Echaniz-Laguna A - Search Results

1

Phenotype-genotype correlation in X-linked Charcot-Marie-Tooth disease: A French cohort study.

Barbat du Closel L, Bonello-Palot N, Delmont E, Péréon Y, Echaniz-Laguna A, Camdessanché JP, Pakleza AN, Chanson JB, Frachet S, Magy L, Cassereau J, Cintas P, Choumert A, Devic P, Louis SL, Tard C, Solé G, Salort-Campana E, Bouhour F, Latour P, Stojkovic T, Attarian S. Barbat du Closel L, et al. Among authors: echaniz laguna a. Eur J Neurol. 2025 Jan;32(1):e16523. doi: 10.1111/ene.16523. Epub 2024 Nov 21. Eur J Neurol. 2025. PMID: 39569692 Free PMC article.

2

[Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy].

Degos B, Echaniz-Laguna A, Latour P, Vandenberghe A, Anheim M, Talmant V, Tranchant C. Degos B, et al. Rev Neurol (Paris). 2004 Dec;160(12):1203-6. doi: 10.1016/s0035-3787(04)71168-6. Rev Neurol (Paris). 2004. PMID: 15602369 French.

3

NDRG1-linked Charcot-Marie-Tooth disease (CMT4D) with central nervous system involvement.

Echaniz-Laguna A, Degos B, Bonnet C, Latour P, Hamadouche T, Lévy N, Leheup B. Echaniz-Laguna A, et al. Neuromuscul Disord. 2007 Feb;17(2):163-8. doi: 10.1016/j.nmd.2006.10.002. Epub 2006 Dec 4. Neuromuscul Disord. 2007. PMID: 17142040

4

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

5

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

6

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

7

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

8

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

9

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

10

The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease.

Laforêt P, Laloui K, Granger B, Hamroun D, Taouagh N, Hogrel JY, Orlikowski D, Bouhour F, Lacour A, Salort-Campana E, Penisson-Besnier I, Sacconi S, Zagnoli F, Chapon F, Eymard B, Desnuelle C, Pouget J; French Pompe Registry Study Group. Laforêt P, et al. Rev Neurol (Paris). 2013 Aug-Sep;169(8-9):595-602. doi: 10.1016/j.neurol.2013.07.002. Epub 2013 Sep 3. Rev Neurol (Paris). 2013. PMID: 24008051

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