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DataTítuloAutor(es)TipoAcesso
2019Lack of KBTBD4 mutations in molecularly classified Brazilian medulloblastomasLeal, Letícia Ferro; Cavagna, Rodrigo de Oliveira; Campanella, Nathalia Cristina, et al.ArtigoAcesso restrito autor
2019Late ophthalmologic referral of anisometropic amblyopia: a retrospective study of different amblyopia subtypesVieira, Maria João; Guimarães, Sandra Viegas; Costa, Patrício Soares, et al.ArtigoAcesso aberto
2016Linking learning contexts: the relationship between students’ civic and political experiences and their self-regulation in schoolMalafaia, Carla; Teixeira, Pedro Miguel Silva Costa Afonso; Neves, Tiago, et al.ArtigoAcesso aberto
2024Longitudinal predictors of online dating aggression: similarities and differences between control and intrusivenessRodríguez-deArriba, María-Luisa; Caridade, Sónia Maria Martins; Del Rey, Rosario, et al.ArtigoAcesso aberto
Jun-2007MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patientsCoutinho, Ana M.; Oliveira, Guiomar; Katz, Cécile, et al.ArtigoAcesso restrito UMinho
2020Medidas hipertensivas em escolares: risco da obesidade central e efeito protetor da atividade física moderada-vigorosaTozo, Tatiana Affornali; Pereira, Beatriz; Menezes Junior, Francisco José de, et al.ArtigoAcesso aberto
2007Molecular alterations of KIT oncogene in gliomasGomes, Ana L.; Reis-Filho, Jorge S.; Lopes, José M., et al.ArtigoAcesso restrito UMinho
Out-2005Molecular strategies for identifying human papillomavirus infection in routinely processed samples: focus on paraffin sectionsNonogaki, Suely; Wakamatsu, Alda; Longatto, Adhemar, et al.ArtigoAcesso restrito UMinho
Mai-2013Morphometry of corpus callosum in Williams syndrome: shape as an index of neural developmentSampaio, Adriana; Bouix, Sylvain; Sousa, Nuno, et al.ArtigoAcesso restrito UMinho
2021A morte de jovens em contexto de urgência: vivências dos enfermeirosTeixeira, Diana FernandesDissertação de mestrado Acesso aberto
30-Jul-2008Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation typeTemudo, Teresa; Ramos, Elisabete; Dias, Karin, et al.ArtigoAcesso restrito UMinho
Out-2010Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesisPinho, Teresa; Silva-Fernandes, Anabela; Bousbaa, Hassan, et al.ArtigoAcesso aberto
Jan-2009Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patientsSantos, Mónica; Temudo, Teresa; Kay, Teresa, et al.ArtigoAcesso aberto
Nov-2008New foci of Buruli ulcer, Angola and Democratic Republic of CongoKibadi, Kapay; Panda, Mbutu; Tamfum, Jean-Jacques Muyembe, et al.ArtigoAcesso aberto
2018New pediatric risk factors for amblyopia: strabismic versus refractiveGuimarães, Sandra; Vieira, Maria; Queirós, Tatiana Sofia Monteiro, et al.ArtigoAcesso aberto
2010Optional screening strategies for cervical cancer using standalone tests and their combinations among low- and medium-income populations in Latin America and Eastern EuropeSarian, Luis Otavio; Derchain, Sophie; Shabalova, Irena, et al.ArtigoAcesso aberto
2018Perianal Crohn's disease - association with significant inflammatory activity in proximal small bowel segmentsXavier, Sofia; Cúrdia Gonçalves, Tiago; Dias de Castro, Francisca, et al.ArtigoAcesso restrito autor
Jul-2009Persistent high-risk human papillomavirus infections and other end-point markers of progressive cervical disease among women prospectively followed up in the New Independent States of the Former Soviet Union and the Latin American Screening study cohortsSyrjänen, Kari; Shabalova, Irena; Naud, Paulo, et al.ArtigoAcesso restrito autor
Out-2013Phenotypic characterization and familial risk in hyperplastic polyposis syndromeCaetano, Ana Célia; Ferreira, Helena; Soares, João, et al.ArtigoAcesso restrito UMinho
4-Set-2018Predicting participation of people with impaired vision in epidemiological studiesRamos, Pedro Lima; Santana, Rui; Moreno, Laura Hernandez, et al.ArtigoAcesso aberto