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Trabalho de evento-resumo
Acurácia do teste de dígitos no ruído do português brasileiro (2024)
Balen, Sheila Andreoli ; Cavalcanti, Hannalice Gottschalck ; Araújo, Arielly Dayane da Silva Nunes ; Silva, Gleyson José Pinheiro Caldeira ; Almeida, Maiara Cristine Oliveira de; Barros, Victor Vasconcelos ; Swanepoel, De Wet ; Smits, Cas ; Ferrari, Deborah Viviane
Source: Anais Científicos. Conference titles: EIA - Encontro Internacional de Audiologia. Unidades: FOB, HRAC
Subjects: PERDA AUDITIVA, RUÍDO NA COMUNICAÇÃO, TESTE DICÓTICO DE DÍGITOS, LÍNGUA PORTUGUESA
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ABNT
BALEN, Sheila Andreoli et al. Acurácia do teste de dígitos no ruído do português brasileiro. 2024, Anais.. São Paulo: Academia Brasileira de Audiologia, 2024. . Acesso em: 04 nov. 2024.
APA
Balen, S. A., Cavalcanti, H. G., Araújo, A. D. da S. N., Silva, G. J. P. C., Almeida, M. C. O. de, Barros, V. V., et al. (2024). Acurácia do teste de dígitos no ruído do português brasileiro. In Anais Científicos. São Paulo: Academia Brasileira de Audiologia.
NLM
Balen SA, Cavalcanti HG, Araújo AD da SN, Silva GJPC, Almeida MCO de, Barros VV, Swanepoel DW, Smits C, Ferrari DV. Acurácia do teste de dígitos no ruído do português brasileiro. Anais Científicos. 2024 ;[citado 2024 nov. 04 ]
Vancouver
Balen SA, Cavalcanti HG, Araújo AD da SN, Silva GJPC, Almeida MCO de, Barros VV, Swanepoel DW, Smits C, Ferrari DV. Acurácia do teste de dígitos no ruído do português brasileiro. Anais Científicos. 2024 ;[citado 2024 nov. 04 ]
Artigo de periodico
The first hybrid international educational comprehensive cleft care workshop (2023)
Kantar, Rami S. ; Esenlik, Elçin ; Al Abyad, Omar S. ; Melhem, Antonio ; Younan, Robert Anthony ; Haddad, Mario ; Keith, Kristen ; Kassam, Serena ; Annan, Beyhan; Vijayakumar, Charanya ; Picard, Arnaud ; Padwa, Bonnie L.; Sommerlad, Brian ; Raposo-Amaral, Cassio Eduardo ; Forrest, Christopher R. ; Gillett, David A. ; Steinbacher, Derek M. ; Runyan, Christopher Michael ; Tanikawa, Daniela Yukie Sakai ; Chong, David K. ; Fisher, David M.; Mark, Hans ; Canter, Halil Ibrahim ; Losee, Joseph E. ; Patel, Krishna G.; Hartzell, Larry D. ; Johnson, Adam B.; Collares, Marcus Vinícius Martins ; Alonso, Nivaldo ; Chen, Philip Kuo-Ting ; Tse, Raymond W. ; Mann, Robert J.; Prada-Madrid, Jose Rolando; Kobayashi, Shinji ; Hussain, Syed Altaf ; Kummer, Ann W. ; Sell, Debbie A. ; Pereira, Valerie Jane ; Mabry, Kelly ; Gonsoulin, Courtney K.; Persson, Martin ; Davies, Gareth; Sethna, Navil F. ; Munoz-Pareja, Jennifer C. ; Kuijpers-Jagtman, Anne Marie ; Grayson, Barry H. ; Grollemund, Bruno ; Garib, Daniela Gamba ; Meazzini, Maria Costanza ; Kharbanda, Om Prakash ; Santiago, Pedro E.; Nalabothu, Prasad ; Batra, Puneet ; Stieber, Erin; Prasad, Dushyant; Brewster, Hugh; Ayala, Ruben E. ; Erbay, Elif; Akçam, Mehmet Okan ; Griot, J. Peter W. Don ; Vyas, Raj M. ; Flores, Roberto L. ; Breugem, Corstiaan C. ; Hamdan, Usama S.
