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Erasmo Barbante Casella
Researcher at University of São Paulo
Publications - 54
Citations - 660
Erasmo Barbante Casella is an academic researcher from University of São Paulo. The author has contributed to research in topics: Attention deficit hyperactivity disorder & Population. The author has an hindex of 14, co-authored 50 publications receiving 573 citations. Previous affiliations of Erasmo Barbante Casella include Albert Einstein Hospital.
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Vitamin B12 deficiency in infancy as a cause of developmental regression.
TL;DR: The clinical symptoms and the brain CT were normalized after vitamin B12 administration, and a 6-month-old infant with insidious developmental regression and brain atrophy showed by CT scan, secondarily to vitamin B 12 deficiency was reported.
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Attention deficit and hyperactivity disorder in people with epilepsy: diagnosis and implications to the treatment.
TL;DR: Some neurobiological and physiopathogenic aspects, common to ADHD and epilepsy, from recent research studies, related to pharmacology, neuroimaging and electroencephalography are presented.
Journal ArticleDOI
Griscelli syndrome: characterization of a new mutation and rescue of T-cytotoxic activity by retroviral transfer of RAB27A gene
João C. S. Bizario,Jérôme Feldmann,Fabíola Attié de Castro,Gaël Ménasché,Cristina Miuki Abe Jacob,Lilian Maria Cristofani,Erasmo Barbante Casella,Júlio César Voltarelli,Geneviève de Saint-Basile,Enilza Maria Espreáfico +9 more
TL;DR: It is shown that cytotoxic activity of the patient's CD8+ T lymphocytes can be rescued in vitro by RAB27A gene transfer mediated by a recombinant retroviral vector, a first step towards a potential treatment of the acute phase of GS2 by R AB27A transduced lymphocytes.
Journal ArticleDOI
Motor profile of children with attention deficit hyperactivity disorder, combined type
Juliana Barbosa Goulardins,Juliana C. Bilhar Marques,Erasmo Barbante Casella,Roseane O Nascimento,Jorge Alberto de Oliveira +4 more
TL;DR: Difficulties in motor performance were observed in the children with ADHD, combined type, and the identification of such deficits may assist in the design of therapeutic protocols for the treatment of children with this type of ADHD.
Journal ArticleDOI
Paralog Studies Augment Gene Discovery: DDX and DHX Genes.
Ingrid S. Paine,Jennifer E. Posey,Christopher M. Grochowski,Shalini N. Jhangiani,Sarah Rosenheck,Robert Kleyner,Taylor Marmorale,Margaret Yoon,Kai Wang,Reid J. Robison,Gerarda Cappuccio,Michele Pinelli,Adriano Magli,Zeynep Coban Akdemir,Joannie Hui,Wai Lan Yeung,Bibiana K Y Wong,Lucia Ortega,Mir Reza Bekheirnia,Tatjana Bierhals,Maja Hempel,Jessika Johannsen,René Santer,Dilek Aktas,Mehmet Alikasifoglu,Sevcan Tug Bozdogan,Hatip Aydin,Ender Karaca,Yavuz Bayram,Hadas Ityel,Michael O. Dorschner,Janson White,Ekkehard Wilichowski,Saskia B. Wortmann,Erasmo Barbante Casella,Joao Paulo Kitajima,Fernando Kok,Fabíola Paoli Monteiro,Donna M. Muzny,Michael J. Bamshad,Richard A. Gibbs,V. Reid Sutton,Hilde Van Esch,Nicola Brunetti-Pierri,Friedhelm Hildebrandt,Ariel Brautbar,Ignatia B. Van den Veyver,Ian A. Glass,Davor Lessel,Gholson J. Lyon,James R. Lupski +50 more
TL;DR: 15 unrelated individuals who have DD and/or ID, central nervous system (CNS) dysfunction, vertebral anomalies, and dysmorphic features and were found to have probably damaging variants in DExD/H-box RNA helicase genes are described.