Martin-Negrier ML - Search Results

1

Primitive malignant fibrous histiocytoma of the neck with carotid occlusion and multiple cerebral ischemic lesions.

Martin-Negrier ML, Belleannee G, Vital C, Orgogozo JM. Martin-Negrier ML, et al. Stroke. 1996 Mar;27(3):536-7. doi: 10.1161/01.str.27.3.536. Stroke. 1996. PMID: 8610325

2

[Oncocytic carcinoma of the parotid gland].

Martin Negrier ML, Rivel J, Vital C, Pinsolle J. Martin Negrier ML, et al. Ann Pathol. 1991;11(5-6):359-62. Ann Pathol. 1991. PMID: 1804158 French.

3

Simultaneous development of two different B-cell lymphomas in a patient with acquired immune deficiency syndrome evidenced by molecular analysis.

Dubus P, MacGrogan G, Vital C, Martin-Négrier ML, Morlat P, Ragnaud JM, de Mascarel A, Bloch B, Merlio JP. Dubus P, et al. Mod Pathol. 1995 Oct;8(8):825-9. Mod Pathol. 1995. PMID: 8552570

4

Peripheral neuropathy associated with mitochondrial disorders: 8 cases and review of the literature.

Bouillot S, Martin-Négrier ML, Vital A, Ferrer X, Lagueny A, Vincent D, Coquet M, Orgogozo JM, Bloch B, Vita C. Bouillot S, et al. J Peripher Nerv Syst. 2002 Dec;7(4):213-20. doi: 10.1046/j.1529-8027.2002.02027.x. J Peripher Nerv Syst. 2002. PMID: 12477166 Review.

5

Concurrent herpes simplex type 1 necrotizing encephalitis, cytomegalovirus ventriculoencephalitis and cerebral lymphoma in an AIDS patient.

Vital C, Monlun E, Vital A, Martin-Negrier ML, Cales V, Leger F, Longy-Boursier M, Le Bras M, Bloch B. Vital C, et al. Acta Neuropathol. 1995;89(1):105-8. doi: 10.1007/BF00294267. Acta Neuropathol. 1995. PMID: 7709722

6

Lhermitte-Duclos type cerebellum hamartoma and Cowden disease.

Vital A, Vital C, Martin-Negrier ML, McGrogan G, Bioulac P, Trojani M, Loiseau H, Rougier A. Vital A, et al. Clin Neuropathol. 1994 Jul-Aug;13(4):229-31. Clin Neuropathol. 1994. PMID: 7955671

7

Parkinsonism in a patient with Leber hereditary optic neuropathy (LHON).

Vital C, Julien J, Martin-Negrier ML, Lagueny A, Ferrer X, Vital A. Vital C, et al. Rev Neurol (Paris). 2015 Sep;171(8-9):679-80. doi: 10.1016/j.neurol.2015.03.011. Epub 2015 Apr 24. Rev Neurol (Paris). 2015. PMID: 25917160 Review. No abstract available.

8

TWINKLE gene mutation: report of a French family with an autosomal dominant progressive external ophthalmoplegia and literature review.

Martin-Negrier ML, Sole G, Jardel C, Vital C, Ferrer X, Vital A. Martin-Negrier ML, et al. Eur J Neurol. 2011 Mar;18(3):436-41. doi: 10.1111/j.1468-1331.2010.03171.x. Epub 2010 Sep 29. Eur J Neurol. 2011. PMID: 20880070 Review.

9

Ontogeny of the striatal neurons expressing neuropeptide genes in the human fetus and neonate.

Brana C, Charron G, Aubert I, Carles D, Martin-Negrier ML, Trouette H, Fournier MC, Vital C, Bloch B. Brana C, et al. J Comp Neurol. 1995 Sep 25;360(3):488-505. doi: 10.1002/cne.903600310. J Comp Neurol. 1995. PMID: 8543654

10

[Diagnostic procedure of limb girdle muscular dystrophies 2A or calpainopathies: French cohort from a neuromuscular center (Bordeaux)].

Perez F, Vital A, Martin-Negrier ML, Ferrer X, Sole G. Perez F, et al. Rev Neurol (Paris). 2010 May;166(5):502-8. doi: 10.1016/j.neurol.2009.10.015. Epub 2009 Dec 30. Rev Neurol (Paris). 2010. PMID: 20044116 French.

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