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Artigo de periodico
Association of thoracic spine deformity and cardiovascular disease in a mouse model for Marfan syndrome (2019)
Souza, Rodrigo Barbosa de ; Farinha-Arcieri, Luis Ernesto ; Catroxo, Márcia Helena Braga ; Martins, Ana Maria Cristina Rebelo Pinto da Fonseca ; Tedesco, Roberto Carlos; Alonso, Luís Garcia; Koh, Ivan Hong Jun ; Pereira, Lygia da Veiga
Source: PLOS ONE. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, COLUNA VERTEBRAL, SISTEMA CARDIOVASCULAR, MODELOS ANIMAIS DE DOENÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUZA, Rodrigo Barbosa de et al. Association of thoracic spine deformity and cardiovascular disease in a mouse model for Marfan syndrome. PLOS ONE, v. No 2019, n. 11, 2019Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0224581. Acesso em: 26 maio 2024.
APA
Souza, R. B. de, Farinha-Arcieri, L. E., Catroxo, M. H. B., Martins, A. M. C. R. P. da F., Tedesco, R. C., Alonso, L. G., et al. (2019). Association of thoracic spine deformity and cardiovascular disease in a mouse model for Marfan syndrome. PLOS ONE, No 2019( 11). doi:10.1371/journal.pone.0224581
NLM
Souza RB de, Farinha-Arcieri LE, Catroxo MHB, Martins AMCRP da F, Tedesco RC, Alonso LG, Koh IHJ, Pereira L da V. Association of thoracic spine deformity and cardiovascular disease in a mouse model for Marfan syndrome [Internet]. PLOS ONE. 2019 ; No 2019( 11):[citado 2024 maio 26 ] Available from: https://doi.org/10.1371/journal.pone.0224581
Vancouver
Souza RB de, Farinha-Arcieri LE, Catroxo MHB, Martins AMCRP da F, Tedesco RC, Alonso LG, Koh IHJ, Pereira L da V. Association of thoracic spine deformity and cardiovascular disease in a mouse model for Marfan syndrome [Internet]. PLOS ONE. 2019 ; No 2019( 11):[citado 2024 maio 26 ] Available from: https://doi.org/10.1371/journal.pone.0224581
Artigo de periodico
Anatomic an dynamic aspects of stomatognathic structures in osteogenesis imperfecta: a case report (2007)
Ortega, Adriana de Oliveira Lira; Rosa, Vera L. M; Zwir, Liete Maria Liarte Figueiredo; Ciamponi, Ana Lídia; Guimarães, Antônio Sérgio; Alonso, Luís Garcia
Source: The Journal of Craniomandibular Practice. Unidade: FO
Subjects: OSTEOGÊNESE IMPERFEITA, DISFUNÇÃO TEMPOROMANDIBULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ORTEGA, Adriana de Oliveira Lira et al. Anatomic an dynamic aspects of stomatognathic structures in osteogenesis imperfecta: a case report. The Journal of Craniomandibular Practice, v. 25, n. 2, p. 144-149, 2007Tradução . . Acesso em: 26 maio 2024.
APA
Ortega, A. de O. L., Rosa, V. L. M., Zwir, L. M. L. F., Ciamponi, A. L., Guimarães, A. S., & Alonso, L. G. (2007). Anatomic an dynamic aspects of stomatognathic structures in osteogenesis imperfecta: a case report. The Journal of Craniomandibular Practice, 25( 2), 144-149.
NLM
Ortega A de OL, Rosa VLM, Zwir LMLF, Ciamponi AL, Guimarães AS, Alonso LG. Anatomic an dynamic aspects of stomatognathic structures in osteogenesis imperfecta: a case report. The Journal of Craniomandibular Practice. 2007 ; 25( 2): 144-149.[citado 2024 maio 26 ]
Vancouver
Ortega A de OL, Rosa VLM, Zwir LMLF, Ciamponi AL, Guimarães AS, Alonso LG. Anatomic an dynamic aspects of stomatognathic structures in osteogenesis imperfecta: a case report. The Journal of Craniomandibular Practice. 2007 ; 25( 2): 144-149.[citado 2024 maio 26 ]
Artigo de periodico
Morphological analysis of the vestibular aqueduct by computerized tomography images (2007)
Marques, Sergio Ricardo; Smith, Ricardo Luiz; Isotani, Sadao; Alonso, Luís Garcia; Anadão, Carlos Augusto; Prates, José Carlos; Lederman, Henrique Manoel
Source: European Journal of Radiology. Unidade: IF
Subjects: TOMOGRAFIA, ANATOMIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARQUES, Sergio Ricardo et al. Morphological analysis of the vestibular aqueduct by computerized tomography images. European Journal of Radiology, v. 61, n. 1, p. 79-83, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.clinimag.2007.04.007. Acesso em: 26 maio 2024.
