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Derniers dépôts
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Romain Didier, Lucie Garnier, Gauthier Duloquin, Alexandre Meloux, Audrey Sagnard, et al.. Distribution of atrial cardiomyopathy markers and association with atrial fibrillation detected after ischaemic stroke in the SAFAS study. Stroke and Vascular Neurology, 2023, 9, pp.165 - 173. ⟨10.1136/svn-2023-002447⟩. ⟨hal-04591992⟩
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Angelos Gerassimopoulos, Céline Michaud, Mélanie Gaillet, Cyril Rousseau, Adriana Gonzalez, et al.. Santé et recours aux soins et à la prévention des travailleuses du sexe dominicaines vivant le long du fleuve Maroni. 6e journées des travaux scientifiques des soignant.e.s de Guyane, May 2023, Cayenne, Guyane française. ⟨hal-04585175⟩
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Joe-Elie Salem, Marie Bretagne, Baptiste Abbar, Sarah Leonard-Louis, Stéphane Ederhy, et al.. Abatacept/Ruxolitinib and Screening for Concomitant Respiratory Muscle Failure to Mitigate Fatality of Immune-Checkpoint Inhibitor Myocarditis. Cancer Discovery, 2023, 13 (5), pp.1100-1115. ⟨10.1158/2159-8290.CD-22-1180⟩. ⟨hal-04578810⟩
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Antonio Atalaia, Dagmar Wandrei, Nawel Lalout, Rachel Thompson, Adrian Tassoni, et al.. EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disorders. Orphanet Journal of Rare Diseases, 2024, 19 (1), pp.66. ⟨10.1186/s13023-024-03059-3⟩. ⟨hal-04460667⟩
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Vanessa Ueberschlag-Pitiot, Amalia Stantzou, Julien Messéant, Megane Lemaitre, Daniel Owens, et al.. Gonad-related factors promote muscle performance gain during postnatal development in male and female mice. AJP - Endocrinology and Metabolism, 2017, 313 (1), pp.E12-E25. ⟨10.1152/ajpendo.00446.2016⟩. ⟨hal-03677800⟩
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Hubert Smeets, Bram Verbrugge, Xavier Bulbena, Liliya Hristova, Julia Vogt, et al.. European Joint Programme on Rare Diseases workshop: LAMA2-muscular dystrophy: paving the road to therapy March 17–19, 2023, Barcelona, Spain. LAMA2-muscular dystrophy: paving the road to therapy, Neuromuscular Disorders, 36, pp.16 - 22, 2024, ⟨10.1016/j.nmd.2024.01.001⟩. ⟨hal-04546346⟩
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Medhi Hassani, Dylan Moutachi, Mégane Lemaitre, Alexis Boulinguiez, Denis Furling, et al.. Beneficial effects of resistance training on both mild and severe mouse dystrophic muscle function as a preclinical option for Duchenne muscular dystrophy. PLoS ONE, 2024, 19, ⟨10.1371/journal.pone.0295700⟩. ⟨hal-04501283⟩
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Pierre Joanne, Yeranuhi Hovhannisyan, Alexandre Simon, Gaëlle Revet, Romain Diot, et al.. Generation of human induced pluripotent stem cell lines from five patients with Myofibrillar myopathy carrying different heterozygous mutations in the DES gene. Stem Cell Research, 2024, 76, pp.103338. ⟨10.1016/j.scr.2024.103338⟩. ⟨hal-04466294⟩
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Pascal Laforêt, Michio Inoue, Evelyne Goillot, Claire Lefeuvre, Umut Cagin, et al.. Deep morphological analysis of muscle biopsies from type III glycogenesis (GSDIII), debranching enzyme deficiency, revealed stereotyped vacuolar myopathy and autophagy impairment. Acta Neuropathologica Communications, 2019, 7 (1), ⟨10.1186/s40478-019-0815-2⟩. ⟨hal-02414161⟩
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Mechanotransduction
Actin
Humans
Errance diagnostique
Duchenne muscular dystrophy
MBNL
Cancer
Becker muscular dystrophy
Biomarker
CTG repeat contractions
ALS
Congenital myopathy
Centronuclear myopathy
Treatment
Autoimmunity
Muscular dystrophy
Cell therapy
Laminopathie
Brain
Thérapie génique
Male
Neuromuscular junction
RNA interference
Laminopathies
Myoblasts
Calcium
Laminopathy
Antisense oligonucleotides
Dynamin 2
Motoneuron
OPMD
CMS
Diagnosis
COVID-19
Nuclear envelope
Trinucleotide repeat expansion
Genotype phenotype correlation
Satellite cells
FSHD
Inflammation
Autophagy
Regeneration
Clinical trials
Muscle regeneration
Myotonic dystrophy type 1
Thymus
Dystrophin
Myasthenia Gravis MG
Myopathies
Myopathy
Exercise
Myositis
Autoantibodies
Myogenesis
Aged
Rare diseases
Heart failure
Long read sequencing
Cardiomyopathy
Animals
Neuromuscular diseases
Biomarkers
Glutamate
Myotonic Dystrophy type 1
Rare neuromuscular diseases
Dilated cardiomyopathy
Muscle
Lamin A/C
Lamin A/C LMNA gene
Cytokines
LMNA
Myotonic Dystrophy
Myotonic dystrophy
Autoimmune diseases
DMD
Fibrosis
RNA biology
LMNA gene
Congenital muscular dystrophy
AAV
Mouse model
CRISPRi
Dermatomyositis
Outcome measures
Heart
Alternative splicing
PABPN1
Satellite cell
Transcriptomics
Therapy
Fabry disease
Neuromuscular disease
Astrocyte
Cytoskeleton
Gene therapy
Skeletal muscle
Transgenic mouse model
Myasthenia gravis
Aging
Amyotrophic lateral sclerosis