Search Results - "Mello, Claudia Berlim de"

DNA methylation epi-signature and biological age in attention deficit hyperactivity disorder patients by Carvalho, Gleyson Francisco da Silva, Costa, Thais Virginia Moura Machado, Nascimento, Amom Mendes, Wolff, Beatriz Martins, Damasceno, Julian Gabriel, Vieira, Lucas Liro, Almeida, Vanessa Tavares, Oliveira, Yanca Gasparini de, Mello, Claudia Berlim de, Muszkat, Mauro, Kulikowski, Leslie Domenici

“…Attention Deficit/Hyperactivity Disorder (ADHD) is a common behavioral syndrome that begins in childhood and affects 3.4% of children worldwide. Due to its…”
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Influence of blood phenylalanine level variations on the development of executive functions and social cognition in children with phenylketonuria by de Almeida Duarte, Cristiane Mendes, Piazzon, Flavia Balbo, Rocco, Isadora Salvador, de Mello, Claudia Berlim

“…To investigate the performance of 27 children with phenylketonuria (PKU) in tests of Executive Functions (EF) and Social Cognition (SC), and their associations…”
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Neuropsychological Profile of 25 Brazilian Patients with 22q11.2 Deletion Syndrome: Effects of Clinical and Socioeconomic Variables by Pimenta, Larissa Salustiano Evangelista, Mello, Claudia Berlim de, Benedetto, Luciana Mello Di, Soares, Diogo Cordeiro de Queiroz, Kulikowski, Leslie Domenici, Dantas, Anelisa Gollo, Melaragno, Maria Isabel, Kim, Chong Ae

“…The 22q11.2 deletion syndrome (22q11.2DS) is associated with a heterogeneous neurocognitive phenotype, which includes psychiatric disorders. However, few…”
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Executive functions in children with dyslexia by Barbosa, Thais, Rodrigues, Camila Cruz, Mello, Claudia Berlim de, Silva, Mariana Cristina de Souza e, Bueno, Orlando Francisco Amodeo

“…ABSTRACT This study aimed to verify whether children with dyslexia have difficulties in executive functions (shifting, working memory, inhibition). Methods: A…”
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Intelligence Quotient Variability in Klinefelter Syndrome Is Associated With GTPBP6 Expression Under Regulation of X-Chromosome Inactivation Pattern by Simonetti, Luciane, Ferreira, Lucas G. A., Vidi, Angela Cristina, Souza, Janaina Sena de, Kunii, Ilda S., Melaragno, Maria Isabel, Mello, Claudia Berlim de, Carvalheira, Gianna, Dias da Silva, Magnus R.

“…Klinefelter syndrome (KS) displays a broad dysmorphological, endocrinological, and neuropsychological clinical spectrum. We hypothesized that the…”
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Educational status, testosterone replacement, and intelligence outcomes in Klinefelter syndrome by Simonetti, Luciane, Silva, Magnus Regios Dias da, Mello, Claudia Berlim de

“…Most male hypergonadotropic hypogonadism associated with infertility can be attributed to a single genetic condition such as Klinefelter syndrome (KS). This…”
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Response to intervention as an identification strategy of the risk for dyslexia by Medda, Mariana Gobbo, Barbosa, Thais, Rocco, Isadora Salvador, Mello, Claudia Berlim de

“…To develop on intervention process to identify children at risk of dyslexia, based on the Response to Intervention model. Specifically, to identify the pattern…”
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Assessment of Executive Functions after Treatment of Childhood Acute Lymphoid Leukemia: a Systematic Review by Godoy, Priscilla Brandi Gomes, Simionato, Natalia Maria, de Mello, Claudia Berlim, Suchecki, Deborah

“…Individuals treated for childhood acute lymphoblastic leukemia (ALL) have a high survival rate. This fact, however, may lead to neurocognitive impairments in…”
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Numerical cognition in children with cerebral palsy by de Freitas Feldberg, Silvia Cristina, da Silva Gusmão Cardoso, Thiago, Santos, Flavia H., Muszkat, Mauro, Bueno, Orlando Francisco Amodeo, Berlim de Mello, Claudia

“…•Participant’s.•Measured by the Raven Matrices scales.•On the other hand, IQ scores were in typical levels for all groups.•van Rooijen.•Maintain that working…”
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The effect of brain-derived neurotrophic factor Val66Met polymorphism on adolescent activity and rest rhythms, circadian preferences and attentional performance by da Costa Lopes, Luísa, Rollemberg Poyares, Dalva Lucia, Tufik, Sergio, La Banca de Oliveira, Sophia, Ribeiro da Silva Vallim, Julia, Kiyomi Ota, Vanessa, Melaragno, Maria Isabel, Ohayon, Maurice, Berlim de Mello, Claudia

“…Variations in circadian regulating mechanisms generate different individual preferences in respect of sleep and activity timing, which are known as…”
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Downregulation of genes outside the deleted region in individuals with 22q11.2 deletion syndrome by Dantas, Anelisa Gollo, Santoro, Marcos Leite, Nunes, Natalia, de Mello, Claudia Berlim, Pimenta, Larissa Salustiano Evangelista, Meloni, Vera Ayres, Soares, Diogo Cordeiro Queiroz, Belangero, Sintia Nogueira, Carvalheira, Gianna, Kim, Chong Ae, Melaragno, Maria Isabel

