ReP USP - Resultado da busca

Artigo de periodico
High dosage folic acid supplementation, oral cleft recurrence and fetal growth (2013)
Wehby, George L.; Félix, Têmis Maria ; Goco, Norman; Richieri-Costa, Antonio ; Chakraborty, Hrishikesh; Souza, Josiane; Pereira, Rui; Padovani, Carla; Ferreira, Danilo Moretti; Murray, Jeffrey C
Fonte: International Journal of Environmental Research and Public Health. Unidade: HRAC
Assuntos: ÁCIDO FÓLICO, FISSURA LÁBIOPALATINA, RECIDIVA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WEHBY, George L. et al. High dosage folic acid supplementation, oral cleft recurrence and fetal growth. International Journal of Environmental Research and Public Health, v. 10, n. 2, p. 590-605, 2013Tradução . . Disponível em: https://doi.org/10.3390/ijerph10020590. Acesso em: 21 out. 2025.
APA
Wehby, G. L., Félix, T. M., Goco, N., Richieri-Costa, A., Chakraborty, H., Souza, J., et al. (2013). High dosage folic acid supplementation, oral cleft recurrence and fetal growth. International Journal of Environmental Research and Public Health, 10( 2), 590-605. doi:10.3390/ijerph10020590
NLM
Wehby GL, Félix TM, Goco N, Richieri-Costa A, Chakraborty H, Souza J, Pereira R, Padovani C, Ferreira DM, Murray JC. High dosage folic acid supplementation, oral cleft recurrence and fetal growth [Internet]. International Journal of Environmental Research and Public Health. 2013 ; 10( 2): 590-605.[citado 2025 out. 21 ] Available from: https://doi.org/10.3390/ijerph10020590
Vancouver
Wehby GL, Félix TM, Goco N, Richieri-Costa A, Chakraborty H, Souza J, Pereira R, Padovani C, Ferreira DM, Murray JC. High dosage folic acid supplementation, oral cleft recurrence and fetal growth [Internet]. International Journal of Environmental Research and Public Health. 2013 ; 10( 2): 590-605.[citado 2025 out. 21 ] Available from: https://doi.org/10.3390/ijerph10020590
Artigo de periodico
Oral cleft prevention program (OCPP) (2012)
Wehby, George L.; Goco, Norman; Ferreira, Danilo Moretti; Felix, Temis; Richieri-Costa, Antonio ; Padovani, Carla; Queiros, Fernanda; Guimarães, Camilla Vila Nova; Pereira, Rui; Litavecz, Steve; Hartwell, Tyler; Chakraborty, Hrishikesh; Javois, Lorette C; Murray, Jeffrey C
Fonte: BMC Pediatrics. Unidade: HRAC
Assuntos: FISSURA LÁBIOPALATINA (PREVENÇÃO E CONTROLE), ANORMALIDADES CRANIOFACIAIS, ÁCIDO FÓLICO, VITAMINAS
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ABNT
WEHBY, George L. et al. Oral cleft prevention program (OCPP). BMC Pediatrics, v. 12, p. 184, 2012Tradução . . Disponível em: https://doi.org/10.1186/1471-2431-12-184. Acesso em: 21 out. 2025.
APA
Wehby, G. L., Goco, N., Ferreira, D. M., Felix, T., Richieri-Costa, A., Padovani, C., et al. (2012). Oral cleft prevention program (OCPP). BMC Pediatrics, 12, 184. doi:10.1186/1471-2431-12-184
NLM
Wehby GL, Goco N, Ferreira DM, Felix T, Richieri-Costa A, Padovani C, Queiros F, Guimarães CVN, Pereira R, Litavecz S, Hartwell T, Chakraborty H, Javois LC, Murray JC. Oral cleft prevention program (OCPP) [Internet]. BMC Pediatrics. 2012 ; 12 184.[citado 2025 out. 21 ] Available from: https://doi.org/10.1186/1471-2431-12-184
Vancouver
Wehby GL, Goco N, Ferreira DM, Felix T, Richieri-Costa A, Padovani C, Queiros F, Guimarães CVN, Pereira R, Litavecz S, Hartwell T, Chakraborty H, Javois LC, Murray JC. Oral cleft prevention program (OCPP) [Internet]. BMC Pediatrics. 2012 ; 12 184.[citado 2025 out. 21 ] Available from: https://doi.org/10.1186/1471-2431-12-184
Artigo de periodico
Clinical findings in patients with GLI2 mutations: phenotypic variability (2012)
Bertolacini, Claudia Danielli Pereira; Ribeiro-Bicudo, Lucilene Arilho ; Petrin, A.; Richieri-Costa, Antonio ; Murray, Jeffrey C
Fonte: Clinical Genetics. Unidade: HRAC
Assuntos: HOLOPROSENCEFALIA, ANORMALIDADES CRANIOFACIAIS, MUTAÇÃO
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ABNT
BERTOLACINI, Claudia Danielli Pereira et al. Clinical findings in patients with GLI2 mutations: phenotypic variability. Clinical Genetics, v. 81, n. Ja 2012, p. 70-75, 2012Tradução . . Disponível em: https://doi.org/10.1111/j.1399-0004.2010.01606.x. Acesso em: 21 out. 2025.
