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Trabalho de evento-resumo
Concordance between videofluoroscopic severity scales for neurogenic oropharyngeal dysphagia (2012)
Da Silva, Roberta; Motonaga, S.; Cola, P. C.; Gatto, A. R.; Ribeiro, P.; De Carvalho , L. R.; Schelp, A. O.; Jorge, A.; Peres, F.; Dantas, Roberto Oliveira
Conference titles: Annual Meeting of the Dysphagia Research Society. Unidade: FMRP
Subjects: TRANSTORNOS DE DEGLUTIÇÃO, FLUOROSCOPIA
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ABNT
DA SILVA, Roberta et al. Concordance between videofluoroscopic severity scales for neurogenic oropharyngeal dysphagia. 2012, Anais.. Toronto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2012. . Acesso em: 19 jul. 2024.
APA
Da Silva, R., Motonaga, S., Cola, P. C., Gatto, A. R., Ribeiro, P., De Carvalho , L. R., et al. (2012). Concordance between videofluoroscopic severity scales for neurogenic oropharyngeal dysphagia. In . Toronto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Da Silva R, Motonaga S, Cola PC, Gatto AR, Ribeiro P, De Carvalho LR, Schelp AO, Jorge A, Peres F, Dantas RO. Concordance between videofluoroscopic severity scales for neurogenic oropharyngeal dysphagia. 2012 ;[citado 2024 jul. 19 ]
Vancouver
Da Silva R, Motonaga S, Cola PC, Gatto AR, Ribeiro P, De Carvalho LR, Schelp AO, Jorge A, Peres F, Dantas RO. Concordance between videofluoroscopic severity scales for neurogenic oropharyngeal dysphagia. 2012 ;[citado 2024 jul. 19 ]
Trabalho de evento-resumo periodico
Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE) (2011)
França, M.; Jorge, A.; Carvalho, L.; Otto, A.; Corrêa, F.; Costalonga, E.; Mendonça. B.; Arnhold, I.
Source: Hormone Research in Paediatrics. Conference titles: Annual Meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP). Unidade: FM
Subjects: GENES (ANÁLISE), HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA), FENÓTIPOS, RESUMOS (EVENTOS)
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ABNT
FRANÇA, M. et al. Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE). Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf. Acesso em: 19 jul. 2024. , 2011
APA
França, M., Jorge, A., Carvalho, L., Otto, A., Corrêa, F., Costalonga, E., et al. (2011). Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE). Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
NLM
França M, Jorge A, Carvalho L, Otto A, Corrêa F, Costalonga E, Mendonça. B., Arnhold I. Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE) [Internet]. Hormone Research in Paediatrics. 2011 ; 76( suppl. 4): 1.[citado 2024 jul. 19 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
Vancouver
França M, Jorge A, Carvalho L, Otto A, Corrêa F, Costalonga E, Mendonça. B., Arnhold I. Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE) [Internet]. Hormone Research in Paediatrics. 2011 ; 76( suppl. 4): 1.[citado 2024 jul. 19 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
Artigo de periodico
Identification of SHOX gene deletions in patients with disproportional short stature or Léri-Weill dyschondrosteosis: comparison between the fish technique and microsatellite study (2007)
Funari, M.; Jorge, A.; Souza, S.; Mendonça, Berenice Bilharinho de; Nishi, M.
Source: Hormone research. Conference titles: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Subjects: TÉCNICAS DE DIAGNÓSTICO E PROCEDIMENTOS, PESO-ESTATURA, BIOMARCADORES
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ABNT
FUNARI, M. et al. Identification of SHOX gene deletions in patients with disproportional short stature or Léri-Weill dyschondrosteosis: comparison between the fish technique and microsatellite study. Hormone research, v. 68, p. 11, 2007Tradução . . Acesso em: 19 jul. 2024.
APA
Funari, M., Jorge, A., Souza, S., Mendonça, B. B. de, & Nishi, M. (2007). Identification of SHOX gene deletions in patients with disproportional short stature or Léri-Weill dyschondrosteosis: comparison between the fish technique and microsatellite study. Hormone research, 68, 11.
