Global ETD Search

81	Factors emocionals associats a la conducta alimentària en adolescents. Adaptació i validació de l'EES-C i de l'EPI-C Thomas, Mònica 24 July 2012 (has links) Study of the impact of some emotional factors related to food intake. The research is based on the design and observational cross-cultural adaptation and validation of assessment tools for emotional eating (EES-C) and eating behavior (EPI-C) in 379 non-pathological adolescents (14 -18 years old). The factorial structure, the concurrent validity, the discriminant and reliability of the original scales were maintained.  The girls showed a higher emotional intake in AAF in the EES-C and higher scores in DIER and EEAT in the EPI-C. The boys showed the higher scores in PAR. We found significant differences between different types of emotional eating and sex in the AAF, and DEP subscales. A higher percentage of girls belonged to the type II and obtained the highest scores in Diet ChEAT and depressive symptoms by CDI assessment. Diet restriction increased 3 times the risk of eating disorders, and greater parental control increased the risk of TCA twice. / Estudi de la incidència de factors emocionals relacionats amb ingesta alimentaria. Disseny descriptiu, observacional i transversal d’adaptació i validació cultural dels instruments d’avaluació de la ingesta emocional (EES-C) i de la conducta alimentària (EPI-C) en 379 adolescents no clínics (14 -18 anys). Es mantingué estructura factorial, validesa concurrent, discriminant i fiabilitat de les escales originals. Les noies presentaren major ingesta emocional en AAF i UNS de l’EES-C i puntuacions més elevades en DIER i EEAT en l’EPI-C. Els nois presentaren puntuacions més elevades en PAR. Es trobaren diferències significatives entre tipologies d’ingesta emocional en AAF, DEP i UNS i diferències de sexe. Un percentatge més elevat de noies pertanyien a la tipologia II i obtingué puntuacions més elevades en DIETA mesurada pel ChEAT i simptomatologia depressiva avaluada pel CDI. La restricció dietètica augmentà 3 vegades el risc de TCA, i un major control parental n'augmentà el risc 2 vegades. Nutrició Nutrición Nutrition Alimentació Alimentación Diet Alimentació emocional Alimentación emocional Eating patterns EPI-C Eating Pattern Inventory for Children EES-C Emotional Eating Scale for Children Adolescència Adolescencia Adolescence Patrons alimentaris Patrones alimentarios Eating patterns Regulació emocional Regulación emocional Emotional regulation 159.9
82	MR-tomographische Darstellung intracerebraler Blutungen mit und ohne Therapie / Different magnetic resonance imaging of experimentally induced intracerebral hemorrhages with and without therapy Meddour, Miriam 02 February 2011 (has links) No description available. 610 Medizin, Gesundheit Medicine MRT T1 gewichtete Sequenz T2 gewichtete Sequenz PD TSE FLAIR-TSE T2* GE DWI ADC rt-PA PAI MRI T1-weighted imaging T2-weighted TSE protone-density weighted TSE FLAIR-TSE T2*-weighted GE Sequence diffusion-weighted EPI ADC rt-PA PAI 44.64 44.90 MED 371: Radiologie
83	A Novel Approach to Identify Candidate Imprinted Genes in Humans Shapiro, Jonathan 21 March 2012 (has links) Many imprinted genes are necessary for normal human development. Approximately 70 imprinted genes have been identified in humans. I developed a novel approach to identify candidate imprinted genes in humans using the premise that imprinted genes are often associated with nearby parent-of-origin-specific DNA differentially methylated regions (DMRs). I identified parent-of-origin-specific DMRs using sodium bisulfite-based DNA (CpG) methylation profiling of uniparental tissues, mature cystic ovarian teratoma (MCT) and androgenetic complete hydatidiform mole (AnCHM), and biparental tissues, blood and placenta. In support of this approach, the CpG methylation profiling led to the identification of parent-of-origin-specific differentially methylated