ReP USP - Resultado da busca

Artigo de periodico
Craniocervical instability in oculoauriculovertebral spectrum (2023)
Gomes, Luiz Paulo; Ferraz, Beatriz Gonçalves ; Brandão, Michele Madeira ; Alonso, Nivaldo ; Pittoli, Siulan Vendramini ; Tonello, Cristiano
Source: The Journal of Craniofacial Surgery. Unidades: HRAC, FOB, HRACF
Subjects: INSTABILIDADE ARTICULAR, COLUNA VERTEBRAL, SÍNDROME DE GOLDENHAR, ASSIMETRIA FACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, Luiz Paulo et al. Craniocervical instability in oculoauriculovertebral spectrum. The Journal of Craniofacial Surgery, v. 34, n. 4, p. 1283-1286, 2023Tradução . . Disponível em: https://doi.org/10.1097/SCS.0000000000009192. Acesso em: 04 out. 2023.
APA
Gomes, L. P., Ferraz, B. G., Brandão, M. M., Alonso, N., Pittoli, S. V., & Tonello, C. (2023). Craniocervical instability in oculoauriculovertebral spectrum. The Journal of Craniofacial Surgery, 34( 4), 1283-1286. doi:10.1097/SCS.0000000000009192
NLM
Gomes LP, Ferraz BG, Brandão MM, Alonso N, Pittoli SV, Tonello C. Craniocervical instability in oculoauriculovertebral spectrum [Internet]. The Journal of Craniofacial Surgery. 2023 ; 34( 4): 1283-1286.[citado 2023 out. 04 ] Available from: https://doi.org/10.1097/SCS.0000000000009192
Vancouver
Gomes LP, Ferraz BG, Brandão MM, Alonso N, Pittoli SV, Tonello C. Craniocervical instability in oculoauriculovertebral spectrum [Internet]. The Journal of Craniofacial Surgery. 2023 ; 34( 4): 1283-1286.[citado 2023 out. 04 ] Available from: https://doi.org/10.1097/SCS.0000000000009192
Artigo de periodico
Clinical characterization of congenital anophthalmic and microphthalmic cavities in inidviduals with craniofacial anomalies (2023)
Parizotto Paula, Isabella ; Gonçalves Paula, Raul ; Kokitsu, Nancy Mizue ; Alonso, Nivaldo ; Tonello, Cristiano
Source: The Journal of Craniofacial Surgery. Unidades: HRAC, FOB, HRACF
Subjects: OFTALMOPATIAS, ANORMALIDADES CONGÊNITAS, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARIZOTTO PAULA, Isabella et al. Clinical characterization of congenital anophthalmic and microphthalmic cavities in inidviduals with craniofacial anomalies. The Journal of Craniofacial Surgery, v. 34, n. 6, p. e542-e546, 2023Tradução . . Disponível em: https://doi.org/10.1097/SCS.0000000000009557. Acesso em: 04 out. 2023.
APA
Parizotto Paula, I., Gonçalves Paula, R., Kokitsu, N. M., Alonso, N., & Tonello, C. (2023). Clinical characterization of congenital anophthalmic and microphthalmic cavities in inidviduals with craniofacial anomalies. The Journal of Craniofacial Surgery, 34( 6), e542-e546. doi:10.1097/SCS.0000000000009557
NLM
Parizotto Paula I, Gonçalves Paula R, Kokitsu NM, Alonso N, Tonello C. Clinical characterization of congenital anophthalmic and microphthalmic cavities in inidviduals with craniofacial anomalies [Internet]. The Journal of Craniofacial Surgery. 2023 ; 34( 6): e542-e546.[citado 2023 out. 04 ] Available from: https://doi.org/10.1097/SCS.0000000000009557
Vancouver
Parizotto Paula I, Gonçalves Paula R, Kokitsu NM, Alonso N, Tonello C. Clinical characterization of congenital anophthalmic and microphthalmic cavities in inidviduals with craniofacial anomalies [Internet]. The Journal of Craniofacial Surgery. 2023 ; 34( 6): e542-e546.[citado 2023 out. 04 ] Available from: https://doi.org/10.1097/SCS.0000000000009557
