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Artigo de periodico
Core outcomes for orofacial clefts: reconciling traditional and ICHOM minimum datasets (2023)
Mossey, Peter Anthony ; Lai, Jason; Meazzini, Maria Costanza ; Breugem, Corstiaan C. ; Mark, Hans ; Mink van der Molen, Aebele B. ; Persson, Martin ; Davies, Gareth; Ozawa, Terumi Okada
Source: European Journal of Orthodontics. Unidade: HRAC
Subjects: GASOMETRIA, FISSURA LÁBIOPALATINA, ABORDAGEM DE TRATAMENTO INTERDISCIPLINAR
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ABNT
MOSSEY, Peter Anthony et al. Core outcomes for orofacial clefts: reconciling traditional and ICHOM minimum datasets. European Journal of Orthodontics, v. 45, n. 6, p. 671–679, 2023Tradução . . Disponível em: https://doi.org/10.1093/ejo/cjad023. Acesso em: 14 jun. 2024.
APA
Mossey, P. A., Lai, J., Meazzini, M. C., Breugem, C. C., Mark, H., Mink van der Molen, A. B., et al. (2023). Core outcomes for orofacial clefts: reconciling traditional and ICHOM minimum datasets. European Journal of Orthodontics, 45( 6), 671–679. doi:10.1093/ejo/cjad023
NLM
Mossey PA, Lai J, Meazzini MC, Breugem CC, Mark H, Mink van der Molen AB, Persson M, Davies G, Ozawa TO. Core outcomes for orofacial clefts: reconciling traditional and ICHOM minimum datasets [Internet]. European Journal of Orthodontics. 2023 ; 45( 6): 671–679.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1093/ejo/cjad023
Vancouver
Mossey PA, Lai J, Meazzini MC, Breugem CC, Mark H, Mink van der Molen AB, Persson M, Davies G, Ozawa TO. Core outcomes for orofacial clefts: reconciling traditional and ICHOM minimum datasets [Internet]. European Journal of Orthodontics. 2023 ; 45( 6): 671–679.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1093/ejo/cjad023
Artigo de periodico
Self-assembly peptide P11-4 induces mineralization and cell-migration of odontoblast-like cells (2022)
Araújo, Isaac Jordão de Souza; Guimarães, Gustavo Narvaes ; Machado, Renato Assis; Bertassoni, Luiz Eduardo; Davies, Robert Philip Wynn ; Puppin-Rontani, Regina Maria
Source: Journal of Dentistry. Unidade: HRAC
Subjects: BIOMINERALIZAÇÃO, ODONTOBLASTO, PEPTÍDEOS
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ABNT
ARAÚJO, Isaac Jordão de Souza et al. Self-assembly peptide P11-4 induces mineralization and cell-migration of odontoblast-like cells. Journal of Dentistry, v. 121, n. Ja 2022, p. 7 , 2022Tradução . . Disponível em: https://doi.org/10.1016/j.jdent.2022.104111. Acesso em: 14 jun. 2024.
APA
Araújo, I. J. de S., Guimarães, G. N., Machado, R. A., Bertassoni, L. E., Davies, R. P. W., & Puppin-Rontani, R. M. (2022). Self-assembly peptide P11-4 induces mineralization and cell-migration of odontoblast-like cells. Journal of Dentistry, 121( Ja 2022), 7 . doi:10.1016/j.jdent.2022.104111
NLM
Araújo IJ de S, Guimarães GN, Machado RA, Bertassoni LE, Davies RPW, Puppin-Rontani RM. Self-assembly peptide P11-4 induces mineralization and cell-migration of odontoblast-like cells [Internet]. Journal of Dentistry. 2022 ; 121( Ja 2022): 7 .[citado 2024 jun. 14 ] Available from: https://doi.org/10.1016/j.jdent.2022.104111
Vancouver
Araújo IJ de S, Guimarães GN, Machado RA, Bertassoni LE, Davies RPW, Puppin-Rontani RM. Self-assembly peptide P11-4 induces mineralization and cell-migration of odontoblast-like cells [Internet]. Journal of Dentistry. 2022 ; 121( Ja 2022): 7 .[citado 2024 jun. 14 ] Available from: https://doi.org/10.1016/j.jdent.2022.104111
Artigo de periodico
