Open Access
Numéro
Cah. Myol.
Numéro 21, Juin 2020
Page(s) 42 - 62
Section Partenariats /Partnerships
DOI https://doi.org/10.1051/myolog/202021014
Publié en ligne 10 juillet 2020
  1. Gagnon C, Heatwole C, Hébert LJ, Hogrel JY, Laberge L, Leone M, Meola G, Richer L, Sansone V, Kierkegaard M. Report of the third outcome measures in myotonic dystrophy type 1 (OMMYD-3) international workshop Paris, France, June 8, 2015. J Neuromuscul Dis 2018 ; 5 : 523-37. [CrossRef] [PubMed] [Google Scholar]
  2. Gourdon G, Meola G. Myotonic dystrophies: state of the art of new therapeutic developments for the CNS. Fron Neurosci 2017 ; 11 : 101. [Google Scholar]
  3. Angeard N. A neurodevelopmental approach to myotonic dystrophy type 1. Dev Med Child Neurol 2019. doi10.1111/ dmcn.14194. [PubMed] [Google Scholar]
  4. De Die-Smulders C. Congenital and childhood-onset myotonic dystrophy. In : Harper PS, van Engelen B, Eymard B, Wilcox, DE eds. Myotonic dystrophy: present management, future therapy. Oxford University, 2004 : 162-75. [Google Scholar]
  5. Douniol M, Jacquette A, Cohen D, Bodeau N, Rachidi L, Angeard N, et al. Psychiatric and cognitive phenotype of childhood myotonic dystrophy type 1. Dev Med Child Neurol 2012 ; 54 : 905-11. [CrossRef] [PubMed] [Google Scholar]
  6. Cohen D, Plaza M, Angeard N, Lanthier-Gazzano O, Baraud P, Rivière J P, et al. Reading and spelling impairments in children and adolescents with infantile myotonic dystrophy. J Neurolinguistics 2006 ; 19 : 455-65. [Google Scholar]
  7. Angeard N, Jacquette A, Gargiulo M, Radvanyi H, Moutier S, Eymard B, Héron D. A new window on neurocognitive dysfunction in the childhood form of myotonic dystrophy type 1 (DM1). Neuromusc Disord 2011 ; 21 : 468-76. [Google Scholar]
  8. Angeard N, Gargiulo M, Jacquette A, Radvanyi H, Eymard B, Héron D. Cognitive profile in childhood myotonic dystrophy type 1: is there a global impairment? Neuromusc Disord 2007 ; 17 : 451-8. [Google Scholar]
  9. Wozniak JR, Mueller BA, Bell CJ, Muetzel RL, Lim KO, Day JW. Diffusion tensor imaging reveals widespread white matter abnormalities in children and adolescents with myotonic dystrophy type 1. J Neurol 2013 ; 260 : 1122-31. [CrossRef] [PubMed] [Google Scholar]
  10. Wozniak JR, Mueller BA, Ward EE, Lim KO, Day JW. White matter abnormalities and neurocognitive correlates in children and adolescents with myotonic dystrophy type 1: a diffusion tensor imaging study. Neuromusc Disord 2011 ; 21 : 89-96. [Google Scholar]
  11. Jacquette A, Lemaitre H, Angeard N, Eymard B, Whalen S, Desguerre I, Brunelle F, Zilbovicius M, Héron D, Boddaert N. Neuroradiologic findings in a series of 9 patients with childhoodonset form of DM1. Lille, France : 4e Congrès International de Myologie, 2011 May : 9-13. [Google Scholar]
  12. Meola G, Sansone V, Perani D, Scarone S, Cappa S, Dragoni C, et al. Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2). Neuromusc Disord 2003 ; 13 : 813-21. [Google Scholar]
  13. Rubinsztein JS, Rubinsztein DC, McKenna PJ, Goodburn S, Holland, AJ. Mild myotonic dystrophy is associated with memory impairment in the context of normal general intelligence. J Med Genet 1997 ; 34 ; 229-33. [CrossRef] [PubMed] [Google Scholar]
  14. Weber YG, Roebling R, Kassubek J, Hoffmann S, Rosenbohm A, Wolf M, et al. Comparative analysis of brain structure, metabolism, and cognition in myotonic dystrophy 1 and 2. Neurology 2010 ; 74 : 1108-17. [Google Scholar]
