ReP USP - Resultado da busca

Filtros : "Majewski, Jacek" Removido: "Lynch, Danielle C." Limpar

Filtros

Autores
- majewski, jacek (2)
- abramowicz, anna (1)
- aguena, meire (1)
- bareke, eric (1)
- bertola, débora romeo (1)

Autores USP
- annichini, maria sol brassesco (1)
- bertola, débora romeo (1)
- bueno, maria rita dos santos e passos (1)
- jorge, alexander augusto de lima (1)
- kim, chong ae (1)

Ano de publicação
- 2018 (~1)
- 2015 (~1)
Assuntos
- anormalidades cardiovasculares (1)
- anormalidades craniofaciais (1)
- crianças (1)
- cérebro (1)
- doenças cerebrais (1)

Indexado em
- indexado no: scopus (2)
- indexado no: biosis (1)
- indexado no: cab abstracts (1)
- indexado no: embase (1)
- indexado no: medline (1)

Artigo de periodico
Methylome analysis and whole-exome sequencing reveal that brain tumors associated with encephalocraniocutaneous lipomatosis are midline pilocytic astrocytomas (2018)
Valera, Elvis Terci; McConechy, Melissa K.; Gayden, Tenzin; Rivera, Barbara; Jones, David T. W.; Wittmann, Andrea; Han, HyeRim; Bareke, Eric; Nikbakht, Hamid; Mikael, Leonie; Queiroz, Rosane Gomes de Paula; Suazo, Veridiana Kiill; Phi, Ji Hoon; Kim, Seung-Ki; Park, Sung-Hye; Fukaya, Raita; Yum, Mi-Sun; Ko, Tae-Sung; Oliveira, Ricardo Santos de; Machado, Hélio Rubens; Brassesco, Maria Sol; Santos, Antônio Carlos dos; Simão, Gustavo Novelino; Ramalho, Leandra Naíra Zambelli; Neder, Luciano; Scrideli, Carlos Alberto; Tone, Luiz Gonzaga; Majewski, Jacek; Jabado, Nada
Fonte: Acta Neuropathologica. Unidades: FMRP, FFCLRP
Assuntos: DOENÇAS CEREBRAIS, GENÉTICA, CÉREBRO, NEUROLOGIA, CRIANÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VALERA, Elvis Terci et al. Methylome analysis and whole-exome sequencing reveal that brain tumors associated with encephalocraniocutaneous lipomatosis are midline pilocytic astrocytomas. Acta Neuropathologica, v. 136, n. 4, p. 657-660, 2018Tradução . . Disponível em: https://doi.org/10.1007/s00401-018-1898-8. Acesso em: 26 out. 2025.
APA
Valera, E. T., McConechy, M. K., Gayden, T., Rivera, B., Jones, D. T. W., Wittmann, A., et al. (2018). Methylome analysis and whole-exome sequencing reveal that brain tumors associated with encephalocraniocutaneous lipomatosis are midline pilocytic astrocytomas. Acta Neuropathologica, 136( 4), 657-660. doi:10.1007/s00401-018-1898-8
NLM
Valera ET, McConechy MK, Gayden T, Rivera B, Jones DTW, Wittmann A, Han HR, Bareke E, Nikbakht H, Mikael L, Queiroz RG de P, Suazo VK, Phi JH, Kim S-K, Park S-H, Fukaya R, Yum M-S, Ko T-S, Oliveira RS de, Machado HR, Brassesco MS, Santos AC dos, Simão GN, Ramalho LNZ, Neder L, Scrideli CA, Tone LG, Majewski J, Jabado N. Methylome analysis and whole-exome sequencing reveal that brain tumors associated with encephalocraniocutaneous lipomatosis are midline pilocytic astrocytomas [Internet]. Acta Neuropathologica. 2018 ; 136( 4): 657-660.[citado 2025 out. 26 ] Available from: https://doi.org/10.1007/s00401-018-1898-8
Vancouver
Valera ET, McConechy MK, Gayden T, Rivera B, Jones DTW, Wittmann A, Han HR, Bareke E, Nikbakht H, Mikael L, Queiroz RG de P, Suazo VK, Phi JH, Kim S-K, Park S-H, Fukaya R, Yum M-S, Ko T-S, Oliveira RS de, Machado HR, Brassesco MS, Santos AC dos, Simão GN, Ramalho LNZ, Neder L, Scrideli CA, Tone LG, Majewski J, Jabado N. Methylome analysis and whole-exome sequencing reveal that brain tumors associated with encephalocraniocutaneous lipomatosis are midline pilocytic astrocytomas [Internet]. Acta Neuropathologica. 2018 ; 136( 4): 657-660.[citado 2025 out. 26 ] Available from: https://doi.org/10.1007/s00401-018-1898-8
Artigo de periodico
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome (2015)
Yamamoto, Guilherme Lopes; Aguena, Meire; Gos, Monika; Hung, Christina; Pilch, Jacek; Fahiminiya, Somayyeh; Abramowicz, Anna; Cristian, Ingrid; Buscarilli, Michelle; Naslavsky, Michel ; Malaquias, Alexsandra C.; Zatz, Mayana ; Bodamer, Olaf; Majewski, Jacek; Jorge, Alexander A. L.; Pereira, Alexandre C.; Kim, Chong Ae; Passos-Bueno, Maria Rita ; Bertola, Débora Romeo
Fonte: Journal of Medical Genetics. Unidades: FM, IB
Assuntos: ESTUDOS DE COORTES, ESTATÍSTICA (MÉTODOS), ANORMALIDADES CARDIOVASCULARES, ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
YAMAMOTO, Guilherme Lopes et al. Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome. Journal of Medical Genetics, v. 52, n. 6, p. 413-421, 2015Tradução . . Disponível em: https://doi.org/10.1136/jmedgenet-2015-103018. Acesso em: 26 out. 2025.
APA
Yamamoto, G. L., Aguena, M., Gos, M., Hung, C., Pilch, J., Fahiminiya, S., et al. (2015). Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome. Journal of Medical Genetics, 52( 6), 413-421. doi:10.1136/jmedgenet-2015-103018
NLM
Yamamoto GL, Aguena M, Gos M, Hung C, Pilch J, Fahiminiya S, Abramowicz A, Cristian I, Buscarilli M, Naslavsky M, Malaquias AC, Zatz M, Bodamer O, Majewski J, Jorge AAL, Pereira AC, Kim CA, Passos-Bueno MR, Bertola DR. Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome [Internet]. Journal of Medical Genetics. 2015 ; 52( 6): 413-421.[citado 2025 out. 26 ] Available from: https://doi.org/10.1136/jmedgenet-2015-103018
Vancouver
Yamamoto GL, Aguena M, Gos M, Hung C, Pilch J, Fahiminiya S, Abramowicz A, Cristian I, Buscarilli M, Naslavsky M, Malaquias AC, Zatz M, Bodamer O, Majewski J, Jorge AAL, Pereira AC, Kim CA, Passos-Bueno MR, Bertola DR. Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome [Internet]. Journal of Medical Genetics. 2015 ; 52( 6): 413-421.[citado 2025 out. 26 ] Available from: https://doi.org/10.1136/jmedgenet-2015-103018

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