Artigo de periodico
Craniofacial microsomia: new updates in spinal anomalies (2023)
Ferraz, Beatriz Gonçalves ; Vendramini-Pittoli, Siulan ; Gomes, Luiz Paulo; Brandão, Michele Madeira ; Alonso, Nivaldo ; Tonello, Cristiano
Source: The Journal of Craniofacial Surgery. Unidades: HRAC, FOB, HRACF
Subjects: ASSIMETRIA FACIAL, SÍNDROME DE GOLDENHAR, COLUNA VERTEBRAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ, Beatriz Gonçalves et al. Craniofacial microsomia: new updates in spinal anomalies. The Journal of Craniofacial Surgery, v. 34, n. 4, p. e398-e401, 2023Tradução . . Disponível em: https://doi.org/10.1097/scs.0000000000009326. Acesso em: 04 out. 2023.
APA
Ferraz, B. G., Vendramini-Pittoli, S., Gomes, L. P., Brandão, M. M., Alonso, N., & Tonello, C. (2023). Craniofacial microsomia: new updates in spinal anomalies. The Journal of Craniofacial Surgery, 34( 4), e398-e401. doi:10.1097/scs.0000000000009326
NLM
Ferraz BG, Vendramini-Pittoli S, Gomes LP, Brandão MM, Alonso N, Tonello C. Craniofacial microsomia: new updates in spinal anomalies [Internet]. The Journal of Craniofacial Surgery. 2023 ; 34( 4): e398-e401.[citado 2023 out. 04 ] Available from: https://doi.org/10.1097/scs.0000000000009326
Vancouver
Ferraz BG, Vendramini-Pittoli S, Gomes LP, Brandão MM, Alonso N, Tonello C. Craniofacial microsomia: new updates in spinal anomalies [Internet]. The Journal of Craniofacial Surgery. 2023 ; 34( 4): e398-e401.[citado 2023 out. 04 ] Available from: https://doi.org/10.1097/scs.0000000000009326
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 Alberto ; 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: 04 out. 2023.
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 2023 out. 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 2023 out. 04 ] Available from: https://doi.org/10.1002/humu.24375
Artigo de periodico
Tessier 3 and 4 clefts and choanal atresia: an unusual association? (2022)
Tonello, Cristiano ; Martins, Danilo Augusto Nery dos Passos; Baptista, Marco Antonio Ferraz de Barros; Mondelli, Felipe; Nakata, Nancy Mizue Kokitsu ; Feitosa, Leonardo Bezerra ; Alonso, Nivaldo
Source: The Cleft Palate-Craniofacial Journal. Unidades: HRAC, HRACF
Subjects: ANORMALIDADES CRANIOFACIAIS, FISSURA LÁBIOPALATINA, COANAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TONELLO, Cristiano et al. Tessier 3 and 4 clefts and choanal atresia: an unusual association?. The Cleft Palate-Craniofacial Journal, v. 59, n. 10, p. 1228-1232, 2022Tradução . . Disponível em: https://doi.org/10.1177/10556656211042172. Acesso em: 04 out. 2023.
APA
Tonello, C., Martins, D. A. N. dos P., Baptista, M. A. F. de B., Mondelli, F., Nakata, N. M. K., Feitosa, L. B., & Alonso, N. (2022). Tessier 3 and 4 clefts and choanal atresia: an unusual association? The Cleft Palate-Craniofacial Journal, 59( 10), 1228-1232. doi:10.1177/10556656211042172
NLM
Tonello C, Martins DAN dos P, Baptista MAF de B, Mondelli F, Nakata NMK, Feitosa LB, Alonso N. Tessier 3 and 4 clefts and choanal atresia: an unusual association? [Internet]. The Cleft Palate-Craniofacial Journal. 2022 ; 59( 10): 1228-1232.[citado 2023 out. 04 ] Available from: https://doi.org/10.1177/10556656211042172
Vancouver
