Actinomycosis: etiology, clinical features, diagnosis, treatment, and management

F Valour, A Sénéchal, C Dupieux… - Infection and drug …, 2014 - Taylor & Francis
Actinomycosis is a rare chronic disease caused by Actinomyces spp., anaerobic Gram-positive
bacteria that normally colonize the human mouth and digestive and genital tracts. …

Réduction de vibrations de structure complexe par shunts piézoélectriques: application aux turbomachines

A Sénéchal - 2011 - theses.fr
L’objet de cette thèse est d’étudier différents dispositifs d’amortissement de vibrations en
basses fréquences des aubes de rotor de soufflante (" fan") d’un turboréacteur. Les solutions …

[HTML][HTML] Interferon-γ autoantibodies as predisposing factor for nontuberculous mycobacterial infection

F Valour, T Perpoint, A Sénéchal, XF Kong… - Emerging Infectious …, 2016 - ncbi.nlm.nih.gov
To the Editor: Recent advances in the understanding of antimycobacterial immune response
have led to descriptions of predisposing conditions to dissemination of nontuberculous …

COVID-19 in lung transplant recipients

…, S Hirschi, A Nieves, J Le Pavec, A Sénéchal… - …, 2021 - journals.lww.com
Background. A concern about the susceptibility of immunocompromised patients to the
worldwide pandemic of coronavirus disease 2019 (COVID-19) has been raised. We aimed at …

Hardening/softening behavior and reduced order modeling of nonlinear vibrations of rotating cantilever beams

O Thomas, A Sénéchal, JF Deü - Nonlinear dynamics, 2016 - Springer
This work addresses the large amplitude nonlinear vibratory behavior of a rotating cantilever
beam, with applications to turbomachinery and turbopropeller blades. The aim of this work …

[PDF][PDF] Mutations in IMPG1 cause vitelliform macular dystrophies

…, FPM Cremers, JG Hollyfield, A Sénéchal… - The American Journal of …, 2013 - cell.com
Vitelliform macular dystrophies (VMD) are inherited retinal dystrophies characterized by
yellow, round deposits visible upon fundus examination and encountered in individuals with …

[HTML][HTML] Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy

…, G Manes, A Chakraborty, A Sénéchal… - The Journal of …, 2020 - Am Soc Clin Investig
Mutations in genes encoding components of the mitochondrial DNA (mtDNA) replication
machinery cause mtDNA depletion syndromes (MDSs), which associate ocular features with …

[HTML][HTML] X-linked miRNAs associated with gender differences in rheumatoid arthritis

O Khalifa, YM Pers, R Ferreira, A Sénéchal… - International journal of …, 2016 - mdpi.com
Rheumatoid arthritis (RA) is an autoimmune disease that predominantly affects women.
MicroRNAs have emerged as crucial regulators of the immune system, whose expression is …

Relative frequencies of inherited retinal dystrophies and optic neuropathies in Southern France: assessment of 21-year data management

…, G Manes, M Hebrard, A Sénéchal… - Ophthalmic …, 2013 - Taylor & Francis
Purpose: Inherited retinal dystrophies (IRDs) and inherited optic neuropathies (IONs) are
rare diseases defined by specific clinical and molecular features. The relative prevalence of …

[HTML][HTML] Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutations

…, M Hebrard, G Manes, A Sénéchal… - Molecular …, 2013 - ncbi.nlm.nih.gov
Purpose Autosomal recessive retinitis pigmentosa (arRP) is a genetically heterogeneous
disease resulting in progressive loss of photoreceptors that leads to blindness. To date, 36 …