  15. Modoni A, Silvestri G, Pomponi MG, Mangiola F, Tonali PA, Marra C. Characterization of the pattern of cognitive impairment in myotonic dystrophy type 1. Arch Neurol 2004 ; 61 : 1943-7. [CrossRef] [PubMed] [Google Scholar]
  16. Minnerop M, Gliem C, Kornblum C. Current progress in CNS imaging of myotonic dystrophy. Front Neurol 2018 ; 9. [PubMed] [Google Scholar]
  17. Meola G, Sansone V, Perani D, Colleluori A, Cappa S, Cotelli M, et al. Reduced cerebral blood flow and impaired visual-spatial function in proximal myotonic myopathy. Neurology 1999 ; 53 : 1042. [Google Scholar]
  18. Meola G, Sansone V. Cerebral involvement in myotonic dystrophies. Muscle Nerve 2007 ; 36 : 294-306. [Google Scholar]
  19. Romeo V, Pegoraro E, Ferrati C, Squarzanti F, Soraru G, Palmieri A, et al. Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2. J Neurol 2010 ; 257 : 1246-55. [CrossRef] [PubMed] [Google Scholar]
  20. Weber YG, Roebling R, Kassubek J, Hoffmann S, Rosenbohm A, Wolf M, et al. Comparative analysis of brain structure, metabolism, and cognition in myotonic dystrophy 1 and 2. Neurology 2010 ; 74 : 1108-17. [Google Scholar]
  21. Takeda A, Kobayakawa M, Suzuki A, Tsuruya N, Kawamura M. Lowered sensitivity to facial emotions in myotonic dystrophy type 1. J Neurol Sci 2009 ; 280 : 35-9. [CrossRef] [PubMed] [Google Scholar]
  22. Kobayakawa M, Tsuruya N, Takeda A, Suzuki A, Kawamura M. Facial emotion recognition and cerebral white matter lesions in myotonic dystrophy type 1. J Neurol Sci 2010 ; 290 : 48-51. [CrossRef] [PubMed] [Google Scholar]
  23. Winblad S, Lindberg C, Hansen S. Cognitive deficits and CTG repeat expansion size in classical myotonic dystrophy type 1 (DM1). Behav Brain Functions 2006 ; 2 : 16. [Google Scholar]
  24. Kobayakawa M, Tsuruya N, Kawamura M. Theory of mind impairment in adult-onset myotonic dystrophy type 1. Neurosci Res 2012 ; 72 : 341-6. [Google Scholar]
  25. Labayru G, Arenzana I, Aliri J, Zulaica M, de Munain AL, Sistiaga A. Social cognition in myotonic dystrophy type 1: Specific or secondary impairment? PLoS One 2018 ; 13 : e0204227. [CrossRef] [PubMed] [Google Scholar]
  26. Angeard N. Troubles de la cognition sociale dans la forme infantile de la dystrophie myotonique de type 1. Bordeaux : 28e Congrès de la Société Française de Neurologie Pédiatrique, 31 janvier-2 février 2018. [Google Scholar]
  27. Angeard N, Huerta E, Jacquette A, Cohen D, Xavier J, Gargiulo M, et al. Childhood-onset form of myotonic dystrophy type 1 and autism spectrum disorder: Is there comorbidity? Neuromusc Disord 2018 ; 28 : 216-21. [Google Scholar]
  28. Ekström AB, Hakenäs-Plate L, Tulinius M, Wentz E. Cognition and adaptive skills in myotonic dystrophy type 1: a study of 55 individuals with congenital and childhood forms. Dev Med Child Neurol 2009 ; 51 : 982-90. [CrossRef] [PubMed] [Google Scholar]
  29. Gourdon G, Meola G. Myotonic dystrophies: state of the art of new therapeutic developments for the CNS. Front Cell Neurosci 2017 ; 11 : 101. [Google Scholar]
  30. Johnson NE, Aldana EZ, Angeard N, et al. Consensus-based care recommendations for congenital and childhood-onset myotonic dystrophy type 1. Neurol Clin Pract 2019 ; 10 : 1212. [Google Scholar]
  31. Ashizawa T, Gagnon C, Groh WJ, et al. Consensus-based care recommendations for adults with myotonic dystrophy type 1. Neurol Clin Pract 2018 ; 8 : 507-20. [CrossRef] [PubMed] [Google Scholar]

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