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

Year Number of Results
1979 1
1984 2
1985 2
1986 3
1987 3
1988 3
1989 7
1990 1
1991 4
1992 2
1993 2
1994 2
1995 7
1996 5
1997 7
1998 2
1999 7
2000 5
2002 1
2003 5
2004 3
2005 7
2006 4
2007 13
2008 4
2009 9
2010 5
2011 7
2012 7
2013 11
2014 5
2016 3
2017 7
2018 4
2019 5
2020 4
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Publication date

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160 results
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Page 1
EndMT contributes to the onset and progression of cerebral cavernous malformations.
Maddaluno L, Rudini N, Cuttano R, Bravi L, Giampietro C, Corada M, Ferrarini L, Orsenigo F, Papa E, Boulday G, Tournier-Lasserve E, Chapon F, Richichi C, Retta SF, Lampugnani MG, Dejana E. Maddaluno L, et al. Among authors: chapon f. Nature. 2013 Jun 27;498(7455):492-6. doi: 10.1038/nature12207. Epub 2013 Jun 9. Nature. 2013. PMID: 23748444
Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies.
Wahbi K, Ben Yaou R, Gandjbakhch E, Anselme F, Gossios T, Lakdawala NK, Stalens C, Sacher F, Babuty D, Trochu JN, Moubarak G, Savvatis K, Porcher R, Laforêt P, Fayssoil A, Marijon E, Stojkovic T, Béhin A, Leonard-Louis S, Sole G, Labombarda F, Richard P, Metay C, Quijano-Roy S, Dabaj I, Klug D, Vantyghem MC, Chevalier P, Ambrosi P, Salort E, Sadoul N, Waintraub X, Chikhaoui K, Mabo P, Combes N, Maury P, Sellal JM, Tedrow UB, Kalman JM, Vohra J, Androulakis AFA, Zeppenfeld K, Thompson T, Barnerias C, Bécane HM, Bieth E, Boccara F, Bonnet D, Bouhour F, Boulé S, Brehin AC, Chapon F, Cintas P, Cuisset JM, Davy JM, De Sandre-Giovannoli A, Demurger F, Desguerre I, Dieterich K, Durigneux J, Echaniz-Laguna A, Eschalier R, Ferreiro A, Ferrer X, Francannet C, Fradin M, Gaborit B, Gay A, Hagège A, Isapof A, Jeru I, Juntas Morales R, Lagrue E, Lamblin N, Lascols O, Laugel V, Lazarus A, Leturcq F, Levy N, Magot A, Manel V, Martins R, Mayer M, Mercier S, Meune C, Michaud M, Minot-Myhié MC, Muchir A, Nadaj-Pakleza A, Péréon Y, Petiot P, Petit F, Praline J, Rollin A, Sabouraud P, Sarret C, Schaeffer S, Taithe F, Tard C, Tiffreau V, Toutain A, Vatier C, Walther-Louvier U, Eymard B, Charron P, Vigouroux C, Bonne G, Kumar S, Elliott P, Duboc D. Wahbi K, et al. Among authors: chapon f. Circulation. 2019 Jul 23;140(4):293-302. doi: 10.1161/CIRCULATIONAHA.118.039410. Epub 2019 Jun 3. Circulation. 2019. PMID: 31155932
FSHD1 and FSHD2 form a disease continuum.
Sacconi S, Briand-Suleau A, Gros M, Baudoin C, Lemmers RJLF, Rondeau S, Lagha N, Nigumann P, Cambieri C, Puma A, Chapon F, Stojkovic T, Vial C, Bouhour F, Cao M, Pegoraro E, Petiot P, Behin A, Marc B, Eymard B, Echaniz-Laguna A, Laforet P, Salviati L, Jeanpierre M, Cristofari G, van der Maarel SM. Sacconi S, et al. Among authors: chapon f. Neurology. 2019 May 7;92(19):e2273-e2285. doi: 10.1212/WNL.0000000000007456. Epub 2019 Apr 12. Neurology. 2019. PMID: 30979860 Free PMC article.
