Giuliano Tomelleri
Via G. Campi 287
Modena, 41125, Italy
Modena, 41125, Italy
Last Updated: 09/26/2026
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Found 43 publications
A novel in-frame deletion in MYOT causes an early adult onset distal myopathy.
Journal: Clinical genetics
Published: May 30, 2023
Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophy.
Journal: BMC musculoskeletal disorders
Published: May 15, 2023
Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis.
Journal: Scientific reports
Published: August 10, 2020
A 5-year clinical follow-up study from the Italian National Registry for FSHD.
Journal: Journal of neurology
Published: July 02, 2020
Protein Expression of Canine and Feline Muscular Dystrophies.
Journal: Topics in companion animal medicine
Published: June 19, 2020
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: May 04, 2020
Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies.
Journal: International journal of molecular sciences
Published: March 02, 2020
Relapsing-remitting painful masses of the skeletal muscle.
Journal: Journal of clinical pathology
Published: July 11, 2019
Acute Sarcomeric M-Line Disease Associated With ATP Synthase Subunit α Autoantibodies in Ankylosing Spondylitis.
Journal: Journal of neuropathology and experimental neurology
Published: September 15, 2018
Bortezomib-Induced Muscle Toxicity in Multiple Myeloma.
Journal: Journal of neuropathology and experimental neurology
Published: September 03, 2017
Last Updated: 09/26/2026