APA
Bertolacini, C. D. P., Ribeiro-Bicudo, L. A., Petrin, A., Richieri-Costa, A., & Murray, J. C. (2012). Clinical findings in patients with GLI2 mutations: phenotypic variability. Clinical Genetics, 81( Ja 2012), 70-75. doi:10.1111/j.1399-0004.2010.01606.x
NLM
Bertolacini CDP, Ribeiro-Bicudo LA, Petrin A, Richieri-Costa A, Murray JC. Clinical findings in patients with GLI2 mutations: phenotypic variability [Internet]. Clinical Genetics. 2012 ; 81( Ja 2012): 70-75.[citado 2025 out. 21 ] Available from: https://doi.org/10.1111/j.1399-0004.2010.01606.x
Vancouver
Bertolacini CDP, Ribeiro-Bicudo LA, Petrin A, Richieri-Costa A, Murray JC. Clinical findings in patients with GLI2 mutations: phenotypic variability [Internet]. Clinical Genetics. 2012 ; 81( Ja 2012): 70-75.[citado 2025 out. 21 ] Available from: https://doi.org/10.1111/j.1399-0004.2010.01606.x
Artigo de periodico
Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting (2011)
Saadi, Irfan; Alkuraya, Fowzan S.; Gisselbrecht, Stephen S.; Goessling, Wolfram; Cavallesco, Resy; Turbe-Doan, Annick; Petrin, Aline L; Harris, James; Siddiqui, Ursela; Grix Junior, Arthur W.; Hove, Hanne D.; Leboulch, Philippe; Glover, Thomas W.; Morton, Cynthia C; Richieri-Costa, Antonio ; Murray, Jeffrey C; Erickson, Robert P.; Maas, Richard L.
Fonte: American Journal of Human Genetics. Unidade: HRAC
Assuntos: DEFICIÊNCIA DE PROTEÍNA, ANORMALIDADES CRANIOFACIAIS, FENÓTIPOS, DISOSTOSE CRÂNIOFACIAL, FISSURA PALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SAADI, Irfan et al. Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting. American Journal of Human Genetics, v. 89, p. 44-55, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2011.05.023. Acesso em: 21 out. 2025.
APA
Saadi, I., Alkuraya, F. S., Gisselbrecht, S. S., Goessling, W., Cavallesco, R., Turbe-Doan, A., et al. (2011). Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting. American Journal of Human Genetics, 89, 44-55. doi:10.1016/j.ajhg.2011.05.023
NLM
Saadi I, Alkuraya FS, Gisselbrecht SS, Goessling W, Cavallesco R, Turbe-Doan A, Petrin AL, Harris J, Siddiqui U, Grix Junior AW, Hove HD, Leboulch P, Glover TW, Morton CC, Richieri-Costa A, Murray JC, Erickson RP, Maas RL. Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting [Internet]. American Journal of Human Genetics. 2011 ; 89 44-55.[citado 2025 out. 21 ] Available from: https://doi.org/10.1016/j.ajhg.2011.05.023
Vancouver
Saadi I, Alkuraya FS, Gisselbrecht SS, Goessling W, Cavallesco R, Turbe-Doan A, Petrin AL, Harris J, Siddiqui U, Grix Junior AW, Hove HD, Leboulch P, Glover TW, Morton CC, Richieri-Costa A, Murray JC, Erickson RP, Maas RL. Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting [Internet]. American Journal of Human Genetics. 2011 ; 89 44-55.[citado 2025 out. 21 ] Available from: https://doi.org/10.1016/j.ajhg.2011.05.023
Trabalho de evento-resumo
Microarray analysis in Brazilian patients with the oculoauriculovertebral spectrum (2011)
Machado-Paula, Ligiane Alves ; Vendramini-Pittoli, Siulan ; Kokitsu-Nakata, Nancy Mizue ; Ribeiro-Bicudo, Lucilene Arilho ; Richieri-Costa, Antonio ; Murray, Jeffrey C
Fonte: Abstracts. Nome do evento: International Meeting on Craniofacial Anomalies: Clinical Phenotype, Genes Related and New Perspectives. Unidade: HRAC
Assuntos: ANORMALIDADES MÚLTIPLAS, ANORMALIDADES CROMOSSÔMICAS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MACHADO-PAULA, Ligiane Alves et al. Microarray analysis in Brazilian patients with the oculoauriculovertebral spectrum. 2011, Anais.. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2011. Disponível em: https://repositorio.usp.br/directbitstream/6007ea78-c39b-4a8e-b5a0-ce7cd5632b4f/3247768.pdf. Acesso em: 21 out. 2025.
