Latest papers

Reverse protein arrays as novel approach for protein quantification in muscular dystrophies.

Epidermolysis bullosa simplex with muscular dystrophy.

Soft substrates drive optimal differentiation of human healthy and dystrophic myotubes.

Magnetic resonance imaging, ultrasound and real-time ultrasound elastography of the thigh muscles in congenital muscle dystrophy.

Differential expression of utrophin-A and -B promoters in the central nervous system (CNS) of normal and dystrophic mdx mice.

Characterization of genomic structures and expression profiles of three tandem repeats of a mouse double homeobox gene: Duxbl.

Congenital muscular dystrophies: toward molecular therapeutic interventions.

Force exertion capacity measurements in haptic virtual environments.

Perioral skin biopsy to study skeletal muscle protein expression.

Quality of life for primary caregivers of muscular dystrophy patients in South Korea.

A case study on Walker-Warburg syndrome.

[Clinical, molecular pathological and genetic analyses of a Chinese family with congenital muscular dystrophy type 1A].

Caring for young people with chronic illness: a case study.

Mechanical and electrophysiological properties of the sarcolemma of muscle fibers in two murine models of muscle dystrophy: col6a1-/- and mdx.

Caught in the middle: the role of Bag3 in disease.

Current perspectives on muscle regeneration and diseases.

Retinal ectopias and mechanically weakened basement membrane in a mouse model of muscle-eye-brain (MEB) disease congenital muscular dystrophy.

[Caveolae-invaginations in the cell membrane with complex function. Defects in caveolae gene connected to severe congenital diseases].

Anesthesia and perioperative management for a patient with Ullrich syndrome undergoing surgery for scoliosis.

Dystrobrevin isoform expression in patients with neuromuscular disease.