Source: The Cleft Palate Craniofacial Journal. Unidades: FM, HRAC, FOB
Subjects: EVENTOS, SAÚDE BUCAL, CUIDADOS DE ENFERMAGEM, EDUCAÇÃO MÉDICA, EDUCAÇÃO A DISTÂNCIA, COMPETÊNCIA CLÍNICA
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ABNT
KANTAR, Rami S. et al. The first hybrid international educational comprehensive cleft care workshop. The Cleft Palate Craniofacial Journal, v. 60, n. 10, p. 1189-1198, 2023Tradução . . Disponível em: https://doi.org/10.1177/10556656221097820. Acesso em: 04 nov. 2024.
APA
Kantar, R. S., Esenlik, E., Al Abyad, O. S., Melhem, A., Younan, R. A., Haddad, M., et al. (2023). The first hybrid international educational comprehensive cleft care workshop. The Cleft Palate Craniofacial Journal, 60( 10), 1189-1198. doi:10.1177/10556656221097820
NLM
Kantar RS, Esenlik E, Al Abyad OS, Melhem A, Younan RA, Haddad M, Keith K, Kassam S, Annan B, Vijayakumar C, Picard A, Padwa BL, Sommerlad B, Raposo-Amaral CE, Forrest CR, Gillett DA, Steinbacher DM, Runyan CM, Tanikawa DYS, Chong DK, Fisher DM, Mark H, Canter HI, Losee JE, Patel KG, Hartzell LD, Johnson AB, Collares MVM, Alonso N, Chen PK-T, Tse RW, Mann RJ, Prada-Madrid JR, Kobayashi S, Hussain SA, Kummer AW, Sell DA, Pereira VJ, Mabry K, Gonsoulin CK, Persson M, Davies G, Sethna NF, Munoz-Pareja JC, Kuijpers-Jagtman AM, Grayson BH, Grollemund B, Garib DG, Meazzini MC, Kharbanda OP, Santiago PE, Nalabothu P, Batra P, Stieber E, Prasad D, Brewster H, Ayala RE, Erbay E, Akçam MO, Griot JPWD, Vyas RM, Flores RL, Breugem CC, Hamdan US. The first hybrid international educational comprehensive cleft care workshop [Internet]. The Cleft Palate Craniofacial Journal. 2023 ; 60( 10): 1189-1198.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1177/10556656221097820
Vancouver
Kantar RS, Esenlik E, Al Abyad OS, Melhem A, Younan RA, Haddad M, Keith K, Kassam S, Annan B, Vijayakumar C, Picard A, Padwa BL, Sommerlad B, Raposo-Amaral CE, Forrest CR, Gillett DA, Steinbacher DM, Runyan CM, Tanikawa DYS, Chong DK, Fisher DM, Mark H, Canter HI, Losee JE, Patel KG, Hartzell LD, Johnson AB, Collares MVM, Alonso N, Chen PK-T, Tse RW, Mann RJ, Prada-Madrid JR, Kobayashi S, Hussain SA, Kummer AW, Sell DA, Pereira VJ, Mabry K, Gonsoulin CK, Persson M, Davies G, Sethna NF, Munoz-Pareja JC, Kuijpers-Jagtman AM, Grayson BH, Grollemund B, Garib DG, Meazzini MC, Kharbanda OP, Santiago PE, Nalabothu P, Batra P, Stieber E, Prasad D, Brewster H, Ayala RE, Erbay E, Akçam MO, Griot JPWD, Vyas RM, Flores RL, Breugem CC, Hamdan US. The first hybrid international educational comprehensive cleft care workshop [Internet]. The Cleft Palate Craniofacial Journal. 2023 ; 60( 10): 1189-1198.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1177/10556656221097820
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: 04 nov. 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 nov. 04 ] 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 nov. 04 ] Available from: https://doi.org/10.1093/ejo/cjad023
Artigo de periodico
Phenotypic and mutational spectrum of ROR2-related Robinow syndrome (2022)
