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Page 1
Hereditary angioedema in children: Review and practical perspective for clinical management.
Pagnier A, Dermesropian A, Kevorkian-Verguet C, Bourgoin-Heck M, Hoarau C, Reumaux H, Nugues F, Audouin-Pajot C, Blanc S, Carbasse A, Jurquet AL, Voidey M, Villedieu M, Bouillet L, Boccon-Gibod I. Pagnier A, et al. Pediatr Allergy Immunol. 2024 Dec;35(12):e14268. doi: 10.1111/pai.14268. Pediatr Allergy Immunol. 2024. PMID: 39655944 Free PMC article. Review.
Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema.
Deroux A, Boccon-Gibod I, Fain O, Pralong P, Ollivier Y, Pagnier A, Djenouhat K, Du-Thanh A, Gompel A, Faisant C, Launay D, Bouillet L. Deroux A, et al. Among authors: pagnier a. Clin Exp Immunol. 2016 Sep;185(3):332-7. doi: 10.1111/cei.12820. Clin Exp Immunol. 2016. PMID: 27271546 Free PMC article.
Enzymatic assays for the diagnosis of bradykinin-dependent angioedema.
Defendi F, Charignon D, Ghannam A, Baroso R, Csopaki F, Allegret-Cadet M, Ponard D, Favier B, Cichon S, Nicolie B, Fain O, Martin L, Drouet C; National Reference Centre for Angioedema CREAK. Defendi F, et al. PLoS One. 2013 Aug 5;8(8):e70140. doi: 10.1371/journal.pone.0070140. Print 2013. PLoS One. 2013. PMID: 23940538 Free PMC article.
Familial and syndromic lupus share the same phenotype as other early-onset forms of lupus.
Weill O, Decramer S, Malcus C, Kassai B, Rouvet I, Ginhoux T, Crow YJ, Rieux-Laucat F, Soulas-Sprauel P, Pagnier A, Koné-Paut I, Piram M, Galeotti C, Samaille C, Reumaux H, Lanteri A, Dubois SM, Lefebvre H, Burtey S, Maurier F, Carbasse A, Lemelle I, Meinzer U, Despert V, Flodrops H, Fabien N, Ranchin B, Hachulla E, Bader-Meunier B, Belot A. Weill O, et al. Among authors: pagnier a. Joint Bone Spine. 2017 Oct;84(5):589-593. doi: 10.1016/j.jbspin.2016.12.008. Epub 2016 Dec 28. Joint Bone Spine. 2017. PMID: 28039062
Long-Term Follow-Up and Optimization of Interleukin-1 Inhibitors in the Management of Monogenic Autoinflammatory Diseases: Real-Life Data from the JIR Cohort.
Hentgen V, Koné-Paut I, Belot A, Galeotti C, Grateau G, Carbasse A, Pagnier A, Pillet P, Delord M, Hofer M, Georgin-Lavialle S. Hentgen V, et al. Among authors: pagnier a. Front Pharmacol. 2021 Jan 11;11:568865. doi: 10.3389/fphar.2020.568865. eCollection 2020. Front Pharmacol. 2021. PMID: 33505305 Free PMC article.
An appraisal of the frequency and severity of noninfectious manifestations in primary immunodeficiencies: A study of a national retrospective cohort of 1375 patients over 10 years.
Alligon M, Mahlaoui N, Courteille V, Costes L, Afonso V, Randrianomenjanahary P, de Vergnes N, Ranohavimparany A, Vo D, Hafsa I, Bach P, Benoit V, Garcelon N, Fischer A; members of the CEREDIH French PID study group. Alligon M, et al. J Allergy Clin Immunol. 2022 Jun;149(6):2116-2125. doi: 10.1016/j.jaci.2021.12.790. Epub 2022 Jan 12. J Allergy Clin Immunol. 2022. PMID: 35031273
COVID-19 infection among patients with autoinflammatory diseases: a study on 117 French patients compared with 1545 from the French RMD COVID-19 cohort: COVIMAI - the French cohort study of SARS-CoV-2 infection in patient with systemic autoinflammatory diseases.
Bourguiba R, Kyheng M, Koné-Paut I, Rouzaud D, Avouac J, Devaux M, Abdallah NA, Fautrel B, Ferreira-Maldent N, Langlois V, Ledoult E, Nielly H, Queyrel V, Sellam J, Tieulie N, Chazerain P, Evon P, Labreuche J, Savey L, Hentgen V, Grateau G, Georgin-Lavialle S; FAI2R/SFR/SNFMI/SOFREMIP/CRI/IMIDIATE consortium and contributors. Bourguiba R, et al. RMD Open. 2022 May;8(1):e002063. doi: 10.1136/rmdopen-2021-002063. RMD Open. 2022. PMID: 35537796 Free PMC article.
[Vogt-Koyanagi-Harada syndrome: a serious and rare emergency in children].
Venaille A, Palombi K, Templier I, Bouillet L, Pagnier A, Debillon T, Bourdat-Michel G. Venaille A, et al. Among authors: pagnier a. Arch Pediatr. 2011 Jan;18(1):33-6. doi: 10.1016/j.arcped.2010.09.013. Epub 2010 Nov 4. Arch Pediatr. 2011. PMID: 21055910 French.
83 results