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List of works by Ana Ferreiro

A single homozygous point mutation in a 3'untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathy

scientific article

Abnormal distribution of calcium-handling proteins: a novel distinctive marker in core myopathies

scientific article

C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathy

scientific article published in April 2007

Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene.

scientific article

Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy

scientific article

Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy

scientific article

Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies

scientific article

Oxidative stress in SEPN1-related myopathy: from pathophysiology to treatment

scientific article

Selenoproteins and protection against oxidative stress: selenoprotein N as a novel player at the crossroads of redox signaling and calcium homeostasis

scientific article

Severe progressive form of congenital muscular dystrophy with calf pseudohypertrophy, macroglossia and respiratory insufficiency

scientific article published in June 2002

The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease

scientific journal article

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