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Artigo de periodico
Molecular basis of various forms of maple syrup urine disease in Chilean patients (2021)
Campanholi, Diana Ruffato Resende; Margutti, Ana Vitoria Barban; Silva Junior, Wilson Araújo da ; Garcia, Daniel Fantozzi; Molfetta, Greice Andreotti de ; Marques, Adriana A.; Schwartz, Ida Vanessa Doederlein; Cornejo, V.; Hamilton, Valerie; Castro, Gabriela; Sperb-ludwig, Fernanda; Borges, Ester S.; Camelo Júnior, José Simon
Source: Molecular Genetics & Genomic Medicine. Unidade: FMRP
Subjects: AMINOÁCIDOS, ERROS INATOS DO METABOLISMO, LEUCENA, DOENÇA DA URINA DE XAROPE DE BORDO
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ABNT
CAMPANHOLI, Diana Ruffato Resende et al. Molecular basis of various forms of maple syrup urine disease in Chilean patients. Molecular Genetics & Genomic Medicine, v. 9, n. 5, 2021Tradução . . Disponível em: https://doi.org/10.1002/mgg3.1616. Acesso em: 02 nov. 2024.
APA
Campanholi, D. R. R., Margutti, A. V. B., Silva Junior, W. A. da, Garcia, D. F., Molfetta, G. A. de, Marques, A. A., et al. (2021). Molecular basis of various forms of maple syrup urine disease in Chilean patients. Molecular Genetics & Genomic Medicine, 9( 5). doi:10.1002/mgg3.1616
NLM
Campanholi DRR, Margutti AVB, Silva Junior WA da, Garcia DF, Molfetta GA de, Marques AA, Schwartz IVD, Cornejo V, Hamilton V, Castro G, Sperb-ludwig F, Borges ES, Camelo Júnior JS. Molecular basis of various forms of maple syrup urine disease in Chilean patients [Internet]. Molecular Genetics & Genomic Medicine. 2021 ; 9( 5):[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/mgg3.1616
Vancouver
Campanholi DRR, Margutti AVB, Silva Junior WA da, Garcia DF, Molfetta GA de, Marques AA, Schwartz IVD, Cornejo V, Hamilton V, Castro G, Sperb-ludwig F, Borges ES, Camelo Júnior JS. Molecular basis of various forms of maple syrup urine disease in Chilean patients [Internet]. Molecular Genetics & Genomic Medicine. 2021 ; 9( 5):[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/mgg3.1616
Artigo de periodico
Phenotypic IgA deficit (SIgAD) or probably (PIgAD) and related diseases associations during 4 years of research in Latin-American kids (2018)
Fernández, Carmen; Roxo-Junior, Pérsio ; Marina, S. C.; Juan, C. A. B.; Felipe, M. B.; Deysi, L. A. F.; Lorena, B.
Source: Journal of Clinical Immunology and Research. Unidade: FMRP
Subjects: ALERGIA E IMUNOLOGIA, ASMA, LEITE, VITILIGO
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ABNT
FERNÁNDEZ, Carmen et al. Phenotypic IgA deficit (SIgAD) or probably (PIgAD) and related diseases associations during 4 years of research in Latin-American kids. Journal of Clinical Immunology and Research, v. 1, n. 1, p. [5 ], 2018Tradução . . Disponível em: https://www.scitechnol.com/peer-review/phenotypic-iga-deficit-sigad-or-probably-pigad-and-related-diseases-associations-during-4-years-of-research-in-latinamerican-kids-axjk.pdf. Acesso em: 02 nov. 2024.
