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Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample

Clinical genetics, 2009-06, Vol.75 (6), p.550-555

2009

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Phenotypic clustering of lamin A/C mutations in neuromuscular patients

Neurology, 2007-09, Vol.69 (12), p.1285-1292

2007

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Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype

Annals of neurology, 1999-06, Vol.45 (6), p.751-757

1999

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Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes

Journal of medical genetics, 2003-12, Vol.40 (12), p.e132-132

2003

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Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15

Neurology, 1999-07, Vol.53 (1), p.50-50

1999

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Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy

American journal of human genetics, 1998-07, Vol.63 (1), p.181-190

1998

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Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

American journal of human genetics, 2000-04, Vol.66 (4), p.1407-1412

2000

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Facioscapulohumeral muscular dystrophy presenting isolated monomelic lower limb atrophy. Report of two patients with and without 4q35 rearrangement

Neuromuscular disorders : NMD, 2002-11, Vol.12 (9), p.874-877

2002

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Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophy

Neurology, 1998-08, Vol.51 (2), p.592-595

1998

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Chimeric snRNA molecules carrying antisense sequences against the splice junctions of exon 51 of the dystrophin pre-mRNA induce exon skipping and restoration of a dystrophin synthesis in Delta 48-50 DMD cells

Proceedings of the National Academy of Sciences - PNAS, 2002-07, Vol.99 (14), p.9456-9461

2002

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Ultrasound tissue characterization detects preclinical myocardial structural changes in children affected by Duchenne muscular dystrophy

Journal of the American College of Cardiology, 2003-07, Vol.42 (2), p.309

2003

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Integrated Backscatter in Becker Muscular Dystrophy Patients With Functionally Normal Heart: Myocardial Ultrasound Tissue Characterization Study

Journal of the American College of Cardiology, 2006-02, Vol.47 (3), p.686-688

2006

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Italian experience regarding the prevention of Duchenne and Becker muscular dystrophies

European journal of pediatrics, 1988-05, Vol.147 (4), p.412-415

1988

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Clinical study of proximal spinal muscular atrophy. Report on 89 cases

Italian journal of neurological sciences, 1984-12, Vol.5 (4), p.423-432

1984

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Molecular analysis of 4q35 rearrangements in fascioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease

Neuromuscular disorders : NMD, 1999-05, Vol.9 (3), p.190-198

1999

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Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD)

Human genetics, 1994-10, Vol.94 (4), p.367-374

1994

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242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread

Genomics (San Diego, Calif.), 1991, Vol.10 (3), p.631-639

1991

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Detection of immunogenic cell death and its relevance for cancer therapy

Cell death & disease, 2020-11, Vol.11 (11), p.1013-1013, Article 1013

2020

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Autophagy and Mitophagy in Cardiovascular Disease

Circulation research, 2017-05, Vol.120 (11), p.1812-1824

2017

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Apoptosis and Cancer: Force Awakens, Phantom Menace, or Both?

International review of cell and molecular biology, 2018, Vol.337, p.135-152

2018

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Methods to Monitor ROS Production by Fluorescence Microscopy and Fluorometry

Methods in Enzymology, 2014, Vol.542, p.243-262

2014

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Immunostimulation with chemotherapy in the era of immune checkpoint inhibitors

Nature reviews. Clinical oncology, 2020-12, Vol.17 (12), p.725-741

2020

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Calreticulin and cancer

Cell research, 2021-01, Vol.31 (1), p.5-16

2021

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Immunogenic Cell Death in Cancer Therapy

Annual review of immunology, 2013-01, Vol.31 (1), p.51-72

2013

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Molecular Regulation of the Spindle Assembly Checkpoint by Kinases and Phosphatases

International review of cell and molecular biology, 2017-01, Vol.328, p.105-161

2017

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Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample

Phenotypic clustering of lamin A/C mutations in neuromuscular patients

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype

Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes

Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15

Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy

Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

Facioscapulohumeral muscular dystrophy presenting isolated monomelic lower limb atrophy. Report of two patients with and without 4q35 rearrangement

Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophy

Chimeric snRNA molecules carrying antisense sequences against the splice junctions of exon 51 of the dystrophin pre-mRNA induce exon skipping and restoration of a dystrophin synthesis in Delta 48-50 DMD cells

Ultrasound tissue characterization detects preclinical myocardial structural changes in children affected by Duchenne muscular dystrophy

Integrated Backscatter in Becker Muscular Dystrophy Patients With Functionally Normal Heart: Myocardial Ultrasound Tissue Characterization Study

Italian experience regarding the prevention of Duchenne and Becker muscular dystrophies

Clinical study of proximal spinal muscular atrophy. Report on 89 cases

Molecular analysis of 4q35 rearrangements in fascioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease

Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD)

242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread

Detection of immunogenic cell death and its relevance for cancer therapy

Autophagy and Mitophagy in Cardiovascular Disease

Apoptosis and Cancer: Force Awakens, Phantom Menace, or Both?

Methods to Monitor ROS Production by Fluorescence Microscopy and Fluorometry

Immunostimulation with chemotherapy in the era of immune checkpoint inhibitors

Calreticulin and cancer

Immunogenic Cell Death in Cancer Therapy

Molecular Regulation of the Spindle Assembly Checkpoint by Kinases and Phosphatases

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