Martial Mallaret
Overview
Explore the profile of Martial Mallaret including associated specialties, affiliations and a list of published articles.
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20
Citations
295
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Recent Articles
1.
Tankere P, Cascarano E, Raymond C, Mallaret M, Toribio Ruiz C, Herquelot E, et al.
Amyotroph Lateral Scler Frontotemporal Degener
. 2025 Jan;
:1-9.
PMID: 39749674
: This study determined real-life care trajectories before and after initiation of noninvasive ventilation (NIV) in patients with amyotrophic lateral sclerosis (ALS). Caregiver adherence to respiratory management recommendations and the...
2.
Magot A, Reignier A, Binois O, Bedat-Millet A, Davion J, Deberge L, et al.
Orphanet J Rare Dis
. 2024 Dec;
19(1):476.
PMID: 39707482
Background: Spinal muscular atrophy (SMA) patients benefit from pre-mRNA splicing modifiers targeting the SMN2 gene, which aims to increase functional SMN production. The animal toxicity affecting spermatogenesis associated with one...
3.
Theuriet J, Masingue M, Behin A, Ferreiro A, Bassez G, Jaubert P, et al.
Brain
. 2024 May;
147(11):3849-3862.
PMID: 38696726
Congenital myasthenic syndromes (CMS) are clinically and genetically heterogeneous diseases caused by mutations affecting neuromuscular transmission. Even if the first symptoms mainly occur during childhood, adult neurologists must confront this...
4.
Cluse F, Hermier M, Demarquay G, Rogemond V, Mallaret M, Svahn J, et al.
Neurol Neuroimmunol Neuroinflamm
. 2023 Aug;
10(6).
PMID: 37607754
Objectives: Anti-IgLON5 disease (IgLON5-D) may present with a bulbar-onset motor neuron disease-like phenotype, mimicking bulbar-onset amyotrophic lateral sclerosis. Recognition of their distinctive clinical and paraclinical features may help for differential...
5.
Chanson J, Bouhour F, Aube-Nathier A, Mallaret M, Vial C, Hacquard A, et al.
J Neurol
. 2023 Aug;
270(12):5819-5826.
PMID: 37592137
Background: Myasthenia gravis (MG) is an autoimmune disease treated with acetylcholinesterase inhibitors and immunosuppressant/immunomodulatory drugs. MG is frequently diagnosed in elderly patients, a fragile population in which treatment adverse effects...
6.
Pisella L, Fernandes S, Sole G, Stojkovic T, Tard C, Chanson J, et al.
Orphanet J Rare Dis
. 2021 Oct;
16(1):450.
PMID: 34702344
Background: Due to their health condition, patients with neuromuscular diseases (NMD) are at greater risk of developing serious complications with COVID-19. The objective of this study was to analyze the...
7.
Perrin A, Juntas Morales R, Chapon F, Theze C, Lacourt D, Pegeot H, et al.
Ann Clin Transl Neurol
. 2021 Jul;
8(9):1906-1912.
PMID: 34312993
The aim of this study was to analyze patients from two distinct families with a novel distal titinopathy phenotype associated with exactly the same CNV in the TTN gene. We...
8.
Benkirane M, Marelli C, Guissart C, Roubertie A, Ollagnon E, Choumert A, et al.
Genet Med
. 2021 Jul;
23(11):2160-2170.
PMID: 34234304
Purpose: Diagnosis of inherited ataxia and related diseases represents a real challenge given the tremendous heterogeneity and clinical overlap of the various causes. We evaluated the efficacy of molecular diagnosis...
9.
Lornage X, Mallaret M, Silva-Rojas R, Biancalana V, Giovannini D, Dieterich K, et al.
Neurogenetics
. 2021 Jan;
22(1):33-41.
PMID: 33405017
The nuclear envelope (NE) separates the nucleus from the cytoplasm in all eukaryotic cells. A disruption of the NE structure compromises normal gene regulation and leads to severe human disorders...
10.
Bigaut K, Mallaret M, Baloglu S, Nemoz B, Morand P, Baicry F, et al.
Neurol Neuroimmunol Neuroinflamm
. 2020 May;
7(5).
PMID: 32461235
No abstract available.