Lacour A - Search Results

1

Characteristics of Patients With Late-Onset Pompe Disease in France: Insights From the French Pompe Registry in 2022.

Lefeuvre C, De Antonio M, Bouhour F, Tard C, Salort-Campana E, Lagrange E, Behin A, Sole G, Noury JB, Sacconi S, Magot A, Nadaj-Pakleza A, Lacour A, Beltran S, Spinazzi M, Cintas P, Renard D, Michaud M, Bedat-Millet AL, Prigent H, Taouagh N, Arrassi A, Hamroun D, Attarian S, Laforêt P; for Pompe Study Group. Lefeuvre C, et al. Among authors: lacour a. Neurology. 2023 Aug 29;101(9):e966-e977. doi: 10.1212/WNL.0000000000207547. Epub 2023 Jul 7. Neurology. 2023. PMID: 37419682

2

JCV serology in time: 3 years of follow-up.

Cambron M, Hadhoum N, Duhin E, Lacour A, Chouraki A, Vermersch P. Cambron M, et al. Among authors: lacour a. Acta Neurol Scand. 2017 Jul;136(1):54-58. doi: 10.1111/ane.12699. Epub 2016 Oct 20. Acta Neurol Scand. 2017. PMID: 27766611

3

[Economic evaluation of screening for neuroblastoma].

Lacour A, Chauvin F, Duru G, Philip T. Lacour A, et al. Rev Epidemiol Sante Publique. 1994;42(1):24-33. Rev Epidemiol Sante Publique. 1994. PMID: 8134663 French.

4

[West Nile meningoencephalitis in an immunocompromised patient].

Dequatre N, Moreau C, Lacour A, Degardin A, Lionet A, Devos D, Destée A, Defebvre L. Dequatre N, et al. Among authors: lacour a. Rev Neurol (Paris). 2008 Dec;164(12 Suppl):F275-9. doi: 10.1016/S0035-3787(08)75128-2. Rev Neurol (Paris). 2008. PMID: 19268190 French. No abstract available.

5

NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe.

Klebe S, Lacour A, Durr A, Stojkovic T, Depienne C, Forlani S, Poea-Guyon S, Vuillaume I, Sablonniere B, Vermersch P, Brice A, Stevanin G. Klebe S, et al. Among authors: lacour a. Neurogenetics. 2007 Apr;8(2):155-7. doi: 10.1007/s10048-006-0074-9. Epub 2007 Jan 5. Neurogenetics. 2007. PMID: 17205300 No abstract available.

6

Recurrent multiple cranial nerve palsy and anti-GD1a antibodies.

Simon O, Lacour A, Delval A, Beaume A, Vermersch P. Simon O, et al. Among authors: lacour a. Muscle Nerve. 2011 Mar;43(3):447-8. doi: 10.1002/mus.21958. Muscle Nerve. 2011. PMID: 21321960 No abstract available.

7

Novel epsilon subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome.

Outteryck O, Richard P, Lacour A, Fournier E, Zéphir H, Gaudon K, Eymard B, Hantaï D, Vermersch P, Stojkovic T. Outteryck O, et al. Among authors: lacour a. J Neurol Neurosurg Psychiatry. 2009 Apr;80(4):450-1. doi: 10.1136/jnnp.2008.148189. J Neurol Neurosurg Psychiatry. 2009. PMID: 19289485 No abstract available.

8

Occurrence of vismodegib-induced cramps (muscular spasms) in the treatment of basal cell carcinoma: A prospective study in 30 patients.

Girard E, Lacour A, Abi Rached H, Ramdane N, Templier C, Dziwniel V, Desmedt E, Le Rhun E, Mortier L. Girard E, et al. Among authors: lacour a. J Am Acad Dermatol. 2018 Jun;78(6):1213-1216.e2. doi: 10.1016/j.jaad.2017.11.045. Epub 2017 Dec 1. J Am Acad Dermatol. 2018. PMID: 29203435 No abstract available.

9

Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspots.

Beetz C, Schüle R, Klebe S, Klimpe S, Klopstock T, Lacour A, Otto S, Sperfeld AD, van de Warrenburg B, Schöls L, Deufel T. Beetz C, et al. Among authors: lacour a. J Neurol Sci. 2008 May 15;268(1-2):131-5. doi: 10.1016/j.jns.2007.11.015. Epub 2008 Jan 14. J Neurol Sci. 2008. PMID: 18191948

10

Brain Magnetic Susceptibility Changes in Patients with Natalizumab-Associated Progressive Multifocal Leukoencephalopathy.

Hodel J, Outteryck O, Verclytte S, Deramecourt V, Lacour A, Pruvo JP, Vermersch P, Leclerc X. Hodel J, et al. Among authors: lacour a. AJNR Am J Neuroradiol. 2015 Dec;36(12):2296-302. doi: 10.3174/ajnr.A4436. Epub 2015 Aug 27. AJNR Am J Neuroradiol. 2015. PMID: 26316568 Free PMC article.

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