Tonello C, Martins DAN dos P, Baptista MAF de B, Mondelli F, Nakata NMK, Feitosa LB, Alonso N. Tessier 3 and 4 clefts and choanal atresia: an unusual association? [Internet]. The Cleft Palate-Craniofacial Journal. 2022 ; 59( 10): 1228-1232.[citado 2023 out. 04 ] Available from: https://doi.org/10.1177/10556656211042172
Trabalho de evento-resumo
Fissuras raras da face e apêndices finger-like: desorganização em seres humanos (2022)
Serigatto, Henrique Regonaschi ; Virmond, Luiza do Amaral; Kokitsu-Nakata, Nancy Mizue ; Vendramini-Pittoli, Siulan ; Rosenberg, Carla ; Zechi-Ceide, Roseli Maria
Source: Anais. Conference titles: Congresso Médico Acadêmico de Bauru da Universidade de São Paulo - COMAB. Unidades: HRAC, IB, HRACF
Subjects: ANOMALIA FACIAL, TERATOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERIGATTO, Henrique Regonaschi et al. Fissuras raras da face e apêndices finger-like: desorganização em seres humanos. 2022, Anais.. Bauru: Faculdade de Odontologia de Bauru. Universidade de São Paulo, 2022. Disponível em: https://repositorio.usp.br/directbitstream/934b4ccb-9ab6-47a1-b2b4-0066de69de1c/3139253.pdf. Acesso em: 04 out. 2023.
APA
Serigatto, H. R., Virmond, L. do A., Kokitsu-Nakata, N. M., Vendramini-Pittoli, S., Rosenberg, C., & Zechi-Ceide, R. M. (2022). Fissuras raras da face e apêndices finger-like: desorganização em seres humanos. In Anais. Bauru: Faculdade de Odontologia de Bauru. Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/934b4ccb-9ab6-47a1-b2b4-0066de69de1c/3139253.pdf
NLM
Serigatto HR, Virmond L do A, Kokitsu-Nakata NM, Vendramini-Pittoli S, Rosenberg C, Zechi-Ceide RM. Fissuras raras da face e apêndices finger-like: desorganização em seres humanos [Internet]. Anais. 2022 ;[citado 2023 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/934b4ccb-9ab6-47a1-b2b4-0066de69de1c/3139253.pdf
Vancouver
Serigatto HR, Virmond L do A, Kokitsu-Nakata NM, Vendramini-Pittoli S, Rosenberg C, Zechi-Ceide RM. Fissuras raras da face e apêndices finger-like: desorganização em seres humanos [Internet]. Anais. 2022 ;[citado 2023 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/934b4ccb-9ab6-47a1-b2b4-0066de69de1c/3139253.pdf
Trabalho de evento-resumo periodico
MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis (2022)
Zechi-Ceide, Roseli Maria ; Kokitsu-Nakata, Nancy Mizue; Alvarez, Camila Wenceslau ; Migliore, Chiara; Rafacho, Marina Bigeli ; Siemann, Maria Eugênia; Candido-Souza, Rosana Maria; Vendramini-Pittoli, Siulan; Tonello, Cristiano ; Maximino, Luciana Paula ; Meroni, Germana; Guion-Almeida, Maria Leine; Opitz, John M.; Richieri-Costa, Antonio
Source: European Journal of Human Genetics. Conference titles: European Society of Human Genetics. Unidades: HRAC, FOB, HRACF
Subjects: FISSURA LÁBIOPALATINA, HIPERTELORISMO, TRIAGEM, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZECHI-CEIDE, Roseli Maria et al. MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis. European Journal of Human Genetics. London: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Disponível em: https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.pdf. Acesso em: 04 out. 2023. , 2022
APA
Zechi-Ceide, R. M., Kokitsu-Nakata, N. M., Alvarez, C. W., Migliore, C., Rafacho, M. B., Siemann, M. E., et al. (2022). MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis. European Journal of Human Genetics. London: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.pdf
NLM
