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You searched for: Author/Creator Mariot, Virginie

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1. Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy. Issue 3 (3rd July 2015)

2. Downregulation of myostatin pathway in neuromuscular diseases may explain challenges of anti-myostatin therapeutic approaches. Issue 1 (December 2017)

3. Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles. Issue 2 (22nd February 2022)

4. Myostatin inhibition in combination with antisense oligonucleotide therapy improves outcomes in spinal muscular atrophy. Issue 3 (7th February 2020)

7. Quantification of the methylation at the GNAS locus identifies subtypes of sporadic pseudohypoparathyroidism type Ib. Issue 1 (23rd October 2010)

8. RIPK3‐mediated cell death is involved in DUX4‐mediated toxicity in facioscapulohumeral dystrophy. Issue 6 (22nd October 2021)

9. Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo-Humeral Dystrophy: a case report. Issue 1 (December 2016)