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Artigo de periodico
Tessier’s cleft number 6 revisited: a series of 26 new cases and literature review of 44 (2023)
Pellerin, Philippe ; Tonello, Cristiano ; Freitas, Renato da Silva ; Tang, Xiao Jun; Alonso, Nivaldo
Fonte: The Cleft Palate Craniofacial Journal. Unidade: HRAC
Assuntos: MACROSTOMIA, ANOMALIA CRANIOFACIAL, DISOSTOSE MANDIBULOFACIAL, ASSIMETRIA FACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PELLERIN, Philippe et al. Tessier’s cleft number 6 revisited: a series of 26 new cases and literature review of 44. The Cleft Palate Craniofacial Journal, v. 60, n. 8, p. 938-948, 2023Tradução . . Disponível em: https://doi.org/10.1177/10556656221086459. Acesso em: 31 out. 2024.
APA
Pellerin, P., Tonello, C., Freitas, R. da S., Tang, X. J., & Alonso, N. (2023). Tessier’s cleft number 6 revisited: a series of 26 new cases and literature review of 44. The Cleft Palate Craniofacial Journal, 60( 8), 938-948. doi:10.1177/10556656221086459
NLM
Pellerin P, Tonello C, Freitas R da S, Tang XJ, Alonso N. Tessier’s cleft number 6 revisited: a series of 26 new cases and literature review of 44 [Internet]. The Cleft Palate Craniofacial Journal. 2023 ; 60( 8): 938-948.[citado 2024 out. 31 ] Available from: https://doi.org/10.1177/10556656221086459
Vancouver
Pellerin P, Tonello C, Freitas R da S, Tang XJ, Alonso N. Tessier’s cleft number 6 revisited: a series of 26 new cases and literature review of 44 [Internet]. The Cleft Palate Craniofacial Journal. 2023 ; 60( 8): 938-948.[citado 2024 out. 31 ] Available from: https://doi.org/10.1177/10556656221086459
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.
Fonte: The Cleft Palate Craniofacial Journal. Unidades: FM, HRAC, FOB
Assuntos: 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: 31 out. 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 out. 31 ] 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 out. 31 ] Available from: https://doi.org/10.1177/10556656221097820
Artigo de periodico
Crouzon syndrome anatomy, usefulness of vestibular orientation (2022)
Pellerin, Philippe ; Vinchon, Matthieu; Guerreschi, Pierre; Anastassov, Yuri; Zhang, Zhi Yong; Tang, Xiao; Alonso, Nivaldo
Fonte: The Journal of Craniofacial Surgery. Unidades: FM, HRAC
Assuntos: DISOSTOSE CRÂNIOFACIAL, RADIOGRAFIA, ANOMALIA CRANIOFACIAL, DESENVOLVIMENTO CRANIOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PELLERIN, Philippe et al. Crouzon syndrome anatomy, usefulness of vestibular orientation. The Journal of Craniofacial Surgery, v. 33, n. 6, p. Se 2022, 2022Tradução . . Disponível em: https://doi.org/10.1097/SCS.0000000000008644. Acesso em: 31 out. 2024.
