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Epilepsy in NF1: Epidemiologic, Genetic, and Clinical Features. A Monocentric Retrospective Study in a Cohort of 784 Patients.
Cancers (Basel). 2021 Dec 17;13(24):6336. doi: 10.3390/cancers13246336.
Cancers (Basel). 2021.
PMID: 34944956
Free PMC article.
DFNA20/26 and Other ACTG1-Associated Phenotypes: A Case Report and Review of the Literature.
Sorrentino U, Piccolo C, Rigon C, Brasson V, Trevisson E, Boaretto F, Martini A, Cassina M.
Sorrentino U, et al. Among authors: brasson v.
Audiol Res. 2021 Oct 18;11(4):582-593. doi: 10.3390/audiolres11040052.
Audiol Res. 2021.
PMID: 34698053
Free PMC article.
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Epigenetics of pregnancy: looking beyond the DNA code.
Zuccarello D, Sorrentino U, Brasson V, Marin L, Piccolo C, Capalbo A, Andrisani A, Cassina M.
Zuccarello D, et al. Among authors: brasson v.
J Assist Reprod Genet. 2022 Apr;39(4):801-816. doi: 10.1007/s10815-022-02451-x. Epub 2022 Mar 17.
J Assist Reprod Genet. 2022.
PMID: 35301622
Free PMC article.
Review.
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Tuberous sclerosis-associated neuropsychiatric disorders: a paediatric cohort study.
Toldo I, Brasson V, Miscioscia M, Pelizza MF, Manara R, Sartori S, Mantegazza G, Vecchi M, Nosadini M, Gatta M.
Toldo I, et al. Among authors: brasson v.
Dev Med Child Neurol. 2019 Feb;61(2):168-173. doi: 10.1111/dmcn.14055. Epub 2018 Oct 9.
Dev Med Child Neurol. 2019.
PMID: 30298907
Free article.
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