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Presse Medicale (Paris, France : 1983)|May 20, 2006
[Takayasu arteritis]Thomas Quéméneur, Eric Hachulla, Marc Lambert, et al.
Clinical and Experimental Rheumatology|February 22, 2018
No specific imaging pattern can help differentiate IgG4-related disease from idiopathic retroperitoneal fibrosis: 18 histologically proven casesAlexandra Forestier, David Buob, Tristan Mirault, et al.
Medicine|September 30, 2016
Pulmonary arterial hypertension in idiopathic inflammatory myopathies: Data from the French pulmonary hypertension registry and review of the literatureSébastien Sanges, Cécile M Yelnik, Olivier Sitbon, et al.
Journal of Scleroderma and Related Disorders|November 4, 2024
Prevalence, causes, and clinical associations of anemia in patients with systemic sclerosis: A cohort studyBenoit Gachet, Mathieu Jouvray, Vincent Koether, et al.
RMD Open|July 1, 2025
Thrombin generation test as a useful tool for improving disease severity stratification in antiphospholipid syndromeCecile Yelnik, Anne Bauters, Julien Labreuche, et al.
Plos One|May 16, 2018
Clinical phenotypes and survival of pre-capillary pulmonary hypertension in systemic sclerosisDavid Launay, David Montani, Paul M Hassoun, et al.
Rheumatology (Oxford, England)|February 7, 2025
Anti-fibroblast and anti-endothelial cell autoantibodies in pulmonary arterial hypertension (PAH) in patients with connective tissue diseases (CTD)Benjamin Thoreau, Arthur Renaud, Philippe Chafey, et al.
The European Respiratory Journal|September 14, 2018
Haemodynamics and serial risk assessment in systemic sclerosis associated pulmonary arterial hypertensionJason Weatherald, Athénaïs Boucly, David Launay, et al.
Arthritis and Rheumatism|April 29, 2006
Recovery from deafness in a patient with Muckle-Wells syndrome treated with anakinraTristan Mirault, David Launay, Laurence Cuisset, et al.
Chest|August 31, 2017
Pulmonary Arterial Hypertension Associated With Systemic Lupus Erythematosus: Results From the French Pulmonary Hypertension RegistryEric Hachulla, Xavier Jais, Gaël Cinquetti, et al.
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