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Journal of Clinical Immunology|November 1, 2020
Hereditary Angioedema with and Without C1-Inhibitor Deficiency in Postmenopausal WomenAurore Billebeau, Olivier Fain, David Launay, et al.
Annals of Surgery|October 15, 2016
Reemergence of Splenectomy for ITP Second-line Treatment?Charbel Chater, Louis Terriou, Alain Duhamel, et al.
JAMA Neurology|September 13, 2018
Development of a New Classification System for Idiopathic Inflammatory Myopathies Based on Clinical Manifestations and Myositis-Specific AutoantibodiesKubéraka Mariampillai, Benjamin Granger, Damien Amelin, et al.
Rheumatology (Oxford, England)|February 17, 2010
Clinical manifestations of anti-synthetase syndrome positive for anti-alanyl-tRNA synthetase (anti-PL12) antibodies: a retrospective study of 17 casesBaptiste Hervier, Benoit Wallaert, Eric Hachulla, et al.
RMD Open|June 15, 2023
Assessment of type I interferon response in routine practice in France in 2022Anais Nombel, Anne Perrine Foray, Lorna Garnier, et al.
European Journal of Dermatology : EJD|March 3, 2017
Hereditary angioedema with normal C1 inhibitor: clinical characteristics and treatment response with plasma-derived human C1 inhibitor concentrate (Berinert<sup>®</sup>) in a French cohortLaurence Bouillet, Isabelle Boccon-Gibod, Anne Gompel, et al.
British Journal of Haematology|November 20, 2002
Autologous bone marrow transplantation in the treatment of refractory systemic sclerosis: early results from a French multicentre phase I-II studyDominique Farge, Jean Pierre Marolleau, Sarah Zohar, et al.
The Journal of Rheumatology|June 3, 2009
Clinical features of scleroderma patients with or without prior or current ischemic digital ulcers: post-hoc analysis of a nationwide multicenter cohort (ItinérAIR-Sclérodermie)Kiet Phong Tiev, Elisabeth Diot, Pierre Clerson, et al.
Presse Medicale (Paris, France : 1983)|November 23, 2007
[Management of digital ulcers from systemic scleroderma]Camille Francès, Yannick Allanore, Jean Cabane, et al.
Medicine|August 31, 2012
Malignant retroperitoneal fibrosis: MRI characteristics in 50 patientsTristan Mirault, Marc Lambert, Philippe Puech, et al.
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