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Artigo de periodico
Diagnosis and management of biliary complications in pediatric living donor liver transplant recipients (2014)
Feier, Flávia H.; Chapchap, Paulo; Pugliese, Renata; Fonseca, Eduardo A. da; Carnevale, Francisco C.; Moreira, Airton M.; Zurstrassen, Charles; Santos, Aline C.; Miura, Irene K.; Baggio, Vera; Porta, Adriana; Guimarães, Teresa; Cândido, Helry; Benavides, Marcel; Godoy, Andre; Leite, Katia M. R.; Porta, Gilda; Kondo, Mario; Seda-Neto, João
Source: Liver transplantation. Unidades: RUSP, FEARP, FM
Subjects: TRANSPLANTE DE FÍGADO, CRIANÇAS, COMPLICAÇÕES PÓS-OPERATÓRIAS, BIÓPSIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FEIER, Flávia H. et al. Diagnosis and management of biliary complications in pediatric living donor liver transplant recipients. Liver transplantation, v. 20, n. 8, p. 882-892, 2014Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/lt.23896/pdf. Acesso em: 21 out. 2024.
APA
Feier, F. H., Chapchap, P., Pugliese, R., Fonseca, E. A. da, Carnevale, F. C., Moreira, A. M., et al. (2014). Diagnosis and management of biliary complications in pediatric living donor liver transplant recipients. Liver transplantation, 20( 8), 882-892. doi:10.1002/lt.23896
NLM
Feier FH, Chapchap P, Pugliese R, Fonseca EA da, Carnevale FC, Moreira AM, Zurstrassen C, Santos AC, Miura IK, Baggio V, Porta A, Guimarães T, Cândido H, Benavides M, Godoy A, Leite KMR, Porta G, Kondo M, Seda-Neto J. Diagnosis and management of biliary complications in pediatric living donor liver transplant recipients [Internet]. Liver transplantation. 2014 ; 20( 8): 882-892.[citado 2024 out. 21 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/lt.23896/pdf
Vancouver
Feier FH, Chapchap P, Pugliese R, Fonseca EA da, Carnevale FC, Moreira AM, Zurstrassen C, Santos AC, Miura IK, Baggio V, Porta A, Guimarães T, Cândido H, Benavides M, Godoy A, Leite KMR, Porta G, Kondo M, Seda-Neto J. Diagnosis and management of biliary complications in pediatric living donor liver transplant recipients [Internet]. Liver transplantation. 2014 ; 20( 8): 882-892.[citado 2024 out. 21 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/lt.23896/pdf
Artigo de periodico
HCC prevalence and histopathological findings in liver explants of patients with hereditary tyrosinemia type 1 (2014)
Seda Neto, Joao; Leite, Katia M. R.; Porta, Adriana; Fonseca, Eduardo A.; Feier, Flavia H.; Pugliese, Renata; Miura, Irene K.; Chapchap, Paulo; Porta, Gilda
Source: Pediatric Blood Cancer. Unidades: FM, FEARP
Subjects: NEOPLASIAS HEPÁTICAS, CRIANÇAS, DOENÇAS HEREDITÁRIAS, TRANSPLANTE DE FÍGADO, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SEDA NETO, Joao et al. HCC prevalence and histopathological findings in liver explants of patients with hereditary tyrosinemia type 1. Pediatric Blood Cancer, v. 61, n. 9, p. 1584-1589, 2014Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/pbc.25094/pdf. Acesso em: 21 out. 2024.
