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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1958 1
1960 1
1962 1
1966 1
1967 4
1968 2
1973 1
1983 2
1986 4
1988 4
1989 2
1990 3
1991 1
1992 4
1993 2
1994 2
1995 4
1996 6
1997 5
1998 4
1999 5
2000 2
2001 5
2002 3
2003 5
2004 4
2005 4
2006 5
2007 4
2008 7
2009 11
2010 13
2011 9
2012 19
2013 17
2014 20
2015 11
2016 8
2017 16
2018 11
2019 10
2020 15
2021 21
2022 8
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Search Results

265 results
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Page 1
Duchenne Muscular Dystrophy: From Diagnosis to Therapy.
Falzarano MS, Scotton C, Passarelli C, Ferlini A. Falzarano MS, et al. Among authors: ferlini a. Molecules. 2015 Oct 7;20(10):18168-84. doi: 10.3390/molecules201018168. Molecules. 2015. PMID: 26457695 Free PMC article. Review.
A single NGS-based assay covering the entire genomic sequence of the DMD gene facilitates diagnostic and newborn screening confirmatory testing.
Nallamilli BRR, Chaubey A, Valencia CA, Stansberry L, Behlmann AM, Ma Z, Mathur A, Shenoy S, Ganapathy V, Jagannathan L, Ramachander V, Ferlini A, Bean L, Hegde M. Nallamilli BRR, et al. Among authors: ferlini a. Hum Mutat. 2021 May;42(5):626-638. doi: 10.1002/humu.24191. Epub 2021 Mar 19. Hum Mutat. 2021. PMID: 33644936
Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database.
Koeks Z, Bladen CL, Salgado D, van Zwet E, Pogoryelova O, McMacken G, Monges S, Foncuberta ME, Kekou K, Kosma K, Dawkins H, Lamont L, Bellgard MI, Roy AJ, Chamova T, Guergueltcheva V, Chan S, Korngut L, Campbell C, Dai Y, Wang J, Barišić N, Brabec P, Lähdetie J, Walter MC, Schreiber-Katz O, Karcagi V, Garami M, Herczegfalvi A, Viswanathan V, Bayat F, Buccella F, Ferlini A, Kimura E, van den Bergen JC, Rodrigues M, Roxburgh R, Lusakowska A, Kostera-Pruszczyk A, Santos R, Neagu E, Artemieva S, Rasic VM, Vojinovic D, Posada M, Bloetzer C, Klein A, Díaz-Manera J, Gallardo E, Karaduman AA, Oznur T, Topaloğlu H, El Sherif R, Stringer A, Shatillo AV, Martin AS, Peay HL, Kirschner J, Flanigan KM, Straub V, Bushby K, Béroud C, Verschuuren JJ, Lochmüller H. Koeks Z, et al. Among authors: ferlini a. J Neuromuscul Dis. 2017;4(4):293-306. doi: 10.3233/JND-170280. J Neuromuscul Dis. 2017. PMID: 29125504 Free PMC article.
Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types.
Rapezzi C, Merlini G, Quarta CC, Riva L, Longhi S, Leone O, Salvi F, Ciliberti P, Pastorelli F, Biagini E, Coccolo F, Cooke RM, Bacchi-Reggiani L, Sangiorgi D, Ferlini A, Cavo M, Zamagni E, Fonte ML, Palladini G, Salinaro F, Musca F, Obici L, Branzi A, Perlini S. Rapezzi C, et al. Among authors: ferlini a. Circulation. 2009 Sep 29;120(13):1203-12. doi: 10.1161/CIRCULATIONAHA.108.843334. Epub 2009 Sep 14. Circulation. 2009. PMID: 19752327
Biomarkers in rare diseases.
Ferlini A, Scotton C, Novelli G. Ferlini A, et al. Public Health Genomics. 2013;16(6):313-21. doi: 10.1159/000355938. Epub 2014 Feb 3. Public Health Genomics. 2013. PMID: 24503592 Review.
POPDC2 a novel susceptibility gene for conduction disorders.
Rinné S, Ortiz-Bonnin B, Stallmeyer B, Kiper AK, Fortmüller L, Schindler RFR, Herbort-Brand U, Kabir NS, Dittmann S, Friedrich C, Zumhagen S, Gualandi F, Selvatici R, Rapezzi C, Arbustini E, Ferlini A, Fabritz L, Schulze-Bahr E, Brand T, Decher N. Rinné S, et al. Among authors: ferlini a. J Mol Cell Cardiol. 2020 Aug;145:74-83. doi: 10.1016/j.yjmcc.2020.06.005. Epub 2020 Jun 11. J Mol Cell Cardiol. 2020. PMID: 32535041
RNA-targeted drugs for neuromuscular diseases.
Ferlini A, Goyenvalle A, Muntoni F. Ferlini A, et al. Science. 2021 Jan 1;371(6524):29-31. doi: 10.1126/science.aba4515. Science. 2021. PMID: 33384365 Free article. No abstract available.
[Latest news and perspectives in cardiogenetics].
Malagù M, Zaraket F, Gualandi F, Ferlini A, Brieda A, Vitali F, Del Franco A, Balla C, Fucili A, Ferrari R, Bertini M. Malagù M, et al. Among authors: ferlini a. G Ital Cardiol (Rome). 2018 Feb;19(2):91-100. doi: 10.1714/2868.28940. G Ital Cardiol (Rome). 2018. PMID: 29531381 Review. Italian.
265 results