“…The 22q11.2 deletion syndrome (22q11.2DS) is caused by recurrent hemizygous deletions of chromosome 22q11.2. The phenotype of the syndrome is complex and…”
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X-linked intellectual disability related genes disrupted by balanced X-autosome translocations by Moysés-Oliveira, Mariana, Guilherme, Roberta Santos, Meloni, Vera Ayres, Di Battista, Adriana, de Mello, Claudia Berlim, Bragagnolo, Silvia, Moretti-Ferreira, Danilo, Kosyakova, Nadezda, Liehr, Thomas, Carvalheira, Gianna Maria, Melaragno, Maria Isabel

“…Detailed molecular characterization of chromosomal rearrangements involving X‐chromosome has been a key strategy in identifying X‐linked intellectual…”
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Clinical and molecular evaluation of 13 Brazilian patients with Gomez‐López‐Hernández syndrome by Perrone, Eduardo, Perez, Ana Beatriz Alvarez, D'Almeida, Vânia, Mello, Claudia Berlim, Jacobina, Marcela Amaral Avelino, Loureiro, Rafael Maffei, Burlin, Stênio, Migliavacca, Michele, Amaral Virmond, Luiza, Graziadio, Carla, Pedroso, José Luiz, Mendes, Elaine Lustosa, Gomy, Israel, Macena Sobreira, Nara Lygia

“…We aim to characterize patients with Gomez‐López‐Hernández syndrome (GLHS) clinically and to investigate them molecularly. A clinical protocol, including a…”
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Gomez–López–Hernández syndrome: A case report with clinical and molecular evaluation and literature review by Perrone, Eduardo, D'Almeida, Vânia, Macena Sobreira, Nara Lygia, Mello, Claudia Berlim, Oliveira, Allan Chiaratti, Burlin, Stênio, Soares, Maria de Fátima de Faria, Cernach, Mirlene Cecília Soares Pinho, Alvarez Perez, Ana Beatriz

“…Gomez–López–Hernández syndrome (GLHS) is characterized by rhombencephalosynapsis (RES), alopecia, trigeminal anesthesia and a distinctive phenotype, including…”
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A model for pediatric and neuropsychological screening assessment of children with learning disabilities by de Mello, Claudia Berlim, Brunoni, Leila Raquel Russowsky, Pilla, Ana Luiza, Taddei, José Augusto Aguiar Carrazedo, Barbosa, Thais, Sinnes, Elaine Girão, Rodrigues, Camila Cruz, Miranda, Monica Carolina, Muzskat, Mauro, Bueno, Orlando Francisco Amodeo

“…The high frequency of learning difficulties, attention disorders or developmental delay in children in the early years of schooling has resulted in a greater…”
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Versão Abreviada do WISC-III: Correlação entre QI Estimado e QI Total em Crianças Brasileiras by DE MELLO, Claudia Berlim, ARGOLLO, Nayara, SHAVER, Beatriz P. M, ABREU, Neander, GODINHO, Kátya, DURAN, Paula, VARGEM, Fernanda, MUSZKAT, Mauro, MIRANDA, Mônica Carolina, AMODEO BUENO, Orlando Francisco

“…Com o objetivo de correlacionar o QI Estimado com o QI Total, quatro bancos de dados do WISC III de 207 crianças foram associados: 1) crianças com…”
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Resposta à intervenção como estratégia de identificação do risco para dislexia by Medda, Mariana Gobbo, Barbosa, Thais, Rocco, Isadora Salvador, Mello, Claudia Berlim de

“…Resumo Objetivo desenvolver um processo de intervenção para identificação de crianças em risco para dislexia, baseado no modelo de resposta à intervenção…”
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Attentional Profiles and White Matter Correlates in Attention-Deficit/Hyperactivity Disorder Predominantly Inattentive Type by Rossi, Adriana Suzart Ungaretti, de Moura, Luciana Monteiro, de Mello, Claudia Berlim, de Souza, Altay Alves Lino, Muszkat, Mauro, Bueno, Orlando Francisco Amodeo

“…Attention-deficit/hyperactivity disorder (ADHD) is a widely studied neurodevelopmental disorder. It is a highly heterogeneous condition, encompassing different…”
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Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome in an adolescent with complex chromosomal rearrangement and intellectual disability by Oliveira, Mariana Moysés, Meloni, Vera Ayres, Canonaco, Rosane Seidler, Takeno, Sylvia Satomi, Bortolai, Adriana, de Mello, Claudia Berlim, de Lima, Fernanda Teresa, Melaragno, Maria Isabel

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Involution of categorical thinking processes in Alzheimer's disease: Preliminary results by de Mello, Claudia Berlim, Abrisqueta-Gomez, Jacqueline, Xavier, Gilberto Fernando, Bueno, Orlando Francisco Amodeo

“…Alzheimer's disease (AD) is a degenerative brain disorder characterized by progressive losses in cognitive functions, including memory. The sequence of these…”
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