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Page 1
Can paranasal sinus computed tomography screen for cystic fibrosis heterozygotes?
Malagutti N, Cogliandolo C, Franciosi D, Ferlini A, Rimessi P, Ravani A, Bianchini C, Ciorba A, Stomeo F, Pelucchi S. Malagutti N, et al. Among authors: rimessi p. Panminerva Med. 2022 Mar;64(1):116-119. doi: 10.23736/S0031-0808.19.03588-2. Epub 2019 Feb 11. Panminerva Med. 2022. PMID: 30747503 No abstract available.
Exon skipping quantification by real-time PCR.
Ferlini A, Rimessi P. Ferlini A, et al. Among authors: rimessi p. Methods Mol Biol. 2012;867:189-99. doi: 10.1007/978-1-61779-767-5_12. Methods Mol Biol. 2012. PMID: 22454062
A Family with γ-Thalassemia and High Hb A2 Levels.
Parmeggiani G, Gualandi F, Selvatici R, Rimessi P, Bigoni S, Taddei Masieri M, Dolcini B, Venturoli A, Cappabianca MP, Ferlini A, Ravani A. Parmeggiani G, et al. Among authors: rimessi p. Hemoglobin. 2016 Jun;40(3):187-90. doi: 10.3109/03630269.2016.1148613. Hemoglobin. 2016. PMID: 27117568
Workload measurement for molecular genetics laboratory: A survey study.
Tagliafico E, Bernardis I, Grasso M, D'Apice MR, Lapucci C, Botta A, Giachino DF, Marinelli M, Primignani P, Russo S, Sani I, Seia M, Fini S, Rimessi P, Tenedini E, Ravani A, Genuardi M, Ferlini A; Molecular Genetics Working Group of the Italian Society of Human Genetics, SIGU. Tagliafico E, et al. Among authors: rimessi p. PLoS One. 2018 Nov 27;13(11):e0206855. doi: 10.1371/journal.pone.0206855. eCollection 2018. PLoS One. 2018. PMID: 30481188 Free PMC article.
Exon skipping-mediated dystrophin reading frame restoration for small mutations.
Spitali P, Rimessi P, Fabris M, Perrone D, Falzarano S, Bovolenta M, Trabanelli C, Mari L, Bassi E, Tuffery S, Gualandi F, Maraldi NM, Sabatelli-Giraud P, Medici A, Merlini L, Ferlini A. Spitali P, et al. Among authors: rimessi p. Hum Mutat. 2009 Nov;30(11):1527-34. doi: 10.1002/humu.21092. Hum Mutat. 2009. PMID: 19760747
Persistent dystrophin protein restoration 90 days after a course of intraperitoneally administered naked 2'OMePS AON and ZM2 NP-AON complexes in mdx mice.
Bassi E, Falzarano S, Fabris M, Gualandi F, Merlini L, Vattemi G, Perrone D, Marchesi E, Sabatelli P, Sparnacci K, Laus M, Bonaldo P, Rimessi P, Braghetta P, Ferlini A. Bassi E, et al. Among authors: rimessi p. J Biomed Biotechnol. 2012;2012:897076. doi: 10.1155/2012/897076. Epub 2012 Oct 2. J Biomed Biotechnol. 2012. PMID: 23091362 Free PMC article.
Autosomal recessive Bethlem myopathy: A clinical, genetic and functional study.
Caria F, Cescon M, Gualandi F, Pichiecchio A, Rossi R, Rimessi P, Cotti Piccinelli S, Gallo Cassarino S, Gregorio I, Galvagni A, Ferlini A, Padovani A, Bonaldo P, Filosto M. Caria F, et al. Among authors: rimessi p. Neuromuscul Disord. 2019 Sep;29(9):657-663. doi: 10.1016/j.nmd.2019.07.007. Epub 2019 Jul 30. Neuromuscul Disord. 2019. PMID: 31471117
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