Timing of surgery following SARS-CoV-2 infection: an international prospective cohort study (2021)
Nepogodiev, Dmitri; Alonso, Nivaldo ; Santos, Carlos Ferreira dos ; Tonello, Cristiano ; Duarte, Geraldo; Joviliano, Edwaldo Edner; Santos, Carolina Lourenço Gomes dos; Quintana, Silvana Maria; Tamashiro, Edwin ; Valera, Fabiana Cardoso Pereira ; Zaccaro, Marília Veccechi Bijos; Gregorio, Paulo; Mariani, Alessandro Wasum; Minamoto, Fabio; Carvalho, Vladimir C.; Lima, Ana Lucia Munhoz; Oliveira, Priscila R.; Silva, Jorge dos Santos; Murta, Claudio Bovolenta; Salgado Júnior, Wilson; Prado, Caio Antonio de Campos; Moisés, Elaine Christine Dantas ; Suto, Hilda Satié; Yasuda, Alice Gadotti; Kowalski, Luiz Paulo
Source: Anaesthesia: Peri-operative medicine, critical care and pain. Unidades: HRAC, FOB, FMRP, FM, ESALQ
Subjects: COVID-19, IDOSOS, JOVENS, CRIANÇAS EM IDADE PRÉ-ESCOLAR
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ABNT
NEPOGODIEV, Dmitri et al. Timing of surgery following SARS-CoV-2 infection: an international prospective cohort study. Anaesthesia: Peri-operative medicine, critical care and pain, v. 76, n. 6, p. 748-758, 2021Tradução . . Disponível em: https://doi.org/10.1111/anae.15458. Acesso em: 14 jun. 2024.
APA
Nepogodiev, D., Alonso, N., Santos, C. F. dos, Tonello, C., Duarte, G., Joviliano, E. E., et al. (2021). Timing of surgery following SARS-CoV-2 infection: an international prospective cohort study. Anaesthesia: Peri-operative medicine, critical care and pain, 76( 6), 748-758. doi:10.1111/anae.15458
NLM
Nepogodiev D, Alonso N, Santos CF dos, Tonello C, Duarte G, Joviliano EE, Santos CLG dos, Quintana SM, Tamashiro E, Valera FCP, Zaccaro MVB, Gregorio P, Mariani AW, Minamoto F, Carvalho VC, Lima ALM, Oliveira PR, Silva J dos S, Murta CB, Salgado Júnior W, Prado CA de C, Moisés ECD, Suto HS, Yasuda AG, Kowalski LP. Timing of surgery following SARS-CoV-2 infection: an international prospective cohort study [Internet]. Anaesthesia: Peri-operative medicine, critical care and pain. 2021 ; 76( 6): 748-758.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1111/anae.15458
Vancouver
Nepogodiev D, Alonso N, Santos CF dos, Tonello C, Duarte G, Joviliano EE, Santos CLG dos, Quintana SM, Tamashiro E, Valera FCP, Zaccaro MVB, Gregorio P, Mariani AW, Minamoto F, Carvalho VC, Lima ALM, Oliveira PR, Silva J dos S, Murta CB, Salgado Júnior W, Prado CA de C, Moisés ECD, Suto HS, Yasuda AG, Kowalski LP. Timing of surgery following SARS-CoV-2 infection: an international prospective cohort study [Internet]. Anaesthesia: Peri-operative medicine, critical care and pain. 2021 ; 76( 6): 748-758.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1111/anae.15458
Artigo de periodico
Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 (2020)
Pittoli, Siulan Vendramini Paulovich ; Souza, Rosana Maria Candido ; Quiezi, Rodrigo Gonçalves; Zechi-Ceide, Roseli Maria ; Nakata, Nancy Mizue Kokitsu ; Jehee, Fernanda Sarquis; Ribeiro-Bicudo, Lucilene Arilho ; FitzPatrick, David R. ; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: Journal of Pediatric Genetics. Unidades: HRAC, HRACF
Subjects: AGENESIA, FISSURA PALATINA, DELEÇÃO DE GENES
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ABNT
PITTOLI, Siulan Vendramini Paulovich et al. Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2. Journal of Pediatric Genetics, v. 9, n. 4, p. 258-262, 2020Tradução . . Disponível em: https://doi.org/10.1055/s-0039-3402047. Acesso em: 14 jun. 2024.
