sobre o Dr. Condino - CRM: 51204
Médico e pesquisador especializado em imunologia.
Diretor Médico da Clínica Alergológica, do Laboratório Immunogenic e do Centro de Imunodeficiências Primárias Jeffrey Modell, São Paulo, SP. Consultor Científico Sênior no Instituto Jô Clemente e no Instituto Pensi/Hospital Sabará/Alergia Pediátrica - Imunologia. Presidente do Departamento de Imunologia da Sociedade Brasileira de Pediatria, Diretor de Relações Internacionais da Sociedade Brasileira de Alergia e Imunologia e membro de outras sociedades internacionais líderes em Alergia e Imunologia Clínica. Membro do conselho editorial do Journal of Clinical Immunology e do Journal of Allergy and Clinical Immunology. É Editor Associado da Frontiers Immunology / Primary Immunodeficiencies.
Diretor de Relações Internacionais da Associação Brasileira de Alergia e Imunologia
Diretor do Centro Jeffrey Modell de Imunodeficiências - São Paulo
Livre Docente em Alergia, Imunologia e Pneumologia Pediátrica - FCM UNICAMP (2001)
Doutorado em Farmacologia ICB USP (1994)
Residência Pediátrica FCM - Unicamp (1986)
Graduação Medicina FCM - Unicamp (1984)
Diretor Cientifico da SMCC (Sociedade de Medicina e Cirurgia de Campinas)
Presidente do Departamento de Imunologia da Sociedade Brasileira de Pediatria
Professor Titular de Imunologia e Medicina Experimental USP (2009)
Pós-Doutorado em Medicina Molecular na University of Massachusetts Medical School - Estados Unidos (1997)
Mestrado em Imunologia no IB - Unicamp (1990)
Publicações recentes
Confira abaixo publicações científicas recentes do dr. Condino. Utilize os filtros para selecionar resultados. Clique em 'Resumo' sob os títulos de cada publicação para mais detalhes.
2025
do Amaral de Leon, Cristiano; Amantea, Sérgio Luis; Pereira, Renan Augusto; Dantas, Ellen O; Loekmanwidjaja, Jéssica; Costa-Carvalho, Beatriz T; Mazzucchelli, Juliana T L; Aranda, Carolina S; González-Serrano, Maria E; Córdoba, Elizabeth Alejandra De La Cruz; Bezrodnik, Liliana; Moreira, Ileana; Ferreira, Janaira F S; Dantas, Vera M; Sales, Valéria S F; Navarrete, Carmen L; Vilela, Maria M S; Motta, Isabella P; Franco, Jose Luis; Arango, Julio Cesar Orrego; Álvarez-Álvarez, Jesús A; Cardozo, Lina Rocío Riaño; Orellana, Julio C; Condino-Neto, Antonio; Kokron, Cristina M; Barros, Myrthes T; Regairaz, Lorena; Cabanillas, Diana; Suarez, Carmen L N; Rosario, Nelson A; Chong-Neto, Herberto J; Takano, Olga A; Nadaf, Maria I S V; Moraes, Lillian S L; Tavares, Fabiola S; Rabelo, Flaviane; Pino, Jessica; Calderon, Wilmer C; Mendoza-Quispe, Daniel; Goudouris, Ekaterine S; Patiño, Virginia; Montenegro, Cecilia; Souza, Monica S; Branco, Aniela B X C Castelo; Forte, Wilma C N; Carvalho, Flavia A A; Segundo, Gesmar; Cheik, Marina F A; Roxo-Junior, Pérsio; Peres, Maryanna; Oliveira, Annie M; Neto, Arnaldo C P; Ortega-López, Maria Claudia; Lozano, Alejandro; Lozano, Natalia Andrea; Nieto, Leticia H; Grumach, Anete S; Costa, Daniele C; Antunes, Nelma M N; Nudelman, Victor; Pereira, Camila T M; Martinez, Maria D M; Quiroz, Francisco J R; Cardona, Aristoteles A; Nuñez-Nuñez, Maria E; Rodriguez, Jairo A; Cuellar, Célia M; Vijoditz, Gustavo; Bichuetti-Silva, Daniélli C; Prando, Carolina C M
Nutritional status and metabolic alterations in patients with ataxia-telangiectasia Journal Article
Em: Orphanet J Rare Dis, vol. 20, não 1, pp. 330, 2025, ISSN: 1750-1172.