APA
Fernández, C., Roxo-Junior, P., Marina, S. C., Juan, C. A. B., Felipe, M. B., Deysi, L. A. F., & Lorena, B. (2018). Phenotypic IgA deficit (SIgAD) or probably (PIgAD) and related diseases associations during 4 years of research in Latin-American kids. Journal of Clinical Immunology and Research, 1( 1), [5 ]. Recuperado de https://www.scitechnol.com/peer-review/phenotypic-iga-deficit-sigad-or-probably-pigad-and-related-diseases-associations-during-4-years-of-research-in-latinamerican-kids-axjk.pdf
NLM
Fernández C, Roxo-Junior P, Marina SC, Juan CAB, Felipe MB, Deysi LAF, Lorena B. Phenotypic IgA deficit (SIgAD) or probably (PIgAD) and related diseases associations during 4 years of research in Latin-American kids [Internet]. Journal of Clinical Immunology and Research. 2018 ; 1( 1): [5 ].[citado 2024 nov. 02 ] Available from: https://www.scitechnol.com/peer-review/phenotypic-iga-deficit-sigad-or-probably-pigad-and-related-diseases-associations-during-4-years-of-research-in-latinamerican-kids-axjk.pdf
Vancouver
Fernández C, Roxo-Junior P, Marina SC, Juan CAB, Felipe MB, Deysi LAF, Lorena B. Phenotypic IgA deficit (SIgAD) or probably (PIgAD) and related diseases associations during 4 years of research in Latin-American kids [Internet]. Journal of Clinical Immunology and Research. 2018 ; 1( 1): [5 ].[citado 2024 nov. 02 ] Available from: https://www.scitechnol.com/peer-review/phenotypic-iga-deficit-sigad-or-probably-pigad-and-related-diseases-associations-during-4-years-of-research-in-latinamerican-kids-axjk.pdf
Trabalho de evento-resumo periodico
Identification of six new mutations on chilean population with maple syrup urine disease (2017)
Campanholi, Diana; Camelo Júnior, José Simon; Cornejo, Veronica; Schwartz, Ida V. D.; Borges, Ester; Silva Júnior, Wilson Araújo da; Campo, Karen
Source: Journal of Inborn Errors of Metabolism and Screening. Conference titles: International Congress of Inborn Errors of Metabolism. Unidade: FMRP
Subjects: GENÉTICA ANIMAL, GADO NELORE, INTERAÇÃO GENÓTIPO-AMBIENTE
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ABNT
CAMPANHOLI, Diana et al. Identification of six new mutations on chilean population with maple syrup urine disease. Journal of Inborn Errors of Metabolism and Screening. Thousand Oaks: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 02 nov. 2024. , 2017
APA
Campanholi, D., Camelo Júnior, J. S., Cornejo, V., Schwartz, I. V. D., Borges, E., Silva Júnior, W. A. da, & Campo, K. (2017). Identification of six new mutations on chilean population with maple syrup urine disease. Journal of Inborn Errors of Metabolism and Screening. Thousand Oaks: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Campanholi D, Camelo Júnior JS, Cornejo V, Schwartz IVD, Borges E, Silva Júnior WA da, Campo K. Identification of six new mutations on chilean population with maple syrup urine disease. Journal of Inborn Errors of Metabolism and Screening. 2017 ; 5 174-175.[citado 2024 nov. 02 ]
Vancouver
Campanholi D, Camelo Júnior JS, Cornejo V, Schwartz IVD, Borges E, Silva Júnior WA da, Campo K. Identification of six new mutations on chilean population with maple syrup urine disease. Journal of Inborn Errors of Metabolism and Screening. 2017 ; 5 174-175.[citado 2024 nov. 02 ]
Artigo de periodico
Impact of maternal diabetes mellitus on mortality and morbidity of very low birth weight infants: a multicenter Latin America study (2015)
Grandi, Carlos; Tapia, José L.; Cardoso, Viviane Cunha
Source: Jornal de Pediatria. Unidade: FMRP
Subjects: RECÉM-NASCIDO DE MUITO BAIXO PESO, DIABETES MELLITUS, MORBIDADE, MORTALIDADE NEONATAL
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ABNT
GRANDI, Carlos e TAPIA, José L. e CARDOSO, Viviane Cunha. Impact of maternal diabetes mellitus on mortality and morbidity of very low birth weight infants: a multicenter Latin America study. Jornal de Pediatria, v. 91, n. 3, p. 234-241, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.jped.2014.08.007. Acesso em: 02 nov. 2024.
APA
Grandi, C., Tapia, J. L., & Cardoso, V. C. (2015). Impact of maternal diabetes mellitus on mortality and morbidity of very low birth weight infants: a multicenter Latin America study. Jornal de Pediatria, 91( 3), 234-241. doi:10.1016/j.jped.2014.08.007
NLM
Grandi C, Tapia JL, Cardoso VC. Impact of maternal diabetes mellitus on mortality and morbidity of very low birth weight infants: a multicenter Latin America study [Internet]. Jornal de Pediatria. 2015 ; 91( 3): 234-241.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.jped.2014.08.007
Vancouver
Grandi C, Tapia JL, Cardoso VC. Impact of maternal diabetes mellitus on mortality and morbidity of very low birth weight infants: a multicenter Latin America study [Internet]. Jornal de Pediatria. 2015 ; 91( 3): 234-241.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.jped.2014.08.007
Artigo de periodico
Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry (2015)
Oliveira-Junior, Edgar Borges de; Zurro, Nuria Bengala; Prando, Carolina; Cabral-Marques, Otavio; Pereira, Paulo Vitor Soeiro; Schimke, Lena-Friederick; Klaver, Stefanie; Buzolin, Marcia; Blancas-Galicia, Lizbeth; Santos-Argumedo, Leopoldo; Pietropaolo-Cienfuegos, Dino Roberto; Espinosa-Rosales, Francisco; King, Alejandra; Sorensen, Ricardo; Porras, Oscar; Roxo Junior, Persio; Forte, Wilma Carvalho Neves; Orellana, Julio Cesar; Lozano, Alejandro; Galicchio, Miguel; Regairaz, Lorena; Grumach, Anete Sevciovic; Costa-Carvalho, Beatriz Tavares; Bustamante, Jacinta; Bezrodnik, Liliana; Oleastro, Matias; Danielian, Silvia; Condino Neto, Antonio
Source: Pediatric Blood & Cancer. Unidades: FMRP, ICB
Subjects: GENÉTICA MÉDICA, MUTAÇÃO, INFECÇÕES BACTERIANAS
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ABNT
OLIVEIRA-JUNIOR, Edgar Borges de et al. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry. Pediatric Blood & Cancer, v. 62, n. 12, p. 2101-2107, 2015Tradução . . Disponível em: https://doi.org/10.1002/pbc.25674. Acesso em: 02 nov. 2024.
