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Profil bibliographique

Claire Wary

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

75Publications signalées
2106Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Advanced MRI Techniques and ApplicationsMuscle Physiology and DisordersCardiovascular and exercise physiologyGlycogen Storage Diseases and MyoclonusMitochondrial Function and Pathology

Les publications récentes

Accès ouvert 2016 article OpenAlex

Longitudinal functional and NMR assessment of upper limbs in Duchenne muscular dystrophy

Jean‐Yves Hogrel, Claire Wary, Amélie Moraux, Noura Azzabou et autres

OBJECTIVE: To explore the value of nuclear magnetic resonance (NMR) and functional assessments for follow-up of ambulatory and nonambulatory patients with Duchenne muscular dystrophy (DMD). METHODS: Twenty-five 53-skippable patients with DMD were included in this study; 15 were nonambulatory at baseline. All …

fr (code pays fourni par la source)

76 citations Neurology
Accès ouvert 2015 article OpenAlex

Response

Russell S. Richardson, Claire Wary, David Walter Wray, Jan Hoff et autres

Dear Editor-in-Chief, We thank Murias and Paterson (4) for their interest in our work and for raising two important questions about our recent publication (6) in Medicine & Science in Sports & Exercise. This article provides evidence that deoxygenated myoglobin (deoxy-Mb) accumulation, …

us, no, fr (code pays fourni par la source)

0 citations Medicine & Science in Sports & Exercise
2015 article OpenAlex

Quantitative NMRI and NMRS identify augmented disease progression after loss of ambulation in forearms of boys with Duchenne muscular dystrophy

Claire Wary, Noura Azzabou, Céline Giraudeau, Julien Le Louër et autres

Quantitative NMRI and (31)P NMRS indices are reported in the forearms of 24 patients with Duchenne muscular dystrophy (DMD) (6-18 years, 14 non-ambulant) amenable to exon 53 skipping therapy and in 12 age-matched male controls (CONT). Examinations carried out at 3 T …

fr (code pays fourni par la source)

70 citations NMR in Biomedicine
Accès ouvert 2015 article OpenAlex

MRS Evidence of Adequate O2 Supply in Human Skeletal Muscle at the Onset of Exercise

Russell S. Richardson, Claire Wary, David Walter Wray, Jan Hoff et autres

PURPOSE: At exercise onset, intramuscular oxidative energy production responds relatively slowly in comparison with the change in adenosine triphosphate demand. To determine whether the slow kinetics of oxidative adenosine triphosphate production is due to inadequate O2 supply or metabolic inertia, we studied …

us, fr, no (code pays fourni par la source)

36 citations Medicine & Science in Sports & Exercise
Accès ouvert 2015 article OpenAlex

Skeletal muscle quantitative nuclear magnetic resonance imaging follow‐up of adult Pompe patients

Pierre G. Carlier, Noura Azzabou, Paulo Loureiro de Sousa, Arnaud Hicks et autres

Adult late-onset Pompe disease is most often a slowly progressive limb-girdle and spine extensor muscle dystrophy, due to defective lysosomal acid maltase. With the exception of the few patients who present with a dramatically accelerated clinical course, standard diagnostic imaging fail to …

fr (code pays fourni par la source)

109 citations Journal of Inherited Metabolic Disease
Accès ouvert 2014 article OpenAlex

Forelimb Treatment in a Large Cohort of Dystrophic Dogs Supports Delivery of a Recombinant AAV for Exon Skipping in Duchenne Patients

Caroline Le Guiner, Marie Montus, Laurent Servais, Yan Chérel et autres

Duchenne muscular dystrophy (DMD) is a severe muscle-wasting disorder caused by mutations in the dystrophin gene, without curative treatment yet available. Our study provides, for the first time, the overall safety profile and therapeutic dose of a recombinant adeno-associated virus vector, serotype …

fr, us (code pays fourni par la source)

124 citations Molecular Therapy

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