio-Ankle Vascular Index –CAVI-) in a general Mediterranean population and in a Mediterranean intermediate ...

    Factors associats a la incidència de fibril·lació auricular i estudi de l'associació del tractament amb estatines amb la incidència d'aquesta arítmia en població hipertensa sense antecedents de malaltia isquèmica vascular 

    Alves Cabratosa, Lia (Fecha de defensa: 2016-12-16)

    Atrial fibrillation (AF) is the most common arrhythmia in clinical practice and implies a huge social, medical, and economical burden. Analyses of AF risk factors in certain groups of population would allow tailored ...

    WNT5A, SFRP5 y CRTC3: nuevas adipocinas relacionadas con la obesidad en la edad pediátrica 

    Soriano Rodríguez, Pilar (Fecha de defensa: 2015-10-13)

    WNT5A is a protein with proinflammatory properties recently related to insulin resistance. It is believed that this protein might be regulated by SFRP5, which sequesters WNT5A exerting its anti-inflammatory actions and ...

    Bypass gástrico en el tratamiento de la obesidad mórbida. Seguimiento a 5 años de los primeros 300 casos en la provincia de Girona 

    Rodríguez Hermosa, José Ignacio (Fecha de defensa: 2018-12-10)

    A prospective study on 300 morbidly obese patients who underwent gastric bypass in the province of Girona with a follow-up of 5 years.More female (288/12), mean age 43.5 years, mean weight 118.7 kg, mean BMI 46.1 kg/m2. ...

    Nou mecanismes implicats en els dèficits transcripcionals i la pèrdua del BDNF en la malaltia de Huntington: descripció de noves dianes terapèutiques 

    Vidal Sancho, Laura (Fecha de defensa: 2018-01-10)

    Huntington disease is a neurodegenerative disorder characterized by motor, cognitive and psychiatric dysfunction. Huntington disease is caused by an expanded CAG trinucleotide repeat at the exon 1 of the IT15 gen, which ...

    Sistema immunitari i marcadors de risc cardiometabòlic en l'edat pediàtrica 

    Gispert-Saüch Puigdevall, Montse (Fecha de defensa: 2018-03-02)

    We studied the relationship between the circulating levels of the innate immune system molecules (α-defensins and BPI) and the acquired immune system (IgG, IgA and IgM) with obesity and cardiometabolic risk factors in ...

    Papel del diffusion tensor imaging en la resonancia magnética cerebral como marcador predictivo del estado motor y evolución funcional en pacientes con hemorragia intracerebral 

    Terceño Izaga, Mikel (Fecha de defensa: 2018-02-06)

    The present thesis, aims to study whether the evaluation of the CT through DTI and tractography sequences in the first 12 hours from the ICH onset, is able to predict the motor and functional outcome at 3 months. The ...

    Arteopatia perifèrica i factors de risc cardiovascular. Millora de la prevenció secundària dels pacients amb arteriopatia perifèrica en l'atenció primària 

    Llobera Serentill, Àlex (Fecha de defensa: 2018-03-09)

    Cardiovascular risk factors control is low in peripheral artery disease patients. Leukocyte count over7.8 K/mcL or neutrophil count over 4.6 K/mcL are predictors of increased risk for heart coronary disease, cerebral ...

    Detecció de Copy Number Variants mitjançant seqüenciació d'alt rendiment en la Mort Sobtada Cardíaca hereditària 

    Matés Ramírez, Jesús (Fecha de defensa: 2018-01-19)

    Arrhythmogenic cardiac diseases are the main cause of SCD among the population under 35 years of age. Despite the improvements in genetic diagnosis, the percentage of cases that remain unexplained after genetic analysis ...

    Identificació de microRNAs circulants i placentaris en obesitat materna gestacional i la seva relació amb paràmetres metabòlics materns i el creixement pre i postnatal 

    Bonmatí Santané, Alexandra (Fecha de defensa: 2017-11-28)

    Increased metabolic disease in children is a major public health problem.. Epigenetic marks, such as microRNAs, could be one of the mechanisms that regulate the association maternal obesity with the development of metabolic ...

    Arteriopatia perifèrica assimptomàtica: prevalença, detecció i tractament 

    Quesada Sabaté, Miquel (Fecha de defensa: 2017-02-17)

    Background There is few epidemiological data of peripheral arterial disease (PAD) in our environment. The recommendation of screening with ankle brachial index (ABI) in asymptomatic individuals is controversial. Evidence ...

    Relación entre el flujo de la arteria cerebral media y la presión en la arteria carótida interna durante la endarterectomía carotídea 

    Rodríguez Cabeza, Patricia (Fecha de defensa: 2017-10-03)

    Risk of cerebral hypoperfusion during carotid endarterectomy arterial is the main limiting factor of this technique. Shunt allows partial maintenance of cerebral perfusion during clamping. We analyze the hemodynamic ...

    Determinants moleculars de la mort sobtada cardíaca en una gran família de les Illes Canàries 

    Bosch Calero, Cristina (Fecha de defensa: 2016-03-08)

    Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a sudden cardiac death (SCD) associated disease characterized by the presence of polymorphic or bidirectional ventricular tachycardia during emotional or ...

    Eficàcia, seguretat i abandonament del tractament farmacològic del trastorn per dèficit d’atenció amb hiperactivitat en pacients adults 

    Cunill Clotet, Ruth (Fecha de defensa: 2017-05-08)

    There are concerns about the benefit-risk ratio of pharmacologic interventions for ADHD in adults, especially in patients with ADHD and substance use disorder (SUD). Four systematic reviews of randomized placebo-controlled ...

    Els factors GATA4 i GATA5 en la regulació transcripcional del gen que codifica pel canal de sodi cardíac (SCN5A) 

    Tarradas Pou, Anna (Fecha de defensa: 2017-03-14)

    The SCN5A gene encodes the alpha subunit of the cardiac sodium channel (NaV1.5), which is responsible for the influx of sodium ions through membrane of cardiomyocytes. Different evidences suggest that an aberrant expression ...