ReP USP - Resultado da busca

Artigo de periodico
Prevalence of palatal and alveolar cysts in babies with cleft lip and palate (2004)
Alves, Karina Mirela Ribeiro Pinto; Peixoto, Virginia; Gomide, Márcia Ribeiro; Carrara, Cleide Felício de Carvalho; Costa, Beatriz
Source: The Cleft Palate-Craniofacial Journal. Unidade: HRAC
Subjects: PROCESSO ALVEOLAR, FISSURA LÁBIOPALATINA, BEBÊS, CISTO PERIODONTAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVES, Karina Mirela Ribeiro Pinto et al. Prevalence of palatal and alveolar cysts in babies with cleft lip and palate. The Cleft Palate-Craniofacial Journal, v. 41, n. 5, p. 490-493, 2004Tradução . . Acesso em: 31 out. 2024.
APA
Alves, K. M. R. P., Peixoto, V., Gomide, M. R., Carrara, C. F. de C., & Costa, B. (2004). Prevalence of palatal and alveolar cysts in babies with cleft lip and palate. The Cleft Palate-Craniofacial Journal, 41( 5), 490-493.
NLM
Alves KMRP, Peixoto V, Gomide MR, Carrara CF de C, Costa B. Prevalence of palatal and alveolar cysts in babies with cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 5): 490-493.[citado 2024 out. 31 ]
Vancouver
Alves KMRP, Peixoto V, Gomide MR, Carrara CF de C, Costa B. Prevalence of palatal and alveolar cysts in babies with cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 5): 490-493.[citado 2024 out. 31 ]
Artigo de periodico
Rapid maxillary expansion after secondary alveolar bone graft in a patient with bilateral cleft lip and palate (2004)
Cavassan, Arlete de Oliveira; Albuquerque, Marcelo d'Albuquerque de; Capelozza Filho, Leopoldino
Source: The Cleft Palate-Craniofacial Journal. Unidades: HRAC, FOB
Subjects: EXPANSÃO RÁPIDA DA MAXILA, FISSURA LÁBIOPALATINA, ENXERTO ÓSSEO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAVASSAN, Arlete de Oliveira e ALBUQUERQUE, Marcelo d'Albuquerque de e CAPELOZZA FILHO, Leopoldino. Rapid maxillary expansion after secondary alveolar bone graft in a patient with bilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal, v. 41, n. 3, p. 332-339, 2004Tradução . . Acesso em: 31 out. 2024.
APA
Cavassan, A. de O., Albuquerque, M. d'A. de, & Capelozza Filho, L. (2004). Rapid maxillary expansion after secondary alveolar bone graft in a patient with bilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal, 41( 3), 332-339.
NLM
Cavassan A de O, Albuquerque M d'A de, Capelozza Filho L. Rapid maxillary expansion after secondary alveolar bone graft in a patient with bilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 3): 332-339.[citado 2024 out. 31 ]
Vancouver
Cavassan A de O, Albuquerque M d'A de, Capelozza Filho L. Rapid maxillary expansion after secondary alveolar bone graft in a patient with bilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 3): 332-339.[citado 2024 out. 31 ]
Artigo de periodico
Chronology of deciduous teeth eruption in children with cleft lip and palate (2004)
Duque, Cristiane; Dalben, Gisele da Silva; Aranha, Andreza Maria Fábio; Carrara, Cleide Felício de Carvalho; Gomide, Márcia Ribeiro; Costa, Beatriz
Source: The Cleft Palate-Craniofacial Journal. Unidade: HRAC
Subjects: DENTE DECÍDUO, ERUPÇÃO DENTÁRIA, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DUQUE, Cristiane et al. Chronology of deciduous teeth eruption in children with cleft lip and palate. The Cleft Palate-Craniofacial Journal, v. 41, n. 3, p. 285-289, 2004Tradução . . Acesso em: 31 out. 2024.
APA
Duque, C., Dalben, G. da S., Aranha, A. M. F., Carrara, C. F. de C., Gomide, M. R., & Costa, B. (2004). Chronology of deciduous teeth eruption in children with cleft lip and palate. The Cleft Palate-Craniofacial Journal, 41( 3), 285-289.
NLM
Duque C, Dalben G da S, Aranha AMF, Carrara CF de C, Gomide MR, Costa B. Chronology of deciduous teeth eruption in children with cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 3): 285-289.[citado 2024 out. 31 ]
