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Items: 1 to 20 of 61

1.

Molecular diagnosis of inherited peripheral neuropathies by targeted next-generation sequencing: molecular spectrum delineation.

Bacquet J, Stojkovic T, Boyer A, Martini N, Audic F, Chabrol B, Salort-Campana E, Delmont E, Desvignes JP, Verschueren A, Attarian S, Chaussenot A, Delague V, Levy N, Bonello-Palot N.

BMJ Open. 2018 Oct 28;8(10):e021632. doi: 10.1136/bmjopen-2018-021632.

2.

Motor unit number index correlates with disability in Charcot-Marie-Tooth disease.

Bas J, Delmont E, Fatehi F, Salort-Campana E, Verschueren A, Pouget J, Lefebvre MN, Grapperon AM, Attarian S.

Clin Neurophysiol. 2018 Jul;129(7):1390-1396. doi: 10.1016/j.clinph.2018.04.359. Epub 2018 Apr 16.

PMID:
29729594
3.

Region-specific impairment of the cervical spinal cord (SC) in amyotrophic lateral sclerosis: A preliminary study using SC templates and quantitative MRI (diffusion tensor imaging/inhomogeneous magnetization transfer).

Rasoanandrianina H, Grapperon AM, Taso M, Girard OM, Duhamel G, Guye M, Ranjeva JP, Attarian S, Verschueren A, Callot V.

NMR Biomed. 2017 Dec;30(12). doi: 10.1002/nbm.3801. Epub 2017 Sep 19.

PMID:
28926131
4.

Motor unit number index (MUNIX) in patients with anti-MAG neuropathy.

Fatehi F, Delmont E, Grapperon AM, Salort-Campana E, Sévy A, Verschueren A, Boucraut J, Attarian S.

Clin Neurophysiol. 2017 Jul;128(7):1264-1269. doi: 10.1016/j.clinph.2017.04.022. Epub 2017 May 9.

PMID:
28545015
5.

Predictive factors of efficacy of rituximab in patients with anti-MAG neuropathy.

Gazzola S, Delmont E, Franques J, Boucraut J, Salort-Campana E, Verschueren A, Sagui E, Hubert AM, Pouget J, Attarian S.

J Neurol Sci. 2017 Jun 15;377:144-148. doi: 10.1016/j.jns.2017.04.015. Epub 2017 Apr 12.

PMID:
28477685
6.

Motor neuropathies and lower motor neuron syndromes.

Verschueren A.

Rev Neurol (Paris). 2017 May;173(5):320-325. doi: 10.1016/j.neurol.2017.03.018. Epub 2017 Apr 20. Review.

PMID:
28434507
7.

Global motor unit number index sum score for assessing the loss of lower motor neurons in amyotrophic lateral sclerosis.

Grimaldi S, Duprat L, Grapperon AM, Verschueren A, Delmont E, Attarian S.

Muscle Nerve. 2017 Aug;56(2):202-206. doi: 10.1002/mus.25595. Epub 2017 Apr 1.

PMID:
28164325
8.

Motor-evoked potential gain is a helpful test for the detection of corticospinal tract dysfunction in amyotrophic lateral sclerosis.

Duclos Y, Grapperon AM, Jouve E, Truillet R, Zemmour C, Verschueren A, Pouget J, Attarian S.

Clin Neurophysiol. 2017 Feb;128(2):357-364. doi: 10.1016/j.clinph.2016.12.015. Epub 2016 Dec 23.

PMID:
28068522
9.

Updating temporal expectancy of an aversive event engages striatal plasticity under amygdala control.

Dallérac G, Graupner M, Knippenberg J, Martinez RC, Tavares TF, Tallot L, El Massioui N, Verschueren A, Höhn S, Bertolus JB, Reyes A, LeDoux JE, Schafe GE, Diaz-Mataix L, Doyère V.

Nat Commun. 2017 Jan 9;8:13920. doi: 10.1038/ncomms13920.

10.

New strategy for improving the diagnostic sensitivity of repetitive nerve stimulation in myasthenia gravis.

Bou Ali H, Salort-Campana E, Grapperon AM, Gallard J, Franques J, Sevy A, Delmont E, Verschueren A, Pouget J, Attarian S.

Muscle Nerve. 2017 Apr;55(4):532-538. doi: 10.1002/mus.25374. Epub 2017 Jan 3.

PMID:
27511866
11.

Motor unit number index (MUNIX): Is it relevant in chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)?

Delmont E, Benvenutto A, Grimaldi S, Duprat L, Philibert M, Pouget J, Grapperon AM, Salort-Campana E, Sévy A, Verschueren A, Attarian S.

