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Filtros : "Monnier, Nicole" Limpar

Filtros

USP affiliated authors
- arruda, luisa karla de paula (~1)
- dias, marina mendonça (~1)
- silva junior, wilson araújo da (~1)
- vainzof, mariz (~1)
Date published
- 2015 (~1)
- 2013 (~1)
Subjects
- angioedema (1)
- dna (1)
- doenças hereditárias (1)
- doenças neuromusculares (1)
- miopatias congênitas estruturais (1)

Collaboration
Normalized affiliation
- universidade estadual paulista júlio de mesquita filho (unesp) (~1)
Non normalized affiliation
- biochimie et génétique moléculaire, centre hospitalier universitaire grenoble, institut nationale de la santé et de la recherche médicale, u386 grenoble, france (1)
- centre for medical research, the university of western australia, western australian institute for medical research, nedlands, wa 6009, australia (1)
- department of neurology, university of bonn, bonn 53127, germany (1)
- department of physiology, vu university medical centre, 1081 hv amsterdam, the netherlands (1)
- division of biochemistry and biotechnology, department of biosciences, university of helsinki, helsinki, 00029 hus, finland (1)

Artigo de periodico
Coagulation factor XII gene mutation in Brazilian families with hereditary angioedema with normal C1 inhibitor (2015)
Moreno, Adriana Santos; Valle, Solange Oliveira Rodrigues; Levy, Soloni ; França, Alfeu Tavares; Serpa, Faradiba S. ; Arcuri, Helen Andrade; Palma, Mario Sérgio; Campos, Wagner Narciso de; Dias, Marina M. ; Ponard, Denise ; Monnier, Nicole; Lunardi, Joel ; Bork, Konrad ; Silva Júnior, Wilson Araújo da; Arruda, Luisa Karla de Paula
Source: International Archives of Allergy and Immunology. Unidade: FMRP
Subjects: ANGIOEDEMA, DNA, REAÇÃO EM CADEIA POR POLIMERASE, DOENÇAS HEREDITÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MORENO, Adriana Santos et al. Coagulation factor XII gene mutation in Brazilian families with hereditary angioedema with normal C1 inhibitor. International Archives of Allergy and Immunology, v. 166, n. 2, p. 114-120, 2015Tradução . . Disponível em: https://doi.org/10.1159/000376547. Acesso em: 05 nov. 2024.
APA
Moreno, A. S., Valle, S. O. R., Levy, S. , França, A. T., Serpa, F. S. , Arcuri, H. A., et al. (2015). Coagulation factor XII gene mutation in Brazilian families with hereditary angioedema with normal C1 inhibitor. International Archives of Allergy and Immunology, 166( 2), 114-120. doi:10.1159/000376547
NLM
Moreno AS, Valle SOR, Levy S , França AT, Serpa F S , Arcuri HA, Palma MS, Campos WN de, Dias M M , Ponard D , Monnier N, Lunardi J , Bork K , Silva Júnior WA da, Arruda LK de P. Coagulation factor XII gene mutation in Brazilian families with hereditary angioedema with normal C1 inhibitor [Internet]. International Archives of Allergy and Immunology. 2015 ; 166( 2): 114-120.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000376547
Vancouver
Moreno AS, Valle SOR, Levy S , França AT, Serpa F S , Arcuri HA, Palma MS, Campos WN de, Dias M M , Ponard D , Monnier N, Lunardi J , Bork K , Silva Júnior WA da, Arruda LK de P. Coagulation factor XII gene mutation in Brazilian families with hereditary angioedema with normal C1 inhibitor [Internet]. International Archives of Allergy and Immunology. 2015 ; 166( 2): 114-120.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000376547
Artigo de periodico
K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity (2013)
Mokbel, Nancy; Ilkovski, Biljana; Kreissl, Michaela; Memo, Massimiliano; Jeffries, Cy M; Marttila, Minttu; Lehtokari, Vilma-Lotta; Lemola, Elina; Grönholm, Mikaela; Yang, Nan; Menard, Dominique; Marcorelles, Pascale; Echaniz-Laguna, Andoni; Reimann, Jens; Vainzof, Mariz ; Monnier, Nicole; Ravenscroft, Gianina; McNamara, Elyshia; Nowak, Kristen J; Laing, Nigel G; Wallgren-Pettersson, Carina; Trewhella, Jill; Marston, Steve; Ottenheijm, Coen; North, Kathryn N; Clarke, Nigel F
Source: Brain. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, MIOPATIAS CONGÊNITAS ESTRUTURAIS, DOENÇAS NEUROMUSCULARES, PROTEÍNAS MUSCULARES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOKBEL, Nancy et al. K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity. Brain, v. 136, n. 2, p. 494-507, 2013Tradução . . Disponível em: https://doi.org/10.1093/brain/aws348. Acesso em: 05 nov. 2024.
APA
Mokbel, N., Ilkovski, B., Kreissl, M., Memo, M., Jeffries, C. M., Marttila, M., et al. (2013). K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity. Brain, 136( 2), 494-507. doi:10.1093/brain/aws348
NLM
Mokbel N, Ilkovski B, Kreissl M, Memo M, Jeffries CM, Marttila M, Lehtokari V-L, Lemola E, Grönholm M, Yang N, Menard D, Marcorelles P, Echaniz-Laguna A, Reimann J, Vainzof M, Monnier N, Ravenscroft G, McNamara E, Nowak KJ, Laing NG, Wallgren-Pettersson C, Trewhella J, Marston S, Ottenheijm C, North KN, Clarke NF. K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity [Internet]. Brain. 2013 ; 136( 2): 494-507.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1093/brain/aws348
Vancouver
Mokbel N, Ilkovski B, Kreissl M, Memo M, Jeffries CM, Marttila M, Lehtokari V-L, Lemola E, Grönholm M, Yang N, Menard D, Marcorelles P, Echaniz-Laguna A, Reimann J, Vainzof M, Monnier N, Ravenscroft G, McNamara E, Nowak KJ, Laing NG, Wallgren-Pettersson C, Trewhella J, Marston S, Ottenheijm C, North KN, Clarke NF. K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity [Internet]. Brain. 2013 ; 136( 2): 494-507.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1093/brain/aws348

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