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Artigo de periodico
Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities (2022)
Griffero, Mariana; Benedetti, Anna Flavia Figueredo; Perez, Marcela; Carvalho, Luciani; Jorge, Alexander Augusto de Lima ; Xavier, Ana Claudia Latronico ; Mendonca, Berenice Bilharinho de ; Arnhold, Ivo; Mericq, Veronica
Fonte: Journal of pediatric endocrinology & metabolism. Unidade: FM
Assuntos: MUTAGÊNESE, DOENÇAS CONGÊNITAS, PEDIATRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GRIFFERO, Mariana et al. Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities. Journal of pediatric endocrinology & metabolism, v. 35, n. 6, p. 831-835, 2022Tradução . . Disponível em: https://doi.org/10.1515/jpem-2021-0719. Acesso em: 17 out. 2024.
APA
Griffero, M., Benedetti, A. F. F., Perez, M., Carvalho, L., Jorge, A. A. de L., Xavier, A. C. L., et al. (2022). Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities. Journal of pediatric endocrinology & metabolism, 35( 6), 831-835. doi:10.1515/jpem-2021-0719
NLM
Griffero M, Benedetti AFF, Perez M, Carvalho L, Jorge AA de L, Xavier ACL, Mendonca BB de, Arnhold I, Mericq V. Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities [Internet]. Journal of pediatric endocrinology & metabolism. 2022 ; 35( 6): 831-835.[citado 2024 out. 17 ] Available from: https://doi.org/10.1515/jpem-2021-0719
Vancouver
Griffero M, Benedetti AFF, Perez M, Carvalho L, Jorge AA de L, Xavier ACL, Mendonca BB de, Arnhold I, Mericq V. Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities [Internet]. Journal of pediatric endocrinology & metabolism. 2022 ; 35( 6): 831-835.[citado 2024 out. 17 ] Available from: https://doi.org/10.1515/jpem-2021-0719
Artigo de periodico
Gastroschisis: state of the art in translating experimental research to the bedside (2019)
Sbragia, Lourenço ; Figueira, Rebeca Rodrigues Lopes Roslindo ; Costa, Karina Miura da ; Volpe, Fábio Perecim
Fonte: European Journal of Pediatric Surgery. Unidade: FMRP
Assuntos: RECÉM-NASCIDO, TAXA DE SOBREVIVÊNCIA, DOENÇAS CONGÊNITAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SBRAGIA, Lourenço et al. Gastroschisis: state of the art in translating experimental research to the bedside. European Journal of Pediatric Surgery, v. 29, n. 4, p. 342-351, 2019Tradução . . Disponível em: https://doi.org/10.1055/s-0039-1694746. Acesso em: 17 out. 2024.
APA
Sbragia, L., Figueira, R. R. L. R., Costa, K. M. da, & Volpe, F. P. (2019). Gastroschisis: state of the art in translating experimental research to the bedside. European Journal of Pediatric Surgery, 29( 4), 342-351. doi:10.1055/s-0039-1694746
NLM
Sbragia L, Figueira RRLR, Costa KM da, Volpe FP. Gastroschisis: state of the art in translating experimental research to the bedside [Internet]. European Journal of Pediatric Surgery. 2019 ; 29( 4): 342-351.[citado 2024 out. 17 ] Available from: https://doi.org/10.1055/s-0039-1694746
Vancouver
Sbragia L, Figueira RRLR, Costa KM da, Volpe FP. Gastroschisis: state of the art in translating experimental research to the bedside [Internet]. European Journal of Pediatric Surgery. 2019 ; 29( 4): 342-351.[citado 2024 out. 17 ] Available from: https://doi.org/10.1055/s-0039-1694746
Artigo de periodico
The pubo-femoral distance decreases with Pavlik harness treatment for developmental dysplasia of the hip in newborns (2017)
Maranho, Daniel Augusto; Donati, Felipe Nunes; Dalto, Vitor Faeda; Nogueira-Barbosa, Marcello Henrique
Fonte: Skeletal Radiology. Unidade: FMRP
Assuntos: DOENÇAS CONGÊNITAS, QUADRIL, ULTRASSONOGRAFIA, RECÉM-NASCIDO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARANHO, Daniel Augusto et al. The pubo-femoral distance decreases with Pavlik harness treatment for developmental dysplasia of the hip in newborns. Skeletal Radiology, v. 46, n. 9, p. 1201-1207, 2017Tradução . . Disponível em: https://doi.org/10.1007/s00256-017-2668-8. Acesso em: 17 out. 2024.