Zechi-Ceide RM, Kokitsu-Nakata NM, Alvarez CW, Migliore C, Rafacho MB, Siemann ME, Candido-Souza RM, Vendramini-Pittoli S, Tonello C, Maximino LP, Meroni G, Guion-Almeida ML, Opitz JM, Richieri-Costa A. MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis [Internet]. European Journal of Human Genetics. 2022 ; 30 349-350.[citado 2023 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.pdf
Vancouver
Zechi-Ceide RM, Kokitsu-Nakata NM, Alvarez CW, Migliore C, Rafacho MB, Siemann ME, Candido-Souza RM, Vendramini-Pittoli S, Tonello C, Maximino LP, Meroni G, Guion-Almeida ML, Opitz JM, Richieri-Costa A. MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis [Internet]. European Journal of Human Genetics. 2022 ; 30 349-350.[citado 2023 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.pdf
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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 out. 2023.
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 2023 out. 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 2023 out. 04 ] Available from: https://doi.org/10.1002/humu.24349
Artigo de periodico
Eyeball preservation with purse-string conjunctival closure for melting corneal ulcer in rare facial cleft (2021)
Tonello, Cristiano ; Paula, Raul Gonçalves; Paula, Isabella P.; Nunes, Rodrigo B.; Nakata, Nancy Mizue Kokitsu ; Alonso, Nivaldo
Source: The Cleft Palate-Craniofacial Journal. Unidades: HRAC, HRACF
Subjects: MORFOLOGIA (ANATOMIA), OLHO, ANOMALIA CRANIOFACIAL, CÓRNEA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TONELLO, Cristiano et al. Eyeball preservation with purse-string conjunctival closure for melting corneal ulcer in rare facial cleft. The Cleft Palate-Craniofacial Journal, v. 58, n. 9, p. 1195-1200, 2021Tradução . . Disponível em: https://doi.org/10.1177/1055665620980632. Acesso em: 04 out. 2023.
APA
Tonello, C., Paula, R. G., Paula, I. P., Nunes, R. B., Nakata, N. M. K., & Alonso, N. (2021). Eyeball preservation with purse-string conjunctival closure for melting corneal ulcer in rare facial cleft. The Cleft Palate-Craniofacial Journal, 58( 9), 1195-1200. doi:10.1177/1055665620980632
NLM
Tonello C, Paula RG, Paula IP, Nunes RB, Nakata NMK, Alonso N. Eyeball preservation with purse-string conjunctival closure for melting corneal ulcer in rare facial cleft [Internet]. The Cleft Palate-Craniofacial Journal. 2021 ; 58( 9): 1195-1200.[citado 2023 out. 04 ] Available from: https://doi.org/10.1177/1055665620980632
Vancouver
Tonello C, Paula RG, Paula IP, Nunes RB, Nakata NMK, Alonso N. Eyeball preservation with purse-string conjunctival closure for melting corneal ulcer in rare facial cleft [Internet]. The Cleft Palate-Craniofacial Journal. 2021 ; 58( 9): 1195-1200.[citado 2023 out. 04 ] Available from: https://doi.org/10.1177/1055665620980632
Artigo de periodico
Craniofacial and airway morphology of individuals with oculoauriculovertebral spectrum (2021)
Parizotto, Julianna Oliveira Lima ; Peixoto, Adriano Porto; Borsato, Karina Tostes; Bianchi, Jonas ; Pittoli, Siulan Vendramini Paulovich ; Tonello, Cristiano ; Gonçalves, João Roberto
Source: Orthodontics and Craniofacial Research. Unidade: HRAC
Subjects: SÍNDROME DE GOLDENHAR, DESENVOLVIMENTO CRANIOFACIAL, TOMOGRAFIA COMPUTADORIZADA DE EMISSÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARIZOTTO, Julianna Oliveira Lima et al. Craniofacial and airway morphology of individuals with oculoauriculovertebral spectrum. Orthodontics and Craniofacial Research, v. No 2021, n. 4, p. 575-584, 2021Tradução . . Disponível em: https://doi.org/10.1111/ocr.12483. Acesso em: 04 out. 2023.
