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Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome.
Fortugno P, Monetta R, Cinquina V, Rigon C, Boaretto F, De Luca C, Zoppi N, Di Leandro L, De Domenico E, Di Daniele A, Ippoliti R, Angelucci F, Di Cesare E, De Paulis R, Salviati L, Colombi M, Brancati F, Ritelli M. Fortugno P, et al. Among authors: rigon c. Eur J Hum Genet. 2023 May;31(5):596-601. doi: 10.1038/s41431-022-01279-4. Epub 2023 Jan 4. Eur J Hum Genet. 2023. PMID: 36599937 Free PMC article.
Ideal food pyramid for patients with rheumatoid arthritis: A narrative review.
Rondanelli M, Perdoni F, Peroni G, Caporali R, Gasparri C, Riva A, Petrangolini G, Faliva MA, Infantino V, Naso M, Perna S, Rigon C. Rondanelli M, et al. Among authors: rigon c. Clin Nutr. 2021 Mar;40(3):661-689. doi: 10.1016/j.clnu.2020.08.020. Epub 2020 Sep 2. Clin Nutr. 2021. PMID: 32928578 Free article. Review.
The Potential Roles of Very Low Calorie, Very Low Calorie Ketogenic Diets and Very Low Carbohydrate Diets on the Gut Microbiota Composition.
Rondanelli M, Gasparri C, Peroni G, Faliva MA, Naso M, Perna S, Bazire P, Sajuox I, Maugeri R, Rigon C. Rondanelli M, et al. Among authors: rigon c. Front Endocrinol (Lausanne). 2021 May 14;12:662591. doi: 10.3389/fendo.2021.662591. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34054731 Free PMC article. Review.
FBXO28 is a critical gene of the 1q41q42 microdeletion syndrome.
Cassina M, Rigon C, Casarin A, Vicenzi V, Salviati L, Clementi M. Cassina M, et al. Among authors: rigon c. Am J Med Genet A. 2015 Jun;167(6):1418-20. doi: 10.1002/ajmg.a.37033. Epub 2015 Apr 21. Am J Med Genet A. 2015. PMID: 25900767 No abstract available.
6q27 subtelomeric deletions: Is there a specific phenotype?
Rigon C, Salviati L, Mandarano R, Donà M, Clementi M. Rigon C, et al. Am J Med Genet A. 2011 May;155A(5):1213-4. doi: 10.1002/ajmg.a.33877. Epub 2011 Apr 11. Am J Med Genet A. 2011. PMID: 21484997 No abstract available.
36 results