Echaniz-Laguna A - Search Results

1

Clinical, paraclinical and outcome features of 166 patients with acute anti-GQ1b antibody syndrome.

Coly M, Adams D, Attarian S, Bouhour F, Camdessanché JP, Carey G, Cauquil C, Chanson JB, Chrétien P, Créange A, Delmont E, Fargeot G, Frachet S, Gendre T, Kuntzer T, Labeyrie C, Maisonobe T, Michaud M, Moulin M, Nicolas G, Noury JB, Péréon Y, Puma A, Sole G, Taithe F, Tard C, Théaudin M, Timsit S, Venditti L, Echaniz-Laguna A. Coly M, et al. Among authors: echaniz laguna a. J Neurol. 2024 Aug;271(8):4982-4990. doi: 10.1007/s00415-024-12410-4. Epub 2024 May 20. J Neurol. 2024. PMID: 38767661

2

Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations.

Roze E, Apartis E, Clot F, Dorison N, Thobois S, Guyant-Marechal L, Tranchant C, Damier P, Doummar D, Bahi-Buisson N, André-Obadia N, Maltete D, Echaniz-Laguna A, Pereon Y, Beaugendre Y, Dupont S, De Greslan T, Jedynak CP, Ponsot G, Dussaule JC, Brice A, Dürr A, Vidailhet M. Roze E, et al. Neurology. 2008 Mar 25;70(13):1010-6. doi: 10.1212/01.wnl.0000297516.98574.c0. Neurology. 2008. PMID: 18362280

3

A novel variation in the Twinkle linker region causing late-onset dementia.

Echaniz-Laguna A, Chanson JB, Wilhelm JM, Sellal F, Mayençon M, Mohr M, Tranchant C, Mousson de Camaret B. Echaniz-Laguna A, et al. Neurogenetics. 2010 Feb;11(1):21-5. doi: 10.1007/s10048-009-0202-4. Epub 2009 Jun 10. Neurogenetics. 2010. PMID: 19513767

4

TDP43-positive intraneuronal inclusions in a patient with motor neuron disease and Parkinson's disease.

Chanson JB, Echaniz-Laguna A, Vogel T, Mohr M, Benoilid A, Kaltenbach G, Kiesmann M. Chanson JB, et al. Neurodegener Dis. 2010;7(4):260-4. doi: 10.1159/000273591. Epub 2010 Feb 27. Neurodegener Dis. 2010. PMID: 20197650

5

Characteristics of clinical and electrophysiological pattern of Charcot-Marie-Tooth 4C.

Yger M, Stojkovic T, Tardieu S, Maisonobe T, Brice A, Echaniz-Laguna A, Alembik Y, Girard S, Cazeneuve C, Leguern E, Dubourg O. Yger M, et al. J Peripher Nerv Syst. 2012 Mar;17(1):112-22. doi: 10.1111/j.1529-8027.2012.00382.x. J Peripher Nerv Syst. 2012. PMID: 22462672

6

Chronic inflammatory demyelinating polyradiculoneuropathy in solid organ transplant recipients: a prospective study.

Echaniz-Laguna A, de Séze J, Chanson JB. Echaniz-Laguna A, et al. J Neurol Neurosurg Psychiatry. 2012 Jul;83(7):699-705. doi: 10.1136/jnnp-2012-302374. Epub 2012 May 10. J Neurol Neurosurg Psychiatry. 2012. PMID: 22577230

7

A clinical pattern-based etiological diagnostic strategy for sensory neuronopathies: a French collaborative study.

Camdessanché JP, Jousserand G, Franques J, Pouget J, Delmont E, Créange A, Kuntzer T, Maisonobe T, Abba K, Antoine JC; French CIDP study group. Camdessanché JP, et al. J Peripher Nerv Syst. 2012 Sep;17(3):331-40. doi: 10.1111/j.1529-8027.2012.00411.x. J Peripher Nerv Syst. 2012. PMID: 22971095

8

Central nervous system abnormalities in patients with PMP22 gene mutations: a prospective study.

Chanson JB, Echaniz-Laguna A, Blanc F, Lacour A, Ballonzoli L, Kremer S, Namer IJ, Lannes B, Tranchant C, Vermersch P, de Seze J. Chanson JB, et al. J Neurol Neurosurg Psychiatry. 2013 Apr;84(4):392-7. doi: 10.1136/jnnp-2012-303725. Epub 2012 Dec 15. J Neurol Neurosurg Psychiatry. 2013. PMID: 23243264

9

Early electrodiagnostic abnormalities in acute inflammatory demyelinating polyneuropathy: a retrospective study of 58 patients.

Chanson JB, Echaniz-Laguna A. Chanson JB, et al. Clin Neurophysiol. 2014 Sep;125(9):1900-5. doi: 10.1016/j.clinph.2014.01.007. Epub 2014 Jan 27. Clin Neurophysiol. 2014. PMID: 24529487

10

Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy.

Echaniz-Laguna A, Dubourg O, Carlier P, Carlier RY, Sabouraud P, Péréon Y, Chapon F, Thauvin-Robinet C, Laforêt P, Eymard B, Latour P, Stojkovic T. Echaniz-Laguna A, et al. Neurology. 2014 May 27;82(21):1919-26. doi: 10.1212/WNL.0000000000000450. Epub 2014 Apr 30. Neurology. 2014. PMID: 24789864

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