Chateau D - Search Results

1

Functional mitochondrial heterogeneity in heteroplasmic cells carrying the mitochondrial DNA mutation associated with the MELAS syndrome (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes).

Bakker A, Barthélémy C, Frachon P, Chateau D, Sternberg D, Mazat JP, Lombès A. Bakker A, et al. Among authors: chateau d. Pediatr Res. 2000 Aug;48(2):143-50. doi: 10.1203/00006450-200008000-00005. Pediatr Res. 2000. PMID: 10926287

2

Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo.

Rojo M, Legros F, Chateau D, Lombès A. Rojo M, et al. Among authors: chateau d. J Cell Sci. 2002 Apr 15;115(Pt 8):1663-74. doi: 10.1242/jcs.115.8.1663. J Cell Sci. 2002. PMID: 11950885

3

[Exercise intolerance caused by muscular phosphorylase kinase deficiency. Contribution of in vivo metabolic studies].

Laforêt P, Eymard B, Lombès A, Duboc D, Jehenson P, Rocchiccioli F, Chaussain M, Chateau D, Brunet P, Fardeau M. Laforêt P, et al. Among authors: chateau d. Rev Neurol (Paris). 1996 Jun-Jul;152(6-7):458-64. Rev Neurol (Paris). 1996. PMID: 8944243 Review. French.

4

[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene].

Fardeau M, Vicart P, Caron A, Chateau D, Chevallay M, Collin H, Chapon F, Duboc D, Eymard B, Tomé FM, Dupret JM, Paulin D, Guicheney P. Fardeau M, et al. Among authors: chateau d. Rev Neurol (Paris). 2000 May;156(5):497-504. Rev Neurol (Paris). 2000. PMID: 10844369 French.

5

X-linked vacuolated myopathy: complement membrane attack complex on surface membrane of injured muscle fibers.

Villanova M, Louboutin JP, Chateau D, Eymard B, Sagniez M, Tomé FM, Fardeau M. Villanova M, et al. Among authors: chateau d. Ann Neurol. 1995 May;37(5):637-45. doi: 10.1002/ana.410370514. Ann Neurol. 1995. PMID: 7755359

6

A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathy.

Vicart P, Caron A, Guicheney P, Li Z, Prévost MC, Faure A, Chateau D, Chapon F, Tomé F, Dupret JM, Paulin D, Fardeau M. Vicart P, et al. Among authors: chateau d. Nat Genet. 1998 Sep;20(1):92-5. doi: 10.1038/1765. Nat Genet. 1998. PMID: 9731540

7

Multi-minicore disease--searching for boundaries: phenotype analysis of 38 cases.

Ferreiro A, Estournet B, Chateau D, Romero NB, Laroche C, Odent S, Toutain A, Cabello A, Fontan D, dos Santos HG, Haenggeli CA, Bertini E, Urtizberea JA, Guicheney P, Fardeau M. Ferreiro A, et al. Among authors: chateau d. Ann Neurol. 2000 Nov;48(5):745-57. Ann Neurol. 2000. PMID: 11079538

8

Apolipoprotein A-II is catabolized in the kidney as a function of its plasma concentration.

Dugué-Pujol S, Rousset X, Château D, Pastier D, Klein C, Demeurie J, Cywiner-Golenzer C, Chabert M, Verroust P, Chambaz J, Châtelet FP, Kalopissis AD. Dugué-Pujol S, et al. Among authors: chateau d. J Lipid Res. 2007 Oct;48(10):2151-61. doi: 10.1194/jlr.M700089-JLR200. Epub 2007 Jul 24. J Lipid Res. 2007. PMID: 17652309 Free article.

9

Morphological changes in muscle fibers in oculopharyngeal muscular dystrophy.

Tomé FM, Chateau D, Helbling-Leclerc A, Fardeau M. Tomé FM, et al. Among authors: chateau d. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S63-9. doi: 10.1016/s0960-8966(97)00085-0. Neuromuscul Disord. 1997. PMID: 9392019

10

Autosomal dominant late adult onset distal leg myopathy.

Pénisson-Besnier I, Dumez C, Chateau D, Dubas F, Fardeau M. Pénisson-Besnier I, et al. Among authors: chateau d. Neuromuscul Disord. 1998 Oct;8(7):459-66. doi: 10.1016/s0960-8966(98)00063-7. Neuromuscul Disord. 1998. PMID: 9829275

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