APA
Pellerin, P., Vinchon, M., Guerreschi, P., Anastassov, Y., Zhang, Z. Y., Tang, X., & Alonso, N. (2022). Crouzon syndrome anatomy, usefulness of vestibular orientation. The Journal of Craniofacial Surgery, 33( 6), Se 2022. doi:10.1097/SCS.0000000000008644
NLM
Pellerin P, Vinchon M, Guerreschi P, Anastassov Y, Zhang ZY, Tang X, Alonso N. Crouzon syndrome anatomy, usefulness of vestibular orientation [Internet]. The Journal of Craniofacial Surgery. 2022 ; 33( 6): Se 2022.[citado 2024 out. 31 ] Available from: https://doi.org/10.1097/SCS.0000000000008644
Vancouver
Pellerin P, Vinchon M, Guerreschi P, Anastassov Y, Zhang ZY, Tang X, Alonso N. Crouzon syndrome anatomy, usefulness of vestibular orientation [Internet]. The Journal of Craniofacial Surgery. 2022 ; 33( 6): Se 2022.[citado 2024 out. 31 ] Available from: https://doi.org/10.1097/SCS.0000000000008644
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
Fonte: Human Mutation. Unidades: HRACF, HRAC, IB
Assuntos: 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: 31 out. 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 out. 31 ] 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 out. 31 ] Available from: https://doi.org/10.1002/humu.24349
Artigo de periodico
A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects (2021)
Palagano, Eleonora; Gordon, Christopher T; Uva, Paolo ; Strina, Dario ; Dimartino, Clémantine; Villa, Anna; Amiel, Jeanne; Guion-Almeida, Maria Leine; Pittoli, Siulan Vendramini Paulovich ; Nakata, Nancy Mizue Kokitsu ; Zechi-Ceide, Roseli Maria ; Sobacchi, Cristina
Fonte: Bone. Unidade: HRAC
Assuntos: DISOSTOSE MANDIBULOFACIAL, MUTAÇÃO GENÉTICA, FENÓTIPOS, CONVULSÕES
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ABNT
PALAGANO, Eleonora et al. A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects. Bone, v. 153, p. 7 , 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bone.2021.116152. Acesso em: 31 out. 2024.
APA
Palagano, E., Gordon, C. T., Uva, P., Strina, D., Dimartino, C., Villa, A., et al. (2021). A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects. Bone, 153, 7 . doi:10.1016/j.bone.2021.116152
NLM
Palagano E, Gordon CT, Uva P, Strina D, Dimartino C, Villa A, Amiel J, Guion-Almeida ML, Pittoli SVP, Nakata NMK, Zechi-Ceide RM, Sobacchi C. A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects [Internet]. Bone. 2021 ; 153 7 .[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.bone.2021.116152
Vancouver
Palagano E, Gordon CT, Uva P, Strina D, Dimartino C, Villa A, Amiel J, Guion-Almeida ML, Pittoli SVP, Nakata NMK, Zechi-Ceide RM, Sobacchi C. A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects [Internet]. Bone. 2021 ; 153 7 .[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.bone.2021.116152
Artigo de periodico
Turner syndrome in diverse populations (2020)
Kruszka, Paul ; Addissie, Yonit A; Tekendo-Ngongang, Cedrik; Jones, Kelly L ; Savage, Sarah K.; Gupta, Neerja; Sirisena, Nirmala D; Dissanayake, Vajira H. W; Paththinige, C. Sampath; Aravena, Teresa; Nampoothiri, Sheela; Yesodharan, Dhanya; Girisha, Katta M ; Patil, Siddaramappa Jagdish ; Jamuar, Saumya Shekhar ; Goh, Jasmine Chew-Yin; Utari, Agustini ; Sihombing, Nydia; Mishra, Rupesh; Chitrakar, Neer Shoba; Iriele, Brenda C.; Lulseged, Ezana; Megarbane, Andre ; Uwineza, Annette; Oyenusi, Elizabeth Eberechi; Olopade, Oluwarotimi Bolaji; Fasanmade, Olufemi Adetola; Duenas-Roque, Milagros M.; Thong, Meow-Keong; Tung, Joanna Y. L; Mok, Gary T. K; Fleischer, Nicole; Rwegerera, Godfrey M; Herreros, María Beatriz; Watts, Johnathan; Fieggen, Karen; Huckstadt, Victoria; Moresco, Angélica; Obregon, María Gabriela; Hussen, Dalia Farouk; Ashaat, Neveen A ; Ashaat, Engy A. ; Chung, Brian H. Y; Badoe, Eben; Faradz, Sultana M. H; El Ruby, Mona O; Shotelersuk, Vorasuk; Wonkam, Ambroise; Ekure, Ekanem Nsikak; Phadke, Shubha R; Richieri-Costa, Antonio ; Muenke, Maximilian
Fonte: American Journal of Medical Genetics. Part A. Unidade: HRAC
Assuntos: ANÁLISE FACIAL, GENÉTICA DE POPULAÇÕES, FENÓTIPOS, ANORMALIDADES CONGÊNITAS, SÍNDROME DE NOONAN
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ABNT
KRUSZKA, Paul et al. Turner syndrome in diverse populations. American Journal of Medical Genetics. Part A, v. 182A, n. 2, p. 303-313, 2020Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.61461. Acesso em: 31 out. 2024.
