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

Year Number of Results
1987 3
1989 5
1990 3
1991 9
1992 3
1993 2
1994 8
1995 3
1996 6
1997 6
1998 5
1999 2
2000 10
2001 10
2002 6
2003 7
2004 5
2005 6
2006 8
2007 7
2008 6
2009 12
2010 13
2011 14
2012 21
2013 14
2014 12
2015 14
2016 9
2017 14
2018 12
2019 8
2020 13
2021 17
2022 11
2023 9
2024 4

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287 results

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Page 1
GJB2 mutations and degree of hearing loss: a multicenter study.
Snoeckx RL, Huygen PL, Feldmann D, Marlin S, Denoyelle F, Waligora J, Mueller-Malesinska M, Pollak A, Ploski R, Murgia A, Orzan E, Castorina P, Ambrosetti U, Nowakowska-Szyrwinska E, Bal J, Wiszniewski W, Janecke AR, Nekahm-Heis D, Seeman P, Bendova O, Kenna MA, Frangulov A, Rehm HL, Tekin M, Incesulu A, Dahl HH, du Sart D, Jenkins L, Lucas D, Bitner-Glindzicz M, Avraham KB, Brownstein Z, del Castillo I, Moreno F, Blin N, Pfister M, Sziklai I, Toth T, Kelley PM, Cohn ES, Van Maldergem L, Hilbert P, Roux AF, Mondain M, Hoefsloot LH, Cremers CW, Löppönen T, Löppönen H, Parving A, Gronskov K, Schrijver I, Roberson J, Gualandi F, Martini A, Lina-Granade G, Pallares-Ruiz N, Correia C, Fialho G, Cryns K, Hilgert N, Van de Heyning P, Nishimura CJ, Smith RJ, Van Camp G. Snoeckx RL, et al. Among authors: gualandi f. Am J Hum Genet. 2005 Dec;77(6):945-57. doi: 10.1086/497996. Epub 2005 Oct 19. Am J Hum Genet. 2005. PMID: 16380907 Free PMC article.
Brugada Syndrome: More than a Monogenic Channelopathy.
Liantonio A, Bertini M, Mele A, Balla C, Dinoi G, Selvatici R, Mele M, De Luca A, Gualandi F, Imbrici P. Liantonio A, et al. Among authors: gualandi f. Biomedicines. 2023 Aug 18;11(8):2297. doi: 10.3390/biomedicines11082297. Biomedicines. 2023. PMID: 37626795 Free PMC article. Review.
[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: gualandi f. G Ital Cardiol (Rome). 2018 Feb;19(2):91-100. doi: 10.1714/2868.28940. G Ital Cardiol (Rome). 2018. PMID: 29531381 Review. Italian.
Congenital muscular dystrophies: a brief review.
Bertini E, D'Amico A, Gualandi F, Petrini S. Bertini E, et al. Among authors: gualandi f. Semin Pediatr Neurol. 2011 Dec;18(4):277-88. doi: 10.1016/j.spen.2011.10.010. Semin Pediatr Neurol. 2011. PMID: 22172424 Free PMC article. Review.
Hematopoietic stem cell transplantation procedures.
Saccardi R, Gualandi F. Saccardi R, et al. Among authors: gualandi f. Autoimmunity. 2008 Dec;41(8):570-6. doi: 10.1080/08916930802197776. Autoimmunity. 2008. PMID: 18958744 Review.
Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes.
Zanotti S, Magri F, Salani S, Napoli L, Ripolone M, Ronchi D, Fortunato F, Ciscato P, Velardo D, D'Angelo MG, Gualandi F, Nigro V, Sciacco M, Corti S, Comi GP, Piga D. Zanotti S, et al. Among authors: gualandi f. Int J Mol Sci. 2023 Mar 14;24(6):5551. doi: 10.3390/ijms24065551. Int J Mol Sci. 2023. PMID: 36982625 Free PMC article.
Digital health and Clinical Patient Management System (CPMS) platform utility for data sharing of neuromuscular patients: the Italian EURO-NMD experience.
Fortunato F, Bianchi F, Ricci G, Torri F, Gualandi F, Neri M, Farnè M, Giannini F, Malandrini A, Volpi N, Lopergolo D, Silani V, Ticozzi N, Verde F, Pareyson D, Fenu S, Bonanno S, Nigro V, Peduto C, D'Ambrosio P, Zeuli R, Zanobio M, Picillo E, Servidei S, Primiano G, Sancricca C, Sciacco M, Brusa R, Filosto M, Cotti Piccinelli S, Pegoraro E, Mongini T, Solero L, Gadaleta G, Brusa C, Minetti C, Bruno C, Panicucci C, Sansone VA, Lunetta C, Zanolini A, Toscano A, Pugliese A, Nicocia G, Bertini E, Catteruccia M, Diodato D, Atalaia A, Evangelista T, Siciliano G, Ferlini A. Fortunato F, et al. Among authors: gualandi f. Orphanet J Rare Dis. 2023 Jul 21;18(1):196. doi: 10.1186/s13023-023-02776-5. Orphanet J Rare Dis. 2023. PMID: 37480080 Free PMC article.
287 results