ReP USP - Resultado da busca

Artigo de periodico
Gingival recession in individuals with cleft lip and palate: prevalence and severity. (2012)
Almeida, Ana Lúcia Pompéia Fraga de ; Esper, Luis Augusto; Pegoraro, Thiago Amadei; Valle, Accacio Lins do
Source: Cleft Palate-craniofacial Journal. Unidades: FOB, HRAC
Subjects: RETRAÇÃO GENGIVAL, FISSURA LÁBIOPALATINA, PREVALÊNCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALMEIDA, Ana Lúcia Pompéia Fraga de et al. Gingival recession in individuals with cleft lip and palate: prevalence and severity. Cleft Palate-craniofacial Journal, v. 49, n. Ja 2012., p. 92-95, 2012Tradução . . Disponível em: https://doi.org/10.1597/10-052. Acesso em: 03 out. 2024.
APA
Almeida, A. L. P. F. de, Esper, L. A., Pegoraro, T. A., & Valle, A. L. do. (2012). Gingival recession in individuals with cleft lip and palate: prevalence and severity. Cleft Palate-craniofacial Journal, 49( Ja 2012.), 92-95. doi:10.1597/10-052
NLM
Almeida ALPF de, Esper LA, Pegoraro TA, Valle AL do. Gingival recession in individuals with cleft lip and palate: prevalence and severity. [Internet]. Cleft Palate-craniofacial Journal. 2012 ; 49( Ja 2012.): 92-95.[citado 2024 out. 03 ] Available from: https://doi.org/10.1597/10-052
Vancouver
Almeida ALPF de, Esper LA, Pegoraro TA, Valle AL do. Gingival recession in individuals with cleft lip and palate: prevalence and severity. [Internet]. Cleft Palate-craniofacial Journal. 2012 ; 49( Ja 2012.): 92-95.[citado 2024 out. 03 ] Available from: https://doi.org/10.1597/10-052
Artigo de periodico
Variable phenotypic manifestations of a K44N mutation in the TGIF gene (2008)
Richieri-Costa, Antonio; Ribeiro, Lucilene Arilho
Source: Brain & Development. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e RIBEIRO, Lucilene Arilho. Variable phenotypic manifestations of a K44N mutation in the TGIF gene. Brain & Development, v. 30, n. 3, p. 203-205, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.braindev.2007.07.012. Acesso em: 03 out. 2024.
APA
Richieri-Costa, A., & Ribeiro, L. A. (2008). Variable phenotypic manifestations of a K44N mutation in the TGIF gene. Brain & Development, 30( 3), 203-205. doi:10.1016/j.braindev.2007.07.012
NLM
Richieri-Costa A, Ribeiro LA. Variable phenotypic manifestations of a K44N mutation in the TGIF gene [Internet]. Brain & Development. 2008 ; 30( 3): 203-205.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.braindev.2007.07.012
Vancouver
Richieri-Costa A, Ribeiro LA. Variable phenotypic manifestations of a K44N mutation in the TGIF gene [Internet]. Brain & Development. 2008 ; 30( 3): 203-205.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.braindev.2007.07.012
Artigo de periodico
Laryngeal microweb and vocal nodules: clinical study in a brazilian population (2006)
Ruiz, Daniela Maria Cury Ferreira; Pontes, Paulo; Behlau, Mara; Richieri-Costa, Antonio
Source: Folia Phoniatrica et Logopaedica. Unidade: HRAC
Subjects: CORDAS VOCAIS, LARINGOSCOPIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RUIZ, Daniela Maria Cury Ferreira et al. Laryngeal microweb and vocal nodules: clinical study in a brazilian population. Folia Phoniatrica et Logopaedica, v. 58, n. 6, p. 392-399, 2006Tradução . . Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=95000&Ausgabe=232147&ProduktNr=224177&filename=95000.pdf. Acesso em: 03 out. 2024.
