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

Year Number of Results
1989 1
1991 2
1992 5
1993 1
1994 8
1995 2
1996 4
1997 2
1998 2
1999 3
2000 2
2001 3
2002 2
2003 4
2004 6
2005 2
2007 4
2008 3
2009 2
2010 6
2011 3
2012 4
2013 5
2014 4
2015 3
2016 4
2017 9
2018 6
2019 6
2020 5
2021 6
2022 5
2023 1
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117 results
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Page 1
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
Laquerriere A, Jaber D, Abiusi E, Maluenda J, Mejlachowicz D, Vivanti A, Dieterich K, Stoeva R, Quevarec L, Nolent F, Biancalana V, Latour P, Sternberg D, Capri Y, Verloes A, Bessieres B, Loeuillet L, Attie-Bitach T, Martinovic J, Blesson S, Petit F, Beneteau C, Whalen S, Marguet F, Bouligand J, Héron D, Viot G, Amiel J, Amram D, Bellesme C, Bucourt M, Faivre L, Jouk PS, Khung S, Sigaudy S, Delezoide AL, Goldenberg A, Jacquemont ML, Lambert L, Layet V, Lyonnet S, Munnich A, Van Maldergem L, Piard J, Guimiot F, Landrieu P, Letard P, Pelluard F, Perrin L, Saint-Frison MH, Topaloglu H, Trestard L, Vincent-Delorme C, Amthor H, Barnerias C, Benachi A, Bieth E, Boucher E, Cormier-Daire V, Delahaye-Duriez A, Desguerre I, Eymard B, Francannet C, Grotto S, Lacombe D, Laffargue F, Legendre M, Martin-Coignard D, Mégarbané A, Mercier S, Nizon M, Rigonnot L, Prieur F, Quélin C, Ranjatoelina-Randrianaivo H, Resta N, Toutain A, Verhelst H, Vincent M, Colin E, Fallet-Bianco C, Granier M, Grigorescu R, Saada J, Gonzales M, Guiochon-Mantel A, Bessereau JL, Tawk M, Gut I, Gitiaux C, Melki J. Laquerriere A, et al. Among authors: biancalana v. J Med Genet. 2022 Jun;59(6):559-567. doi: 10.1136/jmedgenet-2020-107595. Epub 2021 Apr 5. J Med Genet. 2022. PMID: 33820833 Free PMC article.
An innovative eye-tracker: Main features and demonstrative tests.
Bellizzi L, Bevilacqua G, Biancalana V, Carucci M, Cecchi R, Chessa P, Donniacuo A, Mandalà M, Stiaccini L. Bellizzi L, et al. Among authors: biancalana v. Rev Sci Instrum. 2022 Mar 1;93(3):035006. doi: 10.1063/5.0079779. Rev Sci Instrum. 2022. PMID: 35365022
Clinical massively parallel sequencing for the diagnosis of myopathies.
Gorokhova S, Biancalana V, Lévy N, Laporte J, Bartoli M, Krahn M. Gorokhova S, et al. Among authors: biancalana v. Rev Neurol (Paris). 2015 Jun-Jul;171(6-7):558-71. doi: 10.1016/j.neurol.2015.02.019. Epub 2015 May 26. Rev Neurol (Paris). 2015. PMID: 26022190 Review.
Microsatellites and disease: a new paradigm.
Wrogemann K, Biancalana V, Devys D, Imbert G, Trottier Y, Mandel JL. Wrogemann K, et al. Among authors: biancalana v. EXS. 1993;67:141-52. doi: 10.1007/978-3-0348-8583-6_13. EXS. 1993. PMID: 8400686 Review. No abstract available.
Glycogenin-1 deficiency mimicking limb-girdle muscular dystrophy.
Lefeuvre C, Schaeffer S, Carlier RY, Fournier M, Chapon F, Biancalana V, Nicolas G, Malfatti E, Laforêt P. Lefeuvre C, et al. Among authors: biancalana v. Mol Genet Metab Rep. 2020 May 24;24:100597. doi: 10.1016/j.ymgmr.2020.100597. eCollection 2020 Sep. Mol Genet Metab Rep. 2020. PMID: 32477874 Free PMC article.
Fragile X disease.
Biancalana V, Macpherson J. Biancalana V, et al. Methods Mol Med. 2004;92:157-82. doi: 10.1385/1-59259-432-8:157. Methods Mol Med. 2004. PMID: 14733312 No abstract available.
MTM1 mutations in X-linked myotubular myopathy.
Laporte J, Biancalana V, Tanner SM, Kress W, Schneider V, Wallgren-Pettersson C, Herger F, Buj-Bello A, Blondeau F, Liechti-Gallati S, Mandel JL. Laporte J, et al. Among authors: biancalana v. Hum Mutat. 2000;15(5):393-409. doi: 10.1002/(SICI)1098-1004(200005)15:5<393::AID-HUMU1>3.0.CO;2-R. Hum Mutat. 2000. PMID: 10790201 Review.
117 results