Laforêt P - Search Results

1

Whole-Body Muscle Magnetic Resonance Imaging in Glycogen-Storage Disease Type III.

Tobaly D, Laforêt P, Perry A, Habes D, Labrune P, Decostre V, Masingue M, Petit F, Barp A, Bello L, Carlier P, Carlier RY. Tobaly D, et al. Among authors: laforet p. Muscle Nerve. 2019 Jul;60(1):72-79. doi: 10.1002/mus.26483. Epub 2019 Apr 24. Muscle Nerve. 2019. PMID: 30972778

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

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

4

Muscle glycogenosis due to phosphoglucomutase 1 deficiency.

Stojkovic T, Vissing J, Petit F, Piraud M, Orngreen MC, Andersen G, Claeys KG, Wary C, Hogrel JY, Laforêt P. Stojkovic T, et al. Among authors: laforet p. N Engl J Med. 2009 Jul 23;361(4):425-7. doi: 10.1056/NEJMc0901158. N Engl J Med. 2009. PMID: 19625727 No abstract available.

5

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

6

Investigating glycogenosis type III patients with multi-parametric functional NMR imaging and spectroscopy.

Wary C, Nadaj-Pakleza A, Laforêt P, Claeys KG, Carlier R, Monnet A, Fleury S, Baligand C, Eymard B, Labrune P, Carlier PG. Wary C, et al. Among authors: laforet p. Neuromuscul Disord. 2010 Aug;20(8):548-58. doi: 10.1016/j.nmd.2010.06.011. Neuromuscul Disord. 2010. PMID: 20620060

7

Recombinant human acid alpha-glucosidase (rhGAA) in adult patients with severe respiratory failure due to Pompe disease.

Orlikowski D, Pellegrini N, Prigent H, Laforêt P, Carlier R, Carlier P, Eymard B, Lofaso F, Annane D. Orlikowski D, et al. Among authors: laforet p. Neuromuscul Disord. 2011 Jul;21(7):477-82. doi: 10.1016/j.nmd.2011.04.001. Epub 2011 May 6. Neuromuscul Disord. 2011. PMID: 21550241 Clinical Trial.

8

Whole-body muscle MRI in 20 patients suffering from late onset Pompe disease: Involvement patterns.

Carlier RY, Laforet P, Wary C, Mompoint D, Laloui K, Pellegrini N, Annane D, Carlier PG, Orlikowski D. Carlier RY, et al. Among authors: laforet p. Neuromuscul Disord. 2011 Nov;21(11):791-9. doi: 10.1016/j.nmd.2011.06.748. Epub 2011 Jul 30. Neuromuscul Disord. 2011. PMID: 21803581

9

Juvenile-onset permanent weakness in muscle phosphofructokinase deficiency.

Malfatti E, Birouk N, Romero NB, Piraud M, Petit FM, Hogrel JY, Laforêt P. Malfatti E, et al. Among authors: laforet p. J Neurol Sci. 2012 May 15;316(1-2):173-7. doi: 10.1016/j.jns.2012.01.027. Epub 2012 Feb 23. J Neurol Sci. 2012. PMID: 22364848

10

Muscle MRI findings in limb girdle muscular dystrophy type 2L.

Sarkozy A, Deschauer M, Carlier RY, Schrank B, Seeger J, Walter MC, Schoser B, Reilich P, Leturq F, Radunovic A, Behin A, Laforet P, Eymard B, Schreiber H, Hicks D, Vaidya SS, Gläser D, Carlier PG, Bushby K, Lochmüller H, Straub V. Sarkozy A, et al. Among authors: laforet p. Neuromuscul Disord. 2012 Oct 1;22 Suppl 2:S122-9. doi: 10.1016/j.nmd.2012.05.012. Neuromuscul Disord. 2012. PMID: 22980763

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