Vancouver
Duque C, Dalben G da S, Aranha AMF, Carrara CF de C, Gomide MR, Costa B. Chronology of deciduous teeth eruption in children with cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 3): 285-289.[citado 2024 out. 31 ]
Artigo de periodico
Growth of children with isolated Robin sequence treated by nasopharyngeal intubation: importance of a hypercaloric diet (2004)
Marques, Ilza Lazarini; Peres, Suely Prieto de Barros Almeida; Bettiol, Heloisa; Barbieri, Marco Antonio; Andrea, Mauro; Souza, Luiz de
Source: The Cleft Palate-Craniofacial Journal. Unidades: HRAC, FMRP
Subjects: SÍNDROME DE PIERRE ROBIN, NUTRIÇÃO DA CRIANÇA, NUTRIÇÃO INFANTIL, NASOFARINGE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARQUES, Ilza Lazarini et al. Growth of children with isolated Robin sequence treated by nasopharyngeal intubation: importance of a hypercaloric diet. The Cleft Palate-Craniofacial Journal, v. 41, n. Ja 2004, p. 53-58, 2004Tradução . . Acesso em: 31 out. 2024.
APA
Marques, I. L., Peres, S. P. de B. A., Bettiol, H., Barbieri, M. A., Andrea, M., & Souza, L. de. (2004). Growth of children with isolated Robin sequence treated by nasopharyngeal intubation: importance of a hypercaloric diet. The Cleft Palate-Craniofacial Journal, 41( Ja 2004), 53-58.
NLM
Marques IL, Peres SP de BA, Bettiol H, Barbieri MA, Andrea M, Souza L de. Growth of children with isolated Robin sequence treated by nasopharyngeal intubation: importance of a hypercaloric diet. The Cleft Palate-Craniofacial Journal. 2004 ; 41( Ja 2004): 53-58.[citado 2024 out. 31 ]
Vancouver
Marques IL, Peres SP de BA, Bettiol H, Barbieri MA, Andrea M, Souza L de. Growth of children with isolated Robin sequence treated by nasopharyngeal intubation: importance of a hypercaloric diet. The Cleft Palate-Craniofacial Journal. 2004 ; 41( Ja 2004): 53-58.[citado 2024 out. 31 ]
Artigo de periodico
Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study (2004)
Passos-Bueno, Maria Rita ; Gaspar, Dinamar A.; Kamiya, Tânia Yoshico; Tescarollo, Graziela; Rabanéa, Daniel Saraiva; Richieri-Costa, Antonio; Alonso, Nivaldo; Araújo, Belmino
Source: The Cleft Palate-Craniofacial Journal. Unidades: IB, HRAC
Subjects: GENES, FISSURA LÁBIOPALATINA, GENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal, v. 41, n. 4, p. 387-391, 2004Tradução . . Acesso em: 31 out. 2024.
APA
Passos-Bueno, M. R., Gaspar, D. A., Kamiya, T. Y., Tescarollo, G., Rabanéa, D. S., Richieri-Costa, A., et al. (2004). Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal, 41( 4), 387-391.
NLM
Passos-Bueno MR, Gaspar DA, Kamiya TY, Tescarollo G, Rabanéa DS, Richieri-Costa A, Alonso N, Araújo B. Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 4): 387-391.[citado 2024 out. 31 ]
Vancouver
Passos-Bueno MR, Gaspar DA, Kamiya TY, Tescarollo G, Rabanéa DS, Richieri-Costa A, Alonso N, Araújo B. Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 4): 387-391.[citado 2024 out. 31 ]
Artigo de periodico
Delayed formation of a lower second premolar (2004)
Silva Filho, Omar Gabriel da; Lauris, Rita de Cássia Moura Carvalho; Ferrari Junior, Flávio Mauro; Ozawa, Terumi Okada
Source: The Journal of Clinical Pediatric Dentistry. Unidade: HRAC
Subjects: PRÉ-MOLAR, ODONTOGÊNESE, ORTODONTIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA FILHO, Omar Gabriel da et al. Delayed formation of a lower second premolar. The Journal of Clinical Pediatric Dentistry, v. 28, n. 4, p. 299-301, 2004Tradução . . Disponível em: https://doi.org/10.17796/jcpd.28.4.811nk87718648n43. Acesso em: 31 out. 2024.
APA
Silva Filho, O. G. da, Lauris, R. de C. M. C., Ferrari Junior, F. M., & Ozawa, T. O. (2004). Delayed formation of a lower second premolar. The Journal of Clinical Pediatric Dentistry, 28( 4), 299-301. doi:10.17796/jcpd.28.4.811nk87718648n43
