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Artigo de periodico
Association between draining vein diameters and intracranial arteriovenous malformation hemorrhage: a multicentric retrospective study (2020)
Castro-Afonso, Luis Henrique de; Vanzim, José Ricardo; Trivelato, Felipe Padovani; Rezende, Marco Tulio; Ulhôa, Alexandre Cordeiro; Chodraui Filho, Salomão Faroj ; Mattos, Luiz Gustavo de Abreu; Mounayer, Charbel; Nakiri, Guilherme Seizem ; Colli, Benedicto Oscar ; Abud, Daniel Giansante
Source: Neuroradiology. Unidade: FMRP
Subjects: MALFORMAÇÕES, MALFORMAÇÕES ARTERIOVENOSAS, CÉREBRO, HEMORRAGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO-AFONSO, Luis Henrique de et al. Association between draining vein diameters and intracranial arteriovenous malformation hemorrhage: a multicentric retrospective study. Neuroradiology, v. 62, n. 11, p. 1497-1505, 2020Tradução . . Disponível em: https://doi.org/10.1007/s00234-020-02484-y. Acesso em: 17 nov. 2024.
APA
Castro-Afonso, L. H. de, Vanzim, J. R., Trivelato, F. P., Rezende, M. T., Ulhôa, A. C., Chodraui Filho, S. F., et al. (2020). Association between draining vein diameters and intracranial arteriovenous malformation hemorrhage: a multicentric retrospective study. Neuroradiology, 62( 11), 1497-1505. doi:10.1007/s00234-020-02484-y
NLM
Castro-Afonso LH de, Vanzim JR, Trivelato FP, Rezende MT, Ulhôa AC, Chodraui Filho SF, Mattos LG de A, Mounayer C, Nakiri GS, Colli BO, Abud DG. Association between draining vein diameters and intracranial arteriovenous malformation hemorrhage: a multicentric retrospective study [Internet]. Neuroradiology. 2020 ; 62( 11): 1497-1505.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s00234-020-02484-y
Vancouver
Castro-Afonso LH de, Vanzim JR, Trivelato FP, Rezende MT, Ulhôa AC, Chodraui Filho SF, Mattos LG de A, Mounayer C, Nakiri GS, Colli BO, Abud DG. Association between draining vein diameters and intracranial arteriovenous malformation hemorrhage: a multicentric retrospective study [Internet]. Neuroradiology. 2020 ; 62( 11): 1497-1505.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s00234-020-02484-y
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: 17 nov. 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 nov. 17 ] 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 nov. 17 ] Available from: https://doi.org/10.1210/clinem/dgaa065
Artigo de periodico
Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients (2017)
Garavelli, Livia; Ivanovski, Ivan; Caraffi, Stefano Giuseppe; Santodirocco, Daniela; Pollazzon, Marzia; Cordelli, Duccio Maria; Abdalla, Ebtesam; Accorsi, Patrizia; Adam, Margaret P.; Baldo, Chiara; Bayat, Allan; Belligni, Elga; Bonvicini, Federico; Breckpot, Jeroen; Callewaert, Bert; Cocchi, Guido; Cuturilo, Goran; Devriendt, Koenraad; Dinulos, Mary Beth; Djuric, Olivera; Epifanio, Roberta; Faravelli, Francesca; Formisano, Debora; Giordano, Lucio; Grasso, Marina; Grønborg, Sabine; Iodice, Alessandro; Iughetti, Lorenzo; Lacombe, Didier; Maggi, Massimo; Malbora, Baris; Mammi, Isabella; Moutton, Sebastien; Møller, Rikke; Muschke, Petra; Napoli, Manuela; Pantaleoni, Chiara; Pascarella, Rosario; Pellicciari, Alessandro; Poch-Olive, Maria Luisa; Raviglione, Federico; Rivieri, Francesca; Russo, Carmela; Savasta, Salvatore; Scarano, Gioacchino; Selicorni, Angelo; Silengo, Margherita; Sorge, Giovanni; Tarani, Luigi; Tone, Luiz Gonzaga; Toutain, Annick; Trimouille, Aurelien; Valera, Elvis Terci; Vergano, Samantha Schrier; Zanotta, Nicoletta; Zollino, Marcella; Dobyns, William B; Paciorkowski, Alex R
Source: Genetics in Medicine. Unidade: FMRP
Subjects: DOENÇAS GENÉTICAS, MALFORMAÇÕES, NEUROIMAGEM
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GARAVELLI, Livia et al. Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients. Genetics in Medicine, v. 19, n. 6, p. 691-700, 2017Tradução . . Disponível em: https://doi.org/10.1038/gim.2016.176. Acesso em: 17 nov. 2024.
