Daniele Sabbatini
Padova, Italy
Last Updated: 09/26/2026
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Found 23 publications
Integrating Genetic Modifier Genotype With Serum Proteomics in Duchenne Muscular Dystrophy Clinical Trials Links LTBP4 Genetic Modifier to IL-23/CD93 Pathways in Muscle.
Journal: American journal of medical genetics. Part A
Published: March 24, 2026
Model architecture dominates nutritional estimation accuracy in vision-language systems.
Journal: Scientific reports
Published: December 15, 2025
Wernicke Encephalopathy Complicating a Distinctive POLG Phenotype With MNGIE-Like Features.
Journal: European journal of neurology
Published: May 14, 2025
Genome-wide association for sarcoidosis identifies novel risk loci and genetic heritability in African and European ancestries: a meta-analysis from the Finngen, Million Veteran Program, UK Biobank, and Biobank Japan datasets.
Journal: Orphanet journal of rare diseases
Published: April 28, 2025
Longitudinal Changes of Motor Function in Becker Muscular Dystrophy.
Journal: Neurology. Genetics
Published: December 04, 2024
MEPs and MRI Motor Band Sign as Potential Complementary Markers of Upper Motor Neuron Involvement in Amyotrophic Lateral Sclerosis.
Journal: European journal of neurology
Published: July 26, 2024
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity.
Journal: Brain : a journal of neurology
Published: July 08, 2024
Deep characterization of females with heterozygous Duchenne muscular dystrophy mutations.
Journal: Journal of neurology
Published: July 02, 2024
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy.
Journal: Journal of neuromuscular diseases
Published: February 16, 2024
A Novel MAO-B/SSAO Inhibitor Improves Multiple Aspects of Dystrophic Phenotype in mdx Mice.
Journal: Antioxidants (Basel, Switzerland)
Published: January 31, 2024
Last Updated: 09/26/2026