NLM
Silva Filho OG da, Lauris R de CMC, Ferrari Junior FM, Ozawa TO. Delayed formation of a lower second premolar [Internet]. The Journal of Clinical Pediatric Dentistry. 2004 ; 28( 4): 299-301.[citado 2024 out. 31 ] Available from: https://doi.org/10.17796/jcpd.28.4.811nk87718648n43
Vancouver
Silva Filho OG da, Lauris R de CMC, Ferrari Junior FM, Ozawa TO. Delayed formation of a lower second premolar [Internet]. The Journal of Clinical Pediatric Dentistry. 2004 ; 28( 4): 299-301.[citado 2024 out. 31 ] Available from: https://doi.org/10.17796/jcpd.28.4.811nk87718648n43
Artigo de periodico
TBX22 mutations are a frequent cause of cleft palate (2004)
Marçano, Ana Carolina Braga; Doudney, K.; Braybrook, C.; Squires, R.; Patton, M. A.; Lees, M. M.; Richieri-Costa, Antonio; Lidral, Andrew C.; Murray, Jeffrey C.; Moore, G.E.; Stanier, P.
Source: Journal of Medical Genetics. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, FISSURA PALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARÇANO, Ana Carolina Braga et al. TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics, v. 41, n. Ja 2004, p. 68-74, 2004Tradução . . Acesso em: 31 out. 2024.
APA
Marçano, A. C. B., Doudney, K., Braybrook, C., Squires, R., Patton, M. A., Lees, M. M., et al. (2004). TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics, 41( Ja 2004), 68-74.
NLM
Marçano ACB, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P. TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics. 2004 ; 41( Ja 2004): 68-74.[citado 2024 out. 31 ]
Vancouver
Marçano ACB, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P. TBX22 mutations are a frequent cause of cleft palate. Journal of Medical Genetics. 2004 ; 41( Ja 2004): 68-74.[citado 2024 out. 31 ]
Artigo de periodico
Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? (2004)
Guion-Almeida, Maria Leine; Paula, Ligiane Alves Machado; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e PAULA, Ligiane Alves Machado e RICHIERI-COSTA, Antonio. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome?. American Journal of Medical Genetics, v. 129A, n. 2, p. 156-161, 2004Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30153. Acesso em: 31 out. 2024.
APA
Guion-Almeida, M. L., Paula, L. A. M., & Richieri-Costa, A. (2004). Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? American Journal of Medical Genetics, 129A( 2), 156-161. doi:10.1002/ajmg.a.30153
NLM
Guion-Almeida ML, Paula LAM, Richieri-Costa A. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? [Internet]. American Journal of Medical Genetics. 2004 ; 129A( 2): 156-161.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.30153
Vancouver
Guion-Almeida ML, Paula LAM, Richieri-Costa A. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? [Internet]. American Journal of Medical Genetics. 2004 ; 129A( 2): 156-161.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.30153
Artigo de periodico
Behavior of partially formed roots of teeth submitted to orthodontic movement (2004)
Silva Filho, Omar Gabriel da; Mendes, Olivia de Freitas; Ozawa, Terumi Okada; Ferrari Junior, Flávio Mauro; Corrêa, Tatiana Mattosinho
Source: Journal of Clinical Pediatric Dentistry. Unidade: HRAC
Subjects: DENTIÇÃO MISTA, ORTODONTIA INTERCEPTORA, MOVIMENTAÇÃO DENTÁRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA FILHO, Omar Gabriel da et al. Behavior of partially formed roots of teeth submitted to orthodontic movement. Journal of Clinical Pediatric Dentistry, v. 28, n. 2, p. 147-154, 2004Tradução . . Disponível em: https://doi.org/10.17796/jcpd.28.2.56n643558770p763. Acesso em: 31 out. 2024.
APA
