Gaetano A. Vattemi

Verona, Italy

Last Updated: 09/26/2026

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Found 66 publications

Immune-mediated necrotizing myopathies: clinico-serological features and treatment outcomes of a large Italian cohort of patients.

Immune-mediated necrotizing myopathies: clinico-serological features and treatment outcomes of a large Italian cohort of patients.

Journal: Journal of neurology
Published: May 04, 2026

X-linked Emery-Dreifuss muscular dystrophy: a multicenter, Italian, cohort study.

X-linked Emery-Dreifuss muscular dystrophy: a multicenter, Italian, cohort study.

Journal: Journal of neurology
Published: January 21, 2026

Recurrent CAPN3 p.Asp753Asn Variant Supports a Potential Dominant Calpainopathy with Variable Clinical Expressivity.

Recurrent CAPN3 p.Asp753Asn Variant Supports a Potential Dominant Calpainopathy with Variable Clinical Expressivity.

Journal: International journal of molecular sciences
Published: October 31, 2025

Assessment of IBM-FRS total score and specific functional domains in a large cohort of inclusion body myositis patients.

Assessment of IBM-FRS total score and specific functional domains in a large cohort of inclusion body myositis patients.

Journal: Journal of neurology
Published: September 08, 2025

CryAB-driven amyloidogenesis in Drosophila muscle engages extracellular vesicle pathways for cellular release.

CryAB-driven amyloidogenesis in Drosophila muscle engages extracellular vesicle pathways for cellular release.

Journal: iScience
Published: August 18, 2025

Profibrotic Molecules Are Reduced in CRISPR-Edited Emery-Dreifuss Muscular Dystrophy Fibroblasts.

Profibrotic Molecules Are Reduced in CRISPR-Edited Emery-Dreifuss Muscular Dystrophy Fibroblasts.

Journal: Cells
Published: July 18, 2025

TDP-43 pathology induces CD8+ T cell activation through cryptic epitope recognition.

TDP-43 pathology induces CD8+ T cell activation through cryptic epitope recognition.

Journal: bioRxiv : the preprint server for biology
Published: July 16, 2025

Nucleolar FRG2 lncRNAs inhibit rRNA transcription and cytoplasmic translation, linking FSHD to dysregulation of muscle-specific protein synthesis.

Nucleolar FRG2 lncRNAs inhibit rRNA transcription and cytoplasmic translation, linking FSHD to dysregulation of muscle-specific protein synthesis.

Journal: Nucleic acids research
Published: April 14, 2025

Evaluation of aggrephagy markers in myofibrillar myopathies.

Evaluation of aggrephagy markers in myofibrillar myopathies.

Journal: Acta neuropathologica communications
Published: March 04, 2025

Premature skeletal muscle aging in VPS13A deficiency relates to impaired autophagy.

Premature skeletal muscle aging in VPS13A deficiency relates to impaired autophagy.

Journal: Acta neuropathologica communications
Published: February 18, 2025

A novel de novo GFAP variant causes a juvenile-onset Alexander disease with bilateral vocal cord paralysis.

A novel de novo GFAP variant causes a juvenile-onset Alexander disease with bilateral vocal cord paralysis.

Journal: Gene
Published: December 16, 2024

Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies: Experience From the Italian Network.

Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies: Experience From the Italian Network.

Journal: Neurology
Published: August 05, 2024
Showing 1-12 of 66

Last Updated: 09/26/2026