List of works - Lucia Morandi

A large cohort of myotonia congenita probands: novel mutations and a high-frequency mutation region in exons 4 and 5 of the CLCN1 gene

scientific article published on 6 June 2013

Anti-fibrotic effect of pirfenidone in muscle derived-fibroblasts from Duchenne muscular dystrophy patients.

scientific article published on 8 December 2015

Autophagy, inflammation and innate immunity in inflammatory myopathies

scientific article

Botulinum toxin type A affects the transcriptome of cell cultures derived from muscle biopsies of controls and spastic patients

scientific article published on 6 March 2018

Calsequestrin and junctin immunoreactivity in hexagonally cross-linked tubular arrays myopathy

scientific article published on 07 March 2010

Central core disease and susceptibility to malignant hyperthermia in a single family

scientific article published on 28 February 2009

Complete stable remission and autoantibody specificity in myasthenia gravis

scientific article

Decorin and biglycan expression is differentially altered in several muscular dystrophies

scientific article published on 23 September 2005

Human Neurotrophin Receptor p75NTR Defines Differentiation-Oriented Skeletal Muscle Precursor Cells: Implications for Muscle Regeneration

LAMA2 gene analysis in congenital muscular dystrophy: new mutations, prenatal diagnosis, and founder effect.

scientific article

Muscle inflammation and MHC class I up-regulation in muscular dystrophy with lack of dysferlin: an immunopathological study

scientific article (publication date: September 2003)

Myasthenia gravis (MG): epidemiological data and prognostic factors

scientific article

Opposing roles of miR-21 and miR-29 in the progression of fibrosis in Duchenne muscular dystrophy.

scientific article published on 17 April 2015

Osteopontin is highly expressed in severely dystrophic muscle and seems to play a role in muscle regeneration and fibrosis.

scientific article published in December 2011

The Kinesin Superfamily Motor Protein KIF4 Is Associated With Immune Cell Activation in Idiopathic Inflammatory Myopathies

scientific article published on 01 June 2008

Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression.

scientific article published on 31 August 2017

Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2.

scientific article

List of works by Lucia Morandi

A large cohort of myotonia congenita probands: novel mutations and a high-frequency mutation region in exons 4 and 5 of the CLCN1 gene

Anti-fibrotic effect of pirfenidone in muscle derived-fibroblasts from Duchenne muscular dystrophy patients.

Autophagy, inflammation and innate immunity in inflammatory myopathies

Botulinum toxin type A affects the transcriptome of cell cultures derived from muscle biopsies of controls and spastic patients

Calsequestrin and junctin immunoreactivity in hexagonally cross-linked tubular arrays myopathy

Central core disease and susceptibility to malignant hyperthermia in a single family

Complete stable remission and autoantibody specificity in myasthenia gravis

Decorin and biglycan expression is differentially altered in several muscular dystrophies

Human Neurotrophin Receptor p75NTR Defines Differentiation-Oriented Skeletal Muscle Precursor Cells: Implications for Muscle Regeneration

LAMA2 gene analysis in congenital muscular dystrophy: new mutations, prenatal diagnosis, and founder effect.

Muscle inflammation and MHC class I up-regulation in muscular dystrophy with lack of dysferlin: an immunopathological study

Myasthenia gravis (MG): epidemiological data and prognostic factors

Opposing roles of miR-21 and miR-29 in the progression of fibrosis in Duchenne muscular dystrophy.

Osteopontin is highly expressed in severely dystrophic muscle and seems to play a role in muscle regeneration and fibrosis.

The Kinesin Superfamily Motor Protein KIF4 Is Associated With Immune Cell Activation in Idiopathic Inflammatory Myopathies

Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression.

Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2.