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Items: 1 to 20 of 33

1.

Penumbral imaging and functional outcome in patients with anterior circulation ischaemic stroke treated with endovascular thrombectomy versus medical therapy: a meta-analysis of individual patient-level data.

Campbell BCV, Majoie CBLM, Albers GW, Menon BK, Yassi N, Sharma G, van Zwam WH, van Oostenbrugge RJ, Demchuk AM, Guillemin F, White P, Dávalos A, van der Lugt A, Butcher KS, Cherifi A, Marquering HA, Cloud G, Macho Fernández JM, Madigan J, Oppenheim C, Donnan GA, Roos YBWEM, Shankar J, Lingsma H, Bonafé A, Raoult H, Hernández-Pérez M, Bharatha A, Jahan R, Jansen O, Richard S, Levy EI, Berkhemer OA, Soudant M, Aja L, Davis SM, Krings T, Tisserand M, San Román L, Tomasello A, Beumer D, Brown S, Liebeskind DS, Bracard S, Muir KW, Dippel DWJ, Goyal M, Saver JL, Jovin TG, Hill MD, Mitchell PJ; HERMES collaborators.

Lancet Neurol. 2019 Jan;18(1):46-55. doi: 10.1016/S1474-4422(18)30314-4. Epub 2018 Nov 6. Erratum in: Lancet Neurol. 2019 Mar;18(3):e2.

PMID:
30413385
2.

Imaging features and safety and efficacy of endovascular stroke treatment: a meta-analysis of individual patient-level data.

Román LS, Menon BK, Blasco J, Hernández-Pérez M, Dávalos A, Majoie CBLM, Campbell BCV, Guillemin F, Lingsma H, Anxionnat R, Epstein J, Saver JL, Marquering H, Wong JH, Lopes D, Reimann G, Desal H, Dippel DWJ, Coutts S, du Mesnil de Rochemont R, Yavagal D, Ferre JC, Roos YBWEM, Liebeskind DS, Lenthall R, Molina C, Al Ajlan FS, Reddy V, Dowlatshahi D, Sourour NA, Oppenheim C, Mitha AP, Davis SM, Weimar C, van Oostenbrugge RJ, Cobo E, Kleinig TJ, Donnan GA, van der Lugt A, Demchuk AM, Berkhemer OA, Boers AMM, Ford GA, Muir KW, Brown BS, Jovin T, van Zwam WH, Mitchell PJ, Hill MD, White P, Bracard S, Goyal M; HERMES collaborators.

Lancet Neurol. 2018 Oct;17(10):895-904. doi: 10.1016/S1474-4422(18)30242-4. Epub 2018 Sep 18. Erratum in: Lancet Neurol. 2018 Dec;17(12):e2-e3.

PMID:
30264728
3.

Effect of general anaesthesia on functional outcome in patients with anterior circulation ischaemic stroke having endovascular thrombectomy versus standard care: a meta-analysis of individual patient data.

Campbell BCV, van Zwam WH, Goyal M, Menon BK, Dippel DWJ, Demchuk AM, Bracard S, White P, Dávalos A, Majoie CBLM, van der Lugt A, Ford GA, de la Ossa NP, Kelly M, Bourcier R, Donnan GA, Roos YBWEM, Bang OY, Nogueira RG, Devlin TG, van den Berg LA, Clarençon F, Burns P, Carpenter J, Berkhemer OA, Yavagal DR, Pereira VM, Ducrocq X, Dixit A, Quesada H, Epstein J, Davis SM, Jansen O, Rubiera M, Urra X, Micard E, Lingsma HF, Naggara O, Brown S, Guillemin F, Muir KW, van Oostenbrugge RJ, Saver JL, Jovin TG, Hill MD, Mitchell PJ; HERMES collaborators.

Lancet Neurol. 2018 Jan;17(1):47-53. doi: 10.1016/S1474-4422(17)30407-6. Epub 2017 Dec 16. Erratum in: Lancet Neurol. 2019 Mar;18(3):e2.

PMID:
29263006
4.

[Nosology and etiologies of acute longitudinally extensive transverse myelitis].

Collongues N, Papeix C, Zéphir H, Audoin B, Cotton F, Durand-Dubief F, Vukusic S, Brassat D, Laplaud D, Marignier R; Groupe Nomadmus.

Rev Neurol (Paris). 2014 Jan;170(1):6-12. doi: 10.1016/j.neurol.2013.04.008. Epub 2013 Nov 21. French.

PMID:
24269116
5.

Compound heterozygous mutations of the TNXB gene cause primary myopathy.

Pénisson-Besnier I, Allamand V, Beurrier P, Martin L, Schalkwijk J, van Vlijmen-Willems I, Gartioux C, Malfait F, Syx D, Macchi L, Marcorelles P, Arbeille B, Croué A, De Paepe A, Dubas F.

Neuromuscul Disord. 2013 Aug;23(8):664-9. doi: 10.1016/j.nmd.2013.04.009. Epub 2013 Jun 12.

