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Francois Jerome Authier
Francois Jerome Authier
INSERM University Paris Est-Creteil IMRB U955-Team 10
在 u-pec.fr 的电子邮件经过验证 - 首页
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Dysregulation of muscle cholesterol transport in amyotrophic lateral sclerosis
D Sapaly, F Cheguillaume, L Weill, Z Clerc, O Biondi, S Bendris, C Buon, ...
Brain, awae270, 2024
2024
Muscle involvement in systemic sclerosis: high mortality not associated with nature of histological lesions
N Le Gouellec, L Zaidan, B Chaigne, B Periou, E Cailliau, R Dhote, ...
Rheumatology, keae407, 2024
2024
Widespread Myalgia and Chronic Fatigue: Phagocytes from Macrophagic Myofasciitis Patients Exposed to Aluminum Oxyhydroxide-Adjuvanted Vaccine Exhibit Specific Inflammatory …
JD Masson, G Badran, RK Gherardi, FJ Authier, G Crépeaux
Toxics 12 (7), 491, 2024
2024
Atteinte musculaire au cours de la sclérodermie systémique: la mortalité n’est pas associée à la nature des lésions histologiques
N Le Gouellec, L Zaidan, B Chaigne, B Periou, E Cailliau, R Dhôte, ...
La Revue de Médecine Interne 45, A58, 2024
2024
Rhabdomyolyse induite par l’examen clinique
S Souvannanorath, FJ Authier
Revue Neurologique 180, S124, 2024
2024
An up-to-date myopathologic characterisation of facioscapulohumeral muscular dystrophy type 1 muscle biopsies shows sarcolemmal complement membrane attack complex deposits and …
L Hubregtse, K Bouman, C Lama, S Lassche, N de Graaf, V Taglietti, ...
Neuromuscular Disorders 36, 6-15, 2024
2024
Characterizing acute-onset small fiber neuropathy
T Gendre, JP Lefaucheur, T Nordine, Y Baba-Amer, FJ Authier, J Devaux, ...
Neurology: Neuroimmunology & Neuroinflammation 11 (2), e200195, 2024
42024
L’expression myocytaire de MHC-2 est un biomarqueur de myosite de chevauchement et de myosite à inclusions
C Hou, J Aouizerate, YB Amer, E Malfatti, L Martin, J Authier
Morphologie 107 (359), 100639, 2023
2023
Interferon-gamma-mediated JAK/STAT1 signalling triggers muscle damage in Inclusion Body Myositis
C Hou, B Periou, M Gervais, J Berthier, YB Amer, E Malfatti, ...
Morphologie 107 (359), 100625, 2023
2023
Anti-SAE autoantibody in dermatomyositis: original comparative study and review of the literature
J Demortier, M Vautier, O Chosidow, L Gallay, D Bessis, A Berezne, ...
Rheumatology 62 (12), 3932-3939, 2023
82023
Receptor interacting protein kinase‐3 mediates both myopathy and cardiomyopathy in preclinical animal models of Duchenne muscular dystrophy
M Bencze, B Periou, I Punzón, I Barthélémy, V Taglietti, C Hou, L Zaidan, ...
Journal of Cachexia, Sarcopenia and Muscle 14 (6), 2520-2531, 2023
12023
Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling
N Schuermans, S El Chehadeh, D Hemelsoet, J Gautheron, ...
Nature genetics 55 (11), 1929-1940, 2023
72023
Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cells
N Cardone, V Taglietti, S Baratto, K Kefi, B Periou, C Gitiaux, C Barnerias, ...
Acta Neuropathologica Communications 11 (1), 167, 2023
92023
Myalgic encephalomyelitis/chronic fatigue syndrome: Presentation, cognitive profile, and support perspectives
MA Sebaiti, Y Gounden, FJ Authier, M Hainselin
Revue de neuropsychologie 15 (4), 247-257, 2023
2023
An early onset benign myopathy with glycogen storage caused by a de novo 1.4 Mb-deletion of chromosome 14
G Severa, A Pennisi, C Barnerias, C Fiorillo, M Scala, V Taglietti, ...
Neuromuscular Disorders 33 (10), 817-821, 2023
2023
P342 An early onset benign myopathy with glycogen storage caused by a de novo 1.3 microdeletion of chromosome 14
G Severa, C Fiorillo, M Scala, V Taglietti, A Cojocaru, G Tachdjian, ...
Neuromuscular Disorders 33, S180-S181, 2023
2023
Changes in amyloidosis phenotype over 11 years in a cardiac amyloidosis referral centre cohort in France
T Damy, A Zaroui, M de Tournemire, M Kharoubi, R Gounot, A Galat, ...
Archives of cardiovascular diseases 116 (10), 433-446, 2023
22023
Dysferlinopathy in Tunisia: clinical spectrum, genetic background and prognostic profile
I Belhassen, S Laroussi, S Sakka, S Rekik, L Lahkim, M Dammak, ...
Neuromuscular Disorders 33 (10), 718-727, 2023
2023
Hemifacial myohyperplasia is due to somatic muscular PIK3CA gain-of-function mutations and responds to pharmacological inhibition
C Bayard, E Segna, M Taverne, A Fraissenon, Q Hennocq, B Periou, ...
Journal of Experimental Medicine 220 (11), e20230926, 2023
32023
Revisiting idiopathic eosinophilic myositis: towards a clinical-pathological continuum from the muscle to the fascia and skin
C Fermon, LER Lessard, T Fenouil, A Meyer, M Faruch-Bilfeld, M Robert, ...
Rheumatology 62 (6), 2220-2229, 2023
22023
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