APA
Pittoli, S. V. P., Souza, R. M. C., Quiezi, R. G., Zechi-Ceide, R. M., Nakata, N. M. K., Jehee, F. S., et al. (2020). Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2. Journal of Pediatric Genetics, 9( 4), 258-262. doi:10.1055/s-0039-3402047
NLM
Pittoli SVP, Souza RMC, Quiezi RG, Zechi-Ceide RM, Nakata NMK, Jehee FS, Ribeiro-Bicudo LA, FitzPatrick DR, Guion-Almeida ML, Richieri-Costa A. Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 [Internet]. Journal of Pediatric Genetics. 2020 ; 9( 4): 258-262.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1055/s-0039-3402047
Vancouver
Pittoli SVP, Souza RMC, Quiezi RG, Zechi-Ceide RM, Nakata NMK, Jehee FS, Ribeiro-Bicudo LA, FitzPatrick DR, Guion-Almeida ML, Richieri-Costa A. Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 [Internet]. Journal of Pediatric Genetics. 2020 ; 9( 4): 258-262.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1055/s-0039-3402047
Artigo de periodico
Insight into the ontogeny of GnRH neurons from patients born without a nose (2020)
Delaney, Angela; Volochayev, Rita; Meader, Brooke; Lee, Janice; Almpani, Konstantinia; Noukelak, Germaine Y.; Henkind, Jennifer; Chalmers, Laura; Law, Jennifer R.; Williamson, Kathleen A.; Jacobsen, Christina M.; Buitrago, Tatiana Pineda; Perez, Orlando; Cho, Chie-Hee; Kaindl, Angela; Rauch, Anita; Steindl, Katharina; Garcia, Jose Elias; Russell, Bianca E.; Prasad, Rameshwar; Mondal, Uttam K.; Reigstad, Hallvard M.; Clements, Scott; Kim, Susan; Inoue, Kaoru; Arora, Gazal; Salnikov, Kathryn B.; DiOrio, Nicole P.; Prada, Rolando; Capri, Yline; Morioka, Kosuke; Mizota, Michiyo; Zechi-Ceide, Roseli Maria ; Nakata, Nancy Mizue Kokitsu ; Tonello, Cristiano ; Pittoli, Siulan Vendramini Paulovich ; Dalben, Gisele da Silva ; Balasubramanian, Ravikumar; Dwyer, Andrew A.; Seminara, Stephanie B.; Crowley Júnior, William F.; Plummer, Lacey; Hall, Janet E.; Graham Júnior, John M.; Lin, Angela E.; Shaw, Natalie D.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: HRAC
Subjects: HORMÔNIO LIBERADOR DE GONADOTROFINAS, AGENESIA, NARIZ (ANATOMIA), MALFORMAÇÕES, FENÓTIPOS
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ABNT
DELANEY, Angela et al. Insight into the ontogeny of GnRH neurons from patients born without a nose. Journal of Clinical Endocrinology and Metabolism, v. 105, n. 5, p. 1538-1551, 2020Tradução . . Disponível em: https://doi.org/10.1210/clinem/dgaa065. Acesso em: 14 jun. 2024.
