Laforêt P - Search Results

1

The role of electrodiagnosis with long exercise test in mcardle disease.

Semplicini C, Hézode-Arzel M, Laforêt P, Béhin A, Leonard-Louis S, Hogrel JY, Petit F, Eymard B, Stojkovic T, Fournier E. Semplicini C, et al. Among authors: laforet p. Muscle Nerve. 2018 Jan 19. doi: 10.1002/mus.26074. Online ahead of print. Muscle Nerve. 2018. PMID: 29350794

2

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

3

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.

4

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

5

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

6

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

7

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

8

Long-term results of cricopharyngeal myotomy in oculopharyngeal muscular dystrophy.

Coiffier L, Périé S, Laforêt P, Eymard B, St Guily JL. Coiffier L, et al. Among authors: laforet p. Otolaryngol Head Neck Surg. 2006 Aug;135(2):218-22. doi: 10.1016/j.otohns.2006.03.015. Otolaryngol Head Neck Surg. 2006. PMID: 16890071

9

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

10

Severe neonatal myasthenia due to maternal anti-MuSK antibodies.

Béhin A, Mayer M, Kassis-Makhoul B, Jugie M, Espil-Taris C, Ferrer X, Chatenoud L, Laforêt P, Eymard B. Béhin A, et al. Among authors: laforet p. Neuromuscul Disord. 2008 Jun;18(6):443-6. doi: 10.1016/j.nmd.2008.03.006. Epub 2008 Apr 22. Neuromuscul Disord. 2008. PMID: 18434154

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