Laforêt P - Search Results

1

Genetic Mutations and Demographic, Clinical, and Morphological Aspects of Myofibrillar Myopathy in a French Cohort.

Carvalho AAS, Lacene E, Brochier G, Labasse C, Madelaine A, Silva VGD, Corazzini R, Papadopoulos K, Behin A, Laforêt P, Stojkovic T, Eymard B, Fardeau M, Romero N. Carvalho AAS, et al. Among authors: laforet p. Genet Test Mol Biomarkers. 2018 Jun;22(6):374-383. doi: 10.1089/gtmb.2018.0004. Genet Test Mol Biomarkers. 2018. PMID: 29924655

2

Evaluation of muscle glycogen content by 13C NMR spectroscopy in adult-onset acid maltase deficiency.

Wary C, Laforêt P, Eymard B, Fardeau M, Leroy-Willig A, Bassez G, Leroy JP, Caillaud C, Poenaru L, Carlier PG. Wary C, et al. Among authors: laforet p. Neuromuscul Disord. 2003 Sep;13(7-8):545-53. doi: 10.1016/s0960-8966(03)00069-5. Neuromuscul Disord. 2003. PMID: 12921791

3

Clinical study of chronic pain in hereditary myopathies.

Delorme T, Boureau F, Eymard B, Laforet P, Cottrel F. Delorme T, et al. Among authors: laforet p. Eur J Pain. 2004 Feb;8(1):55-61. doi: 10.1016/S1090-3801(03)00076-4. Eur J Pain. 2004. PMID: 14690675

4

Electromyography guides toward subgroups of mutations in muscle channelopathies.

Fournier E, Arzel M, Sternberg D, Vicart S, Laforet P, Eymard B, Willer JC, Tabti N, Fontaine B. Fournier E, et al. Among authors: laforet p. Ann Neurol. 2004 Nov;56(5):650-61. doi: 10.1002/ana.20241. Ann Neurol. 2004. PMID: 15389891 Clinical Trial.

5

Exercise tolerance and daily life in McArdle's disease.

Ollivier K, Hogrel JY, Gomez-Merino D, Romero NB, Laforêt P, Eymard B, Portero P. Ollivier K, et al. Among authors: laforet p. Muscle Nerve. 2005 May;31(5):637-41. doi: 10.1002/mus.20251. Muscle Nerve. 2005. PMID: 15614801

6

Mutations in dynamin 2 cause dominant centronuclear myopathy.

Bitoun M, Maugenre S, Jeannet PY, Lacène E, Ferrer X, Laforêt P, Martin JJ, Laporte J, Lochmüller H, Beggs AH, Fardeau M, Eymard B, Romero NB, Guicheney P. Bitoun M, et al. Among authors: laforet p. Nat Genet. 2005 Nov;37(11):1207-9. doi: 10.1038/ng1657. Epub 2005 Oct 16. Nat Genet. 2005. PMID: 16227997 Free article.

7

A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis.

Laforêt P, Richard P, Said MA, Romero NB, Lacene E, Leroy JP, Baussan C, Hogrel JY, Lavergne T, Wahbi K, Hainque B, Duboc D. Laforêt P, et al. Neuromuscul Disord. 2006 Mar;16(3):178-82. doi: 10.1016/j.nmd.2005.12.004. Epub 2006 Feb 17. Neuromuscul Disord. 2006. PMID: 16487706

8

Characterization of the muscle involvement in dynamin 2-related centronuclear myopathy.

Fischer D, Herasse M, Bitoun M, Barragán-Campos HM, Chiras J, Laforêt P, Fardeau M, Eymard B, Guicheney P, Romero NB. Fischer D, et al. Among authors: laforet p. Brain. 2006 Jun;129(Pt 6):1463-9. doi: 10.1093/brain/awl071. Epub 2006 Apr 3. Brain. 2006. PMID: 16585051

9

Cold extends electromyography distinction between ion channel mutations causing myotonia.

Fournier E, Viala K, Gervais H, Sternberg D, Arzel-Hézode M, Laforêt P, Eymard B, Tabti N, Willer JC, Vial C, Fontaine B. Fournier E, et al. Among authors: laforet p. Ann Neurol. 2006 Sep;60(3):356-65. doi: 10.1002/ana.20905. Ann Neurol. 2006. PMID: 16786525

10

Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression?

Auré K, Ogier de Baulny H, Laforêt P, Jardel C, Eymard B, Lombès A. Auré K, et al. Among authors: laforet p. Brain. 2007 Jun;130(Pt 6):1516-24. doi: 10.1093/brain/awm067. Epub 2007 Apr 17. Brain. 2007. PMID: 17439982

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