APA
Machado-Paula, L. A., Vendramini-Pittoli, S., Kokitsu-Nakata, N. M., Ribeiro-Bicudo, L. A., Richieri-Costa, A., & Murray, J. C. (2011). Microarray analysis in Brazilian patients with the oculoauriculovertebral spectrum. In Abstracts. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/6007ea78-c39b-4a8e-b5a0-ce7cd5632b4f/3247768.pdf
NLM
Machado-Paula LA, Vendramini-Pittoli S, Kokitsu-Nakata NM, Ribeiro-Bicudo LA, Richieri-Costa A, Murray JC. Microarray analysis in Brazilian patients with the oculoauriculovertebral spectrum [Internet]. Abstracts. 2011 ;[citado 2025 out. 21 ] Available from: https://repositorio.usp.br/directbitstream/6007ea78-c39b-4a8e-b5a0-ce7cd5632b4f/3247768.pdf
Vancouver
Machado-Paula LA, Vendramini-Pittoli S, Kokitsu-Nakata NM, Ribeiro-Bicudo LA, Richieri-Costa A, Murray JC. Microarray analysis in Brazilian patients with the oculoauriculovertebral spectrum [Internet]. Abstracts. 2011 ;[citado 2025 out. 21 ] Available from: https://repositorio.usp.br/directbitstream/6007ea78-c39b-4a8e-b5a0-ce7cd5632b4f/3247768.pdf
Trabalho de evento-resumo
Duplication in splicing site of intron 2 of gene PTCH1 in seven patients with holoprosencephaly (2011)
Bertolacini, Claudia Danielli Pereira; Ribeiro-Bicudo, Lucilene Arilho ; Petrin, A; Legnaro, Chiara de Campos; Goes, L. D; Ramalho, R; Richieri-Costa, Antonio ; Murray, Jeffrey C
Fonte: Abstracts. Nome do evento: International Meeting on Craniofacial Anomalies: Clinical Phenotype, Genes Related and New Perspectives. Unidade: HRAC
Assuntos: HOLOPROSENCEFALIA, MUTAÇÃO GENÉTICA, ANORMALIDADES CONGÊNITAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERTOLACINI, Claudia Danielli Pereira et al. Duplication in splicing site of intron 2 of gene PTCH1 in seven patients with holoprosencephaly. 2011, Anais.. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2011. Disponível em: https://repositorio.usp.br/directbitstream/b433a5d9-e9ce-46e3-b97b-ae96cd6f76a9/3247647.pdf. Acesso em: 21 out. 2025.