APA
Kruszka, P., Addissie, Y. A., Tekendo-Ngongang, C., Jones, K. L., Savage, S. K., Gupta, N., et al. (2020). Turner syndrome in diverse populations. American Journal of Medical Genetics. Part A, 182A( 2), 303-313. doi:10.1002/ajmg.a.61461
NLM
Kruszka P, Addissie YA, Tekendo-Ngongang C, Jones KL, Savage SK, Gupta N, Sirisena ND, Dissanayake VHW, Paththinige CS, Aravena T, Nampoothiri S, Yesodharan D, Girisha KM, Patil SJ, Jamuar SS, Goh JC-Y, Utari A, Sihombing N, Mishra R, Chitrakar NS, Iriele BC, Lulseged E, Megarbane A, Uwineza A, Oyenusi EE, Olopade OB, Fasanmade OA, Duenas-Roque MM, Thong M-K, Tung JYL, Mok GTK, Fleischer N, Rwegerera GM, Herreros MB, Watts J, Fieggen K, Huckstadt V, Moresco A, Obregon MG, Hussen DF, Ashaat NA, Ashaat EA, Chung BHY, Badoe E, Faradz SMH, El Ruby MO, Shotelersuk V, Wonkam A, Ekure EN, Phadke SR, Richieri-Costa A, Muenke M. Turner syndrome in diverse populations [Internet]. American Journal of Medical Genetics. Part A. 2020 ; 182A( 2): 303-313.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.61461
Vancouver
Kruszka P, Addissie YA, Tekendo-Ngongang C, Jones KL, Savage SK, Gupta N, Sirisena ND, Dissanayake VHW, Paththinige CS, Aravena T, Nampoothiri S, Yesodharan D, Girisha KM, Patil SJ, Jamuar SS, Goh JC-Y, Utari A, Sihombing N, Mishra R, Chitrakar NS, Iriele BC, Lulseged E, Megarbane A, Uwineza A, Oyenusi EE, Olopade OB, Fasanmade OA, Duenas-Roque MM, Thong M-K, Tung JYL, Mok GTK, Fleischer N, Rwegerera GM, Herreros MB, Watts J, Fieggen K, Huckstadt V, Moresco A, Obregon MG, Hussen DF, Ashaat NA, Ashaat EA, Chung BHY, Badoe E, Faradz SMH, El Ruby MO, Shotelersuk V, Wonkam A, Ekure EN, Phadke SR, Richieri-Costa A, Muenke M. Turner syndrome in diverse populations [Internet]. American Journal of Medical Genetics. Part A. 2020 ; 182A( 2): 303-313.[citado 2024 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.61461
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.
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: HRAC
Assuntos: 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: 31 out. 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 out. 31 ] 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 out. 31 ] Available from: https://doi.org/10.1210/clinem/dgaa065
Artigo de periodico
Common 3-dimensional coordinate system for assessment of directional changes (2016)
Ruellas, Antonio Carlos de Oliveira; Tonello, Cristiano; Gomes, Liliane Rosas; Yatabe, Marilia Sayako; Macron, Lucie; Lopinto, Julia; Gonçalves, João Roberto; Carreira, Daniela Gamba Garib; Alonso, Nivaldo; Souki, Bernardo Quiroga; Coqueiro, Raildo da Silva; Cevidanes, Lucia Helena Soares
Fonte: American Journal of Orthodontics and Dentofacial Orthopedics. Unidades: HRAC, FOB, FM
Assuntos: TERCEIRA DIMENSÃO, COORDENADAS, TOMOGRAFIA COMPUTADORIZADA POR RAIOS X
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ABNT
RUELLAS, Antonio Carlos de Oliveira et al. Common 3-dimensional coordinate system for assessment of directional changes. American Journal of Orthodontics and Dentofacial Orthopedics, v. 149, n. 5, p. 645–656, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.ajodo.2015.10.021. Acesso em: 31 out. 2024.
