Ferre M - Search Results

1

Hereditary optic neuropathies share a common mitochondrial coupling defect.

Chevrollier A, Guillet V, Loiseau D, Gueguen N, de Crescenzo MA, Verny C, Ferre M, Dollfus H, Odent S, Milea D, Goizet C, Amati-Bonneau P, Procaccio V, Bonneau D, Reynier P. Chevrollier A, et al. Among authors: ferre m. Ann Neurol. 2008 Jun;63(6):794-8. doi: 10.1002/ana.21385. Ann Neurol. 2008. PMID: 18496845 Free article.

2

Sporadic optic atrophy due to synonymous codon change altering mRNA splicing of OPA1.

Amati-Bonneau P, Pasquier L, Lainey E, Ferré M, Odent S, Malthièry Y, Bonneau D, Reynier P. Amati-Bonneau P, et al. Among authors: ferre m. Clin Genet. 2005 Jan;67(1):102-3. doi: 10.1111/j.1399-0004.2004.00358.x. Clin Genet. 2005. PMID: 15617556 No abstract available.

3

Mitochondrial diseases preferentially involve proteins with prokaryote homologues.

Tourmen Y, Ferré M, Malthièry Y, Dessen P, Reynier P. Tourmen Y, et al. Among authors: ferre m. C R Biol. 2004 Dec;327(12):1095-101. doi: 10.1016/j.crvi.2004.09.005. C R Biol. 2004. PMID: 15656352 Free article.

4

eOPA1: an online database for OPA1 mutations.

Ferré M, Amati-Bonneau P, Tourmen Y, Malthièry Y, Reynier P. Ferré M, et al. Hum Mutat. 2005 May;25(5):423-8. doi: 10.1002/humu.20161. Hum Mutat. 2005. PMID: 15832306

5

Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease.

Loiseau D, Chevrollier A, Verny C, Guillet V, Gueguen N, Pou de Crescenzo MA, Ferré M, Malinge MC, Guichet A, Nicolas G, Amati-Bonneau P, Malthièry Y, Bonneau D, Reynier P. Loiseau D, et al. Among authors: ferre m. Ann Neurol. 2007 Apr;61(4):315-23. doi: 10.1002/ana.21086. Ann Neurol. 2007. PMID: 17444508

6

Carotid artery dissection in an adult with the Simpson-Golabi-Behmel syndrome.

Pénisson-Besnier I, Lebouvier T, Moizard MP, Ferré M, Barth M, Marc G, Raynaud M, Bonneau D. Pénisson-Besnier I, et al. Among authors: ferre m. Am J Med Genet A. 2008 Feb 15;146A(4):464-7. doi: 10.1002/ajmg.a.32154. Am J Med Genet A. 2008. PMID: 18203194

7

Reversible optic neuropathy with OPA1 exon 5b mutation.

Cornille K, Milea D, Amati-Bonneau P, Procaccio V, Zazoun L, Guillet V, El Achouri G, Delettre C, Gueguen N, Loiseau D, Muller A, Ferré M, Chevrollier A, Wallace DC, Bonneau D, Hamel C, Reynier P, Lenaers G. Cornille K, et al. Among authors: ferre m. Ann Neurol. 2008 May;63(5):667-71. doi: 10.1002/ana.21376. Ann Neurol. 2008. PMID: 18360822 Free article.

8

Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).

Cassereau J, Chevrollier A, Gueguen N, Malinge MC, Letournel F, Nicolas G, Richard L, Ferre M, Verny C, Dubas F, Procaccio V, Amati-Bonneau P, Bonneau D, Reynier P. Cassereau J, et al. Among authors: ferre m. Neurogenetics. 2009 Apr;10(2):145-50. doi: 10.1007/s10048-008-0166-9. Epub 2008 Dec 17. Neurogenetics. 2009. PMID: 19089472

9

Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.

Ferré M, Bonneau D, Milea D, Chevrollier A, Verny C, Dollfus H, Ayuso C, Defoort S, Vignal C, Zanlonghi X, Charlin JF, Kaplan J, Odent S, Hamel CP, Procaccio V, Reynier P, Amati-Bonneau P. Ferré M, et al. Hum Mutat. 2009 Jul;30(7):E692-705. doi: 10.1002/humu.21025. Hum Mutat. 2009. PMID: 19319978 Free article.

10

Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect.

Nochez Y, Arsene S, Gueguen N, Chevrollier A, Ferré M, Guillet V, Desquiret V, Toutain A, Bonneau D, Procaccio V, Amati-Bonneau P, Pisella PJ, Reynier P. Nochez Y, et al. Among authors: ferre m. Mol Vis. 2009;15:598-608. Epub 2009 Mar 27. Mol Vis. 2009. PMID: 19325939 Free PMC article.

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