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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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Thérapie génique
Cytokines
Laminopathie
Transgenic mouse model
Myotonic Dystrophy
Lamin A/C LMNA gene
CMS
Regeneration
Neuromuscular diseases
Myasthenia gravis
Aging
Laminopathies
Trinucleotide repeat expansion
OPMD
Biomarkers
PABPN1
Myogenesis
Satellite cell
Amyotrophic lateral sclerosis
Exercise
Myotonic Dystrophy type 1
Diagnosis
Animals
Nuclear envelope
Satellite cells
Muscle
Muscular dystrophy
Becker muscular dystrophy
Lamin A/C
Alternative splicing
Clinical trials
FSHD
CRISPRi
COVID-19
Cytoskeleton
Treatment
Mechanotransduction
ALS
Laminopathy
Mouse model
RNA interference
Myotonic dystrophy type 1
Myotonic dystrophy
Duchenne muscular dystrophy
Myopathies
Muscle regeneration
LMNA
Neuromuscular junction
Actin
Fibrosis
Antisense oligonucleotides
DMD
Fabry disease
AAV
Cancer
Dynamin 2
Neuromuscular disease
Thymus
Heart
Therapy
Astrocyte
Humans
Transcriptomics
Dermatomyositis
Genotype phenotype correlation
Rare neuromuscular diseases
MBNL
Gene therapy
Autoimmunity
Cell therapy
Outcome measures
Glutamate
LMNA gene
Brain
Autoimmune diseases
Calcium
Congenital myopathy
Male
Cardiomyopathy
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Myoblasts
Centronuclear myopathy
Rare diseases
Dystrophin
Autoantibodies
Motoneuron
Dilated cardiomyopathy
Inflammation
RNA biology
Skeletal muscle
Aged
Myasthenia Gravis MG
Biomarker
Autophagy
Myopathy
CTG repeat contractions
Congenital muscular dystrophy
Long read sequencing
Heart failure
Errance diagnostique