Lima, Ariadne R.; Ferreira, Barbara M.; Zhang, Chaofan; Jolly, Angad; Du, Haowei ; White, Janson J.; Dawood, Moez; Lins, Tulio C.; Chiabai, Marcela A.; van Beusekom, Ellen; Cordoba, Mara S.; Rosa, Erica C. C. Caldas; Kayserili, Hulya; Kimonis, Virginia; Wu, Erica; Mellado, Cecilia; Aggarwal, Vineet; Richieri-Costa, Antonio ; Brunoni, Décio; Canó, Talyta M.; Jorge, Alexander A. L. ; Kim, Chong Ae ; Honjo, Rachel ; Bertola, Débora R. ; Dandalo-Girardi, Raissa M.; Bayram, Yavuz; Gezdirici, Alper; Yilmaz-Gulec, Elif; Gumus, Evren; Yilmaz, Gülay C.; Okamoto, Nobuhiko ; Ohashi, Hirofumi; Coban–Akdemir, Zeynep; Mitani, Tadahiro; Jhangiani, Shalini N.; Muzny, Donna M.; Regattieri, Neysa A. P. ; Pogue, Robert ; Pereira, Rinaldo W.; Otto, Paulo A ; Gibbs, Richard A.; Ali, Bassam R.; van Bokhoven, Hans; Brunner, Han G.; Sutton, V. Reid; Lupski, James R. ; Vianna-Morgante, Angela M ; Carvalho, Claudia M. B. ; Mazzeu, Juliana F.
Source: Human Mutation. Unidades: HRAC, FM, IB
Subjects: FENÓTIPOS, MORFOLOGIA (ANATOMIA), SEQUENCIAMENTO GENÉTICO
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ABNT
LIMA, Ariadne R. et al. Phenotypic and mutational spectrum of ROR2-related Robinow syndrome. Human Mutation, v. 43, n. 7, p. 900-918, 2022Tradução . . Disponível em: https://doi.org/10.1002/humu.24375. Acesso em: 04 nov. 2024.
APA
Lima, A. R., Ferreira, B. M., Zhang, C., Jolly, A., Du, H., White, J. J., et al. (2022). Phenotypic and mutational spectrum of ROR2-related Robinow syndrome. Human Mutation, 43( 7), 900-918. doi:10.1002/humu.24375
NLM
Lima AR, Ferreira BM, Zhang C, Jolly A, Du H, White JJ, Dawood M, Lins TC, Chiabai MA, van Beusekom E, Cordoba MS, Rosa ECCC, Kayserili H, Kimonis V, Wu E, Mellado C, Aggarwal V, Richieri-Costa A, Brunoni D, Canó TM, Jorge AAL, Kim CA, Honjo R, Bertola DR, Dandalo-Girardi RM, Bayram Y, Gezdirici A, Yilmaz-Gulec E, Gumus E, Yilmaz GC, Okamoto N, Ohashi H, Coban–Akdemir Z, Mitani T, Jhangiani SN, Muzny DM, Regattieri NAP, Pogue R, Pereira RW, Otto PA, Gibbs RA, Ali BR, van Bokhoven H, Brunner HG, Sutton VR, Lupski JR, Vianna-Morgante AM, Carvalho CMB, Mazzeu JF. Phenotypic and mutational spectrum of ROR2-related Robinow syndrome [Internet]. Human Mutation. 2022 ; 43( 7): 900-918.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/humu.24375
Vancouver
Lima AR, Ferreira BM, Zhang C, Jolly A, Du H, White JJ, Dawood M, Lins TC, Chiabai MA, van Beusekom E, Cordoba MS, Rosa ECCC, Kayserili H, Kimonis V, Wu E, Mellado C, Aggarwal V, Richieri-Costa A, Brunoni D, Canó TM, Jorge AAL, Kim CA, Honjo R, Bertola DR, Dandalo-Girardi RM, Bayram Y, Gezdirici A, Yilmaz-Gulec E, Gumus E, Yilmaz GC, Okamoto N, Ohashi H, Coban–Akdemir Z, Mitani T, Jhangiani SN, Muzny DM, Regattieri NAP, Pogue R, Pereira RW, Otto PA, Gibbs RA, Ali BR, van Bokhoven H, Brunner HG, Sutton VR, Lupski JR, Vianna-Morgante AM, Carvalho CMB, Mazzeu JF. Phenotypic and mutational spectrum of ROR2-related Robinow syndrome [Internet]. Human Mutation. 2022 ; 43( 7): 900-918.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/humu.24375
Artigo de periodico
Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases (2022)
