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KMT2A: Umbrella Gene for Multiple Diseases.
Castiglioni S, Di Fede E, Bernardelli C, Lettieri A, Parodi C, Grazioli P, Colombo EA, Ancona S, Milani D, Ottaviano E, Borghi E, Massa V, Ghelma F, Vignoli A, Lesma E, Gervasini C. Castiglioni S, et al. Among authors: vignoli a. Genes (Basel). 2022 Mar 15;13(3):514. doi: 10.3390/genes13030514. Genes (Basel). 2022. PMID: 35328068 Free PMC article. Review.
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
Rett Syndrome: A Focus on Gut Microbiota.
Borghi E, Borgo F, Severgnini M, Savini MN, Casiraghi MC, Vignoli A. Borghi E, et al. Among authors: vignoli a. Int J Mol Sci. 2017 Feb 7;18(2):344. doi: 10.3390/ijms18020344. Int J Mol Sci. 2017. PMID: 28178201 Free PMC article.
Deep phenotyping of patients with Tuberous Sclerosis Complex and no mutation identified in TSC1 and TSC2.
Peron A, Vignoli A, Briola F, Morenghi E, Tansini L, Alfano RM, Bulfamante G, Terraneo S, Ghelma F, Banderali G, Viskochil DH, Carey JC, Canevini MP; TSC Study Group of the San Paolo Hospital of Milan. Peron A, et al. Among authors: vignoli a. Eur J Med Genet. 2018 Jul;61(7):403-410. doi: 10.1016/j.ejmg.2018.02.005. Epub 2018 Feb 9. Eur J Med Genet. 2018. PMID: 29432982
246 results