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Page 1
Decreasing Attacks and Improving Quality of Life through a Systematic Management Program for Patients with Hereditary Angioedema.
Nunes FL, Ferriani MPL, Moreno AS, Langer SS, Maia LSM, Ferraro MF, Sarti W, Bessa Junior J, Cunha D, Suffritti C, Dias MM, Januário YC, daSilva LLP, Aragon DC, Caballero T, Arruda LK. Nunes FL, et al. Among authors: maia lsm. Int Arch Allergy Immunol. 2021;182(8):697-708. doi: 10.1159/000513896. Epub 2021 Mar 3. Int Arch Allergy Immunol. 2021. PMID: 33657571
Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families.
Veronez CL, Moreno AS, Constantino-Silva RN, Maia LSM, Ferriani MPL, Castro FFM, Valle SR, Nakamura VK, Cagini N, Gonçalves RF, Mansour E, Serpa FS, Coelho Dias GA, Piccirillo MA, Toledo E, de Souza Bernardes M, Cichon S, Stieber C, Arruda LK, Pesquero JB, Grumach AS. Veronez CL, et al. Among authors: maia lsm. J Allergy Clin Immunol Pract. 2018 Jul-Aug;6(4):1209-1216.e8. doi: 10.1016/j.jaip.2017.09.025. Epub 2017 Nov 8. J Allergy Clin Immunol Pract. 2018. PMID: 29128335
Serum Baseline Tryptase Level as a Marker for the Severity of Anaphylaxis.
Aniceto V, Dias MM, Melo JML, Trevisan-Neto O, Aragon DC, Maia LSM, Moreno AS, Arruda LK. Aniceto V, et al. Among authors: maia lsm. Int Arch Allergy Immunol. 2019;179(3):201-208. doi: 10.1159/000497235. Epub 2019 Mar 20. Int Arch Allergy Immunol. 2019. PMID: 30893687
Genotype-phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency.
Maia LSM, Moreno AS, Ferriani MPL, Nunes FL, Ferraro MF, Dias MM, Roxo-Junior P, Dias FC, Valle SOR, Levy S, Alonso MLO, França AT, Serpa FS, Motta AA, Maia FGM, Aragon DC, Sarti W, Silva WA Jr, Cichon S, Bork K, Arruda LK. Maia LSM, et al. Allergy. 2019 May;74(5):1013-1016. doi: 10.1111/all.13699. Epub 2019 Jan 22. Allergy. 2019. PMID: 30556912 No abstract available.
Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis.
Giavina-Bianchi P, Arruda LK, Aun MV, Campos RA, Chong-Neto HJ, Constantino-Silva RN, Fernandes FR, Ferraro MF, Ferriani MPL, França AT, Fusaro G, Garcia JFB, Komninakis S, Maia LSM, Mansour E, Moreno AS, Motta AA, Pesquero JB, Portilho N, Rosário NA, Serpa FS, Solé D, Takejima P, Toledo E, Valle SO, Veronez CL, Grumach AS. Giavina-Bianchi P, et al. Among authors: maia lsm. Clinics (Sao Paulo). 2018;73:e310. doi: 10.6061/clinics/2018/e310. Epub 2018 May 3. Clinics (Sao Paulo). 2018. PMID: 29723342 Free PMC article.
Corrigendum to "Gene mapping strategy for Alu elements rearrangements: Detection of new large deletions in the SERPING1 gene causing hereditary angioedema in Brazilian families" [Gene 685C (2019) 179-185].
Nicolicht P, Faria DOS, Martins-Silva L, Maia LSM, Moreno AS, Arruda LK, Motta AA, Grumach AS, Pesquero JB. Nicolicht P, et al. Among authors: maia lsm. Gene. 2020 Jan 30;725:143896. doi: 10.1016/j.gene.2019.05.047. Epub 2019 May 29. Gene. 2020. PMID: 31153634 No abstract available.
11 results