APA
Parizotto, J. O. L., Peixoto, A. P., Borsato, K. T., Bianchi, J., Pittoli, S. V. P., Tonello, C., & Gonçalves, J. R. (2021). Craniofacial and airway morphology of individuals with oculoauriculovertebral spectrum. Orthodontics and Craniofacial Research, No 2021( 4), 575-584. doi:10.1111/ocr.12483
NLM
Parizotto JOL, Peixoto AP, Borsato KT, Bianchi J, Pittoli SVP, Tonello C, Gonçalves JR. Craniofacial and airway morphology of individuals with oculoauriculovertebral spectrum [Internet]. Orthodontics and Craniofacial Research. 2021 ; No 2021( 4): 575-584.[citado 2023 out. 04 ] Available from: https://doi.org/10.1111/ocr.12483
Vancouver
Parizotto JOL, Peixoto AP, Borsato KT, Bianchi J, Pittoli SVP, Tonello C, Gonçalves JR. Craniofacial and airway morphology of individuals with oculoauriculovertebral spectrum [Internet]. Orthodontics and Craniofacial Research. 2021 ; No 2021( 4): 575-584.[citado 2023 out. 04 ] Available from: https://doi.org/10.1111/ocr.12483
Trabalho de evento-resumo
Morfologia da coluna vertebral de indivíduos com espectro oculoauriculo vertebral (2021)
Ferraz, B. G.; Alonso, Nivaldo ; Brandão, Michele Madeira; Gomes, L. P.; Vendramini-Pittoli, Siulan
Source: Anais. Conference titles: JORMED - Jornada da Medicina USP Bauru. Unidades: FM, HRAC, FOB
Subjects: SÍNDROME DE GOLDENHAR, COLUNA VERTEBRAL, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ, B. G. et al. Morfologia da coluna vertebral de indivíduos com espectro oculoauriculo vertebral. 2021, Anais.. Macaé: CONGRESSE.ME, 2021. Disponível em: https://repositorio.usp.br/directbitstream/b47fde5b-623a-4fd7-a491-af9c0c30e972/3125092.pdf. Acesso em: 04 out. 2023.
APA
Ferraz, B. G., Alonso, N., Brandão, M. M., Gomes, L. P., & Vendramini-Pittoli, S. (2021). Morfologia da coluna vertebral de indivíduos com espectro oculoauriculo vertebral. In Anais. Macaé: CONGRESSE.ME. Recuperado de https://repositorio.usp.br/directbitstream/b47fde5b-623a-4fd7-a491-af9c0c30e972/3125092.pdf
NLM
Ferraz BG, Alonso N, Brandão MM, Gomes LP, Vendramini-Pittoli S. Morfologia da coluna vertebral de indivíduos com espectro oculoauriculo vertebral [Internet]. Anais. 2021 ;[citado 2023 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/b47fde5b-623a-4fd7-a491-af9c0c30e972/3125092.pdf
Vancouver
Ferraz BG, Alonso N, Brandão MM, Gomes LP, Vendramini-Pittoli S. Morfologia da coluna vertebral de indivíduos com espectro oculoauriculo vertebral [Internet]. Anais. 2021 ;[citado 2023 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/b47fde5b-623a-4fd7-a491-af9c0c30e972/3125092.pdf
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
Source: Bone. Unidade: HRAC
Subjects: DISOSTOSE MANDIBULOFACIAL, MUTAÇÃO GENÉTICA, FENÓTIPOS, CONVULSÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 04 out. 2023.
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 2023 out. 04 ] 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 2023 out. 04 ] Available from: https://doi.org/10.1016/j.bone.2021.116152
Trabalho de evento-resumo
Fissura craniofacial complexa na síndrome oculoauriculofrontonasal (2021)
