Célia Cristina Barbosa Ventura
AuthID: R-000-3MK
11
TITLE: Conventional and novel "omics"-based approaches to the study of carbon nanotubes pulmonary toxicity. Conventional and “Omics” CNT Toxicity Studies Full Text
AUTHORS: Celia Ventura; Antonio Sousa-Uva ; Joao Lavinha; Maria Joao Silva;
PUBLISHED: 2018, SOURCE: ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, VOLUME: 59, ISSUE: 4
AUTHORS: Celia Ventura; Antonio Sousa-Uva ; Joao Lavinha; Maria Joao Silva;
PUBLISHED: 2018, SOURCE: ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, VOLUME: 59, ISSUE: 4
12
TITLE: PROS1 novel splice-site variant decreases protein S expression in patients from two families with thrombotic disease
AUTHORS: Juliane Menezes; Celia Ventura; Joao Matos Costa; Elsa Parreira; Luisa Romao; Joao Goncalves;
PUBLISHED: 2017, SOURCE: CLINICAL CASE REPORTS, VOLUME: 5, ISSUE: 12
AUTHORS: Juliane Menezes; Celia Ventura; Joao Matos Costa; Elsa Parreira; Luisa Romao; Joao Goncalves;
PUBLISHED: 2017, SOURCE: CLINICAL CASE REPORTS, VOLUME: 5, ISSUE: 12
INDEXED IN: 
WOS
WOS13
TITLE: Genetic defects in Portuguese families with inherited protein C deficiency Full Text
AUTHORS: Dezso David; Cristina Ferreira; Celia Ventura; Isabel Freire; Isabel Moreira; Teresa Gago;
PUBLISHED: 2011, SOURCE: THROMBOSIS RESEARCH, VOLUME: 128, ISSUE: 3
AUTHORS: Dezso David; Cristina Ferreira; Celia Ventura; Isabel Freire; Isabel Moreira; Teresa Gago;
PUBLISHED: 2011, SOURCE: THROMBOSIS RESEARCH, VOLUME: 128, ISSUE: 3
14
TITLE: Female haemophiliac homozygous for the factor VIII intron 22 inversion mutation, with transcriptional inactivation of one of the factor VIII alleles Full Text
AUTHORS: David, D; Morais, S; Ventura, C; Campos, M;
PUBLISHED: 2003, SOURCE: HAEMOPHILIA, VOLUME: 9, ISSUE: 1
AUTHORS: David, D; Morais, S; Ventura, C; Campos, M;
PUBLISHED: 2003, SOURCE: HAEMOPHILIA, VOLUME: 9, ISSUE: 1
