Dagma Venturini Marques Abramides

Identification of a microdeletion at the 7q33‐q35 disrupting the <i>CNTNAP2</i> gene in a Brazilian stuttering case

Aline Petrin, Célia Maria Giacheti, Luciana Paula Maximino et al. · American Journal of Medical Genetics Part A · 2010 · 83 citations · Full text

Developmental language disorder associated with polymicrogyria

Marilisa M. Guerreiro, Simone Rocha de Vasconcellos Hage, Catarina A. Guimarães et al. · Neurology · 2002 · 74 citations

Specific language impairment: linguistic and neurobiological aspects

Simone Rocha de Vasconcellos Hage, Fernando Cendes, Maria Augusta Montenegro et al. · Arquivos de Neuro-Psiquiatria · 2006 · 68 citations · Full text

Neuropsychology, Neurological Disorder, Neurolinguistics +16

Apert and Crouzon syndromes—Cognitive development, brain abnormalities, and molecular aspects

Marilyse B. L. Fernandes, Luciana Paula Maximino, Gimol Benzaquen Perosa et al. · American Journal of Medical Genetics Part A · 2016 · 45 citations

Apert syndrome: factors involved in the cognitive development

Adriano Yacubian Fernandes, Aristides Palhares, Alcir Giglio et al. · Arquivos de Neuro-Psiquiatria · 2005 · 39 citations · Full text