APA
Delaney, A., Volochayev, R., Meader, B., Lee, J., Almpani, K., Noukelak, G. Y., et al. (2020). Insight into the ontogeny of GnRH neurons from patients born without a nose. Journal of Clinical Endocrinology and Metabolism, 105( 5), 1538-1551. doi:10.1210/clinem/dgaa065
NLM
Delaney A, Volochayev R, Meader B, Lee J, Almpani K, Noukelak GY, Henkind J, Chalmers L, Law JR, Williamson KA, Jacobsen CM, Buitrago TP, Perez O, Cho C-H, Kaindl A, Rauch A, Steindl K, Garcia JE, Russell BE, Prasad R, Mondal UK, Reigstad HM, Clements S, Kim S, Inoue K, Arora G, Salnikov KB, DiOrio NP, Prada R, Capri Y, Morioka K, Mizota M, Zechi-Ceide RM, Nakata NMK, Tonello C, Pittoli SVP, Dalben G da S, Balasubramanian R, Dwyer AA, Seminara SB, Crowley Júnior WF, Plummer L, Hall JE, Graham Júnior JM, Lin AE, Shaw ND. Insight into the ontogeny of GnRH neurons from patients born without a nose [Internet]. Journal of Clinical Endocrinology and Metabolism. 2020 ; 105( 5): 1538-1551.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1210/clinem/dgaa065
Vancouver
Delaney A, Volochayev R, Meader B, Lee J, Almpani K, Noukelak GY, Henkind J, Chalmers L, Law JR, Williamson KA, Jacobsen CM, Buitrago TP, Perez O, Cho C-H, Kaindl A, Rauch A, Steindl K, Garcia JE, Russell BE, Prasad R, Mondal UK, Reigstad HM, Clements S, Kim S, Inoue K, Arora G, Salnikov KB, DiOrio NP, Prada R, Capri Y, Morioka K, Mizota M, Zechi-Ceide RM, Nakata NMK, Tonello C, Pittoli SVP, Dalben G da S, Balasubramanian R, Dwyer AA, Seminara SB, Crowley Júnior WF, Plummer L, Hall JE, Graham Júnior JM, Lin AE, Shaw ND. Insight into the ontogeny of GnRH neurons from patients born without a nose [Internet]. Journal of Clinical Endocrinology and Metabolism. 2020 ; 105( 5): 1538-1551.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1210/clinem/dgaa065
Artigo de periodico
Simulation-based comprehensive cleft care workshops: a reproducible model for sustainable education (2020)
Kantar, Rami S. ; Breugem, Corstiaan C. ; Keith, Kristen ; Kassam, Serena ; Vijayakumar, Charanya ; Bow, Mikaela; Alfonso, Allyson R. ; Chahine, Elsa M. ; Ghotmi, Lilian H.; Patel, Krishna G.; Shetye, Pradip R.; Santiago, Pedro E.; Losee, Joseph E. ; Steinbacher, Derek M. ; Rossell-Perry, Percy ; Garib, Daniela Gamba ; Alonso, Nivaldo ; Mann, Robert J.; Prada-Madrid, Jose Rolando; Esenlik, Elçin ; Pamplona, María del Carmen ; Collares, Marcus Vinícius Martins ; Bennun, Ricardo D.; Kummer, Ann W. ; Giugliano, Carlos; Padwa, Bonnie L.; Raposo-Amaral, Cassio Eduardo; Tse, Raymond W. ; Sommerlad, Brian ; Flores, Roberto L. ; Hamdan, Usama S.
Source: The Cleft Palate-Craniofacial Journal. Unidades: FOB, HRAC
Subjects: SAÚDE BUCAL, FISSURA LÁBIOPALATINA, SIMULAÇÃO (APRENDIZAGEM)
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ABNT
KANTAR, Rami S. et al. Simulation-based comprehensive cleft care workshops: a reproducible model for sustainable education. The Cleft Palate-Craniofacial Journal, v. 57, n. 10, p. 1238-1246, 2020Tradução . . Disponível em: https://doi.org/10.1177/1055665620944781. Acesso em: 14 jun. 2024.