Serigatto, Henrique Regonaschi; Tonello, Cristiano ; Moura, Priscila Padilha; Peixoto, Adriano Porto ; Vendramini-Pittoli, Siulan; Kokitsu-Nakata, Nancy Mizue; Zechi-Ceide, Roseli Maria
Source: Anais. Conference titles: JORMED - Jornada da Medicina USP Bauru. Unidades: HRAC, HRACF
Subjects: CRÂNIO, FACE, TOMOGRAFIA COMPUTADORIZADA POR RAIOS X
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERIGATTO, Henrique Regonaschi et al. Fissura craniofacial complexa na síndrome oculoauriculofrontonasal. 2021, Anais.. Macaé: CONGRESSE.ME, 2021. Disponível em: https://repositorio.usp.br/directbitstream/a4e3b218-8714-4bf7-b67b-db14832b88b5/3125711.pdf. Acesso em: 04 out. 2023.
APA
Serigatto, H. R., Tonello, C., Moura, P. P., Peixoto, A. P., Vendramini-Pittoli, S., Kokitsu-Nakata, N. M., & Zechi-Ceide, R. M. (2021). Fissura craniofacial complexa na síndrome oculoauriculofrontonasal. In Anais. Macaé: CONGRESSE.ME. Recuperado de https://repositorio.usp.br/directbitstream/a4e3b218-8714-4bf7-b67b-db14832b88b5/3125711.pdf
NLM
Serigatto HR, Tonello C, Moura PP, Peixoto AP, Vendramini-Pittoli S, Kokitsu-Nakata NM, Zechi-Ceide RM. Fissura craniofacial complexa na síndrome oculoauriculofrontonasal [Internet]. Anais. 2021 ;[citado 2023 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/a4e3b218-8714-4bf7-b67b-db14832b88b5/3125711.pdf
Vancouver
Serigatto HR, Tonello C, Moura PP, Peixoto AP, Vendramini-Pittoli S, Kokitsu-Nakata NM, Zechi-Ceide RM. Fissura craniofacial complexa na síndrome oculoauriculofrontonasal [Internet]. Anais. 2021 ;[citado 2023 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/a4e3b218-8714-4bf7-b67b-db14832b88b5/3125711.pdf
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
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: ANÁLISE FACIAL, GENÉTICA DE POPULAÇÕES, FENÓTIPOS, ANORMALIDADES CONGÊNITAS, SÍNDROME DE NOONAN
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 04 out. 2023.
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 2023 out. 04 ] 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 2023 out. 04 ] Available from: https://doi.org/10.1002/ajmg.a.61461
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 04 out. 2023.
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 2023 out. 04 ] 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 2023 out. 04 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 04 out. 2023.
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 2023 out. 04 ] 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 2023 out. 04 ] Available from: https://doi.org/10.1210/clinem/dgaa065
Artigo de periodico
Craniofacial morphology in patients with opitz G/BBB syndrome (2019)
Dalben, Gisele da Silva ; Garib, Daniela Gamba ; Pinto, Rayane de Oliveira ; Richieri-Costa, Antonio ; Taveira, Luís Antônio de Assis
Source: Cleft Palate-Craniofacial Journal. Unidades: HRAC, FOB
Subjects: CEFALOMETRIA, FISSURA LÁBIOPALATINA, ANOMALIA CRANIOFACIAL, MORFOLOGIA (ANATOMIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DALBEN, Gisele da Silva et al. Craniofacial morphology in patients with opitz G/BBB syndrome. Cleft Palate-Craniofacial Journal, v. no 2019, n. 10, p. 1366-1372, 2019Tradução . . Disponível em: https://doi.org/10.1177/1055665619857001. Acesso em: 04 out. 2023.
APA
Dalben, G. da S., Garib, D. G., Pinto, R. de O., Richieri-Costa, A., & Taveira, L. A. de A. (2019). Craniofacial morphology in patients with opitz G/BBB syndrome. Cleft Palate-Craniofacial Journal, no 2019( 10), 1366-1372. doi:10.1177/1055665619857001
