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So far UNIMORE has created 4 blog entries.

Unveiling a new culprit in muscular dystrophy: UNIMORE study redefines Facioscapulohumeral Muscular Dystrophy mechanism

By , |2025-07-30T09:42:59+00:00August 4, 2025|blog post, News|

A groundbreaking study from the University of Modena and Reggio Emilia (UNIMORE) is changing our understanding of facioscapulohumeral muscular dystrophy (FSHD), a prevalent hereditary muscle disorder. Published in the esteemed journal Nucleic Acids Research, the research identifies a novel molecular mechanism involving a long non-coding RNA (lncRNA) called FRG2A-t, shedding new light on how [...]

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New horizons in neuromuscular diagnosis with AI: CoMPaSS-NMD meets patients in Modena

By , |2025-05-14T09:08:46+00:00May 14, 2025|blog post, Events, News|

In Modena, an event brought together individuals affected by neuromuscular conditions to explore the potential of artificial intelligence in achieving more precise diagnoses and offering hope for future advancements. On Saturday, 10th May, Modena hosted an event entitled “Precision Diagnosis and Artificial Intelligence for Neuromuscular Patients: New Tools and New Possibilities”, dedicated to patients, [...]

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Genes, muscles, and answers: how genetic counseling can help with neuromuscular diseases

By , |2025-02-24T10:16:46+00:00February 28, 2025|News, Post blog|

Neuromuscular diseases (NMDs) encompass a wide range of disorders that can affect the muscles and the nerves controlling them. From Duchenne muscular dystrophy to spinal muscular atrophy (SMA), these diseases present significant challenges for patients and their families, especially in understanding the underlying causes, disease progression, and available treatment options. One crucial element of [...]

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Individual genetic background: the architect of human diversity

By , |2024-12-10T10:49:41+00:00December 4, 2024|News|

What can our genetic background reveal? Unlocking new possibilities for neuromuscular disorder care through CoMPaSS-NMD approach. Our genetic background acts as an "instruction manual" for how we develop, function, and express various traits, including susceptibility to diseases, physical features, and even behaviors. For patients with neuromuscular disorders, this genetic diversity plays a crucial role [...]

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DISCLAIMER

This project has received funding from the European Union under Grant Agreement n° 101080874. Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union or the European Commission. Neither the European Union nor the granting authority can be held responsible for them.

 

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Project Coordinator
Rossella Tupler
rossella.tupler@unimore.it

Communication manager
Annalisa De Angelis
annalisa.deangelis@dblue.it

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