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A clinical screening tool for objective and subjective cognitive disorders in multiple sclerosis.
Guilloton L, Camdessanche JP, Latombe D, Neuschwander P, Cantalloube S, Thomas-Anterion C, Mercier B, Roggerone S, Maucort-Boulch D, Roche S, Jacquin-Courtois S; “Cognition-MS” group of the Rhône-Alpes MS network. Guilloton L, et al. Among authors: roggerone s. Ann Phys Rehabil Med. 2020 Mar;63(2):116-122. doi: 10.1016/j.rehab.2018.11.005. Epub 2019 Jan 29. Ann Phys Rehabil Med. 2020. PMID: 30703524 Free article.
History of multiple sclerosis in 2 successive pregnancies: A French and Italian cohort.
Benoit A, Durand-Dubief F, Amato MP, Portaccio E, Casey R, Roggerone S, Androdias G, Gignoux L, Ionescu I, Marrosu MG, Cocco E, Ghezzi A, Annovazzi P, Trojano M, Simone M, Marignier R, Confavreux C, Vukusic S. Benoit A, et al. Among authors: roggerone s. Neurology. 2016 Sep 27;87(13):1360-7. doi: 10.1212/WNL.0000000000003036. Epub 2016 Jul 27. Neurology. 2016. PMID: 27466470
[New therapies in multiple sclerosis].
Roggerone S, Chenevier F, Confavreux C, Vukusic S. Roggerone S, et al. Rev Prat. 2012 Oct;62(8):1057-60. Rev Prat. 2012. PMID: 23227596 French.
Reliability of longitudinal brain volume loss measurements between 2 sites in patients with multiple sclerosis: comparison of 7 quantification techniques.
Durand-Dubief F, Belaroussi B, Armspach JP, Dufour M, Roggerone S, Vukusic S, Hannoun S, Sappey-Marinier D, Confavreux C, Cotton F. Durand-Dubief F, et al. Among authors: roggerone s. AJNR Am J Neuroradiol. 2012 Nov;33(10):1918-24. doi: 10.3174/ajnr.A3107. Epub 2012 Jul 12. AJNR Am J Neuroradiol. 2012. PMID: 22790248 Free PMC article.
Wernicke's encephalopathy with atypical cortical damage.
Alberti N, Bocquet J, Molinier S, Veron A, Roggerone S, Pinsard L, Arnaud FX, Dousset V. Alberti N, et al. Among authors: roggerone s. Diagn Interv Imaging. 2012 Oct;93(10):804-7. doi: 10.1016/j.diii.2012.04.014. Diagn Interv Imaging. 2012. PMID: 23078833 Free article. No abstract available.
Disentangling molecular and clinical stratification patterns in beta-galactosidase deficiency.
Tebani A, Sudrié-Arnaud B, Dabaj I, Torre S, Domitille L, Snanoudj S, Heron B, Levade T, Caillaud C, Vergnaud S, Saugier-Veber P, Coutant S, Dranguet H, Froissart R, Al Khouri M, Alembik Y, Baruteau J, Arnoux JB, Brassier A, Brehin AC, Busa T, Cano A, Chabrol B, Coubes C, Desguerre I, Doco-Fenzy M, Drenou B, Elcioglu NH, Elsayed S, Fouilhoux A, Poirsier C, Goldenberg A, Jouvencel P, Kuster A, Labarthe F, Lazaro L, Pichard S, Rivera S, Roche S, Roggerone S, Roubertie A, Sigaudy S, Spodenkiewicz M, Tardieu M, Vanhulle C, Marret S, Bekri S. Tebani A, et al. Among authors: roggerone s. J Med Genet. 2022 Apr;59(4):377-384. doi: 10.1136/jmedgenet-2020-107510. Epub 2021 Mar 18. J Med Genet. 2022. PMID: 33737400
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