Vegas, Nancy ; Demir, Zeynep; Gordon, Christopher T.; Breton, Sylvain; Tavares, Vanessa Luiza Romanelli ; Moisset, Hugo; Zechi-Ceide, Roseli Maria ; Kokitsu-Nakata, Nancy M.; Kido, Yasuhiro; Marlin, Sandrine; Halem, Souad Gherbi; Meerschaut, Ilse; Callewaert, Bert; Chung, Brian ; Revencu, Nicole; Lehalle, Daphné; Petit, Florence ; Propst, Evan J.; Papsin, Blake C.; Phillips, John H.; Jakobsen, Linda; Tanno, Pauline Le; Thévenon, Julien; McGaughran, Julie; Gerkes, Erica H.; Leoni, Chiara; Kroisel, Peter; Tan, Tiong Y.; Henderson, Alex; Terhal, Paulien; Basel-Salmon, Lina; Alkindy, Adila; White, Susan M.; Passos-Bueno, Maria Rita ; Pingault, Véronique; Pontual, Loïc De; Amiel, Jeanne
Source: Human Mutation. Unidades: HRACF, HRAC, IB
Subjects: DOENÇAS MUSCULOSQUELÉTICAS, ANORMALIDADES CRANIOFACIAIS, GENÉTICA
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ABNT
VEGAS, Nancy et al. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, v. 43, n. 5, p. 582-594, 2022Tradução . . Disponível em: https://doi.org/10.1002/humu.24349. Acesso em: 04 nov. 2024.
APA
Vegas, N., Demir, Z., Gordon, C. T., Breton, S., Tavares, V. L. R., Moisset, H., et al. (2022). Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, 43( 5), 582-594. doi:10.1002/humu.24349
NLM
Vegas N, Demir Z, Gordon CT, Breton S, Tavares VLR, Moisset H, Zechi-Ceide RM, Kokitsu-Nakata NM, Kido Y, Marlin S, Halem SG, Meerschaut I, Callewaert B, Chung B, Revencu N, Lehalle D, Petit F, Propst EJ, Papsin BC, Phillips JH, Jakobsen L, Tanno PL, Thévenon J, McGaughran J, Gerkes EH, Leoni C, Kroisel P, Tan TY, Henderson A, Terhal P, Basel-Salmon L, Alkindy A, White SM, Passos-Bueno MR, Pingault V, Pontual LD, Amiel J. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/humu.24349
Vancouver
Vegas N, Demir Z, Gordon CT, Breton S, Tavares VLR, Moisset H, Zechi-Ceide RM, Kokitsu-Nakata NM, Kido Y, Marlin S, Halem SG, Meerschaut I, Callewaert B, Chung B, Revencu N, Lehalle D, Petit F, Propst EJ, Papsin BC, Phillips JH, Jakobsen L, Tanno PL, Thévenon J, McGaughran J, Gerkes EH, Leoni C, Kroisel P, Tan TY, Henderson A, Terhal P, Basel-Salmon L, Alkindy A, White SM, Passos-Bueno MR, Pingault V, Pontual LD, Amiel J. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/humu.24349
Trabalho de evento-resumo
Submicroscopic chromosomal rearrangements in complex craniofacial syndromes (2019)
Souza, Rosana Maria Candido ; Zechi-Ceide, Roseli Maria ; Jehee, Fernanda Maria Sarquis; Richieri-Costa, Antonio
Source: Anais. Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas: A fronteira do conhecimento na reabilitação das anomalias craniofaciais. Unidades: HRAC, HRACF
Subjects: ANOMALIA CRANIOFACIAL, CROMOSSOMOS, ACONSELHAMENTO GENÉTICO
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ABNT
SOUZA, Rosana Maria Candido et al. Submicroscopic chromosomal rearrangements in complex craniofacial syndromes. 2019, Anais.. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2019. Disponível em: https://repositorio.usp.br/directbitstream/07fd33fc-2eab-467f-b5ba-4ef8e178054f/3193145.pdf. Acesso em: 04 nov. 2024.
