ReP USP - Resultado da busca

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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 01 jun. 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 jun. 01 ] 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 jun. 01 ] Available from: https://doi.org/10.1177/10556656221097820
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 01 jun. 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 jun. 01 ] 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 jun. 01 ] Available from: https://doi.org/10.1002/humu.24375
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)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 01 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. 01 ] 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. 01 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 01 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. 01 ] 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. 01 ] Available from: https://doi.org/10.1038/s41431-017-0010-5

USP Schools

ReP

Filtros

Departament

Authors

USP affiliated authors

Subjects

Funding Agencies

Indexado em

Non normalized affiliation

Countries of institutions of collaboration