Vignoli A - Search Results

1

Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and Chromatinopathies.

Parodi C, Di Fede E, Peron A, Viganò I, Grazioli P, Castiglioni S, Finnell RH, Gervasini C, Vignoli A, Massa V. Parodi C, et al. Among authors: vignoli a. Front Cell Dev Biol. 2021 Apr 20;9:654467. doi: 10.3389/fcell.2021.654467. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33959609 Free PMC article. Review.

2

Medical care of adolescents and women with Rett syndrome: an Italian study.

Vignoli A, La Briola F, Peron A, Turner K, Savini M, Cogliati F, Russo S, Canevini MP. Vignoli A, et al. Am J Med Genet A. 2012 Jan;158A(1):13-8. doi: 10.1002/ajmg.a.34367. Epub 2011 Dec 2. Am J Med Genet A. 2012. PMID: 22139899 Free article.

3

Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature.

Vignoli A, Borgatti R, Peron A, Zucca C, Ballarati L, Bonaglia C, Bellini M, Giordano L, Romaniello R, Bedeschi MF, Epifanio R, Russo S, Caselli R, Giardino D, Darra F, La Briola F, Banderali G, Canevini MP. Vignoli A, et al. Epilepsia. 2012 Jul;53(7):1146-55. doi: 10.1111/j.1528-1167.2012.03501.x. Epub 2012 May 11. Epilepsia. 2012. PMID: 22578097 Free article. Review.

4

Interstitial 6q microdeletion syndrome and epilepsy: a new patient and review of the literature.

Vignoli A, Scornavacca GF, Peron A, La Briola F, Canevini MP. Vignoli A, et al. Am J Med Genet A. 2013 Aug;161A(8):2009-15. doi: 10.1002/ajmg.a.35993. Epub 2013 Jun 21. Am J Med Genet A. 2013. PMID: 23794236 Review.

5

Hot water epilepsy: a video case of European boy with positive family history and subsequent non-reflex epilepsy.

Vignoli A, Savini MN, La Briola F, Chiesa V, Zambrelli E, Peron A, Canevini MP. Vignoli A, et al. Epileptic Disord. 2014 Mar;16(1):96-100. doi: 10.1684/epd.2014.0640. Epileptic Disord. 2014. PMID: 24691301 Free article.

6

Glioblastoma multiforme in a child with tuberous sclerosis complex.

Vignoli A, Lesma E, Alfano RM, Peron A, Scornavacca GF, Massimino M, Schiavello E, Ancona S, Cerati M, Bulfamante G, Gorio A, Canevini MP. Vignoli A, et al. Am J Med Genet A. 2015 Oct;167A(10):2388-93. doi: 10.1002/ajmg.a.37158. Epub 2015 May 6. Am J Med Genet A. 2015. PMID: 25946256

7

7p22.1 microduplication syndrome: Clinical and molecular characterization of an adult case and review of the literature.

Caselli R, Ballarati L, Vignoli A, Peron A, Recalcati MP, Catusi I, Larizza L, Giardino D. Caselli R, et al. Among authors: vignoli a. Eur J Med Genet. 2015 Nov;58(11):578-83. doi: 10.1016/j.ejmg.2015.08.003. Epub 2015 Aug 19. Eur J Med Genet. 2015. PMID: 26297194 Review.

8

Autism spectrum disorder in tuberous sclerosis complex: searching for risk markers.

Vignoli A, La Briola F, Peron A, Turner K, Vannicola C, Saccani M, Magnaghi E, Scornavacca GF, Canevini MP. Vignoli A, et al. Orphanet J Rare Dis. 2015 Dec 2;10:154. doi: 10.1186/s13023-015-0371-1. Orphanet J Rare Dis. 2015. PMID: 26631248 Free PMC article.

9

Do patients with tuberous sclerosis complex have an increased risk for malignancies?

Peron A, Vignoli A, La Briola F, Volpi A, Montanari E, Morenghi E, Ghelma F, Bulfamante G, Cefalo G, Canevini MP. Peron A, et al. Among authors: vignoli a. Am J Med Genet A. 2016 Jun;170(6):1538-44. doi: 10.1002/ajmg.a.37644. Epub 2016 Apr 7. Am J Med Genet A. 2016. PMID: 27061015

10

Long-term outcome of epilepsy with onset in the first three years of life: Findings from a large cohort of patients.

Vignoli A, Peron A, Turner K, Scornavacca GF, La Briola F, Chiesa V, Zambrelli E, Canevini MP. Vignoli A, et al. Eur J Paediatr Neurol. 2016 Jul;20(4):566-72. doi: 10.1016/j.ejpn.2016.03.008. Epub 2016 Mar 26. Eur J Paediatr Neurol. 2016. PMID: 27071723

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