PMID:
23768946
6.

Myopathy caused by anoctamin 5 mutations and necrotizing vasculitis.

Pénisson-Besnier I, Saint-André JP, Hicks D, Sarkozy A, Croué A, Hudson J, Lochmüller H, Dubas F.

J Neurol. 2012 Sep;259(9):1988-90. doi: 10.1007/s00415-012-6502-x. Epub 2012 Apr 19. No abstract available.

PMID:
22527239
7.

Axon cytoskeleton ultrastructure in chronic inflammatory demyelinating polyneuropathy.

Fressinaud C, Dubas F.

Muscle Nerve. 2011 Sep;44(3):332-9. doi: 10.1002/mus.22069.

PMID:
21996792
8.

The neural substrates of script knowledge deficits as revealed by a PET study in Huntington's disease.

Allain P, Gaura V, Fasotti L, Chauviré V, Prundean A, Sherer-Gagou C, Bonneau D, Bachoud-Levi AC, Dubas F, Remy P, Le Gall D, Verny C.

Neuropsychologia. 2011 Jul;49(9):2673-84. doi: 10.1016/j.neuropsychologia.2011.05.015. Epub 2011 May 30.

9.

Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations.

Cassereau J, Chevrollier A, Gueguen N, Desquiret V, Verny C, Nicolas G, Dubas F, Amati-Bonneau P, Reynier P, Bonneau D, Procaccio V.

Exp Neurol. 2011 Jan;227(1):31-41. doi: 10.1016/j.expneurol.2010.09.006. Epub 2010 Sep 21. Review.

PMID:
20849849
10.

Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation.

Verny C, Guegen N, Desquiret V, Chevrollier A, Prundean A, Dubas F, Cassereau J, Ferre M, Amati-Bonneau P, Bonneau D, Reynier P, Procaccio V.

Mitochondrion. 2011 Jan;11(1):70-5. doi: 10.1016/j.mito.2010.07.006. Epub 2010 Jul 22.

PMID:
20656066
11.

Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathy.

Lamirel C, Cassereau J, Cochereau I, Vignal-Clermont C, Pajot O, Tanguy JY, Zanlonghi X, Reynier P, Amati-Bonneau P, Dubas F, Bonneau D, Verny C.

J Neurol Neurosurg Psychiatry. 2010 May;81(5):578-80. doi: 10.1136/jnnp.2009.174953.

PMID:
20460595
12.

[Multiple sclerosis].

Scherer C, Dubas F.

Rev Prat. 2009 May 20;59(5):695-701. French. No abstract available.

PMID:
19552212
13.

Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).

Cassereau J, Chevrollier A, Gueguen N, Malinge MC, Letournel F, Nicolas G, Richard L, Ferre M, Verny C, Dubas F, Procaccio V, Amati-Bonneau P, Bonneau D, Reynier P.

Neurogenetics. 2009 Apr;10(2):145-50. doi: 10.1007/s10048-008-0166-9. Epub 2008 Dec 17.

PMID:
19089472
14.

Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African origin.

Cassereau J, Lavigne C, Letournel F, Ghali A, Verny C, Dubas F, Devière F, Nicolas G.

J Peripher Nerv Syst. 2008 Sep;13(3):251-4. doi: 10.1111/j.1529-8027.2008.00185.x. No abstract available.

PMID:
18844793
15.

Leukodystrophies: clinical and therapeutic aspects.

Letournel F, Dubas F.

Handb Clin Neurol. 2008;89:725-35. doi: 10.1016/S0072-9752(07)01265-1. No abstract available.

PMID:
18631791
16.

Script representation in patients with Alzheimer's disease.

Allain P, Le Gall D, Foucher C, Etcharry-Bouyx F, Barré J, Dubas F, Berrut G.

Cortex. 2008 Mar;44(3):294-304. doi: 10.1016/j.cortex.2006.07.003. Epub 2007 Nov 17.

PMID:
18387558
17.

[Executive functioning and normal aging: a study of arithmetic word-problem-solving].

Allain P, Kauffmann M, Dubas F, Berrut G, Le Gall D.

Psychol Neuropsychiatr Vieil. 2007 Dec;5(4):315-25. French.

18.

Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome.

Ricard-Mousnier B, N'Guyen S, Dubas F, Pouplard F, Guichet A.

Epileptic Disord. 2007 Sep;9(3):327-31. Epub 2007 Sep 20.

19.

[Nontraumatic coma].

Dubas F.

Rev Prat. 2007 Feb 15;57(3):321-6. French. No abstract available.

PMID:
17578035
20.

Executive functions in normal aging: an examination of script sequencing, script sorting, and script monitoring.

Allain P, Berrut G, Etcharry-Bouyx F, Barré J, Dubas F, Le Gall D.

J Gerontol B Psychol Sci Soc Sci. 2007 May;62(3):P187-90.

PMID:
17507587

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