APA
Bertolacini, C. D. P., Ribeiro-Bicudo, L. A., Petrin, A., Legnaro, C. de C., Goes, L. D., Ramalho, R., et al. (2011). Duplication in splicing site of intron 2 of gene PTCH1 in seven patients with holoprosencephaly. In Abstracts. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/b433a5d9-e9ce-46e3-b97b-ae96cd6f76a9/3247647.pdf
NLM
Bertolacini CDP, Ribeiro-Bicudo LA, Petrin A, Legnaro C de C, Goes LD, Ramalho R, Richieri-Costa A, Murray JC. Duplication in splicing site of intron 2 of gene PTCH1 in seven patients with holoprosencephaly [Internet]. Abstracts. 2011 ;[citado 2025 out. 21 ] Available from: https://repositorio.usp.br/directbitstream/b433a5d9-e9ce-46e3-b97b-ae96cd6f76a9/3247647.pdf
Vancouver
Bertolacini CDP, Ribeiro-Bicudo LA, Petrin A, Legnaro C de C, Goes LD, Ramalho R, Richieri-Costa A, Murray JC. Duplication in splicing site of intron 2 of gene PTCH1 in seven patients with holoprosencephaly [Internet]. Abstracts. 2011 ;[citado 2025 out. 21 ] Available from: https://repositorio.usp.br/directbitstream/b433a5d9-e9ce-46e3-b97b-ae96cd6f76a9/3247647.pdf
Trabalho de evento-resumo
Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate (2009)
Paula, Ligiane Alves Machado; Petrin, Aline Lourenço; Ribeiro-Bicudo, Lucilene Arilho ; Moretti Ferreira, Danilo ; Marazita, Mary L; Cooper, M. E; Mossey, Peter A; Richieri-Costa, Antonio ; Murray, Jeffrey C
Fonte: Anais. Nome do evento: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Assuntos: FISSURA LÁBIOPALATINA, METABOLISMO, GENES
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ABNT
PAULA, Ligiane Alves Machado et al. Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate. 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/406a1218-98e4-4427-805d-1550691acd19/3099699.pdf. Acesso em: 21 out. 2025.
APA
Paula, L. A. M., Petrin, A. L., Ribeiro-Bicudo, L. A., Moretti Ferreira, D., Marazita, M. L., Cooper, M. E., et al. (2009). Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate. In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/406a1218-98e4-4427-805d-1550691acd19/3099699.pdf
NLM
Paula LAM, Petrin AL, Ribeiro-Bicudo LA, Moretti Ferreira D, Marazita ML, Cooper ME, Mossey PA, Richieri-Costa A, Murray JC. Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate [Internet]. Anais. 2009 ;[citado 2025 out. 21 ] Available from: https://repositorio.usp.br/directbitstream/406a1218-98e4-4427-805d-1550691acd19/3099699.pdf
Vancouver
Paula LAM, Petrin AL, Ribeiro-Bicudo LA, Moretti Ferreira D, Marazita ML, Cooper ME, Mossey PA, Richieri-Costa A, Murray JC. Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate [Internet]. Anais. 2009 ;[citado 2025 out. 21 ] Available from: https://repositorio.usp.br/directbitstream/406a1218-98e4-4427-805d-1550691acd19/3099699.pdf
Trabalho de evento-resumo
Triopia associated with a large facial cleft: report on a brazilian patient (2001)
Moretti Ferreira, Danilo ; Lima, Renata Lúcia Leite Ferreira de; Murray, Jeffrey C; Richieri-Costa, Antonio
Fonte: Programme & Abstracts. Nome do evento: International Congress on Cleft Palate and Related Craniofacial Anomalies. Unidade: HRAC
Assunto: ANOMALIA CRANIOFACIAL
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ABNT
MORETTI FERREIRA, Danilo et al. Triopia associated with a large facial cleft: report on a brazilian patient. 2001, Anais.. Goteborg: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2001. Disponível em: https://repositorio.usp.br/directbitstream/11fb802c-7472-4676-9bc0-854a0a1820fe/3167153.pdf. Acesso em: 21 out. 2025.
APA
Moretti Ferreira, D., Lima, R. L. L. F. de, Murray, J. C., & Richieri-Costa, A. (2001). Triopia associated with a large facial cleft: report on a brazilian patient. In Programme & Abstracts. Goteborg: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/11fb802c-7472-4676-9bc0-854a0a1820fe/3167153.pdf
NLM
Moretti Ferreira D, Lima RLLF de, Murray JC, Richieri-Costa A. Triopia associated with a large facial cleft: report on a brazilian patient [Internet]. Programme & Abstracts. 2001 ;[citado 2025 out. 21 ] Available from: https://repositorio.usp.br/directbitstream/11fb802c-7472-4676-9bc0-854a0a1820fe/3167153.pdf
Vancouver
Moretti Ferreira D, Lima RLLF de, Murray JC, Richieri-Costa A. Triopia associated with a large facial cleft: report on a brazilian patient [Internet]. Programme & Abstracts. 2001 ;[citado 2025 out. 21 ] Available from: https://repositorio.usp.br/directbitstream/11fb802c-7472-4676-9bc0-854a0a1820fe/3167153.pdf

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