Silva Filho, O. G. da, Mendes, O. de F., Ozawa, T. O., Ferrari Junior, F. M., & Corrêa, T. M. (2004). Behavior of partially formed roots of teeth submitted to orthodontic movement. Journal of Clinical Pediatric Dentistry, 28( 2), 147-154. doi:10.17796/jcpd.28.2.56n643558770p763
NLM
Silva Filho OG da, Mendes O de F, Ozawa TO, Ferrari Junior FM, Corrêa TM. Behavior of partially formed roots of teeth submitted to orthodontic movement [Internet]. Journal of Clinical Pediatric Dentistry. 2004 ; 28( 2): 147-154.[citado 2024 out. 31 ] Available from: https://doi.org/10.17796/jcpd.28.2.56n643558770p763
Vancouver
Silva Filho OG da, Mendes O de F, Ozawa TO, Ferrari Junior FM, Corrêa TM. Behavior of partially formed roots of teeth submitted to orthodontic movement [Internet]. Journal of Clinical Pediatric Dentistry. 2004 ; 28( 2): 147-154.[citado 2024 out. 31 ] Available from: https://doi.org/10.17796/jcpd.28.2.56n643558770p763
Artigo de periodico
Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment (2004)
Fernandes, Adriano Yacubian; Palhares Neto, Aristides; Giglio, Alcir; Gabarra, Roberto Colichio; Zanini, Silvio Antonio; Portela, Luis; Plese, José Píndaro Pereira
Source: Journal of Neuroradiologie. Unidades: HRAC, FM
Subjects: ANORMALIDADES CRANIOFACIAIS, CÉREBRO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERNANDES, Adriano Yacubian et al. Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment. Journal of Neuroradiologie, v. 31, n. 2, p. 116-122, 2004Tradução . . Disponível em: https://doi.org/10.1016/s0150-9861(04)96978-7. Acesso em: 31 out. 2024.
APA
Fernandes, A. Y., Palhares Neto, A., Giglio, A., Gabarra, R. C., Zanini, S. A., Portela, L., & Plese, J. P. P. (2004). Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment. Journal of Neuroradiologie, 31( 2), 116-122. doi:10.1016/s0150-9861(04)96978-7
NLM
Fernandes AY, Palhares Neto A, Giglio A, Gabarra RC, Zanini SA, Portela L, Plese JPP. Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment [Internet]. Journal of Neuroradiologie. 2004 ; 31( 2): 116-122.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/s0150-9861(04)96978-7
Vancouver
Fernandes AY, Palhares Neto A, Giglio A, Gabarra RC, Zanini SA, Portela L, Plese JPP. Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment [Internet]. Journal of Neuroradiologie. 2004 ; 31( 2): 116-122.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/s0150-9861(04)96978-7
Artigo de periodico
Acrofrontofacionasal dysostosis: report of the third Brazilian family (2003)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: DISOSTOSE CRÂNIOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Acrofrontofacionasal dysostosis: report of the third Brazilian family. American Journal of Medical Genetics, v. 119A, n. 2, p. 238-241, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10444. Acesso em: 31 out. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (2003). Acrofrontofacionasal dysostosis: report of the third Brazilian family. American Journal of Medical Genetics, 119A( 2), 238-241. doi:10.1002/ajmg.a.10444
NLM
Guion-Almeida ML, Richieri-Costa A. Acrofrontofacionasal dysostosis: report of the third Brazilian family [Internet]. American Journal of Medical Genetics. 2003 ; 119A( 2): 238-241.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.10444
Vancouver
Guion-Almeida ML, Richieri-Costa A. Acrofrontofacionasal dysostosis: report of the third Brazilian family [Internet]. American Journal of Medical Genetics. 2003 ; 119A( 2): 238-241.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.10444
Artigo de periodico
Blepharocheilodontic (BCD) syndrome:: expanding the phenotype? (2003)
Lopes, Vera Lúcia Gil da Silva; Guion-Almeida, Maria Leine; Rodini, Elaine Sbroggio de Oliveira
