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Page 1
The genetics of hereditary cancer risk syndromes in Brazil: a comprehensive analysis of 1682 patients.
Eur J Hum Genet. 2022 Jul;30(7):818-823. doi: 10.1038/s41431-022-01098-7. Epub 2022 May 9.
Eur J Hum Genet. 2022.
PMID: 35534704
Free PMC article.
The Brazilian Rare Genomes Project: Validation of Whole Genome Sequencing for Rare Diseases Diagnosis.
Coelho AVC, Mascaro-Cordeiro B, Lucon DR, Nóbrega MS, Reis RS, de Alexandre RB, Moura LMS, de Oliveira GS, Guedes RLM, Caraciolo MP, Zurro NB, Cervato MC, Oliveira JB.
Coelho AVC, et al. Among authors: zurro nb.
Front Mol Biosci. 2022 May 2;9:821582. doi: 10.3389/fmolb.2022.821582. eCollection 2022.
Front Mol Biosci. 2022.
PMID: 35586190
Free PMC article.
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The Role of AIRE in the Immunity Against Candida Albicans in a Model of Human Macrophages.
de Albuquerque JAT, Banerjee PP, Castoldi A, Ma R, Zurro NB, Ynoue LH, Arslanian C, Barbosa-Carvalho MUW, Correia-Deur JEM, Weiler FG, Dias-da-Silva MR, Lazaretti-Castro M, Pedroza LA, Câmara NOS, Mace E, Orange JS, Condino-Neto A.
de Albuquerque JAT, et al. Among authors: zurro nb.
Front Immunol. 2018 Mar 21;9:567. doi: 10.3389/fimmu.2018.00567. eCollection 2018.
Front Immunol. 2018.
PMID: 29666621
Free PMC article.
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A Novel Mutation in the NCF2 Gene in a CGD Patient With Chronic Recurrent Pneumopathy.
de Albuquerque JAT, Lima AM, de Oliveira Junior EB, Ishizuka EK, Aragão-Filho WC, Bengala Zurro N, Mayumi Chiba S, Fernandes FR, Condino-Neto A.
de Albuquerque JAT, et al. Among authors: bengala zurro n.
Front Pediatr. 2019 Sep 27;7:391. doi: 10.3389/fped.2019.00391. eCollection 2019.
Front Pediatr. 2019.
PMID: 31612120
Free PMC article.
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Correction to: Unusual Severe Seborrheic Dermatitis in Two Siblings with Autosomal Recessive Chronic Granulomatous Disease.
Zurro NB, de Oliveira Junior EB, França TT, Dantas VM, Tavares de Albuquerque JA, Condino-Neto A.
Zurro NB, et al.
J Clin Immunol. 2019 Nov;39(8):860. doi: 10.1007/s10875-019-00701-9.
J Clin Immunol. 2019.
PMID: 31676980
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Clinical and Genotypic Spectrum of Chronic Granulomatous Disease in 71 Latin American Patients: First Report from the LASID Registry.
de Oliveira-Junior EB, Zurro NB, Prando C, Cabral-Marques O, Pereira PV, Schimke LF, Klaver S, Buzolin M, Blancas-Galicia L, Santos-Argumedo L, Pietropaolo-Cienfuegos DR, Espinosa-Rosales F, King A, Sorensen R, Porras O, Roxo-Junior P, Forte WC, Orellana JC, Lozano A, Galicchio M, Regairaz L, Grumach AS, Costa-Carvalho BT, Bustamante J, Bezrodnik L, Oleastro M, Danielian S, Condino-Neto A.
de Oliveira-Junior EB, et al. Among authors: zurro nb.
Pediatr Blood Cancer. 2015 Dec;62(12):2101-7. doi: 10.1002/pbc.25674. Epub 2015 Jul 15.
Pediatr Blood Cancer. 2015.
PMID: 26185101
Clinical Trial.
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A C126R de novo Mutation in CYBB Leads to X-linked Chronic Granulomatous Disease With Recurrent Pneumonia and BCGitis.
de Albuquerque JAT, de Oliveira Junior EB, Zurro NB, Vendramini P, Ishizuka EK, Borgli DSP, de Souza MS, Condino-Neto A.
de Albuquerque JAT, et al. Among authors: zurro nb.
Front Pediatr. 2018 Sep 11;6:248. doi: 10.3389/fped.2018.00248. eCollection 2018.
Front Pediatr. 2018.
PMID: 30255005
Free PMC article.
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