Lyon-Caen O - Search Results

1

Biotin-responsive basal ganglia disease in ethnic Europeans with novel SLC19A3 mutations.

Debs R, Depienne C, Rastetter A, Bellanger A, Degos B, Galanaud D, Keren B, Lyon-Caen O, Brice A, Sedel F. Debs R, et al. Arch Neurol. 2010 Jan;67(1):126-30. doi: 10.1001/archneurol.2009.293. Arch Neurol. 2010. PMID: 20065143

2

Therapy insight: inborn errors of metabolism in adult neurology--a clinical approach focused on treatable diseases.

Sedel F, Lyon-Caen O, Saudubray JM. Sedel F, et al. Nat Clin Pract Neurol. 2007 May;3(5):279-90. doi: 10.1038/ncpneuro0494. Nat Clin Pract Neurol. 2007. PMID: 17479075 Review.

3

Rapid onset frontal leukodystrophy with decreased diffusion coefficient and neuroaxonal spheroids.

Maillart E, Rousseau A, Galanaud D, Gray F, Polivka M, Labauge P, Hauw JJ, Lyon-Caen O, Gout O, Sedel F. Maillart E, et al. J Neurol. 2009 Oct;256(10):1649-54. doi: 10.1007/s00415-009-5172-9. Epub 2009 May 21. J Neurol. 2009. PMID: 19458985 Review.

4

High doses of biotin in chronic progressive multiple sclerosis: a pilot study.

Sedel F, Papeix C, Bellanger A, Touitou V, Lebrun-Frenay C, Galanaud D, Gout O, Lyon-Caen O, Tourbah A. Sedel F, et al. Among authors: lyon caen o. Mult Scler Relat Disord. 2015 Mar;4(2):159-69. doi: 10.1016/j.msard.2015.01.005. Epub 2015 Jan 24. Mult Scler Relat Disord. 2015. PMID: 25787192 Free article. Clinical Trial.

5

Portosystemic shunts: an underdiagnosed but treatable cause of neurological and psychiatric disorders.

Degos B, Daelman L, Huberfeld G, Meppiel E, Rabier D, Galanaud D, Magis AS, Lyon-Caen O, Samuel D, Sedel F. Degos B, et al. Among authors: lyon caen o. J Neurol Sci. 2012 Oct 15;321(1-2):58-64. doi: 10.1016/j.jns.2012.07.050. Epub 2012 Aug 17. J Neurol Sci. 2012. PMID: 22906583 Review.

6

POLG mutations associated with remitting/relapsing neurological events.

Degos B, Laforêt P, Jardel C, Sedel F, Jossay-Winter M, Romero NB, Lyon-Caen O, Tourbah A. Degos B, et al. Among authors: lyon caen o. J Clin Neurosci. 2014 Jan;21(1):186-8. doi: 10.1016/j.jocn.2013.03.019. Epub 2013 Jul 2. J Clin Neurosci. 2014. PMID: 23830586

7

The adult form of Niemann-Pick disease type C.

Sévin M, Lesca G, Baumann N, Millat G, Lyon-Caen O, Vanier MT, Sedel F. Sévin M, et al. Brain. 2007 Jan;130(Pt 1):120-33. doi: 10.1093/brain/awl260. Epub 2006 Sep 26. Brain. 2007. PMID: 17003072 Review.

8

Hereditary spastic paraparesis in adults associated with inborn errors of metabolism: a diagnostic approach.

Sedel F, Fontaine B, Saudubray JM, Lyon-Caen O. Sedel F, et al. J Inherit Metab Dis. 2007 Nov;30(6):855-64. doi: 10.1007/s10545-007-0745-1. Epub 2007 Oct 22. J Inherit Metab Dis. 2007. PMID: 17957490 Review.

9

[Treatable hereditary neuro-metabolic diseases].

Sedel F, Lyon-Caen O, Saudubray JM. Sedel F, et al. Rev Neurol (Paris). 2007 Oct;163(10):884-96. doi: 10.1016/s0035-3787(07)92631-4. Rev Neurol (Paris). 2007. PMID: 18033024 Review. French.

10

The phenotype of "pure" autosomal dominant spastic paraplegia.

Dürr A, Brice A, Serdaru M, Rancurel G, Derouesné C, Lyon-Caen O, Agid Y, Fontaine B. Dürr A, et al. Neurology. 1994 Jul;44(7):1274-7. doi: 10.1212/wnl.44.7.1274. Neurology. 1994. PMID: 8035929

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