Lyon-Caen O - Search Results

1

[A case of mitochondrial cytopathy (MERFF) without ragged red fibers at the onset].

Gignoux L, Maisonobe T, Laforet P, Lombès A, Lyon-Caen O, Fontaine B. Gignoux L, et al. Rev Neurol (Paris). 2001 Apr;157(4):427-9. Rev Neurol (Paris). 2001. PMID: 11398016 French.

2

[Immunology of multiple sclerosis. Recent data and therapeutic perspectives].

Tourbah A, Fontaine B, Lyon-Caen O. Tourbah A, et al. Rev Neurol (Paris). 1993;149(6-7):373-84. Rev Neurol (Paris). 1993. PMID: 8303156 Review. French.

3

[Andermann syndrome in an Algerian family: suggestion of phenotype and genetic homogeneity].

Lesca G, Cournu-Rebeix I, Azoulay-Cayla A, Lyon-Caen O, Barois A, Dulac O, Fontaine B. Lesca G, et al. Rev Neurol (Paris). 2001 Oct;157(10):1279-81. Rev Neurol (Paris). 2001. PMID: 11885521 French.

4

[Acute optic neuritis: clinical and MRI prognostic factors. Study of fifty patients].

Deschamps R, Gout O, Fontaine B, Rigolet MH, Cabanis EA, Lyon-Caen O, Tourbah A. Deschamps R, et al. Rev Neurol (Paris). 2002 Apr;158(4):446-52. Rev Neurol (Paris). 2002. PMID: 11984487 French.

5

[Adult onset hereditary leukoencephalopathies].

Sedel F, Tourbah A, Baumann N, Fontaine B, Aubourg P, Lubetzki C, Lyon-Caen O. Sedel F, et al. Rev Neurol (Paris). 2005 Oct;161(10):916-31. doi: 10.1016/s0035-3787(05)85155-0. Rev Neurol (Paris). 2005. PMID: 16365621 Review. French.

6

[Trigeminal neuralgia. Diagnosis].

Fontaine B, Lyon-Caen O. Fontaine B, et al. Rev Prat. 1995 Apr 15;45(8):999-1000. Rev Prat. 1995. PMID: 7761785 French. No abstract available.

7

[Symptomatic heterozygotic adrenoleukodystrophy in adults. 10 cases].

Ménage P, Carreau V, Tourbah A, Fontaine B, Paturneau-Jouas M, Gout O, Lubetzki C, Baumann N, Lyon-Caen O. Ménage P, et al. Rev Neurol (Paris). 1993;149(8-9):445-54. Rev Neurol (Paris). 1993. PMID: 8009141 Review. French.

8

[Nitric-oxide triggered neurological disorders in subjects with vitamin B12 deficiency].

Cohen Aubart F, Sedel F, Vicart S, Lyon-Caen O, Fontaine B. Cohen Aubart F, et al. Rev Neurol (Paris). 2007 Mar;163(3):362-4. doi: 10.1016/s0035-3787(07)90409-9. Rev Neurol (Paris). 2007. PMID: 17404524 French.

9

Hereditary thermosensitive neuropathy: an autosomal dominant disorder of the peripheral nervous system.

Magy L, Birouk N, Vallat JM, Gouider R, Maisonobe T, Bouche P, Lyon-Caen O, Fontaine B. Magy L, et al. Neurology. 1997 Jun;48(6):1684-90. doi: 10.1212/wnl.48.6.1684. Neurology. 1997. PMID: 9191787

10

[Prognosis of multiple sclerosis could be related to damage in white matter with a normal MRI appearance].

Tourbah A, Fontaine B, Cabanis EA, Lyon-Caen O. Tourbah A, et al. Rev Neurol (Paris). 2000 Jul;156(6-7):591-3. Rev Neurol (Paris). 2000. PMID: 10891792 French. No abstract available.

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