Laforêt P - Search Results

1

Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry).

Pinós T, Andreu AL, Bruno C, Hadjigeorgiou GM, Haller RG, Laforêt P, Lucía A, Martín MA, Martinuzzi A, Navarro C, Oflazer P, Pouget J, Quinlivan R, Sacconi S, Scalco RS, Toscano A, Vissing J, Vorgerd M, Wakelin A, Martí R; EUROMAC Consortium. Pinós T, et al. Among authors: laforet p. Orphanet J Rare Dis. 2020 Oct 15;15(1):187. doi: 10.1186/s13023-020-01455-z. Orphanet J Rare Dis. 2020. PMID: 33054807 Free PMC article.

2

Permanent muscle weakness in McArdle disease.

Nadaj-Pakleza AA, Vincitorio CM, Laforêt P, Eymard B, Dion E, Teijeira S, Vietez I, Jeanpierre M, Navarro C, Stojkovic T. Nadaj-Pakleza AA, et al. Among authors: laforet p. Muscle Nerve. 2009 Sep;40(3):350-7. doi: 10.1002/mus.21351. Muscle Nerve. 2009. PMID: 19670320

3

162nd ENMC International Workshop: Disorders of muscle lipid metabolism in adults 28-30 November 2008, Bussum, The Netherlands.

Laforêt P, Vianey-Saban C, Vissing J. Laforêt P, et al. Neuromuscul Disord. 2010 Apr;20(4):283-9. doi: 10.1016/j.nmd.2010.01.010. Epub 2010 Mar 23. Neuromuscul Disord. 2010. PMID: 20335037 No abstract available.

4

Molecular and clinical study of McArdle's disease in a cohort of 123 European patients. Identification of 20 novel mutations.

Vieitez I, Teijeira S, Fernandez JM, San Millan B, Miranda S, Ortolano S, Louis S, Laforet P, Navarro C. Vieitez I, et al. Among authors: laforet p. Neuromuscul Disord. 2011 Dec;21(12):817-23. doi: 10.1016/j.nmd.2011.07.002. Epub 2011 Jul 29. Neuromuscul Disord. 2011. PMID: 21802952

5

Blocked muscle fat oxidation during exercise in neutral lipid storage disease.

Laforêt P, Ørngreen M, Preisler N, Andersen G, Vissing J. Laforêt P, et al. Arch Neurol. 2012 Apr;69(4):530-3. doi: 10.1001/archneurol.2011.631. Arch Neurol. 2012. PMID: 22491199

6

Fat and carbohydrate metabolism during exercise in late-onset Pompe disease.

Preisler N, Laforet P, Madsen KL, Hansen RS, Lukacs Z, Ørngreen MC, Lacour A, Vissing J. Preisler N, et al. Among authors: laforet p. Mol Genet Metab. 2012 Nov;107(3):462-8. doi: 10.1016/j.ymgme.2012.08.019. Epub 2012 Aug 31. Mol Genet Metab. 2012. PMID: 22981821

7

Exercise intolerance in Glycogen Storage Disease Type III: weakness or energy deficiency?

Preisler N, Pradel A, Husu E, Madsen KL, Becquemin MH, Mollet A, Labrune P, Petit F, Hogrel JY, Jardel C, Maillot F, Vissing J, Laforêt P. Preisler N, et al. Among authors: laforet p. Mol Genet Metab. 2013 May;109(1):14-20. doi: 10.1016/j.ymgme.2013.02.008. Epub 2013 Feb 19. Mol Genet Metab. 2013. PMID: 23507172

8

Fat and carbohydrate metabolism during exercise in phosphoglucomutase type 1 deficiency.

Preisler N, Laforêt P, Echaniz-Laguna A, Ørngreen MC, Lonsdorfer-Wolf E, Doutreleau S, Geny B, Stojkovic T, Piraud M, Petit FM, Vissing J. Preisler N, et al. Among authors: laforet p. J Clin Endocrinol Metab. 2013 Jul;98(7):E1235-40. doi: 10.1210/jc.2013-1651. Epub 2013 Jun 18. J Clin Endocrinol Metab. 2013. PMID: 23780368

9

Bezafibrate in skeletal muscle fatty acid oxidation disorders: a randomized clinical trial.

Ørngreen MC, Madsen KL, Preisler N, Andersen G, Vissing J, Laforêt P. Ørngreen MC, et al. Among authors: laforet p. Neurology. 2014 Feb 18;82(7):607-13. doi: 10.1212/WNL.0000000000000118. Epub 2014 Jan 22. Neurology. 2014. PMID: 24453079 Free PMC article. Clinical Trial.

10

Atrio-ventricular block requiring pacemaker in patients with late onset Pompe disease.

Sacconi S, Wahbi K, Theodore G, Garcia J, Salviati L, Bouhour F, Vial C, Duboc D, Laforêt P, Desnuelle C. Sacconi S, et al. Among authors: laforet p. Neuromuscul Disord. 2014 Jul;24(7):648-50. doi: 10.1016/j.nmd.2014.04.005. Epub 2014 Apr 24. Neuromuscul Disord. 2014. PMID: 24844452

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