CpG sites (DMCpGs) in known parent-of-origin-specific DMRs. I found new DMRs for known imprinted genes NAP1L5 and ZNF597. Most importantly, I discovered many new DMCpGs, which were associated with nearby genes, i.e., candidate imprinted genes. Allelic expression analyses of one candidate imprinted gene, AXL, suggested polymorphic imprinting of AXL in human blood. Allele Allele-specific DNA Methylation Allele-specific Gene Expression Allele-specific Expression Allele-specific Methylation AnCHM Androgenetic Androgenetic Mole Mole Complete Mole Hydatidiform Mole Complete Hydatidiform Mole Androgenetic Hydatidiform Mole Androgenetic Complete Hydatidiform Mole Biparental Tissue Bisulfite Bisulphite Blood Blood DNA Computational Biology DNA Methylation DNA Methylation Profiling Epigenetic Epi-genetic Epigenomic Epi-genomic Expression Expression Regulation Gene Expression Gene Expression Regulation Genetic Genetic Imprint Genetic Imprinting Genomic Genomic DNA Genomic Imprint Genomic Imprinting Human Imprint Imprinting Teratoma Ovarian Teratoma Cystic Teratoma Mature Teratoma Mature Cystic Teratoma Mature Ovarian Teratoma Cystic Ovarian Teratoma Mature Cystic Ovarian Teratoma MCT Methylation Cytosine Methylation Microarray Neoplasm Ovarian Neoplasm Placenta Profiling Promoter Promoter Region Sodium Bisulfite Sodium Bisulphite Uniparental Tissue WB WBC Imprinted Gene Polymorphic Imprinting Parent-of-origin Parent-of-origin-specific Methylation Parent-of-origin-specific Expression 0369 0307
84	A Novel Approach to Identify Candidate Imprinted Genes in Humans Shapiro, Jonathan 21 March 2012 (has links) Many imprinted genes are necessary for normal human development. Approximately 70 imprinted genes have been identified in humans. I developed a novel approach to identify candidate imprinted genes in humans using the premise that imprinted genes are often associated with nearby parent-of-origin-specific DNA differentially methylated regions (DMRs). I identified parent-of-origin-specific DMRs using sodium bisulfite-based DNA (CpG) methylation profiling of uniparental tissues, mature cystic ovarian teratoma (MCT) and androgenetic complete hydatidiform mole (AnCHM), and biparental tissues, blood and placenta. In support of this approach, the CpG methylation profiling led to the identification of parent-of-origin-specific differentially methylated CpG sites (DMCpGs) in known parent-of-origin-specific DMRs. I found new DMRs for known imprinted genes NAP1L5 and ZNF597. Most importantly, I discovered many new DMCpGs, which were associated with nearby genes, i.e., candidate imprinted genes. Allelic expression analyses of one candidate imprinted gene, AXL, suggested polymorphic imprinting of AXL in human blood. Allele Allele-specific DNA Methylation Allele-specific Gene Expression Allele-specific Expression Allele-specific Methylation AnCHM Androgenetic Androgenetic Mole Mole Complete Mole Hydatidiform Mole Complete Hydatidiform Mole Androgenetic Hydatidiform Mole Androgenetic Complete Hydatidiform Mole Biparental Tissue Bisulfite Bisulphite Blood Blood DNA Computational Biology DNA Methylation DNA Methylation Profiling Epigenetic Epi-genetic Epigenomic Epi-genomic Expression Expression Regulation Gene Expression Gene Expression Regulation Genetic Genetic Imprint Genetic Imprinting Genomic Genomic DNA Genomic Imprint Genomic Imprinting Human Imprint Imprinting Teratoma Ovarian Teratoma Cystic Teratoma Mature Teratoma Mature Cystic Teratoma Mature Ovarian Teratoma Cystic Ovarian Teratoma Mature Cystic Ovarian Teratoma MCT Methylation Cytosine Methylation Microarray Neoplasm Ovarian Neoplasm Placenta Profiling Promoter Promoter Region Sodium Bisulfite Sodium Bisulphite Uniparental Tissue WB WBC Imprinted Gene Polymorphic Imprinting Parent-of-origin Parent-of-origin-specific Methylation Parent-of-origin-specific Expression 0369 0307

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