APA
Kantar, R. S., Breugem, C. C., Keith, K., Kassam, S., Vijayakumar, C., Bow, M., et al. (2020). Simulation-based comprehensive cleft care workshops: a reproducible model for sustainable education. The Cleft Palate-Craniofacial Journal, 57( 10), 1238-1246. doi:10.1177/1055665620944781
NLM
Kantar RS, Breugem CC, Keith K, Kassam S, Vijayakumar C, Bow M, Alfonso AR, Chahine EM, Ghotmi LH, Patel KG, Shetye PR, Santiago PE, Losee JE, Steinbacher DM, Rossell-Perry P, Garib DG, Alonso N, Mann RJ, Prada-Madrid JR, Esenlik E, Pamplona M del C, Collares MVM, Bennun RD, Kummer AW, Giugliano C, Padwa BL, Raposo-Amaral CE, Tse RW, Sommerlad B, Flores RL, Hamdan US. Simulation-based comprehensive cleft care workshops: a reproducible model for sustainable education [Internet]. The Cleft Palate-Craniofacial Journal. 2020 ; 57( 10): 1238-1246.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1177/1055665620944781
Vancouver
Kantar RS, Breugem CC, Keith K, Kassam S, Vijayakumar C, Bow M, Alfonso AR, Chahine EM, Ghotmi LH, Patel KG, Shetye PR, Santiago PE, Losee JE, Steinbacher DM, Rossell-Perry P, Garib DG, Alonso N, Mann RJ, Prada-Madrid JR, Esenlik E, Pamplona M del C, Collares MVM, Bennun RD, Kummer AW, Giugliano C, Padwa BL, Raposo-Amaral CE, Tse RW, Sommerlad B, Flores RL, Hamdan US. Simulation-based comprehensive cleft care workshops: a reproducible model for sustainable education [Internet]. The Cleft Palate-Craniofacial Journal. 2020 ; 57( 10): 1238-1246.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1177/1055665620944781
Artigo de periodico
Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome (2018)
Kievit, Anneke; Tessadori, Federico; Douben, Hannie; Jordens, Ingrid; Maurice, Madelon; Hoogeboom, Jeannette; Hennekam, Raoul; Nampoothiri, Sheela; Kayserili, Hülya; Castori, Marco; Whiteford, Margo; Motter, Connie; Melver, Catherine; Cunningham, Michael; Hing, Anne; Nakata, Nancy Mizue Kokitsu; Pittoli, Siulan Vendramini Paulovich; Richieri-Costa, Antonio; Baas, Annette F.; Breugem, Corstiaan C. ; Duran, Karen; Massink, Maarten; Derksen, Patrick W. B.; IJcken, Wilfred F. J. van; Unen, Leontine van; Simarro, Fernando Santos; Lapunzina, Pablo; Lopes, Vera Lúcia Gil da Silva; Mendes, Elaine Lustosa; Krall, Max; Slavotinek, Anne; Victor Martinez-Glez; Bakkers, Jeroen; Gassen, Koen L. I. van; Klein, Annelies de; Boogaard, Marie-José H. van den; Haaften, Gijs van
Source: European Journal of Human Genetics. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, ANOMALIA DENTÁRIA, FISSURA LÁBIOPALATINA, ANORMALIDADES CRANIOFACIAIS
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ABNT
KIEVIT, Anneke et al. Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome. European Journal of Human Genetics, v. 26, n. 2, p. 210-219, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41431-017-0010-5. Acesso em: 14 jun. 2024.
APA
Kievit, A., Tessadori, F., Douben, H., Jordens, I., Maurice, M., Hoogeboom, J., et al. (2018). Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome. European Journal of Human Genetics, 26( 2), 210-219. doi:10.1038/s41431-017-0010-5
NLM
Kievit A, Tessadori F, Douben H, Jordens I, Maurice M, Hoogeboom J, Hennekam R, Nampoothiri S, Kayserili H, Castori M, Whiteford M, Motter C, Melver C, Cunningham M, Hing A, Nakata NMK, Pittoli SVP, Richieri-Costa A, Baas AF, Breugem CC, Duran K, Massink M, Derksen PWB, IJcken WFJ van, Unen L van, Simarro FS, Lapunzina P, Lopes VLG da S, Mendes EL, Krall M, Slavotinek A, Victor Martinez-Glez, Bakkers J, Gassen KLI van, Klein A de, Boogaard M-JH van den, Haaften G van. Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome [Internet]. European Journal of Human Genetics. 2018 ; 26( 2): 210-219.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1038/s41431-017-0010-5
Vancouver
Kievit A, Tessadori F, Douben H, Jordens I, Maurice M, Hoogeboom J, Hennekam R, Nampoothiri S, Kayserili H, Castori M, Whiteford M, Motter C, Melver C, Cunningham M, Hing A, Nakata NMK, Pittoli SVP, Richieri-Costa A, Baas AF, Breugem CC, Duran K, Massink M, Derksen PWB, IJcken WFJ van, Unen L van, Simarro FS, Lapunzina P, Lopes VLG da S, Mendes EL, Krall M, Slavotinek A, Victor Martinez-Glez, Bakkers J, Gassen KLI van, Klein A de, Boogaard M-JH van den, Haaften G van. Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome [Internet]. European Journal of Human Genetics. 2018 ; 26( 2): 210-219.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1038/s41431-017-0010-5
Artigo de periodico
Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome (2014)
Gordon, Christopher T.; Cunniff, Christopher M.; Green, Glenn E.; Zechi-Ceide, Roseli Maria ; Johnson, Jason M.; Henderson, Alex; Petit, Florence; Nakata, Nancy Mizue Kokitsu ; Guion-Almeida, Maria Leine; Munnich, Arnold; Cunningham, Michael L.; Lyonnet, Stanislas; Amiel, Jeanne
Source: American Journal of Medical Genetics Part A. Unidade: HRAC
Subjects: DESENVOLVIMENTO MAXILOFACIAL, ANORMALIDADES CRANIOFACIAIS, FENÓTIPOS
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ABNT
GORDON, Christopher T. et al. Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome. American Journal of Medical Genetics Part A, v. 164, n. 7, p. 1850-1853, 2014Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36505. Acesso em: 14 jun. 2024.
