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From diagnosis to prognosis: Revisiting the meaning of muscle ISG15 overexpression in juvenile inflammatory myopathies
Hou C, Durrleman C, Periou B, et al.
Arthritis & rheumatology (Hoboken, N.J.), 2020
Circulating interferon-alpha measured with a highly sensitive assay as a biomarker for juvenile inflammatory myositis activity
Melki I, Devilliers H, Gitiaux C, et al.
Arthritis & rheumatology (Hoboken, N.J.), 2020, 72, 1, p 195
Severe Abdominal Manifestations in Juvenile Dermatomyositis
Besnard C, Gitiaux C, Girard M, et al.
Journal of pediatric gastroenterology and nutrition, 2019
Anti-MDA5 juvenile idiopathic inflammatory myopathy: a specific subgroup defined by differentially enhanced interferon-alpha signalling
Melki I, Devilliers H, Gitiaux C, et al.
Rheumatology (Oxford, England), 2019
Inhibition of IFNalpha secretion in cells from patients with juvenile dermatomyositis under TBK1 inhibitor treatment revealed by single-molecular assay technology
Gitiaux C, Bondet V, Bekaddour N, et al.
Rheumatology (Oxford, England), 2019
A child with severe juvenile dermatomyositis treated with ruxolitinib
Aeschlimann FA, Aeschlimann FA, Fremond ML, et al.
Brain : a journal of neurology, 2018, 141, 11
Muscle ischaemia associated with NXP2 autoantibodies: a severe subtype of juvenile dermatomyositis
Aouizerate J, De Antonio M, Bader-Meunier B, et al.
Rheumatology (Oxford, England), 2018, 57, 5, p 873
Presentations and outcomes of juvenile dermatomyositis patients admitted to intensive care units
Besançon A, Brochard K, Dupic L, et al.
Rheumatology (Oxford, England), 2017, 56, 10, p 1814
Vasculopathy-related clinical and pathological features are associated with severe juvenile dermatomyositis
Gitiaux C, De Antonio M, Aouizerate J, et al.
Rheumatology (Oxford), 2016, 55, 3, p 470
Safety and efficacy of rituximab in severe juvenile dermatomyositis: results from 9 patients from the french autoimmunity and rituximab registry
Bader-Meunier B, Decaluwe H, Barnerias C, et al.
Journal of rheumatology, 2011, 38, 7, p. 1436-1440
CEMARA : a Web dynamic application within a N-tier architecture for rare diseases
Messiaen C, Le Mignot L, Rath A, et al.
Studies in Health Technology and Informatics, 2008, 136, p. 51-56
Genetic bases of severe junctional epidermolysis bullosa presenting spontaneous amelioration with aging
Gache Y, Allegra M, Bodemer C, et al.
Human molecular genetics, 2001, 10, 21, p 2453
Reduced expression of the epithelial adhesion ligand laminin 5 in the skin causes intradermal tissue separation
Spirito F, Chanavas S, Prost-Squarcioni C, et al.
Journal of biological chemistry (The), 2001, 276, 22, p 18828
