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1. Assessment of diaphragm motion using ultrasonography in a patient with facio-scapulo-humeral dystrophy: A case report. Issue 4 (January 2019)

2. Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiency. (December 2017)

3. Clinical profiles and prognosis of acute heart failure in adult patients with dystrophinopathies on home mechanical ventilation. (18th May 2017)

4. Cognitive profile of patients with glycogen storage disease type III: a clinical description of seven cases. Issue 3 (12th November 2014)

5. Determinants of diaphragm inspiratory motion, diaphragm thickening, and its performance for predicting respiratory restrictive pattern in Duchenne muscular dystrophy. Issue 1 (25th October 2021)

7. Genetic Characterization of a French Cohort of GNE‐mutation negative inclusion body myopathy patients with exome sequencing. Issue 5 (7th April 2017)

8. High-resolution breakpoint junction mapping of proximally extended D4Z4 deletions in FSHD1 reveals evidence for a founder effect. Issue 5 (24th September 2021)

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