Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Debora M, Miranda"'
Autor:
Alexandre Paim Diaz, Andre Braule Pinto, Maria Isabel Chaves Araújo, Rui Mateus Joaquim, Danielle de Souza Costa, Alexandre Luiz de Oliveira Serpa, Anthony R. Pisani, Yeates Conwell, Debora M. Miranda, Leandro F. Malloy-Diniz, Antonio G. da Silva
Publikováno v:
Brazilian Journal of Psychiatry, Vol 46 (2024)
Objective: The risk of suicide is higher among health care workers than other workers. This study investigated the association between social support and suicidal ideation and behavior during the COVID-19 pandemic among Brazilian health care workers.
Externí odkaz:
https://doaj.org/article/cb62f770af3e49c3a5cd6fac68a44a24
Autor:
Danielle S. Costa, Carlo Cianchetti, Deborah Dewey, Antônio Marcos Alvim-Soares, Iane Kestelman, Antônio Geraldo da Silva, Leandro F. Malloy-Diniz, Debora M. Miranda, Jonas J. de Paula
Publikováno v:
Jornal de Pediatria, Vol 100, Iss 5, Pp 557- (2024)
Externí odkaz:
https://doaj.org/article/d1610f7ebf5d4b2495d0c4d8e2cdb0b1
Autor:
Danielle S. Costa, Carlo Cianchetti, Deborah Dewey, Antônio Marcos Alvim-Soares Alvim-Soares, Iane Kestelman, Antônio Geraldo da Silva, Leandro F. Malloy-Diniz, Debora M. Miranda, Jonas J. de Paula
Publikováno v:
Jornal de Pediatria, Vol 99, Iss 4, Pp 413-422 (2023)
Objective: The Child and Adolescent Behavior Inventory (CABI) is a cost-free 75 question-questionnaire developed by an Italian group to collect information from parents on the behavior of children and adolescents aged 6 to 18 years. It assesses diffe
Externí odkaz:
https://doaj.org/article/db41fc15fa904b01bb4d8fb9bb1f38af
Autor:
Rui M. Joaquim, André L.C.B. Pinto, Rafaela F. Guatimosim, Jonas J. de Paula, Danielle Souza Costa, Alexandre Paim Diaz, Antônio G. da Silva, Mayra I.C. Pinheiro, Alexandre L.O. Serpa, Debora M. Miranda, Leandro F. Malloy-Diniz
Publikováno v:
Current Research in Behavioral Sciences, Vol 2, Iss , Pp 100019- (2021)
The COVID-19 pandemic has been a disturbing experience of proximity to death. As the pandemic goes on, the mixed experience of loss of a close family or friends added to the unpredictability of economic changes and the social isolation can elicit neg
Externí odkaz:
https://doaj.org/article/24de91c6229d48ed9094e940932f5197
Autor:
Jonas J. de Paula, Fabio L. S. Duran, Geraldo Busatto, Debora M. Miranda, Marco A. Romano-Silva
Publikováno v:
Molecular Psychiatry. 28:538-540
Autor:
Debora M. Miranda, Zilma S.N. Reis, Marco A. Romano-Silva, Leandro Malloy-Diniz, Antônio Geraldo da Silva
Publikováno v:
Brazilian Journal of Psychiatry, Vol 43, Iss 4, Pp 347-348 (2020)
Externí odkaz:
https://doaj.org/article/ac3eee9461084e6fb252205d97808ad5
Autor:
Eduardo A. Oliveira, Ana Cristina Simões e Silva, Maria Christina L. Oliveira, Enrico A. Colosimo, Robert H. Mak, Mariana A. Vasconcelos, Debora M. Miranda, Daniella B. Martelli, Ludmila R. Silva, Clara C. Pinhati, Hercílio Martelli-Júnior
Publikováno v:
The Journal of Pediatrics. 244:178-185.e3
Autor:
Debora M, Miranda, Augusto Cesar, Dos Santos, Helena C, Sarubi, Luciana, Bastos-Rodrigues, Daniela Valadão, Rosa, Izabella S, Freitas, Luiz Armando, De Marco, Eduardo A, Oliveira, Ana Cristina, Simões e Silva
Publikováno v:
Nephrology (Carlton, Vic.). 19(11)
The angiotensin type 2 (AT2 ) receptor takes part in the process of ureteric bud during kidney development. Therefore, the gene encoding AT2 receptor, the AGTR2 gene located in the X chromosome, is a potential candidate for genetic association with C
Autor:
Luciana N, Almeida, Rachel, Melilo-Carolino, Carlos E, Veloso, Patrícia A, Pereira, Luciana, Bastos-Rodrigues, Helena, Sarubi, Debora M, Miranda, Gisele, Soubrane, Luiz, De Marco, Marcio B, Nehemy
Publikováno v:
Ophthalmic research. 50(2)
To investigate the association between the CFH and ARMS2 gene polymorphisms and age-related macular degeneration (AMD) in a Brazilian cohort.We examined 163 individuals with AMD and 154 controls recruited at the Department of Ophthalmology of the Uni
Autor:
Debora M, Miranda, Bernardo L, Wajchenberg, Maria R, Calsolari, Marcos J, Aguiar, José M C L, Silva, Marcia G, Ribeiro, Cristina, Fonseca, Daniela, Amaral, Wolfanga L, Boson, Bruna A, Resende, Luiz, De Marco
Publikováno v:
Clinical endocrinology. 71(4)
Congenital generalized lipodystrophy, or Berardinelli-Seip syndrome, is a rare autosomal recessive disease caused by mutations in either the BSCL2 or AGPAT2 genes. This syndrome is characterized by an almost complete loss of adipose tissue usually di