APA
Gordon, C. T., Cunniff, C. M., Green, G. E., Zechi-Ceide, R. M., Johnson, J. M., Henderson, A., et al. (2014). Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome. American Journal of Medical Genetics Part A, 164( 7), 1850-1853. doi:10.1002/ajmg.a.36505
NLM
Gordon CT, Cunniff CM, Green GE, Zechi-Ceide RM, Johnson JM, Henderson A, Petit F, Nakata NMK, Guion-Almeida ML, Munnich A, Cunningham ML, Lyonnet S, Amiel J. Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome [Internet]. American Journal of Medical Genetics Part A. 2014 ; 164( 7): 1850-1853.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1002/ajmg.a.36505
Vancouver
Gordon CT, Cunniff CM, Green GE, Zechi-Ceide RM, Johnson JM, Henderson A, Petit F, Nakata NMK, Guion-Almeida ML, Munnich A, Cunningham ML, Lyonnet S, Amiel J. Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome [Internet]. American Journal of Medical Genetics Part A. 2014 ; 164( 7): 1850-1853.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1002/ajmg.a.36505
Artigo de periodico
A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects (2014)
Favaro, Francine Pinheiro; Alvizi, Lucas ; Zechi-Ceide, Roseli Maria; Bertola, Débora Romeo; Félix, Têmis Maria ; Souza, Josiane de; Raskin, Salmo; Twigg, Stephen R. F; Weiner, Andrea M. J; Armas, Pablo; Margarit, Ezequiel; Calcaterra, Nora B; Andersen, Gregers R; McGowan, Simon J; Wilkie, Andrew O. M; Richieri-Costa, Antonio; Almeida, Maria Leine Guion de; Passos-Bueno, Maria Rita
Source: American Journal of Human Genetics. Unidades: HRAC, IB, HRACF
Subjects: ANORMALIDADES CRANIOFACIAIS, MUTAÇÃO GENÉTICA, MALFORMAÇÕES, FISSURA PALATINA, MODELOS ANIMAIS, GENOMAS
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ABNT
FAVARO, Francine Pinheiro et al. A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects. American Journal of Human Genetics, v. 94, n. Ja 2014, p. 120-128, 2014Tradução . . Acesso em: 14 jun. 2024.
APA
Favaro, F. P., Alvizi, L., Zechi-Ceide, R. M., Bertola, D. R., Félix, T. M., Souza, J. de, et al. (2014). A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects. American Journal of Human Genetics, 94( Ja 2014), 120-128.
NLM
Favaro FP, Alvizi L, Zechi-Ceide RM, Bertola DR, Félix TM, Souza J de, Raskin S, Twigg SRF, Weiner AMJ, Armas P, Margarit E, Calcaterra NB, Andersen GR, McGowan SJ, Wilkie AOM, Richieri-Costa A, Almeida MLG de, Passos-Bueno MR. A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects. American Journal of Human Genetics. 2014 ; 94( Ja 2014): 120-128.[citado 2024 jun. 14 ]
Vancouver
Favaro FP, Alvizi L, Zechi-Ceide RM, Bertola DR, Félix TM, Souza J de, Raskin S, Twigg SRF, Weiner AMJ, Armas P, Margarit E, Calcaterra NB, Andersen GR, McGowan SJ, Wilkie AOM, Richieri-Costa A, Almeida MLG de, Passos-Bueno MR. A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects. American Journal of Human Genetics. 2014 ; 94( Ja 2014): 120-128.[citado 2024 jun. 14 ]
Artigo de periodico
Prevalence of a Simonart’s band in patients with complete cleft lip and alveolus and complete cleft lip and palate (2006)
Silva Filho, Omar Gabriel da; Santamaria Junior, Milton ; Dalben, Gisele da Silva ; Semb, Gunvor
Source: The Cleft Palate-Craniofacial Journal. Unidades: HRAC, FOB
Subjects: FISSURA LÁBIOPALATINA, BANDA ORTODÔNTICA, PROCESSO ALVEOLAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA FILHO, Omar Gabriel da et al. Prevalence of a Simonart’s band in patients with complete cleft lip and alveolus and complete cleft lip and palate. The Cleft Palate-Craniofacial Journal, v. 43, n. 4, p. 442-445, 2006Tradução . . Disponível em: https://doi.org/10.1597/05-0302.1. Acesso em: 14 jun. 2024.
