Labauge P - Search Results

1

[Natural history of adult-onset eIF2B-related disorders: a multicentric survey of 24 cases].

Carra-Dalliere C, Horzinski L, Ayrignac X, Vukusic S, Rodriguez D, Mauguiere F, Peter L, Goizet C, Bouhour F, Denier C, Confavreux C, Obadia M, Blanc F, de Seze J, Sedel F, Guennoc AM, Sartori E, Laplaud D, Antoine JC, Fogli A, Boespflug-Tanguy O, Labauge P. Carra-Dalliere C, et al. Among authors: labauge p. Rev Neurol (Paris). 2011 Nov;167(11):802-11. doi: 10.1016/j.neurol.2011.03.008. Epub 2011 Jun 14. Rev Neurol (Paris). 2011. PMID: 21676421 French.

2

[Demyelinating nervous lesions in myalgia-eosinophilia syndrome induced by L Tryptophan].

Labauge P, Moulonguet A, Penaud D, Lessana-Leibowitch M, Kahn MF, Said G. Labauge P, et al. Rev Neurol (Paris). 1993;149(4):278-82. Rev Neurol (Paris). 1993. PMID: 8235226 Review. French.

3

[Friedreich's ataxia and hereditary vitamin E deficiency. Case study].

Labauge P, Cavalier L, Ichalalène L, Castelnovo G. Labauge P, et al. Rev Neurol (Paris). 1998 May;154(4):339-41. Rev Neurol (Paris). 1998. PMID: 9773063 French.

4

[Meningo encephalitis revealing Q fever: two cases and a review of the literature].

Castelnovo G, Sotto A, Bouly S, Vladut M, Janbon F, Labauge P. Castelnovo G, et al. Among authors: labauge p. Rev Neurol (Paris). 2002 Jan;158(1):77-80. Rev Neurol (Paris). 2002. PMID: 11938327 Review. French.

5

Ovarian failure related to eukaryotic initiation factor 2B mutations.

Fogli A, Rodriguez D, Eymard-Pierre E, Bouhour F, Labauge P, Meaney BF, Zeesman S, Kaneski CR, Schiffmann R, Boespflug-Tanguy O. Fogli A, et al. Among authors: labauge p. Am J Hum Genet. 2003 Jun;72(6):1544-50. doi: 10.1086/375404. Epub 2003 Apr 21. Am J Hum Genet. 2003. PMID: 12707859 Free PMC article.

6

[Spontaneous thrombosis of lesion-free carotid arteries: a retrospective analysis of eight patients].

Bouly S, Le Bayon A, Blard JM, Touzé E, Leys D, Mas JL, Neau JP, Dauzat M, Gautier V, Delhaume O, Castelnovo G, Labauge P. Bouly S, et al. Among authors: labauge p. Rev Neurol (Paris). 2005 Jan;161(1):61-6. doi: 10.1016/s0035-3787(05)84974-4. Rev Neurol (Paris). 2005. PMID: 15678002 French.

7

Dominant form of vanishing white matter-like leukoencephalopathy.

Labauge P, Fogli A, Castelnovo G, Le Bayon A, Horzinski L, Nicoli F, Cozzone P, Pagès M, Briere C, Marty-Double C, Delhaume O, Gelot A, Boespflug-Tanguy O, Rodriguez D. Labauge P, et al. Ann Neurol. 2005 Oct;58(4):634-9. doi: 10.1002/ana.20573. Ann Neurol. 2005. PMID: 16047349

8

Frequency of retinal cavernomas in 60 patients with familial cerebral cavernomas: a clinical and genetic study.

Labauge P, Krivosic V, Denier C, Tournier-Lasserve E, Gaudric A. Labauge P, et al. Arch Ophthalmol. 2006 Jun;124(6):885-6. doi: 10.1001/archopht.124.6.885. Arch Ophthalmol. 2006. PMID: 16769843

9

Autosomal dominant leukodystrophy and childhood ataxia with central nervous system hypomyelination syndrome.

Labauge P, Gelot A, Fogli A, Boespflug-Tanguy O, Rodriguez D. Labauge P, et al. Ann Neurol. 2006 Oct;60(4):485; author reply 485-6. doi: 10.1002/ana.20930. Ann Neurol. 2006. PMID: 16847948 No abstract available.

10

Genetics of cavernous angiomas.

Labauge P, Denier C, Bergametti F, Tournier-Lasserve E. Labauge P, et al. Lancet Neurol. 2007 Mar;6(3):237-44. doi: 10.1016/S1474-4422(07)70053-4. Lancet Neurol. 2007. PMID: 17303530 Review.

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