APA
Souza, R. M. C., Zechi-Ceide, R. M., Jehee, F. M. S., & Richieri-Costa, A. (2019). Submicroscopic chromosomal rearrangements in complex craniofacial syndromes. In Anais. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/07fd33fc-2eab-467f-b5ba-4ef8e178054f/3193145.pdf
NLM
Souza RMC, Zechi-Ceide RM, Jehee FMS, Richieri-Costa A. Submicroscopic chromosomal rearrangements in complex craniofacial syndromes [Internet]. Anais. 2019 ;[citado 2024 nov. 04 ] Available from: https://repositorio.usp.br/directbitstream/07fd33fc-2eab-467f-b5ba-4ef8e178054f/3193145.pdf
Vancouver
Souza RMC, Zechi-Ceide RM, Jehee FMS, Richieri-Costa A. Submicroscopic chromosomal rearrangements in complex craniofacial syndromes [Internet]. Anais. 2019 ;[citado 2024 nov. 04 ] Available from: https://repositorio.usp.br/directbitstream/07fd33fc-2eab-467f-b5ba-4ef8e178054f/3193145.pdf
Artigo de periodico
Effects of the natural peptide crotamine from a South American rattlesnake on Candida auris, an emergent multidrug antifungal resistant human pathogen (2019)
Dal Mas, Caroline; Rossato, Luana; Shimizu, Thaís; Oliveira, Eduardo Boaventura; Silva Junior, Pedro Ismael da; Meis, Jacques F.; Colombo, Arnaldo Lopes; Hayashi, Mirian A. F.
Source: Biomolecules. Unidade: HRAC
Subjects: MEDICAMENTO, PEPTÍDEOS, ANTIFÚNGICOS, CANDIDA, VENENOS DE ORIGEM ANIMAL, FUNGOS
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ABNT
DAL MAS, Caroline et al. Effects of the natural peptide crotamine from a South American rattlesnake on Candida auris, an emergent multidrug antifungal resistant human pathogen. Biomolecules, v. 9, n. 6, p. [10] , 2019Tradução . . Disponível em: https://doi.org/10.3390/biom9060205. Acesso em: 04 nov. 2024.
APA
Dal Mas, C., Rossato, L., Shimizu, T., Oliveira, E. B., Silva Junior, P. I. da, Meis, J. F., et al. (2019). Effects of the natural peptide crotamine from a South American rattlesnake on Candida auris, an emergent multidrug antifungal resistant human pathogen. Biomolecules, 9( 6), [10] . doi:10.3390/biom9060205
NLM
Dal Mas C, Rossato L, Shimizu T, Oliveira EB, Silva Junior PI da, Meis JF, Colombo AL, Hayashi MAF. Effects of the natural peptide crotamine from a South American rattlesnake on Candida auris, an emergent multidrug antifungal resistant human pathogen [Internet]. Biomolecules. 2019 ; 9( 6): [10] .[citado 2024 nov. 04 ] Available from: https://doi.org/10.3390/biom9060205
Vancouver
Dal Mas C, Rossato L, Shimizu T, Oliveira EB, Silva Junior PI da, Meis JF, Colombo AL, Hayashi MAF. Effects of the natural peptide crotamine from a South American rattlesnake on Candida auris, an emergent multidrug antifungal resistant human pathogen [Internet]. Biomolecules. 2019 ; 9( 6): [10] .[citado 2024 nov. 04 ] Available from: https://doi.org/10.3390/biom9060205
Artigo de periodico
Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome (2019)
Richieri-Costa, Antonio ; Zechi-Ceide, Roseli Maria ; Souza, Rosana Maria Candido ; Monteiro, Rejane Alves de Carvalho; Tonello, Cristiano; Freitas, Mariana L. de; Nakata, Nancy Mizue Kokitsu ; Pittoli, Siulan Vendramini Paulovich ; Mazzeu, Juliana F; Overes, Madelief; Ali-Amin, Roza; van Slegtenhorst, Marjon; Hoefsloot, Lies H; Jehee, Fernanda S
Source: American Journal of Medical Genetics. Unidades: HRAC, HRACF
Subjects: GENÉTICA, HOLOPROSENCEFALIA, FISSURA LÁBIOPALATINA, ANORMALIDADES CRANIOFACIAIS
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ABNT
RICHIERI-COSTA, Antonio et al. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome. American Journal of Medical Genetics, v. No 2019, n. 11, p. 2170-2177, 2019Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.61305. Acesso em: 04 nov. 2024.