APA
Oliveira-Junior, E. B. de, Zurro, N. B., Prando, C., Cabral-Marques, O., Pereira, P. V. S., Schimke, L. -F., et al. (2015). Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry. Pediatric Blood & Cancer, 62( 12), 2101-2107. doi:10.1002/pbc.25674
NLM
Oliveira-Junior EB de, Zurro NB, Prando C, Cabral-Marques O, Pereira PVS, Schimke L-F, 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 WCN, Orellana JC, Lozano A, Galicchio M, Regairaz L, Grumach AS, Costa-Carvalho BT, Bustamante J, Bezrodnik L, Oleastro M, Danielian S, Condino Neto A. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry [Internet]. Pediatric Blood & Cancer. 2015 ; 62( 12): 2101-2107.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/pbc.25674
Vancouver
Oliveira-Junior EB de, Zurro NB, Prando C, Cabral-Marques O, Pereira PVS, Schimke L-F, 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 WCN, Orellana JC, Lozano A, Galicchio M, Regairaz L, Grumach AS, Costa-Carvalho BT, Bustamante J, Bezrodnik L, Oleastro M, Danielian S, Condino Neto A. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry [Internet]. Pediatric Blood & Cancer. 2015 ; 62( 12): 2101-2107.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/pbc.25674
Artigo de periodico
Long-term effect of imiglucerase in Latin American children with Gaucher disease type 1: lessons from the International Collaborative Gaucher Group Gaucher Registry (2014)
Camelo Junior, José Simon; Cabello, Juan Francisco; Drelichman, Guillermo G.; Kerstenetzky, Marcelo M.; Sarmiento, Isabel C.; Ordoñez, Soledad Suarez; Taylor, John S.; Gwosdow, Andrea R.; Linares, Adriana
Source: BMC Hematology. Unidade: FMRP
Subjects: CRIANÇAS, HEMATOLOGIA (RESULTADOS)
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ABNT
CAMELO JUNIOR, José Simon et al. Long-term effect of imiglucerase in Latin American children with Gaucher disease type 1: lessons from the International Collaborative Gaucher Group Gaucher Registry. BMC Hematology, v. 14, 2014Tradução . . Disponível em: https://doi.org/10.1186/2052-1839-14-10. Acesso em: 02 nov. 2024.
APA
Camelo Junior, J. S., Cabello, J. F., Drelichman, G. G., Kerstenetzky, M. M., Sarmiento, I. C., Ordoñez, S. S., et al. (2014). Long-term effect of imiglucerase in Latin American children with Gaucher disease type 1: lessons from the International Collaborative Gaucher Group Gaucher Registry. BMC Hematology, 14. doi:10.1186/2052-1839-14-10
NLM
Camelo Junior JS, Cabello JF, Drelichman GG, Kerstenetzky MM, Sarmiento IC, Ordoñez SS, Taylor JS, Gwosdow AR, Linares A. Long-term effect of imiglucerase in Latin American children with Gaucher disease type 1: lessons from the International Collaborative Gaucher Group Gaucher Registry [Internet]. BMC Hematology. 2014 ; 14[citado 2024 nov. 02 ] Available from: https://doi.org/10.1186/2052-1839-14-10
Vancouver
Camelo Junior JS, Cabello JF, Drelichman GG, Kerstenetzky MM, Sarmiento IC, Ordoñez SS, Taylor JS, Gwosdow AR, Linares A. Long-term effect of imiglucerase in Latin American children with Gaucher disease type 1: lessons from the International Collaborative Gaucher Group Gaucher Registry [Internet]. BMC Hematology. 2014 ; 14[citado 2024 nov. 02 ] Available from: https://doi.org/10.1186/2052-1839-14-10

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