APA
Maranho, D. A., Donati, F. N., Dalto, V. F., & Nogueira-Barbosa, M. H. (2017). The pubo-femoral distance decreases with Pavlik harness treatment for developmental dysplasia of the hip in newborns. Skeletal Radiology, 46( 9), 1201-1207. doi:10.1007/s00256-017-2668-8
NLM
Maranho DA, Donati FN, Dalto VF, Nogueira-Barbosa MH. The pubo-femoral distance decreases with Pavlik harness treatment for developmental dysplasia of the hip in newborns [Internet]. Skeletal Radiology. 2017 ; 46( 9): 1201-1207.[citado 2024 out. 17 ] Available from: https://doi.org/10.1007/s00256-017-2668-8
Vancouver
Maranho DA, Donati FN, Dalto VF, Nogueira-Barbosa MH. The pubo-femoral distance decreases with Pavlik harness treatment for developmental dysplasia of the hip in newborns [Internet]. Skeletal Radiology. 2017 ; 46( 9): 1201-1207.[citado 2024 out. 17 ] Available from: https://doi.org/10.1007/s00256-017-2668-8
Artigo de periodico
Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues (2017)
Biancalana, Valérie; Zanoteli, Edmar
Fonte: Acta neuropathologica. Unidade: FM
Assuntos: MIOPATIAS CONGÊNITAS ESTRUTURAIS, MUTAÇÃO GENÉTICA, DIAGNÓSTICO, DOENÇAS CONGÊNITAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BIANCALANA, Valérie e ZANOTELI, Edmar. Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues. Acta neuropathologica, v. 134, p. 889-904, 2017Tradução . . Disponível em: https://doi.org/10.1007/s00401-017-1748-0. Acesso em: 17 out. 2024.
APA
Biancalana, V., & Zanoteli, E. (2017). Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues. Acta neuropathologica, 134, 889-904. doi:10.1007/s00401-017-1748-0
NLM
Biancalana V, Zanoteli E. Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues [Internet]. Acta neuropathologica. 2017 ; 134 889-904.[citado 2024 out. 17 ] Available from: https://doi.org/10.1007/s00401-017-1748-0
Vancouver
Biancalana V, Zanoteli E. Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues [Internet]. Acta neuropathologica. 2017 ; 134 889-904.[citado 2024 out. 17 ] Available from: https://doi.org/10.1007/s00401-017-1748-0
Artigo de periodico
Management of fetal teratomas (2016)
Peiró, Jose L.; Sbragia, Lourenço; Scorletti, Federico; Lim, Foong Y.; Shaaban, Aimen
Fonte: Pediatric Surgery International. Unidade: FMRP
Assuntos: TERATOMA, DIAGNÓSTICO PRÉ-NATAL, FETO, DOENÇAS CONGÊNITAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEIRÓ, Jose L. et al. Management of fetal teratomas. Pediatric Surgery International, v. 32, n. 7, p. 635-647, 2016Tradução . . Disponível em: https://doi.org/10.1007/s00383-016-3892-3. Acesso em: 17 out. 2024.
APA
Peiró, J. L., Sbragia, L., Scorletti, F., Lim, F. Y., & Shaaban, A. (2016). Management of fetal teratomas. Pediatric Surgery International, 32( 7), 635-647. doi:10.1007/s00383-016-3892-3
NLM
Peiró JL, Sbragia L, Scorletti F, Lim FY, Shaaban A. Management of fetal teratomas [Internet]. Pediatric Surgery International. 2016 ; 32( 7): 635-647.[citado 2024 out. 17 ] Available from: https://doi.org/10.1007/s00383-016-3892-3
Vancouver
Peiró JL, Sbragia L, Scorletti F, Lim FY, Shaaban A. Management of fetal teratomas [Internet]. Pediatric Surgery International. 2016 ; 32( 7): 635-647.[citado 2024 out. 17 ] Available from: https://doi.org/10.1007/s00383-016-3892-3
Artigo de periodico
Congenital Absence of the Portal Vein: A Complex Disease with Multiple Manifestations and Types of Treatment (2011)
Tannuri, U.; Galvão, F.; Leal, A. J. G.; Gibelli, N. E.; Tannuri, A. C.
Fonte: European Journal of Pediatric Surgery. Unidade: FM
Assuntos: DOENÇAS CONGÊNITAS, DOENÇAS RARAS, VEIA PORTA (ANORMALIDADES), IMAGEM POR RESSONÂNCIA MAGNÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TANNURI, U. et al. Congenital Absence of the Portal Vein: A Complex Disease with Multiple Manifestations and Types of Treatment. European Journal of Pediatric Surgery, v. 21, n. 4, p. 269-272, 2011Tradução . . Disponível em: https://doi.org/10.1055/s-0031-1275675. Acesso em: 17 out. 2024.
APA
Tannuri, U., Galvão, F., Leal, A. J. G., Gibelli, N. E., & Tannuri, A. C. (2011). Congenital Absence of the Portal Vein: A Complex Disease with Multiple Manifestations and Types of Treatment. European Journal of Pediatric Surgery, 21( 4), 269-272. doi:10.1055/s-0031-1275675
NLM
Tannuri U, Galvão F, Leal AJG, Gibelli NE, Tannuri AC. Congenital Absence of the Portal Vein: A Complex Disease with Multiple Manifestations and Types of Treatment [Internet]. European Journal of Pediatric Surgery. 2011 ; 21( 4): 269-272.[citado 2024 out. 17 ] Available from: https://doi.org/10.1055/s-0031-1275675
Vancouver
Tannuri U, Galvão F, Leal AJG, Gibelli NE, Tannuri AC. Congenital Absence of the Portal Vein: A Complex Disease with Multiple Manifestations and Types of Treatment [Internet]. European Journal of Pediatric Surgery. 2011 ; 21( 4): 269-272.[citado 2024 out. 17 ] Available from: https://doi.org/10.1055/s-0031-1275675

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