APA
Richieri-Costa, A., Zechi-Ceide, R. M., Souza, R. M. C., Monteiro, R. A. de C., Tonello, C., Freitas, M. L. de, et al. (2019). Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome. American Journal of Medical Genetics, No 2019( 11), 2170-2177. doi:10.1002/ajmg.a.61305
NLM
Richieri-Costa A, Zechi-Ceide RM, Souza RMC, Monteiro RA de C, Tonello C, Freitas ML de, Nakata NMK, Pittoli SVP, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome [Internet]. American Journal of Medical Genetics. 2019 ; No 2019( 11): 2170-2177.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/ajmg.a.61305
Vancouver
Richieri-Costa A, Zechi-Ceide RM, Souza RMC, Monteiro RA de C, Tonello C, Freitas ML de, Nakata NMK, Pittoli SVP, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome [Internet]. American Journal of Medical Genetics. 2019 ; No 2019( 11): 2170-2177.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/ajmg.a.61305
Trabalho de evento-resumo
Unique phenotype in a Brazilian girl with syndromic Robin sequence and a 5.6 mb deletion in xp11.4p11.3 (2019)
Nakata, Nancy Mizue Kokitsu ; Jehee, F; Sandri, R; Pittoli, Siulan Vendramini Paulovich ; Alvarez, Camila Wenceslau ; Monteiro, R; Mazzeu, J; Zechi-Ceide, Roseli Maria ; Richieri-Costa, Antonio
Source: Utrecht: European Cleft Palate Craniofacial Association, 2019. Conference titles: European Cleft Palate Craniofacial Association Congress. Unidade: HRAC
Subjects: FENÓTIPOS, SÍNDROME DE PIERRE ROBIN, DELEÇÃO DE GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAKATA, Nancy Mizue Kokitsu et al. Unique phenotype in a Brazilian girl with syndromic Robin sequence and a 5.6 mb deletion in xp11.4p11.3. 2019, Anais.. Utrecht: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2019. Disponível em: https://repositorio.usp.br/directbitstream/2f17e911-522c-4ebf-b07d-80b7f922a17c/2963227.pdf. Acesso em: 04 nov. 2024.