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, FISSURA LÁBIOPALATINA, HIPOTIREOIDISMO, ANOMALIA DENTÁRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOPES, Vera Lúcia Gil da Silva e GUION-ALMEIDA, Maria Leine e RODINI, Elaine Sbroggio de Oliveira. Blepharocheilodontic (BCD) syndrome:: expanding the phenotype?. American Journal of Medical Genetics, v. 121A, n. 3, p. 266-270, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.20223. Acesso em: 31 out. 2024.
APA
Lopes, V. L. G. da S., Guion-Almeida, M. L., & Rodini, E. S. de O. (2003). Blepharocheilodontic (BCD) syndrome:: expanding the phenotype? American Journal of Medical Genetics, 121A( 3), 266-270. doi:10.1002/ajmg.a.20223
NLM
Lopes VLG da S, Guion-Almeida ML, Rodini ES de O. Blepharocheilodontic (BCD) syndrome:: expanding the phenotype? [Internet]. American Journal of Medical Genetics. 2003 ; 121A( 3): 266-270.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.20223
Vancouver
Lopes VLG da S, Guion-Almeida ML, Rodini ES de O. Blepharocheilodontic (BCD) syndrome:: expanding the phenotype? [Internet]. American Journal of Medical Genetics. 2003 ; 121A( 3): 266-270.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.20223
Artigo de periodico
Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients (2003)
Tabith Junior, Alfredo; Gonçalves, Cristina Guedes de Azevedo Bento
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: LARINGE, MALFORMAÇÕES, VOZ (FISIOLOGIA), ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TABITH JUNIOR, Alfredo e GONÇALVES, Cristina Guedes de Azevedo Bento. Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients. American Journal of Medical Genetics, v. 122A, n. 2, p. 133-138, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10227. Acesso em: 31 out. 2024.
APA
Tabith Junior, A., & Gonçalves, C. G. de A. B. (2003). Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients. American Journal of Medical Genetics, 122A( 2), 133-138. doi:10.1002/ajmg.a.10227
NLM
Tabith Junior A, Gonçalves CG de AB. Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients [Internet]. American Journal of Medical Genetics. 2003 ; 122A( 2): 133-138.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.10227
Vancouver
Tabith Junior A, Gonçalves CG de AB. Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: description of two new patients [Internet]. American Journal of Medical Genetics. 2003 ; 122A( 2): 133-138.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.10227
Artigo de periodico
Clinical and microbiological evaluation of the periodontal status of children with unilateral complete cleft lip and palate (2003)
Costa, Beatriz; Lima, José Eduardo de Oliveira; Gomide, Márcia Ribeiro; Rosa, Odila Pereira da Silva
Source: The Cleft Palate-Craniofacial Journal. Unidades: HRAC, FOB
Subjects: BACTÉRIAS AERÓBICAS, FISSURA LÁBIOPALATINA COMPLETA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, Beatriz et al. Clinical and microbiological evaluation of the periodontal status of children with unilateral complete cleft lip and palate. The Cleft Palate-Craniofacial Journal, v. No, n. 6, p. 585-589, 2003Tradução . . Acesso em: 31 out. 2024.
APA
Costa, B., Lima, J. E. de O., Gomide, M. R., & Rosa, O. P. da S. (2003). Clinical and microbiological evaluation of the periodontal status of children with unilateral complete cleft lip and palate. The Cleft Palate-Craniofacial Journal, No( 6), 585-589.
NLM
Costa B, Lima JE de O, Gomide MR, Rosa OP da S. Clinical and microbiological evaluation of the periodontal status of children with unilateral complete cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2003 ; No( 6): 585-589.[citado 2024 out. 31 ]
Vancouver
Costa B, Lima JE de O, Gomide MR, Rosa OP da S. Clinical and microbiological evaluation of the periodontal status of children with unilateral complete cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2003 ; No( 6): 585-589.[citado 2024 out. 31 ]
Artigo de periodico