APA
Seda Neto, J., Leite, K. M. R., Porta, A., Fonseca, E. A., Feier, F. H., Pugliese, R., et al. (2014). HCC prevalence and histopathological findings in liver explants of patients with hereditary tyrosinemia type 1. Pediatric Blood Cancer, 61( 9), 1584-1589. doi:10.1002/pbc.25094
NLM
Seda Neto J, Leite KMR, Porta A, Fonseca EA, Feier FH, Pugliese R, Miura IK, Chapchap P, Porta G. HCC prevalence and histopathological findings in liver explants of patients with hereditary tyrosinemia type 1 [Internet]. Pediatric Blood Cancer. 2014 ; 61( 9): 1584-1589.[citado 2024 out. 21 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/pbc.25094/pdf
Vancouver
Seda Neto J, Leite KMR, Porta A, Fonseca EA, Feier FH, Pugliese R, Miura IK, Chapchap P, Porta G. HCC prevalence and histopathological findings in liver explants of patients with hereditary tyrosinemia type 1 [Internet]. Pediatric Blood Cancer. 2014 ; 61( 9): 1584-1589.[citado 2024 out. 21 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/pbc.25094/pdf
Artigo de periodico
Pompe disease in a Brazilian series:: clinical and molecular analyses with identification of nine new mutations (2009)
Oba-Shinjo, Sueli M.; Basso-Silva, Roseli ; Andrade, Fernanda G.; Palmer, Rachel E.; Pomponio, Robert J.; Ciociola, Kristina M.; Carvalho, Mary S.; Gutierrez, Paulo S.; Porta, Gilda; Marrone, Carlo D.; Munoz, Verônica; Grzesiuk, Anderson K.; Llerena Júnior, Juan C.; Berditchevsky, Célia R.; Sobreira, Cláudia Ferreira da Rosa; Horovitz, Dafne; Hatem, Thamine P.; Frota, Elizabeth Regina Comini; Pecchini, Rogerio; Kouyoumdjian, João Aris; Werneck, Lineu; Amado, Verônica M.; Camelo Júnior, José Simon; Mattaliano, Robert; Marie, Suely Kazue Nagahashi
Source: Journal of Neurology. Unidades: FM, FEARP, FMRP
Subjects: MUTAÇÃO GENÉTICA, NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OBA-SHINJO, Sueli M. et al. Pompe disease in a Brazilian series:: clinical and molecular analyses with identification of nine new mutations. Journal of Neurology, v. 256, n. 11, p. 1881-1890, 2009Tradução . . Disponível em: https://doi.org/10.1007/s00415-009-5219-y. Acesso em: 21 out. 2024.
APA
Oba-Shinjo, S. M., Basso-Silva, R., Andrade, F. G., Palmer, R. E., Pomponio, R. J., Ciociola, K. M., et al. (2009). Pompe disease in a Brazilian series:: clinical and molecular analyses with identification of nine new mutations. Journal of Neurology, 256( 11), 1881-1890. doi:10.1007/s00415-009-5219-y
NLM
Oba-Shinjo SM, Basso-Silva R, Andrade FG, Palmer RE, Pomponio RJ, Ciociola KM, Carvalho MS, Gutierrez PS, Porta G, Marrone CD, Munoz V, Grzesiuk AK, Llerena Júnior JC, Berditchevsky CR, Sobreira CF da R, Horovitz D, Hatem TP, Frota ERC, Pecchini R, Kouyoumdjian JA, Werneck L, Amado VM, Camelo Júnior JS, Mattaliano R, Marie SKN. Pompe disease in a Brazilian series:: clinical and molecular analyses with identification of nine new mutations [Internet]. Journal of Neurology. 2009 ; 256( 11): 1881-1890.[citado 2024 out. 21 ] Available from: https://doi.org/10.1007/s00415-009-5219-y
Vancouver
Oba-Shinjo SM, Basso-Silva R, Andrade FG, Palmer RE, Pomponio RJ, Ciociola KM, Carvalho MS, Gutierrez PS, Porta G, Marrone CD, Munoz V, Grzesiuk AK, Llerena Júnior JC, Berditchevsky CR, Sobreira CF da R, Horovitz D, Hatem TP, Frota ERC, Pecchini R, Kouyoumdjian JA, Werneck L, Amado VM, Camelo Júnior JS, Mattaliano R, Marie SKN. Pompe disease in a Brazilian series:: clinical and molecular analyses with identification of nine new mutations [Internet]. Journal of Neurology. 2009 ; 256( 11): 1881-1890.[citado 2024 out. 21 ] Available from: https://doi.org/10.1007/s00415-009-5219-y

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