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Medecine Sciences : M/S|January 11, 2021
[Limb-Girdle Muscular Dystrophy type R9 linked to the FKRP gene: state of the art and therapeutic perspectives]Rocío Nur Villar Quiles, Isabelle Richard, Céline Bouchet-Seraphin, et al.
Neuromuscular Disorders : NMD|January 11, 2025
Chronic pain as a presenting feature of dysferlinopathyLucia Sanchez-Casado, Teresinha Evangelista, Juliette Nectoux, et al.
Skeletal Radiology|May 8, 2010
Morphologic imaging in muscular dystrophies and inflammatory myopathiesAdrian Degardin, David Morillon, Arnaud Lacour, et al.
Muscle & Nerve|March 28, 2003
Phrenic nerve palsy as a feature of chronic inflammatory demyelinating polyradiculoneuropathyTanya Stojkovic, Jérôme De Seze, Jean-François Hurtevent, et al.
Skeletal Muscle|September 28, 2011
ColVI myopathies: where do we stand, where do we go?Valérie Allamand, Laura Briñas, Pascale Richard, et al.
Muscle & Nerve|February 23, 2017
Rigid spine syndrome associated with sensory-motor axonal neuropathy resembling Charcot-Marie-Tooth disease is characteristic of Bcl-2-associated athanogene-3 gene mutations even without cardiac involvementJean-Baptiste Noury, Thierry Maisonobe, Pascale Richard, et al.
Neurogenetics|February 4, 2018
WES homozygosity mapping in a recessive form of Charcot-Marie-Tooth neuropathy reveals intronic GDAP1 variant leading to a premature stop codonMarion Masingue, Jimmy Perrot, Robert-Yves Carlier, et al.
Neuromuscular Disorders : NMD|April 9, 2008
A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: clinical and pathological findingsMarc Bitoun, Tanya Stojkovic, Bernard Prudhon, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|June 20, 2003
Multiple sclerosis and depression: influence of interferon beta therapyHélène Zephir, Jérôme De Seze, Tanya Stojkovic, et al.
Neurology|December 25, 2016
Correlation between PABPN1 genotype and disease severity in oculopharyngeal muscular dystrophyPascale Richard, Capucine Trollet, Tanya Stojkovic, et al.
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