NLM
Dalben G da S, Garib DG, Pinto R de O, Richieri-Costa A, Taveira LA de A. Craniofacial morphology in patients with opitz G/BBB syndrome [Internet]. Cleft Palate-Craniofacial Journal. 2019 ; no 2019( 10): 1366-1372.[citado 2023 out. 04 ] Available from: https://doi.org/10.1177/1055665619857001
Vancouver
Dalben G da S, Garib DG, Pinto R de O, Richieri-Costa A, Taveira LA de A. Craniofacial morphology in patients with opitz G/BBB syndrome [Internet]. Cleft Palate-Craniofacial Journal. 2019 ; no 2019( 10): 1366-1372.[citado 2023 out. 04 ] Available from: https://doi.org/10.1177/1055665619857001
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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 out. 2023.
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 2023 out. 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 2023 out. 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 out. 2023.
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 2023 out. 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 2023 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/2f17e911-522c-4ebf-b07d-80b7f922a17c/2963227.pdf
Trabalho de evento-resumo
Robin sequence, atypical face and intellectual disability in Brazilian siblings (2019)
Sandri, Rosana Maria Cândido de Souza ; Rafacho, Marina Bigeli ; Maximino, Luciana Paula ; Richieri-Costa, Antonio ; Zechi-Ceide, Roseli Maria
Source: Abstract Book. Conference titles: European Cleft Palate Craniofacial Association Congress. Unidades: FOB, HRAC, HRACF
Subjects: SÍNDROME DE PIERRE ROBIN, PESSOAS COM DEFICIÊNCIA INTELECTUAL, GÊMEOS, ANOMALIA FACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANDRI, Rosana Maria Cândido de Souza et al. Robin sequence, atypical face and intellectual disability in Brazilian siblings. 2019, Anais.. Utrecht: Faculdade de Odontologia de Bauru, Universidade de São Paulo, 2019. Disponível em: https://repositorio.usp.br/directbitstream/fcef6e1b-d54d-4744-95d4-4ad712b7610f/2962403.pdf. Acesso em: 04 out. 2023.
APA
Sandri, R. M. C. de S., Rafacho, M. B., Maximino, L. P., Richieri-Costa, A., & Zechi-Ceide, R. M. (2019). Robin sequence, atypical face and intellectual disability in Brazilian siblings. In Abstract Book. Utrecht: Faculdade de Odontologia de Bauru, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/fcef6e1b-d54d-4744-95d4-4ad712b7610f/2962403.pdf
NLM
Sandri RMC de S, Rafacho MB, Maximino LP, Richieri-Costa A, Zechi-Ceide RM. Robin sequence, atypical face and intellectual disability in Brazilian siblings [Internet]. Abstract Book. 2019 ;[citado 2023 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/fcef6e1b-d54d-4744-95d4-4ad712b7610f/2962403.pdf
Vancouver
Sandri RMC de S, Rafacho MB, Maximino LP, Richieri-Costa A, Zechi-Ceide RM. Robin sequence, atypical face and intellectual disability in Brazilian siblings [Internet]. Abstract Book. 2019 ;[citado 2023 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/fcef6e1b-d54d-4744-95d4-4ad712b7610f/2962403.pdf

USP Schools

ReP

Filtros

USP Schools

Departament

Authors

USP affiliated authors

Date published

Subjects

Source title

Publisher

Conference titles

Countries/Territories

Funding Agencies

Indexado em

Non normalized affiliation

Countries of institutions of collaboration