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Page 1
Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients.
Ayrignac X, Carra-Dalliere C, Menjot de Champfleur N, Denier C, Aubourg P, Bellesme C, Castelnovo G, Pelletier J, Audoin B, Kaphan E, de Seze J, Collongues N, Blanc F, Chanson JB, Magnin E, Berger E, Vukusic S, Durand-Dubief F, Camdessanche JP, Cohen M, Lebrun-Frenay C, Brassat D, Clanet M, Vermersch P, Zephir H, Outteryck O, Wiertlewski S, Laplaud DA, Ouallet JC, Brochet B, Goizet C, Debouverie M, Pittion S, Edan G, Deburghgraeve V, Le Page E, Verny C, Amati-Bonneau P, Bonneau D, Hannequin D, Guyant-Maréchal L, Derache N, Defer GL, Moreau T, Giroud M, Guennoc AM, Clavelou P, Taithe F, Mathis S, Neau JP, Magy L, Devoize JL, Bataillard M, Masliah-Planchon J, Dorboz I, Tournier-Lasserve E, Levade T, Boespflug Tanguy O, Labauge P. Ayrignac X, et al. Brain. 2015 Feb;138(Pt 2):284-92. doi: 10.1093/brain/awu353. Epub 2014 Dec 19. Brain. 2015. PMID: 25527826
Evaluation of CSF1R-related adult onset leukoencephalopathy with axonal spheroids and pigmented glia diagnostic criteria.
Ayrignac X, Carra-Dallière C, Codjia P, Mouzat K, Castelnovo G, Ellie E, Etcharry-Bouyx F, Belliard S, Marelli C, Portet F, Le Ber I, Durand-Dubief F, Mathey G, Stankoff B, Dorboz I, Drunat S, Boespflug-Tanguy O, Menjot de Champfleur N, Lumbroso S, Mochel F, Labauge P. Ayrignac X, et al. Eur J Neurol. 2022 Jan;29(1):329-334. doi: 10.1111/ene.15115. Epub 2021 Sep 28. Eur J Neurol. 2022. PMID: 34541732
Cystic leukoencephalopathy with cortical dysplasia related to LAMB1 mutations.
Tonduti D, Dorboz I, Renaldo F, Masliah-Planchon J, Elmaleh-Bergès M, Dalens H, Rodriguez D, Boespflug-Tanguy O. Tonduti D, et al. Neurology. 2015 May 26;84(21):2195-7. doi: 10.1212/WNL.0000000000001607. Epub 2015 Apr 29. Neurology. 2015. PMID: 25925986 No abstract available.
A novel autosomal dominant leukodystrophy with specific MRI pattern.
Corlobé A, Taithe F, Clavelou P, Pierre E, Carra-Dallière C, Ayrignac X, Mouzat K, Lumbroso S, Menjot de Champfleur N, Koenig M, Boespflug-Tanguy O, Labauge P. Corlobé A, et al. J Neurol. 2015;262(4):988-91. doi: 10.1007/s00415-015-7660-4. Epub 2015 Feb 17. J Neurol. 2015. PMID: 25683759
[Genetic demyelinating diseases].
Labauge P, Boespflug-Tanguy O. Labauge P, et al. Presse Med. 2010 Mar;39(3):363-70. doi: 10.1016/j.lpm.2009.11.011. Epub 2010 Feb 18. Presse Med. 2010. PMID: 20167452 French.
4H syndrome: a rare cause of leukodystrophy.
Outteryck O, Devos D, Jissendi P, Boespflug-Tanguy O, Hopes L, Renard D, Ferri J, Vermersch P, Labauge P. Outteryck O, et al. J Neurol. 2010 Oct;257(10):1759-61. doi: 10.1007/s00415-010-5598-0. Epub 2010 May 30. J Neurol. 2010. PMID: 20512583 No abstract available.
MRI pattern approach of adult-onset inherited leukoencephalopathies.
Labauge P, Carra-Dalliere C, Menjot de Champfleur N, Ayrignac X, Boespflug-Tanguy O. Labauge P, et al. Neurol Clin Pract. 2014 Aug;4(4):287-295. doi: 10.1212/CPJ.0000000000000047. Neurol Clin Pract. 2014. PMID: 29473566 Free PMC article.
203 results