APA
Ruellas, A. C. de O., Tonello, C., Gomes, L. R., Yatabe, M. S., Macron, L., Lopinto, J., et al. (2016). Common 3-dimensional coordinate system for assessment of directional changes. American Journal of Orthodontics and Dentofacial Orthopedics, 149( 5), 645–656. doi:10.1016/j.ajodo.2015.10.021
NLM
Ruellas AC de O, Tonello C, Gomes LR, Yatabe MS, Macron L, Lopinto J, Gonçalves JR, Carreira DGG, Alonso N, Souki BQ, Coqueiro R da S, Cevidanes LHS. Common 3-dimensional coordinate system for assessment of directional changes [Internet]. American Journal of Orthodontics and Dentofacial Orthopedics. 2016 ; 149( 5): 645–656.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.ajodo.2015.10.021
Vancouver
Ruellas AC de O, Tonello C, Gomes LR, Yatabe MS, Macron L, Lopinto J, Gonçalves JR, Carreira DGG, Alonso N, Souki BQ, Coqueiro R da S, Cevidanes LHS. Common 3-dimensional coordinate system for assessment of directional changes [Internet]. American Journal of Orthodontics and Dentofacial Orthopedics. 2016 ; 149( 5): 645–656.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.ajodo.2015.10.021
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
Fonte: American Journal of Medical Genetics Part A. Unidade: HRAC
Assuntos: DESENVOLVIMENTO MAXILOFACIAL, ANORMALIDADES CRANIOFACIAIS, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 31 out. 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 out. 31 ] 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 out. 31 ] Available from: https://doi.org/10.1002/ajmg.a.36505
Artigo de periodico
Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears (2013)
Gordon, Christopher J; Petit, Florence; Kroisel, Peter Michael; Jakobsen, Linda; Zechi-Ceide, Roseli Maria ; Oufadem, Myriam; Bole-Feysot, C; Pruvost, Solenn; Masson, Cécile; Tores, Frédéric; Hieu, Thierry; Nitschké, Patrick; Lindholm, Pernille; Pellerin, Philippe; Guion-Almeida, Maria Leine; Nakata, Nancy Mizue Kokitsu ; Pittoli, Siulan Vendramini Paulovich ; Munnich, Arnold; Lyonnet, Stanislas; Holder-Espinasse, Muriel; Amiel, Jeanne
Fonte: American Journal of Human Genetics. Unidade: HRAC
Assuntos: OTOPATIAS, FENÓTIPOS, ENDOTELINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GORDON, Christopher J et al. Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears. American Journal of Human Genetics, v. 93, n. 6, p. 1118-1125, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2013.10.023. Acesso em: 31 out. 2024.
APA
Gordon, C. J., Petit, F., Kroisel, P. M., Jakobsen, L., Zechi-Ceide, R. M., Oufadem, M., et al. (2013). Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears. American Journal of Human Genetics, 93( 6), 1118-1125. doi:10.1016/j.ajhg.2013.10.023
NLM
Gordon CJ, Petit F, Kroisel PM, Jakobsen L, Zechi-Ceide RM, Oufadem M, Bole-Feysot C, Pruvost S, Masson C, Tores F, Hieu T, Nitschké P, Lindholm P, Pellerin P, Guion-Almeida ML, Nakata NMK, Pittoli SVP, Munnich A, Lyonnet S, Holder-Espinasse M, Amiel J. Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears [Internet]. American Journal of Human Genetics. 2013 ; 93( 6): 1118-1125.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.ajhg.2013.10.023
Vancouver
Gordon CJ, Petit F, Kroisel PM, Jakobsen L, Zechi-Ceide RM, Oufadem M, Bole-Feysot C, Pruvost S, Masson C, Tores F, Hieu T, Nitschké P, Lindholm P, Pellerin P, Guion-Almeida ML, Nakata NMK, Pittoli SVP, Munnich A, Lyonnet S, Holder-Espinasse M, Amiel J. Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears [Internet]. American Journal of Human Genetics. 2013 ; 93( 6): 1118-1125.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.ajhg.2013.10.023

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