APA
Marques, S. R., Smith, R. L., Isotani, S., Alonso, L. G., Anadão, C. A., Prates, J. C., & Lederman, H. M. (2007). Morphological analysis of the vestibular aqueduct by computerized tomography images. European Journal of Radiology, 61( 1), 79-83. doi:10.1016/j.clinimag.2007.04.007
NLM
Marques SR, Smith RL, Isotani S, Alonso LG, Anadão CA, Prates JC, Lederman HM. Morphological analysis of the vestibular aqueduct by computerized tomography images [Internet]. European Journal of Radiology. 2007 ; 61( 1): 79-83.[citado 2024 maio 26 ] Available from: https://doi.org/10.1016/j.clinimag.2007.04.007
Vancouver
Marques SR, Smith RL, Isotani S, Alonso LG, Anadão CA, Prates JC, Lederman HM. Morphological analysis of the vestibular aqueduct by computerized tomography images [Internet]. European Journal of Radiology. 2007 ; 61( 1): 79-83.[citado 2024 maio 26 ] Available from: https://doi.org/10.1016/j.clinimag.2007.04.007
Artigo de periodico
Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients (2006)
Jehee, Fernanda Sarquis; Alonso, Luís Garcia; Cavalcanti, Denise Pontes; Kim, Chong A.; Wall, Steven A.; Plast, F. C. S.; Mulliken, John B.; Sun, Miao; Jabs, Ethylin Wang; Boyadjiev, Simeon A.; Wilkie, Andrew O. M.; Passos-Bueno, Maria Rita
Source: Cleft Palate-Craniofacial Journal. Unidade: IB
Subjects: MALFORMAÇÕES, ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JEHEE, Fernanda Sarquis et al. Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients. Cleft Palate-Craniofacial Journal, v. 43, n. 2, p. 148-151, 2006Tradução . . Acesso em: 26 maio 2024.
APA
Jehee, F. S., Alonso, L. G., Cavalcanti, D. P., Kim, C. A., Wall, S. A., Plast, F. C. S., et al. (2006). Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients. Cleft Palate-Craniofacial Journal, 43( 2), 148-151.
NLM
Jehee FS, Alonso LG, Cavalcanti DP, Kim CA, Wall SA, Plast FCS, Mulliken JB, Sun M, Jabs EW, Boyadjiev SA, Wilkie AOM, Passos-Bueno MR. Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients. Cleft Palate-Craniofacial Journal. 2006 ; 43( 2): 148-151.[citado 2024 maio 26 ]
Vancouver
Jehee FS, Alonso LG, Cavalcanti DP, Kim CA, Wall SA, Plast FCS, Mulliken JB, Sun M, Jabs EW, Boyadjiev SA, Wilkie AOM, Passos-Bueno MR. Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients. Cleft Palate-Craniofacial Journal. 2006 ; 43( 2): 148-151.[citado 2024 maio 26 ]
Artigo de periodico
Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different from FGFR, TWIST, and MSX2 (2002)
Passos-Bueno, Maria Rita ; Armelin, Lúcia Maria Libório; Alonso, Luís Garcia; Neustein, Isaac; Sertié, Andréa Laurato; Abe, Kikue Terada; Pavanello, Rita de Cássia M.; Elkis, Livia Cunha; Koiffmann, Celia Priszkulnik
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, CRANIOSSINOSTOSE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different from FGFR, TWIST, and MSX2. American Journal of Medical Genetics, v. 113, p. 200-206, 2002Tradução . . Disponível em: https://doi.org/10.1002/ajmg.10752. Acesso em: 26 maio 2024.
APA
Passos-Bueno, M. R., Armelin, L. M. L., Alonso, L. G., Neustein, I., Sertié, A. L., Abe, K. T., et al. (2002). Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different from FGFR, TWIST, and MSX2. American Journal of Medical Genetics, 113, 200-206. doi:10.1002/ajmg.10752
NLM
Passos-Bueno MR, Armelin LML, Alonso LG, Neustein I, Sertié AL, Abe KT, Pavanello R de CM, Elkis LC, Koiffmann CP. Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different from FGFR, TWIST, and MSX2 [Internet]. American Journal of Medical Genetics. 2002 ; 113 200-206.[citado 2024 maio 26 ] Available from: https://doi.org/10.1002/ajmg.10752
Vancouver
Passos-Bueno MR, Armelin LML, Alonso LG, Neustein I, Sertié AL, Abe KT, Pavanello R de CM, Elkis LC, Koiffmann CP. Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different from FGFR, TWIST, and MSX2 [Internet]. American Journal of Medical Genetics. 2002 ; 113 200-206.[citado 2024 maio 26 ] Available from: https://doi.org/10.1002/ajmg.10752
Artigo de periodico
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia (2000)
Iughetti, Paula; Alonso, Luís Garcia; Wilcox, William; Alonso, Nivaldo
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
IUGHETTI, Paula et al. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia. American Journal of Medical Genetics, n. 95, p. 482-491, 2000Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(20001218)95:5%3C482::aid-ajmg14%3E3.0.co;2-x. Acesso em: 26 maio 2024.
APA
Iughetti, P., Alonso, L. G., Wilcox, W., & Alonso, N. (2000). Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia. American Journal of Medical Genetics, ( 95), 482-491. doi:10.1002/1096-8628(20001218)95:5%3C482::aid-ajmg14%3E3.0.co;2-x
NLM
Iughetti P, Alonso LG, Wilcox W, Alonso N. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia [Internet]. American Journal of Medical Genetics. 2000 ;( 95): 482-491.[citado 2024 maio 26 ] Available from: https://doi.org/10.1002/1096-8628(20001218)95:5%3C482::aid-ajmg14%3E3.0.co;2-x
Vancouver
Iughetti P, Alonso LG, Wilcox W, Alonso N. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia [Internet]. American Journal of Medical Genetics. 2000 ;( 95): 482-491.[citado 2024 maio 26 ] Available from: https://doi.org/10.1002/1096-8628(20001218)95:5%3C482::aid-ajmg14%3E3.0.co;2-x

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