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people:afriaes [2009/09/09 23:10]
afriaes
people:afriaes [2013/11/25 15:55]
afriaes [Current Position]
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   * Applied Chemistry, Biotechnology - FCT/UNL\\   * Applied Chemistry, Biotechnology - FCT/UNL\\
   * MSc in Biotechnology - FCT/UNL\\   * MSc in Biotechnology - FCT/UNL\\
 +  * PhD in Microbiology - Faculdade de Medicina, UL\\
 ===== Current Position ===== ===== Current Position =====
-**Teaching ​Assistant**\\ ​+**Assistant ​Professor**\\ 
 [[http://​www.imm.fm.ul.pt/​web/​imm/​molecularmicrobiologyandinfection|Molecular Microbiology and Infection Unit]], [[http://​www.imm.fm.ul.pt/​web/​imm/​home|Instituto de Medicina Molecular]]\\ [[http://​www.imm.fm.ul.pt/​web/​imm/​molecularmicrobiologyandinfection|Molecular Microbiology and Infection Unit]], [[http://​www.imm.fm.ul.pt/​web/​imm/​home|Instituto de Medicina Molecular]]\\
 Instituto de Microbiologia,​[[http://​www.fm.ul.pt/​|Faculdade de Medicina de Lisboa]], Universidade de Lisboa\\ ​ Instituto de Microbiologia,​[[http://​www.fm.ul.pt/​|Faculdade de Medicina de Lisboa]], Universidade de Lisboa\\ ​
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 ===== Research Interests ===== ===== Research Interests =====
  
-Microbiology,​ Group A Streptococcus epidemiology,​ pathogenesis,​ and virulence factors; molecular typing methods\\+Microbiology,​ Group A Streptococcus epidemiology,​ pathogenesis,​ and virulence factors; molecular typing methods.\\
  
  
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 ===== Publications ===== ===== Publications =====
 Nonoutbreak surveillance of group A streptococci causing invasive disease in Portugal identified internationally disseminated clones among members of a genetically heterogeneous population. Nonoutbreak surveillance of group A streptococci causing invasive disease in Portugal identified internationally disseminated clones among members of a genetically heterogeneous population.
-__Friães A__, Ramirez M, Melo-Cristino J, Portuguese Group for the Study of Streptococcal Infections+__Friães A__, Ramirez M, Melo-Cristino J, Portuguese Group for the Study of Streptococcal Infections.
 Journal of Clinical Microbiology 2007 45(6):​2044-2047 Journal of Clinical Microbiology 2007 45(6):​2044-2047
  
 Congenital adrenal hyperplasia:​ focus on the molecular basis of 21-hydroxylase deficiency. Congenital adrenal hyperplasia:​ focus on the molecular basis of 21-hydroxylase deficiency.
-Gonçalves J, __Friães A__, Moura L+Gonçalves J, __Friães A__, Moura L.
 Expert Reviews in Molecular Medicine 2007 9(11):1-23 Expert Reviews in Molecular Medicine 2007 9(11):1-23
  
-CYP21A2 mutations in Portuguese patients with congenital adrenal hyperplasia:​ Identification of two novel mutations and characterization of four different partial gene conversions.+//CYP21A2// mutations in Portuguese patients with congenital adrenal hyperplasia:​ Identification of two novel mutations and characterization of four different partial gene conversions.
 __Friães A__, Rêgo AT, Aragüés JM, Moura LF, Mirante A, Mascarenhas MR, Kay TT, Lopes LA, Rodrigues JC, Guerra S, Dias T, Teles AG, Gonçalves J. __Friães A__, Rêgo AT, Aragüés JM, Moura LF, Mirante A, Mascarenhas MR, Kay TT, Lopes LA, Rodrigues JC, Guerra S, Dias T, Teles AG, Gonçalves J.
 Molecular Genetics and Metabolism 2006 88(1):58-65 Molecular Genetics and Metabolism 2006 88(1):58-65
  
  
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