Search Results - "Authier, François‐Jérôme"
-
1
Systematic review and meta-analysis of cognitive impairment in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)
Published in Scientific reports (09-02-2022)“…Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is commonly associated with cognitive complaints. To bring out the neuropsychological…”
Get full text
Journal Article -
2
Systemic light chain amyloidosis myopathy responsive to daratumumab monotherapy
Published in European journal of neurology (01-03-2023)“…Background and purpose Amyloid myopathy is a rare and severe manifestation of systemic light chain (AL) amyloidosis. Early diagnosis and staging are mandatory…”
Get full text
Journal Article -
3
Optimized Flow Cytometry Strategy for Phenotyping Intramuscular Leukocytes: Application to the Evaluation of Myopathological Processes
Published in Journal of neuropathology and experimental neurology (24-02-2022)“…Abstract Phenotyping intramuscular immune cells is essential for the characterization of dysimmune/inflammatory myopathies (DIM). Flow cytometry (FC) is the…”
Get full text
Journal Article -
4
Satellite Cells Attract Monocytes and Use Macrophages as a Support to Escape Apoptosis and Enhance Muscle Growth
Published in The Journal of cell biology (08-12-2003)“…Once escaped from the quiescence niche, precursor cells interact with stromal components that support their survival, proliferation, and differentiation. We…”
Get full text
Journal Article -
5
Automated image-analysis method for the quantification of fiber morphometry and fiber type population in human skeletal muscle
Published in Skeletal muscle (27-05-2019)“…The quantitative analysis of muscle histomorphometry has been growing in importance in both research and clinical settings. Accurate and stringent assessment…”
Get full text
Journal Article -
6
Novel Missense CAPN3 Mutation Responsible for Adult-Onset Limb Girdle Muscular Dystrophy with Calves Hypertrophy
Published in Journal of molecular neuroscience (01-12-2019)“…CAPN3 gene encodes for calpain-3; this protein is a calcium-dependent intracellular protease. Deficiency of this enzyme leads to weakness of the proximal limb…”
Get full text
Journal Article -
7
Systemic Sclerosis-Associated Myopathy
Published in Annals of the New York Academy of Sciences (01-06-2007)“…: Skeletal muscle involvement is a common feature in systemic sclerosis (SSc) because muscle weakness is found in up to 90% SSc patients when systematically…”
Get full text
Journal Article -
8
Distinct interferon signatures stratify inflammatory and dysimmune myopathies
Published in Rheumatic & musculoskeletal diseases open (01-02-2019)“…ObjectiveThe role of interferons (IFN) in the pathophysiology of primary inflammatory and dysimmune myopathies (IDM) is increasingly investigated, notably…”
Get full text
Journal Article -
9
Novel splicing dysferlin mutation causing myopathy with intra-familial heterogeneity
Published in Molecular biology reports (01-08-2020)“…Dysferlinopathies belong to the heterogeneous group of autosomal recessive muscular disorders, caused by mutations in the dysferlin gene and characterized by a…”
Get full text
Journal Article -
10
Myofiber HLA-DR expression is a distinctive biomarker for antisynthetase-associated myopathy
Published in Acta neuropathologica communications (23-10-2014)“…To assess the value of major histocompatibility complex (MHC) class II antigen (HLA-DR) expression to distinguish anti-synthetase myopathy (ASM) from…”
Get full text
Journal Article -
11
Skeletal muscle involvement in human immunodeficiency virus (HIV)-infected patients in the era of highly active antiretroviral therapy (HAART)
Published in Muscle & nerve (01-09-2005)“…Skeletal muscle involvement can occur at all stages of human immunodeficiency virus (HIV) infection, and may represent the first manifestation of the disease…”
Get full text
Journal Article -
12
Clinical and functional characterization of a long survivor congenital titinopathy patient with a novel metatranscript-only titin variant
Published in Acta neuropathologica communications (21-03-2023)“…Congenital titinopathies are an emerging group of a potentially severe form of congenital myopathies caused by biallelic mutations in titin, encoding the…”
Get full text
Journal Article -
13
FDX2 and ISCU Gene Variations Lead to Rhabdomyolysis With Distinct Severity and Iron Regulation
Published in Neurology. Genetics (01-02-2022)“…To determine common clinical and biological traits in 2 individuals with variants in and , displaying severe and recurrent rhabdomyolyses and lactic acidosis…”
Get full text
Journal Article -
14
ADAM12 and α9β1 Integrin Are Instrumental in Human Myogenic Cell Differentiation
Published in Molecular biology of the cell (01-02-2005)“…Knowledge on molecular systems involved in myogenic precursor cell (mpc) fusion into myotubes is fragmentary. Previous studies have implicated the a d…”
Get full text
Journal Article -
15
Vaccination-induced cutaneous pseudolymphoma
Published in Journal of the American Academy of Dermatology (01-04-2005)“…Although mild early cutaneous transient reactions to vaccinations are common, late-onset chronic lesions have been scarcely reported. We report herein a series…”
Get full text
Journal Article -
16
Obesity impairs skeletal muscle repair through NID-1 mediated extracellular matrix remodeling by mesenchymal progenitors
Published in Matrix biology (01-09-2022)“…Obesity triggers skeletal muscle physio-pathological alterations. However, the crosstalk between adipose tissue and myogenic cells remains poorly understood…”
Get full text
Journal Article -
17
From Diagnosis to Prognosis: Revisiting the Meaning of Muscle ISG15 Overexpression in Juvenile Inflammatory Myopathies
Published in Arthritis & rheumatology (Hoboken, N.J.) (01-06-2021)“…Objective Juvenile idiopathic inflammatory/immune myopathies (IIMs) constitute a highly heterogeneous group of disorders with diagnostic difficulties and…”
Get full text
Journal Article -
18
European Network on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (EUROMENE): Expert Consensus on the Diagnosis, Service Provision, and Care of People with ME/CFS in Europe
Published in Medicina (Kaunas, Lithuania) (19-05-2021)“…Designed by a group of ME/CFS researchers and health professionals, the European Network on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (EUROMENE) has…”
Get full text
Journal Article -
19
Anti-MDA5 juvenile idiopathic inflammatory myopathy: a specific subgroup defined by differentially enhanced interferon-α signalling
Published in Rheumatology (01-08-2020)“…Abstract Objectives JDM and juvenile overlap myositis represent heterogeneous subtypes of juvenile idiopathic inflammatory myopathy (JIIM). Chronic evolution…”
Get full text
Journal Article -
20
Al(OH) 3-adjuvanted vaccine-induced macrophagic myofasciitis in rats is influenced by the genetic background
Published in Neuromuscular disorders : NMD (2006)“…Macrophagic myofasciitis (MMF) is a specific histopathologic lesion involved in the persistence for years of aluminum hydroxide [Al(OH) 3] at the site of…”
Get full text
Journal Article