Listar Ciencias de la Salud por autor "Hutz, Mara Helena"
Mostrando ítems 1-11 de 11
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CLOCK polymorphisms in attention-deficit/hyperactivity disorder (ADHD) : further evidence linking sleep and circadian disturbances and ADHD
Carpena, Marina Xavier; Hutz, Mara Helena; Oliveira, Angélica Salatino de; Polanczyk, Guilherme Vanoni; Zeni, Cristian Patrick; Schmitz, Marcelo; Chazan, Rodrigo; Genro, Júlia Pasqualini; Rohde, Luis Augusto Paim; Rodrigues, Luciana Tovo (2019) [Artículo de periódico]Circadian and sleep disorders, short sleep duration, and evening chronotype are often present in attention-deficit/hyperactivity disorder (ADHD). CLOCK, considered the master gene in the circadian rhythm, has been explored ... -
COMT and prenatal maternal smoking in associations with conduct problems and crime : the Pelotas 1993 birth cohort study
Oliveira, Angélica Salatino de; Murray, Joseph; Kieling, Christian Costa; Genro, Júlia Pasqualini; Anselmi, Luciana; Wehrmeister, Fernando César; Barros, Fernando Celso Lopes Fernandes de; Menezes, Ana Maria Baptista; Rohde, Luis Augusto Paim; Hutz, Mara Helena (2016) [Artículo de periódico]Conduct problems in childhood and adolescence are significant precursors of crime and violence in young adulthood. The purpose of the current study is to test the interaction between prenatal maternal smoking and COMT ... -
DRD4 rare variants in attention-deficit/hyperactivity disorder (ADHD) : further evidence from a birth cohort study
Rodrigues, Luciana Tovo; Rohde, Luis Augusto Paim; Menezes, Ana Maria Baptista; Polanczyk, Guilherme Vanoni; Kieling, Christian Costa; Genro, Júlia Pasqualini; Anselmi, Luciana; Hutz, Mara Helena (2013) [Artículo de periódico]The dopamine receptor D4 (DRD4) is one of the most studied candidate genes for Attention-Deficit/Hyperactivity Disorder (ADHD). An excess of rare variants and non-synonymous mutations in the VNTR region of 7R allele in ... -
Genes de suscetibilidade no transtorno de déficit de atenção e hiperatividade
Roman, Tatiana; Rohde, Luis Augusto Paim; Hutz, Mara Helena (2002) [Artículo de periódico]O transtorno de déficit de atenção e hiperatividade (TDAH) é um dos transtornos mais comuns da infância e adolescência, afetando entre 3% a 6% das crianças em idade escolar. Essa patologia caracteriza-se por sintomas de ... -
MAOA is associated with methylphenidate improvement of oppositional symptoms in boys with attention deficit hyperactivity disorder
Guimarães, Ana Paula Miranda; Zeni, Cristian Patrick; Polanczyk, Guilherme Vanoni; Genro, Júlia Pasqualini; Roman, Tatiana; Rohde, Luis Augusto Paim; Hutz, Mara Helena (2009) [Artículo de periódico] -
A role for neurotransmission and neurodevelopment in attention-deficit/hyperactivity disorder
Roman, Tatiana; Rohde, Luis Augusto Paim; Hutz, Mara Helena (2009) [Artículo de periódico]Attention-deficit/hyperactivity disorder (ADHD) has a moderate to high genetic component, probably due to many genes with small effects. Several susceptibility genes have been suggested on the basis of hypotheses that ... -
Shared genetic background between children and adults with attention deficit/hyperactivity disorder
Rovira, Paula; Grevet, Eugenio Horácio; Hutz, Mara Helena; Rovaris, Diego Luiz; Oliveira, Angélica Salatino de; Silva, Bruna Santos da; Bau, Claiton Henrique Dotto; Rohde, Luis Augusto Paim; Ribasés, Marta (2020) [Artículo de periódico]Attention deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder characterized by age-inappropriate symptoms of inattention, impulsivity, and hyperactivity that persist into adulthood in the majority ... -
The brazilian contribution to attention-deficit/hyperactivity disorder molecular genetics in children and adolescents
Genro, Júlia Pasqualini; Roman, Tatiana; Rohde, Luis Augusto Paim; Hutz, Mara Helena (2012) [Artículo de periódico]Attention-Deficit/Hyperactivity Disorder (ADHD) is a common psychiatric condition of children worldwide. This disorder is defined by a combination of symptoms of inattention and hyperactivity/impulsivity. Diagnosis is based ... -
The effects of old and recent migration waves in the distribution of HBB*S globin gene haplotypes
Lindenau, Juliana Dal-Ri; Wagner, Sandrine Comparsi; Castro, Simone Martins de; Hutz, Mara Helena (2016) [Artículo de periódico]Sickle cell hemoglobin is the result of a mutation at the sixth amino acid position of the beta () globin chain. The HBB*S gene is in linkage disequilibrium with five main haplotypes in the -globin-like gene cluster named ... -
The role of MIR9-2 in shared susceptibility of psychiatric disorders during childhood : a population-based birth cohort study
Rodrigues, Luciana Tovo; Callo Quinte, Gabriela; Brum, Clarice Brinck; Ghisleni, Gabriele Cordenonzi; Bastos, Clarissa Ribeiro; Oliveira, Isabel Oliveira de; Barros, Fernando Celso Lopes Fernandes de; Barros, Aluisio Jardim Dornellas de; Santos, Iná da Silva dos; Rohde, Luis Augusto Paim; Hutz, Mara Helena; Matijasevich, Alicia (2019) [Artículo de periódico]Background: It has been suggested that microRNAs (miRNAs; short non-protein-coding RNA molecules that mediate post-transcriptional regulation), including mir-9 and mir-34 families, are important for brain development. ... -
The Val66Met polymorphism at the BDNF gene does not influence Wisconsin Card Sorting Test results in children and adolescents with bipolar disorder
Zeni, Cristian Patrick; Tramontina, Silzá; Zeni, Thamis Aline; Coelho, Roberta Paula Schell; Pheula, Gabriel Ferreira; Bernardi, Julio Mocellin; Maldaner, Ursula; Silva, Talita Lopes; Oliveira, Angélica Salatino de; Hutz, Mara Helena; Rohde, Luis Augusto Paim (2013) [Artículo de periódico]Objectives: To assess the role of the Val66Met polymorphism at the brain-derived neurotrophic factor (BDNF) gene on the performance of children and adolescents with bipolar disorder [juvenile bipolar disorder (JBD)] on the ...