APA
Silva Filho, O. G. da, Santamaria Junior, M., Dalben, G. da S., & Semb, G. (2006). Prevalence of a Simonart’s band in patients with complete cleft lip and alveolus and complete cleft lip and palate. The Cleft Palate-Craniofacial Journal, 43( 4), 442-445. doi:10.1597/05-0302.1
NLM
Silva Filho OG da, Santamaria Junior M, Dalben G da S, Semb G. Prevalence of a Simonart’s band in patients with complete cleft lip and alveolus and complete cleft lip and palate [Internet]. The Cleft Palate-Craniofacial Journal. 2006 ; 43( 4): 442-445.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1597/05-0302.1
Vancouver
Silva Filho OG da, Santamaria Junior M, Dalben G da S, Semb G. Prevalence of a Simonart’s band in patients with complete cleft lip and alveolus and complete cleft lip and palate [Internet]. The Cleft Palate-Craniofacial Journal. 2006 ; 43( 4): 442-445.[citado 2024 jun. 14 ] Available from: https://doi.org/10.1597/05-0302.1
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: 14 jun. 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 jun. 14 ]
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 jun. 14 ]
Trabalho de evento-resumo
Comparison between two surgical protocols for 5 - 6 year - old complete unilateral cleft lip and palate patients: evaluation of the inter-dental arch relationship (2001)
Ozawa, Terumi Okada ; Silva, Marcos Lupercio Novo; Semb, Gunvor
Source: Programme & Abstracts. Conference titles: International Congress on Cleft Palate and Related Craniofacial Anomalies. Unidade: HRAC
Subjects: FISSURA LÁBIOPALATINA, PROTOCOLOS CLÍNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OZAWA, Terumi Okada e SILVA, Marcos Lupercio Novo e SEMB, Gunvor. Comparison between two surgical protocols for 5 - 6 year - old complete unilateral cleft lip and palate patients: evaluation of the inter-dental arch relationship. 2001, Anais.. Goteborg: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2001. Disponível em: https://repositorio.usp.br/directbitstream/0a7dae38-53d8-4abb-9739-b12a338066cf/3167479.pdf. Acesso em: 14 jun. 2024.
APA
Ozawa, T. O., Silva, M. L. N., & Semb, G. (2001). Comparison between two surgical protocols for 5 - 6 year - old complete unilateral cleft lip and palate patients: evaluation of the inter-dental arch relationship. In Programme & Abstracts. Goteborg: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/0a7dae38-53d8-4abb-9739-b12a338066cf/3167479.pdf
NLM
Ozawa TO, Silva MLN, Semb G. Comparison between two surgical protocols for 5 - 6 year - old complete unilateral cleft lip and palate patients: evaluation of the inter-dental arch relationship [Internet]. Programme & Abstracts. 2001 ;[citado 2024 jun. 14 ] Available from: https://repositorio.usp.br/directbitstream/0a7dae38-53d8-4abb-9739-b12a338066cf/3167479.pdf
Vancouver
Ozawa TO, Silva MLN, Semb G. Comparison between two surgical protocols for 5 - 6 year - old complete unilateral cleft lip and palate patients: evaluation of the inter-dental arch relationship [Internet]. Programme & Abstracts. 2001 ;[citado 2024 jun. 14 ] Available from: https://repositorio.usp.br/directbitstream/0a7dae38-53d8-4abb-9739-b12a338066cf/3167479.pdf

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