APA
Ruiz, D. M. C. F., Pontes, P., Behlau, M., & Richieri-Costa, A. (2006). Laryngeal microweb and vocal nodules: clinical study in a brazilian population. Folia Phoniatrica et Logopaedica, 58( 6), 392-399. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=95000&Ausgabe=232147&ProduktNr=224177&filename=95000.pdf
NLM
Ruiz DMCF, Pontes P, Behlau M, Richieri-Costa A. Laryngeal microweb and vocal nodules: clinical study in a brazilian population [Internet]. Folia Phoniatrica et Logopaedica. 2006 ; 58( 6): 392-399.[citado 2024 out. 03 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=95000&Ausgabe=232147&ProduktNr=224177&filename=95000.pdf
Vancouver
Ruiz DMCF, Pontes P, Behlau M, Richieri-Costa A. Laryngeal microweb and vocal nodules: clinical study in a brazilian population [Internet]. Folia Phoniatrica et Logopaedica. 2006 ; 58( 6): 392-399.[citado 2024 out. 03 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=95000&Ausgabe=232147&ProduktNr=224177&filename=95000.pdf
Artigo de periodico
A study of familial stuttering (2006)
Oliveira, Cristiane Moço Canhetti de; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics Part A. Unidade: HRAC
Subjects: GAGUEIRA, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Cristiane Moço Canhetti de e RICHIERI-COSTA, Antonio. A study of familial stuttering. American Journal of Medical Genetics Part A, v. 140A, n. 19, p. 2139-2141, 2006Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31320. Acesso em: 03 out. 2024.
APA
Oliveira, C. M. C. de, & Richieri-Costa, A. (2006). A study of familial stuttering. American Journal of Medical Genetics Part A, 140A( 19), 2139-2141. doi:10.1002/ajmg.a.31320
NLM
Oliveira CMC de, Richieri-Costa A. A study of familial stuttering [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 19): 2139-2141.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ajmg.a.31320
Vancouver
Oliveira CMC de, Richieri-Costa A. A study of familial stuttering [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 19): 2139-2141.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ajmg.a.31320
Artigo de periodico
Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype (2006)
Richieri-Costa, Antonio; Ribeiro, Lucilene Arilho
Source: American Journal of Medical Genetics Part A. Unidade: HRAC
Subjects: FISSURA LÁBIOPALATINA, ANORMALIDADES CRANIOFACIAIS, ANOMALIA DENTÁRIA, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e RIBEIRO, Lucilene Arilho. Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype. American Journal of Medical Genetics Part A, v. 140A, n. 23, p. 2594-2597, 2006Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31379. Acesso em: 03 out. 2024.
APA
Richieri-Costa, A., & Ribeiro, L. A. (2006). Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype. American Journal of Medical Genetics Part A, 140A( 23), 2594-2597. doi:10.1002/ajmg.a.31379
NLM
Richieri-Costa A, Ribeiro LA. Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2594-2597.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ajmg.a.31379
Vancouver
Richieri-Costa A, Ribeiro LA. Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2594-2597.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ajmg.a.31379
Artigo de periodico
Holoprosencephaly: clinical evaluation on audiological and brainstem electrophysiological profiles (2006)
Antoneli, Melissa Zattoni; Zanchetta, Sthella; Zorzetto, Neivo Luiz; Ribeiro, Lucilene Arilho; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics Part A. Unidades: HRAC, HRACF
Subjects: HOLOPROSENCEFALIA, AUDIOLOGIA, AUDIOMETRIA DE RESPOSTAS EVOCADAS DE TRONCO CEREBRAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANTONELI, Melissa Zattoni et al. Holoprosencephaly: clinical evaluation on audiological and brainstem electrophysiological profiles. American Journal of Medical Genetics Part A, v. 140, n. 19, p. 2142-2145, 2006Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31296. Acesso em: 03 out. 2024.