Resumo | Links | BibTeX | Tags: ataxia-telangiectasia, nutrição
@article{pmid40597142,
title = {Nutritional status and metabolic alterations in patients with ataxia-telangiectasia},
author = {Cristiano do Amaral de Leon and Sérgio Luis Amantea and Renan Augusto Pereira and Ellen O Dantas and Jéssica Loekmanwidjaja and Beatriz T Costa-Carvalho and Juliana T L Mazzucchelli and Carolina S Aranda and Maria E González-Serrano and Elizabeth Alejandra De La Cruz Córdoba and Liliana Bezrodnik and Ileana Moreira and Janaira F S Ferreira and Vera M Dantas and Valéria S F Sales and Carmen L Navarrete and Maria M S Vilela and Isabella P Motta and Jose Luis Franco and Julio Cesar Orrego Arango and Jesús A Álvarez-Álvarez and Lina Rocío Riaño Cardozo and Julio C Orellana and Antonio Condino-Neto and Cristina M Kokron and Myrthes T Barros and Lorena Regairaz and Diana Cabanillas and Carmen L N Suarez and Nelson A Rosario and Herberto J Chong-Neto and Olga A Takano and Maria I S V Nadaf and Lillian S L Moraes and Fabiola S Tavares and Flaviane Rabelo and Jessica Pino and Wilmer C Calderon and Daniel Mendoza-Quispe and Ekaterine S Goudouris and Virginia Patiño and Cecilia Montenegro and Monica S Souza and Aniela B X C Castelo Branco and Wilma C N Forte and Flavia A A Carvalho and Gesmar Segundo and Marina F A Cheik and Pérsio Roxo-Junior and Maryanna Peres and Annie M Oliveira and Arnaldo C P Neto and Maria Claudia Ortega-López and Alejandro Lozano and Natalia Andrea Lozano and Leticia H Nieto and Anete S Grumach and Daniele C Costa and Nelma M N Antunes and Victor Nudelman and Camila T M Pereira and Maria D M Martinez and Francisco J R Quiroz and Aristoteles A Cardona and Maria E Nuñez-Nuñez and Jairo A Rodriguez and Célia M Cuellar and Gustavo Vijoditz and Daniélli C Bichuetti-Silva and Carolina C M Prando},
doi = {10.1186/s13023-025-03785-2},
issn = {1750-1172},
year = {2025},
date = {2025-07-01},
urldate = {2025-07-01},
journal = {Orphanet J Rare Dis},
volume = {20},
number = {1},
pages = {330},
abstract = {BACKGROUND: Ataxia-telangiectasia (A-T) is a DNA repair disorder characterized by progressive degeneration, immunodeficiency, cancer predisposition, malnutrition, metabolic disorders, and chronic liver disease. The study aims to describe the nutritional status and plasma levels of biomarkers of lipid status, metabolic profile, and liver function of patients with A-T.nnRESULTS: A total of 218 patients from 9 Latin American countries were included in the study. The distribution of patients according to nutritional status by age group revealed an over-time increase in the proportion of patients with severe thinness (p = 0.016). High glucose and triglyceride levels were observed in 9.5% and 23.6% of patients, respectively. Total cholesterol was high in 31.7, and 34.0% had abnormal LDL-c levels. In the analysis of paired samples, a progressive increase in aspartate aminotransferase was observed over time.nnCONCLUSIONS: The present results are comparable to those of previous studies also showing changes in nutritional status and in lipid, metabolic, and liver profiles over time. These findings confirm a high rate of thinness in patients with A-T and progressive deterioration as the disease progresses, as well as changes in plasma levels of biomarkers of lipid status, metabolic profile, and liver function.},
keywords = {ataxia-telangiectasia, nutrição},
pubstate = {published},
tppubtype = {article}
}
2024
Pereira, Renan A; Dantas, Ellen O; Loekmanwidjaja, Jessica; Mazzucchelli, Juliana T L; Aranda, Carolina S; Serrano, Maria E G; Córdoba, Elisabeth A De La Cruz; Bezrodnik, Liliana; Moreira, Ileana; Ferreira, Janaira F S; Dantas, Vera M; Sales, Valéria S F; Fernandez, Carmen C; Vilela, Maria M S; Motta, Isabela P; Franco, Jose Luis; Arango, Julio Cesar Orrego; Álvarez-Álvarez, Jesús A; Cardozo, Lina Rocío Riaño; Orellana, Julio C; Condino-Neto, Antonio; Kokron, Cristina M; Barros, Myrthes T; Regairaz, Lorena; Cabanillas, Diana; Suarez, Carmen L N; Rosario, Nelson A; Chong-Neto, Herberto J; Takano, Olga A; Nadaf, Maria I S V; Moraes, Lillian S L; Tavares, Fabiola S; Rabelo, Flaviane; Pino, Jessica; Calderon, Wilmer C; Mendoza-Quispe, Daniel; Goudouris, Ekaterini S; Patiño, Virginia; Montenegro, Cecilia; Souza, Monica S; Branco, Aniela BXCCastelo; Forte, Wilma C N; Carvalho, Flavia A A; Segundo, Gesmar; Cheik, Marina F A; Roxo-Junior, Persio; Peres, Maryanna; Oliveira, Annie M; Neto, Arnaldo C P; Ortega-López, Maria Claudia; Lozano, Alejandro; Lozano, Natalia Andrea; Nieto, Leticia H; Grumach, Anete S; Costa, Daniele C; Antunes, Nelma M N; Nudelman, Victor; Pereira, Camila T M; Martinez, Maria D M; Quiroz, Francisco J R; Cardona, Aristoteles A; Nuñez-Nuñez, Maria E; Rodriguez, Jairo A; Cuellar, Célia M; Vijoditz, Gustavo; Bichuetti-Silva, Daniélli C; Prando, Carolina C M; Amantéa, Sérgio L; Costa-Carvalho, Beatriz T
Ataxia-telangiectasia in Latin America: clinical features, immunodeficiency, and mortality in a multicenter study Journal Article
Em: Immunol Res, vol. 72, não 4, pp. 864–873, 2024, ISSN: 1559-0755.
