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Women with TSC: Relationship between Clinical, Lung Function and Radiological Features in a Genotyped Population Investigated for Lymphangioleiomyomatosis.
Di Marco F, Terraneo S, Imeri G, Palumbo G, La Briola F, Tresoldi S, Volpi A, Gualandri L, Ghelma F, Alfano RM, Montanari E, Gorio A, Lesma E, Peron A, Canevini MP, Centanni S. Di Marco F, et al. Among authors: ghelma f. PLoS One. 2016 May 12;11(5):e0155331. doi: 10.1371/journal.pone.0155331. eCollection 2016. PLoS One. 2016. PMID: 27171001 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: ghelma f. 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
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: ghelma f. Genes (Basel). 2022 Mar 15;13(3):514. doi: 10.3390/genes13030514. Genes (Basel). 2022. PMID: 35328068 Free PMC article. Review.
Odontogenic rhinosinusitis and sinonasal complications of dental disease or treatment: prospective validation of a classification and treatment protocol.
Saibene AM, Collurà F, Pipolo C, Bulfamante AM, Lozza P, Maccari A, Arnone F, Ghelma F, Allevi F, Biglioli F, Chiapasco M, Portaleone SM, Scotti A, Borloni R, Felisati G. Saibene AM, et al. Among authors: ghelma f. Eur Arch Otorhinolaryngol. 2019 Feb;276(2):401-406. doi: 10.1007/s00405-018-5220-0. Epub 2018 Nov 27. Eur Arch Otorhinolaryngol. 2019. PMID: 30483941 Free PMC article.
20 results