Clin Neurophysiol. 2016 Mar;127(3):1891-4. doi: 10.1016/j.clinph.2015.12.002. Epub 2015 Dec 12.

PMID:
26750580
12.

Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China.

Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K, Berg-Alonso L, Kageyama Y, Serre V, Moore D, Verschueren A, Rouzier C, Le Ber I, Augé G, Cochaud C, Lespinasse F, N'Guyen K, de Septenville A, Brice A, Yu-Wai-Man P, Sesaki H, Pouget J, Paquis-Flucklinger V.

Brain. 2016 Apr;139(Pt 4):e22. doi: 10.1093/brain/awv368. Epub 2015 Dec 30. No abstract available.

13.

Myofibrillar myopathies: State of the art, present and future challenges.

Béhin A, Salort-Campana E, Wahbi K, Richard P, Carlier RY, Carlier P, Laforêt P, Stojkovic T, Maisonobe T, Verschueren A, Franques J, Attarian S, Maues de Paula A, Figarella-Branger D, Bécane HM, Nelson I, Duboc D, Bonne G, Vicart P, Udd B, Romero N, Pouget J, Eymard B.

Rev Neurol (Paris). 2015 Oct;171(10):715-29. doi: 10.1016/j.neurol.2015.06.002. Epub 2015 Sep 3. Review.

PMID:
26342832
14.

Paraneoplastic subacute lower motor neuron syndrome associated with solid cancer.

Verschueren A, Gallard J, Boucraut J, Honnorat J, Pouget J, Attarian S.

J Neurol Sci. 2015 Nov 15;358(1-2):413-6. doi: 10.1016/j.jns.2015.08.014. Epub 2015 Aug 12.

PMID:
26323521
15.

Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?

Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K, Berg-Alonso L, Kageyama Y, Serre V, Moore D, Verschueren A, Rouzier C, Le Ber I, Augé G, Cochaud C, Lespinasse F, N'Guyen K, de Septenville A, Brice A, Yu-Wai-Man P, Sesaki H, Pouget J, Paquis-Flucklinger V.

Brain. 2015 Oct;138(Pt 10):e386. doi: 10.1093/brain/awv116. Epub 2015 May 7. No abstract available.

PMID:
25953779
16.

Improving molecular diagnosis of distal myopathies by targeted next-generation sequencing.

Sevy A, Cerino M, Gorokhova S, Dionnet E, Mathieu Y, Verschueren A, Franques J, Maues de Paula A, Figarella-Branger D, Lagarde A, Desvignes JP, Béroud C, Attarian S, Levy N, Bartoli M, Krahn M, Campana-Salort E, Pouget J.

J Neurol Neurosurg Psychiatry. 2016 Mar;87(3):340-2. doi: 10.1136/jnnp-2014-309663. Epub 2015 Mar 17. No abstract available.

PMID:
25783436
17.

Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.

Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K, Berg-Alonso L, Kageyama Y, Serre V, Moore D, Verschueren A, Rouzier C, Le Ber I, Augé G, Cochaud C, Lespinasse F, N'Guyen K, de Septenville A, Brice A, Yu-Wai-Man P, Sesaki H, Pouget J, Paquis-Flucklinger V.

Brain. 2015 Sep;138(Pt 9):e377. doi: 10.1093/brain/awv015. Epub 2015 Feb 12. No abstract available.

18.

Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.

Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K, Berg-Alonso L, Kageyama Y, Serre V, Moore D, Verschueren A, Rouzier C, Le Ber I, Augé G, Cochaud C, Lespinasse F, N'Guyen K, de Septenville A, Brice A, Yu-Wai-Man P, Sesaki H, Pouget J, Paquis-Flucklinger V.

Brain. 2015 Aug;138(Pt 8):e373. doi: 10.1093/brain/awu385. Epub 2015 Jan 8. No abstract available.

19.

Triple-stimulation technique improves the diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy.

Attarian S, Franques J, Elisabeth J, Trébuchon A, Duclos Y, Wybrecht D, Verschueren A, Salort-Campana E, Pouget J.

Muscle Nerve. 2015 Apr;51(4):541-8. doi: 10.1002/mus.24352. Epub 2015 Jan 9.

PMID:
25571892
20.

Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K, Berg-Alonso L, Kageyama Y, Serre V, Moore D, Verschueren A, Rouzier C, Le Ber I, Augé G, Cochaud C, Lespinasse F, N'Guyen K, de Septenville A, Brice A, Yu-Wai-Man P, Sesaki H, Pouget J, Paquis-Flucklinger V.

Brain. 2014 Dec;137(Pt 12):e314. doi: 10.1093/brain/awu300. Epub 2014 Oct 27. No abstract available.

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