Frontonasal dysplasia, Poland anomaly and unilateral hypoplasia of lower limb: report on a male patient (2003)
Guion-Almeida, Maria Leine; Lopes, Vera Lúcia Gil da Silva
Source: Clinical Dysmorphology. Unidade: HRAC
Subjects: HIPERTELORISMO, ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e LOPES, Vera Lúcia Gil da Silva. Frontonasal dysplasia, Poland anomaly and unilateral hypoplasia of lower limb: report on a male patient. Clinical Dysmorphology, v. 12, n. 4, p. 233-236, 2003Tradução . . Disponível em: https://doi.org/10.1097/00019605-200310000-00004. Acesso em: 31 out. 2024.
APA
Guion-Almeida, M. L., & Lopes, V. L. G. da S. (2003). Frontonasal dysplasia, Poland anomaly and unilateral hypoplasia of lower limb: report on a male patient. Clinical Dysmorphology, 12( 4), 233-236. doi:10.1097/00019605-200310000-00004
NLM
Guion-Almeida ML, Lopes VLG da S. Frontonasal dysplasia, Poland anomaly and unilateral hypoplasia of lower limb: report on a male patient [Internet]. Clinical Dysmorphology. 2003 ; 12( 4): 233-236.[citado 2024 out. 31 ] Available from: https://doi.org/10.1097/00019605-200310000-00004
Vancouver
Guion-Almeida ML, Lopes VLG da S. Frontonasal dysplasia, Poland anomaly and unilateral hypoplasia of lower limb: report on a male patient [Internet]. Clinical Dysmorphology. 2003 ; 12( 4): 233-236.[citado 2024 out. 31 ] Available from: https://doi.org/10.1097/00019605-200310000-00004
Artigo de periodico
Nasopharyngoscopy in Robin sequence: clinical and predictive value (2003)
Sousa, Telma Vidotto de; Marques, Ilza Lazarini; Carneiro, Araken Fernando; Bettiol, Heloisa; Freitas, José Alberto de Souza
Source: The Cleft Palate-Craniofacial Journal. Unidades: HRAC, FMRP, FOB
Subjects: SÍNDROME DE PIERRE ROBIN, NASOFARINGE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUSA, Telma Vidotto de et al. Nasopharyngoscopy in Robin sequence: clinical and predictive value. The Cleft Palate-Craniofacial Journal, v. No 2003, n. 6, p. 618-623, 2003Tradução . . Acesso em: 31 out. 2024.
APA
Sousa, T. V. de, Marques, I. L., Carneiro, A. F., Bettiol, H., & Freitas, J. A. de S. (2003). Nasopharyngoscopy in Robin sequence: clinical and predictive value. The Cleft Palate-Craniofacial Journal, No 2003( 6), 618-623.
NLM
Sousa TV de, Marques IL, Carneiro AF, Bettiol H, Freitas JA de S. Nasopharyngoscopy in Robin sequence: clinical and predictive value. The Cleft Palate-Craniofacial Journal. 2003 ; No 2003( 6): 618-623.[citado 2024 out. 31 ]
Vancouver
Sousa TV de, Marques IL, Carneiro AF, Bettiol H, Freitas JA de S. Nasopharyngoscopy in Robin sequence: clinical and predictive value. The Cleft Palate-Craniofacial Journal. 2003 ; No 2003( 6): 618-623.[citado 2024 out. 31 ]
Artigo de periodico
Waardenburg syndrome: clinical differentiation between types I and II (2003)
Pardono, Eliete; Bever, Yolande van; Ende, Jenneke van den; Havrenne, Poti Chimetta; Iughetti, Paula; Maestrelli, Sylvia Regina Pedrosa; Costa Filho, Orozimbo Alves; Richieri-Costa, Antonio; Frota-Pessoa, Oswaldo; Otto, Paulo A
Source: American Journal of Medical Genetics. Unidades: FOB, HRAC, IB
Assunto: ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARDONO, Eliete et al. Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, v. 117A, n. 3, p. 223-235, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10193. Acesso em: 31 out. 2024.
APA
Pardono, E., Bever, Y. van, Ende, J. van den, Havrenne, P. C., Iughetti, P., Maestrelli, S. R. P., et al. (2003). Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, 117A( 3), 223-235. doi:10.1002/ajmg.a.10193
NLM
Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.10193
Vancouver
Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.10193
Trabalho de evento-resumo periodico
Breastfeeding and bottle use in cleft babies (2001)
