Lunardi J - Search Results

1

Type III hereditary angio-oedema: clinical and biological features in a French cohort.

Vitrat-Hincky V, Gompel A, Dumestre-Perard C, Boccon-Gibod I, Drouet C, Cesbron JY, Lunardi J, Massot C, Bouillet L. Vitrat-Hincky V, et al. Among authors: lunardi j. Allergy. 2010 Oct;65(10):1331-6. doi: 10.1111/j.1398-9995.2010.02368.x. Epub 2010 Apr 7. Allergy. 2010. PMID: 20384613

2

Characterisation of a new C1 inhibitor mutant in a patient with hepatocellular carcinoma.

Monnier N, Ponard D, Duponchel C, Csopaki F, Bouillet L, Tosi M, Lunardi J, Drouet C. Monnier N, et al. Among authors: lunardi j. Mol Immunol. 2006 Jul;43(14):2161-8. doi: 10.1016/j.molimm.2006.01.006. Epub 2006 Mar 10. Mol Immunol. 2006. PMID: 16529817

3

Bradykinin receptor 2 antagonist (icatibant) for hereditary angioedema type III attacks.

Bouillet L, Boccon-Gibod I, Ponard D, Drouet C, Cesbron JY, Dumestre-Perard C, Monnier N, Lunardi J, Massot C, Gompel A. Bouillet L, et al. Among authors: lunardi j. Ann Allergy Asthma Immunol. 2009 Nov;103(5):448. doi: 10.1016/S1081-1206(10)60369-9. Ann Allergy Asthma Immunol. 2009. PMID: 19927548 No abstract available.

4

Mutational spectrum and phenotypes in Danish families with hereditary angioedema because of C1 inhibitor deficiency.

Bygum A, Fagerberg CR, Ponard D, Monnier N, Lunardi J, Drouet C. Bygum A, et al. Among authors: lunardi j. Allergy. 2011 Jan;66(1):76-84. doi: 10.1111/j.1398-9995.2010.02456.x. Epub 2010 Aug 30. Allergy. 2011. PMID: 20804470

5

Coagulation Factor XII Gene Mutation in Brazilian Families with Hereditary Angioedema with Normal C1 Inhibitor.

Moreno AS, Valle SO, Levy S, França AT, Serpa FS, Arcuri HA, Palma MS, Campos WN, Dias MM, Ponard D, Monnier N, Lunardi J, Bork K, Silva WA Jr, Arruda LK. Moreno AS, et al. Among authors: lunardi j. Int Arch Allergy Immunol. 2015;166(2):114-20. doi: 10.1159/000376547. Epub 2015 Mar 13. Int Arch Allergy Immunol. 2015. PMID: 25790805

6

Human C3 deficiency associated with impairments in dendritic cell differentiation, memory B cells, and regulatory T cells.

Ghannam A, Pernollet M, Fauquert JL, Monnier N, Ponard D, Villiers MB, Péguet-Navarro J, Tridon A, Lunardi J, Gerlier D, Drouet C. Ghannam A, et al. Among authors: lunardi j. J Immunol. 2008 Oct 1;181(7):5158-66. doi: 10.4049/jimmunol.181.7.5158. J Immunol. 2008. PMID: 18802120

7

Presence of two different genetic traits in malignant hyperthermia families: implication for genetic analysis, diagnosis, and incidence of malignant hyperthermia susceptibility.

Monnier N, Krivosic-Horber R, Payen JF, Kozak-Ribbens G, Nivoche Y, Adnet P, Reyford H, Lunardi J. Monnier N, et al. Among authors: lunardi j. Anesthesiology. 2002 Nov;97(5):1067-74. doi: 10.1097/00000542-200211000-00007. Anesthesiology. 2002. PMID: 12411788

8

Mutations in OCRL1 gene in Indian children with Lowe syndrome.

Sethi SK, Bagga A, Gulati A, Hari P, Gupta N, Lunardi J. Sethi SK, et al. Among authors: lunardi j. Clin Exp Nephrol. 2008 Oct;12(5):358-362. doi: 10.1007/s10157-008-0059-0. Epub 2008 May 24. Clin Exp Nephrol. 2008. PMID: 18500547

9

Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome.

Harbuz R, Lespinasse J, Boulet S, Francannet C, Creveaux I, Benkhelifa M, Jouk PS, Lunardi J, Ray PF. Harbuz R, et al. Among authors: lunardi j. Prenat Diagn. 2010 Nov;30(11):1072-8. doi: 10.1002/pd.2613. Prenat Diagn. 2010. PMID: 20842625

10

A new AURKC mutation causing macrozoospermia: implications for human spermatogenesis and clinical diagnosis.

Ben Khelifa M, Zouari R, Harbuz R, Halouani L, Arnoult C, Lunardi J, Ray PF. Ben Khelifa M, et al. Among authors: lunardi j. Mol Hum Reprod. 2011 Dec;17(12):762-8. doi: 10.1093/molehr/gar050. Epub 2011 Jul 6. Mol Hum Reprod. 2011. PMID: 21733974 Free PMC article.

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