Alexandra Belayew
Mons, WAL 7000, Belgium
Last Updated: 09/26/2026
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Found 30 publications
Bridging past and future: the evolution of genetic diagnosis in FSHD and the role of emerging technologies in a globalized framework.
Journal: Neuromuscular disorders : NMD
Published: February 06, 2026
Marion or the metamorphosis: a journey of self-reconstruction and hope in the face of FSHD.
Journal: Neuromuscular disorders : NMD
Published: July 21, 2025
The DUX4-HIF1α Axis in Murine and Human Muscle Cells: A Link More Complex Than Expected.
Journal: International journal of molecular sciences
Published: December 29, 2023
Hypoxia and Hypoxia-Inducible Factor Signaling in Muscular Dystrophies: Cause and Consequences.
Journal: International journal of molecular sciences
Published: May 31, 2021
Correction to: Affinity capillary electrophoresis for identification of active drug candidates in myotonic dystrophy type 1.
Journal: Analytical and bioanalytical chemistry
Published: November 17, 2018
Affinity capillary electrophoresis for identification of active drug candidates in myotonic dystrophy type 1.
Journal: Analytical and bioanalytical chemistry
Published: January 21, 2018
Overexpression of the double homeodomain protein DUX4c interferes with myofibrillogenesis and induces clustering of myonuclei.
Journal: Skeletal muscle
Published: April 06, 2017
Last Updated: 09/26/2026