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2414 news items
Distal hereditary motor neuropathy: identification of the COQ7 gene and coenzyme Q10 supplementation
On 26/01/2023
Until now, the COQ7 gene has only been implicated in very severe coenzyme Q10 deficiencies, for which coenzyme Q10 supplementation has led to stabilisation of…
Paediatric forms of FLNC cardiomyopathy are rare but important to know
On 25/01/2023
Abnormalities of the FLNC gene encoding filamin C have been described in isolated myofibrillar myopathies or cardiomyopathies. Italian researchers conducted a retrospective study of paediatric…
Feedback on innovative therapies for myasthenia gravis
On 25/01/2023
The last five years have seen an unparalleled development of therapies targeting severe and/or refractory forms of myasthenia gravis (MG). US clinicians shared their experiences…
Bacopa-containing food supplement involved in autoimmune necrotizing myopathy
On 25/01/2023
A team from Stanford (USA) has published the case of a 21 year old man with no notable history or long-term treatment: he presented with…
A survey of genetic counselling in neurogenetic diseases, including DM1
On 24/01/2023
A French team conducted a study of 562 patients with autosomal dominant neurological diseases (Huntington’s disease, spinocerebellar ataxias, DM1, etc.). The vast majority of families…
Electrophysiological studies are useful in differentiating CMS
On 24/01/2023
Researchers from the Institute of Myology analysed electroneuromyography data from 120 patients with congenital myasthenic syndromes (CMS) and compared them with the results of genetic…
Evolution of scoliosis in SMA type II in absence of modifying treatment
On 24/01/2023
To address the lack of data on the course of scoliosis without treatment that could be used as a benchmark for clinical trials or modifying…
Quantitative muscle imaging enables early detection of degenerative lesions in calpainopathies
On 23/01/2023
German researchers compared quantitative magnetic resonance imaging (MRI) data of a set of muscles from 19 patients with calpainopathy and 19 healthy subjects. These data…
Institute seminar – Jan 26th – 3pm: Stefan Winblad, PhD. (Sweden)
On 23/01/2023
Cognitive impairments in neuromuscular disorders Thursday, 26 January 2023 – 3pm-4pm Stefan Winblad (University of Gothenburg, Sweden) Amphitheatre C (Ground Floor) 91 Boulevard de…
ERN EURO-NMD webinar, January 26th – Prof. Kristl Claeys (Belgium)
On 23/01/2023
Proximal Weakness 26 January 2023 – 16:00 Paris time Pr Kristl Claeys (University Hospitals Leuven, Belgium) Inscription : https://zoom.us/webinar/register/WN_4pKJp8MYRTGiCJKp4K4x1w Organised by EURO-NMD in collaboration with ERN-RND…
Motor plate analysis relevant to the diagnosis of seronegative myasthenia
On 23/01/2023
A Japanese team evaluated the value of studying the motor plate in people who were negative for anti-RACh and anti-MuSK antibodies. Twenty people with symptoms…
Myasthenia gravis: the role of thymic macrophages is essential
On 20/01/2023
Myasthenia gravis (MG) is a neuromuscular disease related to the deleterious action of autoantibodies directed against elements of the neuromuscular junction, most often against the…
Anti-fibrotic drug therapies in skeletal muscle diseases
On 20/01/2023
Fibrosis is defined as an excessive accumulation of extracellular matrix. It can affect many organs, including the lungs, liver, heart, skin, kidneys and muscles. Muscle…
Depression and anxiety are common in CMT
On 20/01/2023
An analysis of data from the Italian Charcot-Marie-Tooth (CMT) disease registry shows that: 14% suffer from psychological distress, 10% from depression (compared to 4% and…
Molecular improvement and signs of clinical efficacy in the AOC 1001 trial in DM1
On 20/01/2023
Avidity Biosciences announced in a press release the first results of the MARINA phase 1-2 trial of AOC 1001 in 44 people with Steinert’s disease…
Intravenous immunoglobulin (IgIV) therapy does not facilitate corticosteroid dose reduction in corticosteroid-dependent Myasthenia gravis
On 19/01/2023
Intravenous immunoglobulins (IgIV) have shown a cortisone-sparing effect in several autoimmune diseases. An international team conducted a clinical trial to evaluate this effect in myasthenia…
Cytoskeletal involvement in dilated cardiomyopathy caused by LMNA gene mutations – Interview with Caroline Le Dour
On 18/01/2023
Caroline Le Dour is a post-doctoral fellow in the Signaling Pathways & Striated Muscles team led by Antoine Muchir, at the Institute’s Myology Centre for…
Miniaturised “organ-on-chip” for muscle dystrophy modelling
On 18/01/2023
Quantifying functional contraction of skeletal muscle is essential to assess the outcome of therapies in neuromuscular diseases. Three-dimensional muscle “organ-on-chip” models imitate muscle function but…
A new genomic sequencing technique for the diagnosis of FSH
On 18/01/2023
The molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD) is challenging due to the existence of complex alterations in the 4qter chromosomal region and the genetic…
Crossed views on the evaluation and expected benefits of the use of exoskeletons
On 17/01/2023
These videos are obtained from the Ambition Fondation de Myologie website.