Resumo | Links | BibTeX | Tags: ataxia-telangiectasia
@article{pmid38834764,
title = {Ataxia-telangiectasia in Latin America: clinical features, immunodeficiency, and mortality in a multicenter study},
author = {Renan A Pereira and Ellen O Dantas and Jessica Loekmanwidjaja and Juliana T L Mazzucchelli and Carolina S Aranda and Maria E G Serrano and Elisabeth A De La Cruz Córdoba and Liliana Bezrodnik and Ileana Moreira and Janaira F S Ferreira and Vera M Dantas and Valéria S F Sales and Carmen C Fernandez and Maria M S Vilela and Isabela P Motta and Jose Luis Franco and Julio Cesar Orrego Arango and Jesús A Álvarez-Álvarez and Lina Rocío Riaño Cardozo and Julio C Orellana and Antonio Condino-Neto and Cristina M Kokron and Myrthes T Barros and Lorena Regairaz and Diana Cabanillas and Carmen L N Suarez and Nelson A Rosario and Herberto J Chong-Neto and Olga A Takano and Maria I S V Nadaf and Lillian S L Moraes and Fabiola S Tavares and Flaviane Rabelo and Jessica Pino and Wilmer C Calderon and Daniel Mendoza-Quispe and Ekaterini S Goudouris and Virginia Patiño and Cecilia Montenegro and Monica S Souza and Aniela BXCCastelo Branco and Wilma C N Forte and Flavia A A Carvalho and Gesmar Segundo and Marina F A Cheik and Persio Roxo-Junior and Maryanna Peres and Annie M Oliveira and Arnaldo C P Neto and Maria Claudia Ortega-López and Alejandro Lozano and Natalia Andrea Lozano and Leticia H Nieto and Anete S Grumach and Daniele C Costa and Nelma M N Antunes and Victor Nudelman and Camila T M Pereira and Maria D M Martinez and Francisco J R Quiroz and Aristoteles A Cardona and Maria E Nuñez-Nuñez and Jairo A Rodriguez and Célia M Cuellar and Gustavo Vijoditz and Daniélli C Bichuetti-Silva and Carolina C M Prando and Sérgio L Amantéa and Beatriz T Costa-Carvalho},
doi = {10.1007/s12026-024-09494-5},
issn = {1559-0755},
year = {2024},
date = {2024-08-01},
urldate = {2024-08-01},
journal = {Immunol Res},
volume = {72},
number = {4},
pages = {864--873},
abstract = {Ataxia-telangiectasia (AT) is a rare genetic disorder leading to neurological defects, telangiectasias, and immunodeficiency. We aimed to study the clinical and immunological features of Latin American patients with AT and analyze factors associated with mortality. Referral centers from 9 Latin American countries participated in this retrospective cohort study, and 218 patients were included. Median (IQR) ages at symptom onset and diagnosis were 1.0 (1.0-2.0) and 5.0 (3.0-8.0) years, respectively. Most patients presented recurrent airway infections, which was significantly associated with IgA deficiency. IgA deficiency was observed in 60.8% of patients and IgG deficiency in 28.6%. T- and B-lymphopenias were also present in most cases. Mean survival was 24.2 years, and Kaplan-Meier 20-year-survival rate was 52.6%, with higher mortality associated with female gender and low IgG levels. These findings suggest that immunologic status should be investigated in all patients with AT.},
keywords = {ataxia-telangiectasia},
pubstate = {published},
tppubtype = {article}
}