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List of works by Paolo Broda

Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathies

scientific article

Clinical and molecular consequences of exon 78 deletion in DMD gene

scientific article published on 19 March 2018

Expanding the histopathological spectrum of CFL2-related myopathies.

scientific article published on 19 February 2018

Hyperactivation of oxidative mitochondrial metabolism in epithelial cancer cells in situ: visualizing the therapeutic effects of metformin in tumor tissue

scientific article published on December 2011

Impairment of caveolae formation and T-system disorganization in human muscular dystrophy with caveolin-3 deficiency

scientific article published on January 2002

Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophy

scientific article published on 01 August 1999

MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients.

scientific article published on 07 July 2016

Mutation in the CAV3 gene causes partial caveolin-3 deficiency and persistent elevated levels of serum creatine kinase

scientific article (publication date: 28 March 2000)

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

scientific article

POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum

scientific article published in October 2006

POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes.

scientific article

Spinal motor neuron involvement in a patient with homozygous PRUNE mutation

scientific article published on 18 December 2017