Gomide, Márcia Ribeiro; Dalben, Gisele da Silva; Costa, Beatriz; Neves, Lucimara Teixeira das
Source: Journal of Dental Research. Conference titles: Reunião Anual da Sociedade Brasileira de Pesquisa Odontológica. Unidade: HRAC
Subjects: ALEITAMENTO MATERNO, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMIDE, Márcia Ribeiro et al. Breastfeeding and bottle use in cleft babies. Journal of Dental Research. Chicago: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. . Acesso em: 31 out. 2024. , 2001
APA
Gomide, M. R., Dalben, G. da S., Costa, B., & Neves, L. T. das. (2001). Breastfeeding and bottle use in cleft babies. Journal of Dental Research. Chicago: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo.
NLM
Gomide MR, Dalben G da S, Costa B, Neves LT das. Breastfeeding and bottle use in cleft babies. Journal of Dental Research. 2001 ; 80( 4): 1086.[citado 2024 out. 31 ]
Vancouver
Gomide MR, Dalben G da S, Costa B, Neves LT das. Breastfeeding and bottle use in cleft babies. Journal of Dental Research. 2001 ; 80( 4): 1086.[citado 2024 out. 31 ]
Artigo de periodico
Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia (2000)
Suzuki, Koji; Hu, Diane; Bustos, Tania; Zlotogora, Joel; Richieri-Costa, Antonio; Helms, Jill A.; Spritz, Richard A.
Source: Nature Genetics. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, GENES, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SUZUKI, Koji et al. Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia. Nature Genetics, v. 25, p. 427-430, 2000Tradução . . Disponível em: https://doi.org/10.1038/78119. Acesso em: 31 out. 2024.
APA
Suzuki, K., Hu, D., Bustos, T., Zlotogora, J., Richieri-Costa, A., Helms, J. A., & Spritz, R. A. (2000). Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia. Nature Genetics, 25, 427-430. doi:10.1038/78119
NLM
Suzuki K, Hu D, Bustos T, Zlotogora J, Richieri-Costa A, Helms JA, Spritz RA. Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia [Internet]. Nature Genetics. 2000 ; 25 427-430.[citado 2024 out. 31 ] Available from: https://doi.org/10.1038/78119
Vancouver
Suzuki K, Hu D, Bustos T, Zlotogora J, Richieri-Costa A, Helms JA, Spritz RA. Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia [Internet]. Nature Genetics. 2000 ; 25 427-430.[citado 2024 out. 31 ] Available from: https://doi.org/10.1038/78119
Artigo de periodico
Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? (1997)
Passos-Bueno, Maria Rita ; Sertié, Andréa Laurato; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidades: IB, HRAC
Subjects: SÍNDROMES OROFACIODIGITAIS, MUTAÇÃO, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita e SERTIÉ, Andréa Laurato e RICHIERI-COSTA, Antonio. Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene?. American Journal of Medical Genetics, v. 71, n. 2, p. 243-245, 1997Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d. Acesso em: 31 out. 2024.
APA
Passos-Bueno, M. R., Sertié, A. L., & Richieri-Costa, A. (1997). Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? American Journal of Medical Genetics, 71( 2), 243-245. doi:10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d
NLM
Passos-Bueno MR, Sertié AL, Richieri-Costa A. Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? [Internet]. American Journal of Medical Genetics. 1997 ; 71( 2): 243-245.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d
Vancouver
Passos-Bueno MR, Sertié AL, Richieri-Costa A. Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? [Internet]. American Journal of Medical Genetics. 1997 ; 71( 2): 243-245.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d

USP Schools

ReP

Filtros

Departament

Authors

USP affiliated authors

Date published

Subjects

Source title

Indexado em

Non normalized affiliation

Countries of institutions of collaboration