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Progressive ataxia related to PRRT2 gene mutation.
Castelnovo G, Renard D, De Verdal M, Luc J, Thouvenot E, Riant F. Castelnovo G, et al. Among authors: de verdal m. J Neurol Sci. 2016 Aug 15;367:220-1. doi: 10.1016/j.jns.2016.05.058. Epub 2016 May 31. J Neurol Sci. 2016. PMID: 27423591 No abstract available.
Diffuse brain stem glioma.
Renard D, Le Floch A, Collombier L, De Verdal M, Campello C, Labauge P. Renard D, et al. Among authors: de verdal m. Arch Neurol. 2010 Mar;67(3):368-9. doi: 10.1001/archneurol.2010.12. Arch Neurol. 2010. PMID: 20212241 No abstract available.
Ipsilateral uveitis and optic neuritis in multiple sclerosis.
Thouvenot E, Mura F, De Verdal M, Carlander B, Charif M, Schneider C, Navarre S, Camu W. Thouvenot E, et al. Among authors: de verdal m. Mult Scler Int. 2012;2012:372361. doi: 10.1155/2012/372361. Epub 2012 Nov 19. Mult Scler Int. 2012. PMID: 23213530 Free PMC article.
Cortical abnormalities on MRI: what a neurologist should know.
Renard D, Castelnovo G, Bouly S, Le Floch A, Waconge A, De Verdal M, Thouvenot E. Renard D, et al. Among authors: de verdal m. Pract Neurol. 2015 Aug;15(4):257-65. doi: 10.1136/practneurol-2015-001113. Epub 2015 Apr 28. Pract Neurol. 2015. PMID: 25922540 Review.
123I-FP-CIT SPECT imaging in blepharospasm.
De Verdal M, Renard D, Collombier L, Castelnovo G. De Verdal M, et al. Rev Neurol (Paris). 2017 Dec;173(10):645-649. doi: 10.1016/j.neurol.2017.05.006. Epub 2017 Jun 16. Rev Neurol (Paris). 2017. PMID: 28629634 Clinical Trial.
Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes.
Schramm C, Charbonnier C, Zaréa A, Lacour M, Wallon D; CNRMAJ collaborators; Boland A, Deleuze JF, Olaso R; ADES consortium; Alarcon F, Campion D, Nuel G, Nicolas G. Schramm C, et al. Genome Med. 2022 Jun 28;14(1):69. doi: 10.1186/s13073-022-01070-6. Genome Med. 2022. PMID: 35761418 Free PMC article.
13 results