Echaniz-Laguna A - Search Results

1

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

2

[Neuronal ceroid lipofuscinosis. An unknown overload disease].

Echaniz-Laguna A, Tranchant C, Boehm N, Warter JM. Echaniz-Laguna A, et al. Presse Med. 1996 May 25;25(18):853-6. Presse Med. 1996. PMID: 8692764 Review. French.

3

Is clonidine growth hormone stimulation a good test to differentiate multiple system atrophy from idiopathic Parkinson's disease?

Tranchant C, Guiraud-Chaumeil C, Echaniz-Laguna A, Warter JM. Tranchant C, et al. J Neurol. 2000 Nov;247(11):853-6. doi: 10.1007/s004150070072. J Neurol. 2000. PMID: 11151417

4

The Miller Fisher syndrome: neurophysiological and MRI evidence of both peripheral and central origin in one case.

Echaniz-Laguna A, Battaglia F, Heymann R, Tranchant C, Warter JM. Echaniz-Laguna A, et al. J Neurol. 2000 Dec;247(12):980-2. doi: 10.1007/s004150070061. J Neurol. 2000. PMID: 11200697 No abstract available.

5

Homozygous exon 7 deletion of the SMN centromeric gene (SMN2): a potential susceptibility factor for adult-onset lower motor neuron disease.

Echaniz-Laguna A, Guiraud-Chaumeil C, Tranchant C, Reeber A, Melki J, Warter JM. Echaniz-Laguna A, et al. J Neurol. 2002 Mar;249(3):290-3. doi: 10.1007/s004150200007. J Neurol. 2002. PMID: 11993528

6

Mitochondrial respiratory chain function in skeletal muscle of ALS patients.

Echaniz-Laguna A, Zoll J, Ribera F, Tranchant C, Warter JM, Lonsdorfer J, Lampert E. Echaniz-Laguna A, et al. Ann Neurol. 2002 Nov;52(5):623-7. doi: 10.1002/ana.10357. Ann Neurol. 2002. PMID: 12402260

7

[Primary Moyamoya disease].

Echaniz-Laguna A, Degos B, Fleury MC, Beaujeux R, Tranchant C. Echaniz-Laguna A, et al. Rev Neurol (Paris). 2002 Nov;158(11):1129-31. Rev Neurol (Paris). 2002. PMID: 12451349 French. No abstract available.

8

A carpenter with dementia.

Degos B, Echaniz-Laguna A, Tranchant C. Degos B, et al. Lancet. 2003 Nov 15;362(9396):1647. doi: 10.1016/S0140-6736(03)14799-X. Lancet. 2003. PMID: 14630447 No abstract available.

9

[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.

10

A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy.

Echaniz-Laguna A, Rousso E, Anheim M, Cossée M, Tranchant C. Echaniz-Laguna A, et al. Neurology. 2005 Apr 26;64(8):1458-60. doi: 10.1212/01.WNL.0000158617.41819.F3. Neurology. 2005. PMID: 15851746

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