Couvert P - Search Results

1

Tuberous xanthomatosis is not necessarily associated with increased plasma concentrations of cholestanol in cerebrotendinous xanthomatosis.

Bonnet JB, Couvert P, Di-Filippo M, Boissiere F, Cristol JP, Sutra T, Cheillan D, Moulin P, Sultan A. Bonnet JB, et al. Among authors: couvert p. J Intern Med. 2023 Jan;293(1):121-123. doi: 10.1111/joim.13568. Epub 2022 Sep 20. J Intern Med. 2023. PMID: 36085581 Free article. No abstract available.

2

COVID-19-associated collapsing glomerulopathy: a report of two cases and literature review.

Izzedine H, Brocheriou I, Arzouk N, Seilhean D, Couvert P, Cluzel P, Pha M, Le Monnier O, Varnous S, Andreelli F, Amoura Z, Mathian A. Izzedine H, et al. Among authors: couvert p. Intern Med J. 2020 Dec;50(12):1551-1558. doi: 10.1111/imj.15041. Intern Med J. 2020. PMID: 33354883 Review.

3

Myoclonus and dystonia in cerebrotendinous xanthomatosis.

Lagarde J, Roze E, Apartis E, Pothalil D, Sedel F, Couvert P, Vidailhet M, Degos B. Lagarde J, et al. Among authors: couvert p. Mov Disord. 2012 Dec;27(14):1805-10. doi: 10.1002/mds.25206. Epub 2012 Oct 31. Mov Disord. 2012. PMID: 23115103 Review.

4

Natural history of cerebrotendinous xanthomatosis: a paediatric disease diagnosed in adulthood.

Degos B, Nadjar Y, Amador Mdel M, Lamari F, Sedel F, Roze E, Couvert P, Mochel F. Degos B, et al. Among authors: couvert p. Orphanet J Rare Dis. 2016 Apr 16;11:41. doi: 10.1186/s13023-016-0419-x. Orphanet J Rare Dis. 2016. PMID: 27084087 Free PMC article.

5

Leukodystrophy with a cerebellar cystic aspect and intracranial atherosclerosis: an atypical presentation of cerebrotendinous xanthomatosis.

Androdias G, Vukusic S, Gignoux L, Boespflug-Tanguy O, Acquaviva C, Zabot MT, Couvert P, Carrie A, Confavreux C, Labauge P. Androdias G, et al. Among authors: couvert p. J Neurol. 2012 Feb;259(2):364-6. doi: 10.1007/s00415-011-6167-x. Epub 2011 Jul 19. J Neurol. 2012. PMID: 21769531 No abstract available.

6

Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease.

Zyss J, Béhin A, Couvert P, Bouhour F, Sassolas A, Kolev I, Denys V, Vial C, Lacour A, Carrié A, Stojkovic T. Zyss J, et al. Among authors: couvert p. J Neurol. 2012 Jun;259(6):1222-6. doi: 10.1007/s00415-011-6340-2. Epub 2011 Dec 17. J Neurol. 2012. PMID: 22179783

7

Lewis-Sumner syndrome and Tangier disease.

Théaudin M, Couvert P, Fournier E, Bouige D, Bruckert E, Perrotte P, Vaschalde Y, Maisonobe T, Bonnefont-Rousselot D, Carrié A, Le Forestier N. Théaudin M, et al. Among authors: couvert p. Arch Neurol. 2008 Jul;65(7):968-70. doi: 10.1001/archneur.65.7.968. Arch Neurol. 2008. PMID: 18625867

8

Ablation of DNA-methyltransferase 3A in skeletal muscle does not affect energy metabolism or exercise capacity.

Small L, Ingerslev LR, Manitta E, Laker RC, Hansen AN, Deeney B, Carrié A, Couvert P, Barrès R. Small L, et al. Among authors: couvert p. PLoS Genet. 2021 Jan 29;17(1):e1009325. doi: 10.1371/journal.pgen.1009325. eCollection 2021 Jan. PLoS Genet. 2021. PMID: 33513138 Free PMC article.

9

Parental origin of de novo MECP2 mutations in Rett syndrome.

Girard M, Couvert P, Carrié A, Tardieu M, Chelly J, Beldjord C, Bienvenu T. Girard M, et al. Among authors: couvert p. Eur J Hum Genet. 2001 Mar;9(3):231-6. doi: 10.1038/sj.ejhg.5200618. Eur J Hum Genet. 2001. PMID: 11313764

10

Loss of parental-specific methylation at the IGF2 locus in human hepatocellular carcinoma.

Poirier K, Chalas C, Tissier F, Couvert P, Mallet V, Carrié A, Marchio A, Sarli D, Gicquel C, Chaussade S, Beljord C, Chelly J, Kerjean A, Terris B. Poirier K, et al. Among authors: couvert p. J Pathol. 2003 Nov;201(3):473-9. doi: 10.1002/path.1477. J Pathol. 2003. PMID: 14595760

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