APA
Nakata, N. M. K., Jehee, F., Sandri, R., Pittoli, S. V. P., Alvarez, C. W., Monteiro, R., et al. (2019). Unique phenotype in a Brazilian girl with syndromic Robin sequence and a 5.6 mb deletion in xp11.4p11.3. In Utrecht: European Cleft Palate Craniofacial Association, 2019. Utrecht: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/2f17e911-522c-4ebf-b07d-80b7f922a17c/2963227.pdf
NLM
Nakata NMK, Jehee F, Sandri R, Pittoli SVP, Alvarez CW, Monteiro R, Mazzeu J, Zechi-Ceide RM, Richieri-Costa A. Unique phenotype in a Brazilian girl with syndromic Robin sequence and a 5.6 mb deletion in xp11.4p11.3 [Internet]. Utrecht: European Cleft Palate Craniofacial Association, 2019. 2019 ;[citado 2024 nov. 04 ] Available from: https://repositorio.usp.br/directbitstream/2f17e911-522c-4ebf-b07d-80b7f922a17c/2963227.pdf
Vancouver
Nakata NMK, Jehee F, Sandri R, Pittoli SVP, Alvarez CW, Monteiro R, Mazzeu J, Zechi-Ceide RM, Richieri-Costa A. Unique phenotype in a Brazilian girl with syndromic Robin sequence and a 5.6 mb deletion in xp11.4p11.3 [Internet]. Utrecht: European Cleft Palate Craniofacial Association, 2019. 2019 ;[citado 2024 nov. 04 ] Available from: https://repositorio.usp.br/directbitstream/2f17e911-522c-4ebf-b07d-80b7f922a17c/2963227.pdf
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: 04 nov. 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 nov. 04 ] 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 nov. 04 ] Available from: https://doi.org/10.1038/s41431-017-0010-5
Artigo de periodico
Rapid maxillary expansion after alveolar bone grafting with rhBMP-2 in UCLP evaluated by means of CBCT (2017)
Garib, Daniela Gamba ; Miranda, Felicia ; Sathler, Renata ; Kuijpers-Jagtman, Anne Marie ; Aiello, Carlos Alberto
Source: Cleft Palate-Craniofacial Journal. Unidades: FOB, HRAC
Subjects: EXPANSÃO RÁPIDA DA MAXILA, FISSURA LÁBIOPALATINA, TÉCNICA DE EXPANSÃO PALATINA, ENXERTO ÓSSEO, TOMOGRAFIA COMPUTADORIZADA POR RAIOS X
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ABNT
GARIB, Daniela Gamba et al. Rapid maxillary expansion after alveolar bone grafting with rhBMP-2 in UCLP evaluated by means of CBCT. Cleft Palate-Craniofacial Journal, v. 54, n. 4, p. 474-480, 2017Tradução . . Disponível em: https://doi.org/10.1597/15-133. Acesso em: 04 nov. 2024.
APA
Garib, D. G., Miranda, F., Sathler, R., Kuijpers-Jagtman, A. M., & Aiello, C. A. (2017). Rapid maxillary expansion after alveolar bone grafting with rhBMP-2 in UCLP evaluated by means of CBCT. Cleft Palate-Craniofacial Journal, 54( 4), 474-480. doi:10.1597/15-133
NLM
Garib DG, Miranda F, Sathler R, Kuijpers-Jagtman AM, Aiello CA. Rapid maxillary expansion after alveolar bone grafting with rhBMP-2 in UCLP evaluated by means of CBCT [Internet]. Cleft Palate-Craniofacial Journal. 2017 ; 54( 4): 474-480.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1597/15-133
Vancouver
Garib DG, Miranda F, Sathler R, Kuijpers-Jagtman AM, Aiello CA. Rapid maxillary expansion after alveolar bone grafting with rhBMP-2 in UCLP evaluated by means of CBCT [Internet]. Cleft Palate-Craniofacial Journal. 2017 ; 54( 4): 474-480.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1597/15-133
Artigo de periodico
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect (2015)
Tavares, Vanessa Luiza Romanelli ; Gordon, Christopher T; Zechi-Ceide, Roseli Maria ; Nakata, Nancy Mizue Kokitsu ; Voisin, Norine; Tan, Tiong Y; Heggie, Andrew A; Pittoli, Siulan Vendramini Paulovich ; Propst, Evan J; Papsin, Blake C; Torres, Tatiana Teixeira ; Buermans, Henk; Capelo, Luciane Portas; Den Dunnen, Johan T; Guion-Almeida, Maria Leine; Lyonnet, Stanislas; Amiel, Jeanne; Passos-Bueno, Maria Rita
Source: European Journal of Human Genetics. Unidades: HRAC, IB
Subjects: ANORMALIDADES CRANIOFACIAIS, DOENÇAS GENÉTICAS, GENES
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ABNT
TAVARES, Vanessa Luiza Romanelli et al. Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect. European Journal of Human Genetics, v. 23, n. 4, p. 481-485, 2015Tradução . . Disponível em: https://doi.org/10.1038/ejhg.2014.132. Acesso em: 04 nov. 2024.
