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389 results

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Page 1
Guillain-Barre syndrome, influenzalike illnesses, and influenza vaccination during seasons with and without circulating A/H1N1 viruses.
Grimaldi-Bensouda L, Alpérovitch A, Besson G, Vial C, Cuisset JM, Papeix C, Lyon-Caen O, Benichou J, Rossignol M; Lucien Abenhaim for the GBS-PGRx Study Group. Grimaldi-Bensouda L, et al. Among authors: vial c. Am J Epidemiol. 2011 Aug 1;174(3):326-35. doi: 10.1093/aje/kwr072. Epub 2011 Jun 7. Am J Epidemiol. 2011. PMID: 21652600
Absence of airway secretion accumulation predicts tolerance of noninvasive ventilation in subjects with amyotrophic lateral sclerosis.
Vandenberghe N, Vallet AE, Petitjean T, Le Cam P, Peysson S, Guérin C, Dailler F, Jay S, Cadiergue V, Bouhour F, Court-Fortune I, Camdessanche JP, Antoine JC, Philit F, Beuret P, Bin-Dorel S, Vial C, Broussolle E. Vandenberghe N, et al. Among authors: vial c. Respir Care. 2013 Sep;58(9):1424-32. doi: 10.4187/respcare.02103. Epub 2013 Jan 15. Respir Care. 2013. PMID: 23322888 Free article.
Neurological features in adult Triple-A (Allgrove) syndrome.
Vallet AE, Verschueren A, Petiot P, Vandenberghe N, Nicolino M, Roman S, Pouget J, Vial C. Vallet AE, et al. Among authors: vial c. J Neurol. 2012 Jan;259(1):39-46. doi: 10.1007/s00415-011-6115-9. Epub 2011 Jun 9. J Neurol. 2012. PMID: 21656342
Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study.
Salort-Campana E, Nguyen K, Bernard R, Jouve E, Solé G, Nadaj-Pakleza A, Niederhauser J, Charles E, Ollagnon E, Bouhour F, Sacconi S, Echaniz-Laguna A, Desnuelle C, Tranchant C, Vial C, Magdinier F, Bartoli M, Arne-Bes MC, Ferrer X, Kuntzer T, Levy N, Pouget J, Attarian S. Salort-Campana E, et al. Among authors: vial c. Orphanet J Rare Dis. 2015 Jan 21;10:2. doi: 10.1186/s13023-014-0218-1. Orphanet J Rare Dis. 2015. PMID: 25603992 Free PMC article.
Testing the validity of a set of diagnostic criteria for sensory neuronopathies: a francophone collaborative study.
Antoine JC, Robert-Varvat F, Maisonobe T, Créange A, Franques J, Mathis S, Delmont E, Kuntzer T, Lefaucheur JP, Pouget J, Viala K, Desnuelle C, Echaniz-Laguna A, Rotolo F, Camdessanché JP; French CIDP study group. Antoine JC, et al. J Neurol. 2014 Nov;261(11):2093-100. doi: 10.1007/s00415-014-7423-7. Epub 2014 Aug 10. J Neurol. 2014. PMID: 25108558
Convergence of patient- and physician-reported outcomes in the French National Registry of Facioscapulohumeral Dystrophy.
Sanson B, Stalens C, Guien C, Villa L, Eng C, Rabarimeriarijaona S, Bernard R, Cintas P, Solé G, Tiffreau V, Echaniz-Laguna A, Magot A, Juntas Morales R, Boyer FC, Nadaj-Pakleza A, Jacquin-Piques A, Béroud C, Sacconi S; French FSHD registry collaboration group. Sanson B, et al. Orphanet J Rare Dis. 2022 Mar 2;17(1):96. doi: 10.1186/s13023-021-01793-6. Orphanet J Rare Dis. 2022. PMID: 35236385 Free PMC article.
The French national protocol for Kennedy's disease (SBMA): consensus diagnostic and management recommendations.
Pradat PF, Bernard E, Corcia P, Couratier P, Jublanc C, Querin G, Morélot Panzini C, Salachas F, Vial C, Wahbi K, Bede P, Desnuelle C; French Kennedy’s Disease Writing Group. Pradat PF, et al. Among authors: vial c. Orphanet J Rare Dis. 2020 Apr 10;15(1):90. doi: 10.1186/s13023-020-01366-z. Orphanet J Rare Dis. 2020. PMID: 32276665 Free PMC article.
Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteria.
Robert-Varvat F, Jousserand G, Bouhour F, Vial C, Cintas P, Echaniz-Laguna A, Delmont E, Clavelou P, Chauplannaz G, Jomir L, Pereon Y, Leonard-Louis S, Manel V, Antoine JC, Lacour A, Camdessanche JP. Robert-Varvat F, et al. Among authors: vial c. Muscle Nerve. 2018 Feb;57(2):217-221. doi: 10.1002/mus.25666. Epub 2017 Jun 11. Muscle Nerve. 2018. PMID: 28407266
389 results