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Muscle & Nerve|March 20, 2015
Should patients with asymptomatic pompe disease be treated? A nationwide study in FranceAndoni Echaniz-Laguna, Robert-Yves Carlier, Kenza Laloui, et al.
Skeletal Radiology|June 1, 2014
Whole-body muscle MRI to detect myopathies in non-extrapyramidal bent spine syndromeMickaël Ohana, Marie-Christine Durand, Catherine Marty, et al.
BMC Infectious Diseases|July 18, 2020
Predictive factors for positive disco-vertebral biopsy culture in pyogenic vertebral osteomyelitis, and impact of fluoroscopic versus scanographic guidanceCaroline Diffre, Camille Jousset, Anne-Laure Roux, et al.
Molecular Genetics and Metabolism Reports|June 2, 2020
Glycogenin-1 deficiency mimicking limb-girdle muscular dystrophyClaire Lefeuvre, Stéphane Schaeffer, Robert-Yves Carlier, et al.
Neuromuscular Disorders : NMD|August 2, 2011
Whole-body muscle MRI in 20 patients suffering from late onset Pompe disease: Involvement patternsRobert-Yves Carlier, Pascal Laforet, Claire Wary, et al.
Neuromuscular Disorders : NMD|October 29, 2021
Whole-body muscle MRI in McArdle diseaseDavid Tobaly, Pascal Laforêt, Tanya Stojkovic, et al.
European Journal of Radiology|April 14, 2024
Neurogenic heterotopic ossification of the hip: Magnetic resonance imaging versus computed tomography for pre-surgical assessmentRaphaël Amar, Marjorie Salga, Mickaël Tordjman, et al.
Journal of Medical Genetics|September 9, 2020
RASA1 phenotype overlaps with hereditary haemorrhagic telangiectasia: two case reportsMostafa El Hajjam, Ahmed Mekki, Aurelien Palmyre, et al.
Molecular Genetics and Metabolism|January 22, 2013
Neutral lipid storage disease with myopathy: a whole-body nuclear MRI and metabolic studyPascal Laforêt, Tanya Stojkovic, Guillaume Bassez, et al.
Neuromuscular Disorders : NMD|August 23, 2016
A novel neuromuscular form of glycogen storage disease type IV with arthrogryposis, spinal stiffness and rare polyglucosan bodies in muscleEdoardo Malfatti, Christine Barnerias, Carola Hedberg-Oldfors, et al.
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