APA
Tavares, V. L. R., Gordon, C. T., Zechi-Ceide, R. M., Nakata, N. M. K., Voisin, N., Tan, T. Y., et al. (2015). Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect. European Journal of Human Genetics, 23( 4), 481-485. doi:10.1038/ejhg.2014.132
NLM
Tavares VLR, Gordon CT, Zechi-Ceide RM, Nakata NMK, Voisin N, Tan TY, Heggie AA, Pittoli SVP, Propst EJ, Papsin BC, Torres TT, Buermans H, Capelo LP, Den Dunnen JT, Guion-Almeida ML, Lyonnet S, Amiel J, Passos-Bueno MR. Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect [Internet]. European Journal of Human Genetics. 2015 ; 23( 4): 481-485.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/ejhg.2014.132
Vancouver
Tavares VLR, Gordon CT, Zechi-Ceide RM, Nakata NMK, Voisin N, Tan TY, Heggie AA, Pittoli SVP, Propst EJ, Papsin BC, Torres TT, Buermans H, Capelo LP, Den Dunnen JT, Guion-Almeida ML, Lyonnet S, Amiel J, Passos-Bueno MR. Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect [Internet]. European Journal of Human Genetics. 2015 ; 23( 4): 481-485.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/ejhg.2014.132
Trabalho de evento-resumo
Yardstick for rating nasolabial appearance in bilateral cleft lip and palate (2009)
Dominguez-Gonzalez, Susana; Bartzela, Theodosia N. ; Hagberg, Catharina; Katsaros C; Ozawa, Terumi Okada ; Pinheiro, F; Rizell, Sara; Rønning, Elisabeth; Semb, Gunvor; Shaw W
Source: Anais. Conference titles: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Subjects: FISSURA LÁBIOPALATINA, ORTODONTIA, ANÁLISE FACIAL
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ABNT
DOMINGUEZ-GONZALEZ, Susana et al. Yardstick for rating nasolabial appearance in bilateral cleft lip and palate. 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/c20a95d2-358c-4361-989d-b4b0d3ff0eab/3101492.pdf. Acesso em: 04 nov. 2024.
APA
Dominguez-Gonzalez, S., Bartzela, T. N., Hagberg, C., Katsaros C,, Ozawa, T. O., Pinheiro, F., et al. (2009). Yardstick for rating nasolabial appearance in bilateral cleft lip and palate. In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/c20a95d2-358c-4361-989d-b4b0d3ff0eab/3101492.pdf
NLM
Dominguez-Gonzalez S, Bartzela TN, Hagberg C, Katsaros C, Ozawa TO, Pinheiro F, Rizell S, Rønning E, Semb G, Shaw W. Yardstick for rating nasolabial appearance in bilateral cleft lip and palate [Internet]. Anais. 2009 ;[citado 2024 nov. 04 ] Available from: https://repositorio.usp.br/directbitstream/c20a95d2-358c-4361-989d-b4b0d3ff0eab/3101492.pdf
Vancouver
Dominguez-Gonzalez S, Bartzela TN, Hagberg C, Katsaros C, Ozawa TO, Pinheiro F, Rizell S, Rønning E, Semb G, Shaw W. Yardstick for rating nasolabial appearance in bilateral cleft lip and palate [Internet]. Anais. 2009 ;[citado 2024 nov. 04 ] Available from: https://repositorio.usp.br/directbitstream/c20a95d2-358c-4361-989d-b4b0d3ff0eab/3101492.pdf
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
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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: 04 nov. 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 nov. 04 ] 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 nov. 04 ] Available from: https://doi.org/10.1002/ajmg.a.10193

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