APA
Antoneli, M. Z., Zanchetta, S., Zorzetto, N. L., Ribeiro, L. A., & Richieri-Costa, A. (2006). Holoprosencephaly: clinical evaluation on audiological and brainstem electrophysiological profiles. American Journal of Medical Genetics Part A, 140( 19), 2142-2145. doi:10.1002/ajmg.a.31296
NLM
Antoneli MZ, Zanchetta S, Zorzetto NL, Ribeiro LA, Richieri-Costa A. Holoprosencephaly: clinical evaluation on audiological and brainstem electrophysiological profiles [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140( 19): 2142-2145.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ajmg.a.31296
Vancouver
Antoneli MZ, Zanchetta S, Zorzetto NL, Ribeiro LA, Richieri-Costa A. Holoprosencephaly: clinical evaluation on audiological and brainstem electrophysiological profiles [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140( 19): 2142-2145.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ajmg.a.31296
Artigo de periodico
PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI (2006)
Ribeiro, Lucilene Arilho; Murray, Jeffrey C.; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics Part A. Unidade: HRAC
Subjects: FISSURA LÁBIOPALATINA, ANORMALIDADES MÚLTIPLAS, HOLOPROSENCEFALIA, MUTAÇÃO, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Lucilene Arilho e MURRAY, Jeffrey C. e RICHIERI-COSTA, Antonio. PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI. American Journal of Medical Genetics Part A, v. 140A, n. 23, p. 2584-2586, 2006Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31369. Acesso em: 03 out. 2024.
APA
Ribeiro, L. A., Murray, J. C., & Richieri-Costa, A. (2006). PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI. American Journal of Medical Genetics Part A, 140A( 23), 2584-2586. doi:10.1002/ajmg.a.31369
NLM
Ribeiro LA, Murray JC, Richieri-Costa A. PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2584-2586.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ajmg.a.31369
Vancouver
Ribeiro LA, Murray JC, Richieri-Costa A. PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2584-2586.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ajmg.a.31369
Artigo de periodico
Holoprosencephaly-like phenotype: clinical and genetic perspectives (2006)
Richieri-Costa, Antonio; Ribeiro, Lucilene Arilho
Source: American Journal of Medical Genetics Part A. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, ANORMALIDADES MÚLTIPLAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e RIBEIRO, Lucilene Arilho. Holoprosencephaly-like phenotype: clinical and genetic perspectives. American Journal of Medical Genetics Part A, v. 140A, n. 23, p. 2587-2593, 2006Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31378. Acesso em: 03 out. 2024.
APA
Richieri-Costa, A., & Ribeiro, L. A. (2006). Holoprosencephaly-like phenotype: clinical and genetic perspectives. American Journal of Medical Genetics Part A, 140A( 23), 2587-2593. doi:10.1002/ajmg.a.31378
NLM
Richieri-Costa A, Ribeiro LA. Holoprosencephaly-like phenotype: clinical and genetic perspectives [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2587-2593.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ajmg.a.31378
Vancouver
Richieri-Costa A, Ribeiro LA. Holoprosencephaly-like phenotype: clinical and genetic perspectives [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2587-2593.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ajmg.a.31378
Artigo de periodico
GLI2 mutations in four brazilian patients: how wide is the phenotypic spectrum? (2006)
Rahimov, Fedik; Ribeiro, Lucilene Arilho; Miranda, Esiquiel de; Richieri-Costa, Antonio; Murray, Jeffrey C.
Source: American Journal of Medical Genetics Part A. Unidade: HRAC
Assunto: HOLOPROSENCEFALIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAHIMOV, Fedik et al. GLI2 mutations in four brazilian patients: how wide is the phenotypic spectrum?. American Journal of Medical Genetics Part A, v. 140A, n. 23, p. 2571-2576, 2006Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31370. Acesso em: 03 out. 2024.
APA
Rahimov, F., Ribeiro, L. A., Miranda, E. de, Richieri-Costa, A., & Murray, J. C. (2006). GLI2 mutations in four brazilian patients: how wide is the phenotypic spectrum? American Journal of Medical Genetics Part A, 140A( 23), 2571-2576. doi:10.1002/ajmg.a.31370
NLM
Rahimov F, Ribeiro LA, Miranda E de, Richieri-Costa A, Murray JC. GLI2 mutations in four brazilian patients: how wide is the phenotypic spectrum? [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2571-2576.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ajmg.a.31370
Vancouver
Rahimov F, Ribeiro LA, Miranda E de, Richieri-Costa A, Murray JC. GLI2 mutations in four brazilian patients: how wide is the phenotypic spectrum? [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2571-2576.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ajmg.a.31370

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