APA
Garavelli, L., Ivanovski, I., Caraffi, S. G., Santodirocco, D., Pollazzon, M., Cordelli, D. M., et al. (2017). Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients. Genetics in Medicine, 19( 6), 691-700. doi:10.1038/gim.2016.176
NLM
Garavelli L, Ivanovski I, Caraffi SG, Santodirocco D, Pollazzon M, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Baldo C, Bayat A, Belligni E, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, Devriendt K, Dinulos MB, Djuric O, Epifanio R, Faravelli F, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Lacombe D, Maggi M, Malbora B, Mammi I, Moutton S, Møller R, Muschke P, Napoli M, Pantaleoni C, Pascarella R, Pellicciari A, Poch-Olive ML, Raviglione F, Rivieri F, Russo C, Savasta S, Scarano G, Selicorni A, Silengo M, Sorge G, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zollino M, Dobyns WB, Paciorkowski AR. Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients [Internet]. Genetics in Medicine. 2017 ; 19( 6): 691-700.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1038/gim.2016.176
Vancouver
Garavelli L, Ivanovski I, Caraffi SG, Santodirocco D, Pollazzon M, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Baldo C, Bayat A, Belligni E, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, Devriendt K, Dinulos MB, Djuric O, Epifanio R, Faravelli F, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Lacombe D, Maggi M, Malbora B, Mammi I, Moutton S, Møller R, Muschke P, Napoli M, Pantaleoni C, Pascarella R, Pellicciari A, Poch-Olive ML, Raviglione F, Rivieri F, Russo C, Savasta S, Scarano G, Selicorni A, Silengo M, Sorge G, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zollino M, Dobyns WB, Paciorkowski AR. Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients [Internet]. Genetics in Medicine. 2017 ; 19( 6): 691-700.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1038/gim.2016.176
Artigo de periodico
Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome (2017)
Romanelli Tavares, Vanessa L.; Zechi-Ceide, Roseli M.; Bertola, Debora R.; Gordon, Christopher T.; Ferreira, Simone G.; Hsia, Gabriella S. P.; Yamamoto, Guilherme L.; Ezquina, Suzana A. M.; Kokitsu-Nakata, Nancy M.; Vendramini-Pittoli, Siulan; Freitas, Renato S.; Souza, Josiane; Raposo-Amaral, Cesar A.; Zatz, Mayana ; Amiel, Jeanne; Guion-Almeida, Maria L.; Passos-Bueno, Maria Rita
Source: American Journal of Medical Genetics Part A. Unidades: HRAC, IB
Subjects: ANORMALIDADES CRANIOFACIAIS, MALFORMAÇÕES, DOENÇAS GENÉTICAS, FENÓTIPOS, VARIAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROMANELLI TAVARES, Vanessa L. et al. Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome. American Journal of Medical Genetics Part A, v. 173, n. 4, p. 938-945, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.38101. Acesso em: 17 nov. 2024.
APA
Romanelli Tavares, V. L., Zechi-Ceide, R. M., Bertola, D. R., Gordon, C. T., Ferreira, S. G., Hsia, G. S. P., et al. (2017). Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome. American Journal of Medical Genetics Part A, 173( 4), 938-945. doi:10.1002/ajmg.a.38101
NLM
Romanelli Tavares VL, Zechi-Ceide RM, Bertola DR, Gordon CT, Ferreira SG, Hsia GSP, Yamamoto GL, Ezquina SAM, Kokitsu-Nakata NM, Vendramini-Pittoli S, Freitas RS, Souza J, Raposo-Amaral CA, Zatz M, Amiel J, Guion-Almeida ML, Passos-Bueno MR. Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome [Internet]. American Journal of Medical Genetics Part A. 2017 ;173( 4): 938-945.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.38101
Vancouver
Romanelli Tavares VL, Zechi-Ceide RM, Bertola DR, Gordon CT, Ferreira SG, Hsia GSP, Yamamoto GL, Ezquina SAM, Kokitsu-Nakata NM, Vendramini-Pittoli S, Freitas RS, Souza J, Raposo-Amaral CA, Zatz M, Amiel J, Guion-Almeida ML, Passos-Bueno MR. Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome [Internet]. American Journal of Medical Genetics Part A. 2017 ;173( 4): 938-945.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.38101

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