Detalhe da pesquisa
1.
Angioedema associated with thrombolysis for ischemic stroke: analysis of a case-control study.
J Intern Med
; 286(6): 702-710, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31319000
2.
Comparing acquired angioedema with hereditary angioedema (types I/II): findings from the Icatibant Outcome Survey.
Clin Exp Immunol
; 188(1): 148-153, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-27936514
3.
Mucosal-associated Invariant Cells are Deficient in Systemic Sclerosis.
Scand J Immunol
; 86(4): 216-220, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28727155
4.
Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema.
Clin Exp Immunol
; 185(3): 332-7, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27271546
5.
Quality of life in systemic lupus erythematosus: description in a cohort of French patients and association with blood hydroxychloroquine levels.
Lupus
; 25(7): 735-40, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26876692
6.
Subcutaneous phaeohyphomycosis caused by Exophiala spinifera in a European patient with lymphoma: a rare occurrence case report and literature review.
Mycoses
; 59(11): 691-696, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27456474
7.
Efficacy of anti-TNF alpha in severe and/or refractory Behçet's disease: Multicenter study of 124 patients.
J Autoimmun
; 62: 67-74, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26162757
8.
FDG-PET/CT findings in systemic mastocytosis: a French multicentre study.
Eur J Nucl Med Mol Imaging
; 42(13): 2013-20, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26140850
9.
Awareness is still warranted for ARBs.
J Intern Med
; 285(5): 550-552, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30575158
10.
Tranexamic acid as maintenance treatment for non-histaminergic angioedema: analysis of efficacy and safety in 37 patients.
Clin Exp Immunol
; 178(1): 112-7, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24827773
11.
Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
Allergy
; 69(12): 1659-65, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25134986
12.
Cyclophosphamide vs rituximab for eradicating inhibitors in acquired hemophilia A: A randomized trial in 108 patients.
Thromb Res
; 237: 79-87, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38555718
13.
Benefits of progestin contraception in non-allergic angioedema.
Clin Exp Allergy
; 43(4): 475-82, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23517043
14.
[Hereditary angioedema and its new treatments: An update]. / Mise au point sur les angiÅdèmes héréditaires et leurs nouvelles thérapeutiques.
Rev Med Interne
; 44(7): 344-353, 2023 Jul.
Artigo
em Francês
| MEDLINE | ID: mdl-36872215
15.
French national diagnostic and care protocol for Kawasaki disease.
Rev Med Interne
; 44(7): 354-380, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37349225
16.
Efficacy of rituximab in primary Sjogren's syndrome with peripheral nervous system involvement: results from the AIR registry.
Ann Rheum Dis
; 71(1): 84-7, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21926185
17.
Why are people still dying of drug-susceptible TB in Paris in the 21st century?
Int J Tuberc Lung Dis
; 26(2): 142-149, 2022 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35086626
18.
Syndrome de Cogan.
Rev Med Interne
; 42(4): 269-274, 2021 Apr.
Artigo
em Francês
| MEDLINE | ID: mdl-32773166
19.
[Behçet's-like syndrome and other dysimmunitary manifestations related to myelodysplastic syndromes with trisomy 8]. / Syndrome de pseudo-Behçet et autres manifestations dysimmunitaires associées aux syndromes myélodysplasiques avec trisomie 8.
Rev Med Interne
; 42(3): 170-176, 2021 Mar.
Artigo
em Francês
| MEDLINE | ID: mdl-33139078
20.
[Periodic fever syndrome associated with mutations in the TNF type 1 receptor gene: A differential diagnosis of familial Mediterranean fever that should not be overlooked in patients of Mediterranean origin]. / Le syndrome de fièvre prolongée associée aux mutations du gène du récepteur au TNF de type 1 : un diagnostic différentiel de la fièvre méditerranéenne familiale à ne pas méconnaître chez les patients d'origine méditerranéenne.
Rev Med Interne
; 42(7): 459-464, 2021 Jul.
Artigo
em Francês
| MEDLINE | ID: mdl-33131906