NLM
Funari M, Jorge A, Souza S, Mendonça BB de, Nishi M. Identification of SHOX gene deletions in patients with disproportional short stature or Léri-Weill dyschondrosteosis: comparison between the fish technique and microsatellite study. Hormone research. 2007 ; 68 11.[citado 2024 jul. 19 ]
Vancouver
Funari M, Jorge A, Souza S, Mendonça BB de, Nishi M. Identification of SHOX gene deletions in patients with disproportional short stature or Léri-Weill dyschondrosteosis: comparison between the fish technique and microsatellite study. Hormone research. 2007 ; 68 11.[citado 2024 jul. 19 ]
Artigo de periodico
Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth (2007)
Coutinho, D.; Coletta, R.; Costa, E.; Boguszewski, M.; Pachi, P.; Damiani, D.; Arnhold, I.; Mendonça, Berenice Bilharinho de; Jorge, A.
Source: Hormone research. Conference titles: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Subjects: POLIMORFISMO, ALELOPATIA, CRIANÇAS, RECÉM-NASCIDO PEQUENO PARA IDADE GESTACIONAL
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ABNT
COUTINHO, D. et al. Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth. Hormone research, v. 68, p. 8, 2007Tradução . . Acesso em: 19 jul. 2024.
APA
Coutinho, D., Coletta, R., Costa, E., Boguszewski, M., Pachi, P., Damiani, D., et al. (2007). Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth. Hormone research, 68, 8.
NLM
Coutinho D, Coletta R, Costa E, Boguszewski M, Pachi P, Damiani D, Arnhold I, Mendonça BB de, Jorge A. Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth. Hormone research. 2007 ; 68 8.[citado 2024 jul. 19 ]
Vancouver
Coutinho D, Coletta R, Costa E, Boguszewski M, Pachi P, Damiani D, Arnhold I, Mendonça BB de, Jorge A. Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth. Hormone research. 2007 ; 68 8.[citado 2024 jul. 19 ]
Artigo de periodico
Found in children with idiopathic short stature and NS-associated signs (2007)
Ferreira, L.; Montenegro, L.; Arnhold, I.; Mendonça, Berenice Bilharinho de; Jorge, A.
Source: Hormone research. Conference titles: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Subjects: POLIMORFISMO, PESO-ESTATURA, CRIANÇAS, MUTAÇÃO GENÉTICA
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ABNT
FERREIRA, L. et al. Found in children with idiopathic short stature and NS-associated signs. Hormone research, v. 68, p. 10, 2007Tradução . . Acesso em: 19 jul. 2024.
APA
Ferreira, L., Montenegro, L., Arnhold, I., Mendonça, B. B. de, & Jorge, A. (2007). Found in children with idiopathic short stature and NS-associated signs. Hormone research, 68, 10.
NLM
Ferreira L, Montenegro L, Arnhold I, Mendonça BB de, Jorge A. Found in children with idiopathic short stature and NS-associated signs. Hormone research. 2007 ; 68 10.[citado 2024 jul. 19 ]
Vancouver
Ferreira L, Montenegro L, Arnhold I, Mendonça BB de, Jorge A. Found in children with idiopathic short stature and NS-associated signs. Hormone research. 2007 ; 68 10.[citado 2024 jul. 19 ]
Trabalho de evento
Current phase shifts in poled polycarbonate caused by temperature oscillations (1991)
Jorge, A.; Leal Ferreira, Guilherme Fontes
Source: Proceedings. Conference titles: International Symposium on Electrets. Unidade: IFSC
Subjects: MATÉRIA CONDENSADA (PROPRIEDADES ELÉTRICAS), DIELÉTRICOS
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ABNT
JORGE, A. e LEAL FERREIRA, Guilherme Fontes. Current phase shifts in poled polycarbonate caused by temperature oscillations. 1991, Anais.. New York: IEEE, 1991. . Acesso em: 19 jul. 2024.
APA
Jorge, A., & Leal Ferreira, G. F. (1991). Current phase shifts in poled polycarbonate caused by temperature oscillations. In Proceedings. New York: IEEE.
NLM
Jorge A, Leal Ferreira GF. Current phase shifts in poled polycarbonate caused by temperature oscillations. Proceedings. 1991 ;[citado 2024 jul. 19 ]
Vancouver
Jorge A, Leal Ferreira GF. Current phase shifts in poled polycarbonate caused by temperature oscillations. Proceedings. 1991 ;[citado 2024 jul. 19 ]

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