Sustained Response and Rationale of Programmed Cell Death-1-Targeting for Progressive Multifocal Leukoencephalopathy.
Audemard-Verger A, Gasnault J, Faisant M, Besse MC, Martin-Silva N, Berra M, Fournier L, Boutemy J, Maigne G, De Boysson H, Ruet A, Vabret A, Chapon F, Martin-Blondel G, Aouba A. Audemard-Verger A, et al. Among authors: chapon f. Open Forum Infect Dis. 2019 Sep 30;6(10):ofz374. doi: 10.1093/ofid/ofz374. eCollection 2019 Oct. Open Forum Infect Dis. 2019. PMID: 31660340 Free PMC article.
Isolated Cerebral Alveolar Echinococcosis.
Baldolli A, Bonhomme J, Yera H, Grenouillet F, Chapon F, Barbier C, Hazera P, Verdon R. Baldolli A, et al. Among authors: chapon f. Open Forum Infect Dis. 2018 Dec 14;6(1):ofy349. doi: 10.1093/ofid/ofy349. eCollection 2019 Jan. Open Forum Infect Dis. 2018. PMID: 30740467 Free PMC article.
Neuropathological Hallmarks of Brain Malformations in Extreme Phenotypes Related to DYNC1H1 Mutations.
Laquerriere A, Maillard C, Cavallin M, Chapon F, Marguet F, Molin A, Sigaudy S, Blouet M, Benoist G, Fernandez C, Poirier K, Chelly J, Thomas S, Bahi-Buisson N. Laquerriere A, et al. Among authors: chapon f. J Neuropathol Exp Neurol. 2017 Mar 1;76(3):195-205. doi: 10.1093/jnen/nlw124. J Neuropathol Exp Neurol. 2017. PMID: 28395088
Disruption of a miR-29 binding site leading to COL4A1 upregulation causes pontine autosomal dominant microangiopathy with leukoencephalopathy.
Verdura E, Hervé D, Bergametti F, Jacquet C, Morvan T, Prieto-Morin C, Mackowiak A, Manchon E, Hosseini H, Cordonnier C, Girard-Buttaz I, Rosenstingl S, Hagel C, Kuhlenbaümer G, Leca-Radu E, Goux D, Fleming L, Van Agtmael T, Chabriat H, Chapon F, Tournier-Lasserve E. Verdura E, et al. Among authors: chapon f. Ann Neurol. 2016 Nov;80(5):741-753. doi: 10.1002/ana.24782. Epub 2016 Oct 19. Ann Neurol. 2016. PMID: 27666438
Identification of a novel splice site mutation in the SERAC1 gene responsible for the MEGDHEL syndrome.
Snanoudj S, Mordel P, Dupas Q, Schanen C, Arion A, Gérard M, Read MH, Nait Rabah D, Goux D, Chapon F, Jokic M, Allouche S. Snanoudj S, et al. Among authors: chapon f. Mol Genet Genomic Med. 2019 Aug;7(8):e815. doi: 10.1002/mgg3.815. Epub 2019 Jun 28. Mol Genet Genomic Med. 2019. PMID: 31251474 Free PMC article.
[DM1 with severe fatigue: a cognitive behavioural therapy trial].
Chapon F. Chapon F. Med Sci (Paris). 2018 Nov;34 Hors série n°2:43. doi: 10.1051/medsci/201834s213. Epub 2018 Nov 12. Med Sci (Paris). 2018. PMID: 30418147 Free article. French. No abstract available.
[Risk prediction score for ventricular tachyarrhythmias in LMNA mutations].
Chapon F. Chapon F. Med Sci (Paris). 2019 Nov;35 Hors série n° 2:50. doi: 10.1051/medsci/2019179. Epub 2019 Dec 20. Med Sci (Paris). 2019. PMID: 31859635 Free article. French. No abstract available.
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