Search Results - "Pereira, Marina B. B."

Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’ condition by Martins Custodio, Helena, Clayton, Lisa M, Bellampalli, Ravishankara, Pagni, Susanna, Silvennoinen, Katri, Caswell, Richard, Brunklaus, Andreas, Guerrini, Renzo, Koeleman, Bobby P C, Lemke, Johannes R, Møller, Rikke S, Scheffer, Ingrid E, Weckhuysen, Sarah, Zara, Federico, Zuberi, Sameer, Kuchenbaecker, Karoline, Balestrini, Simona, Mills, James D, Sisodiya, Sanjay M

“…Abstract Dravet syndrome is an archetypal rare severe epilepsy, considered ‘monogenic’, typically caused by loss-of-function SCN1A variants. Despite a…”
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Randomized trial of a photography‐aided behavioural intervention to reduce risk factors for caries and malocclusion in high‐risk infants by Pereira, Marina B. B., Pereira, Vinícius B. P., Pereira, Vitor B. P., Pereira, Vanessa G. F., Paula, Viviane M. B., Caetano, Aline P. F., Amaral, Waldemar N.

“…Objective To assess the efficacy of a photography‐aided behavioural intervention in reducing risk factors for dental caries and malocclusion in high‐risk…”
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