Dezso David
AuthID: R-000-470
11
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
12
TITLE: A pathogenic breakpoint at 566.8 kb from the 3 ' end of the SATB2 leads to a 2q33.1 microdeletion-like phenotype Full Text
AUTHORS: Dezso David; Ines Santos; Barbara Marques; Hildeberto Correia; Filomena Teixeira;
PUBLISHED: 2011, SOURCE: CHROMOSOME RESEARCH, VOLUME: 19
AUTHORS: Dezso David; Ines Santos; Barbara Marques; Hildeberto Correia; Filomena Teixeira;
PUBLISHED: 2011, SOURCE: CHROMOSOME RESEARCH, VOLUME: 19
INDEXED IN: 
WOS
WOS13
TITLE: Characterization of two ectrodactyly-associated translocation breakpoints separated by 2.5 Mb on chromosome 2q14.1-q14.2 Full Text
AUTHORS: Dezso David; Barbara Marques; Cristina Ferreira; Paula Vieira; Alfredo Corona Rivera; Jose Carlos Ferreira; Hans van Bokhoven;
PUBLISHED: 2009, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 17, ISSUE: 8
AUTHORS: Dezso David; Barbara Marques; Cristina Ferreira; Paula Vieira; Alfredo Corona Rivera; Jose Carlos Ferreira; Hans van Bokhoven;
PUBLISHED: 2009, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 17, ISSUE: 8
14
TITLE: The spectrum of mutations and molecular pathogenesis of hemophilia A in 181 Portuguese patients Full Text
AUTHORS: David, D; Ventura, C; Moreira, I; Diniz, MJ; Antunes, M; Tavares, A; Araujo, F ; Morais, S; Campos, M; Lavinha, J; Kemball Cook, G;
PUBLISHED: 2006, SOURCE: HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, VOLUME: 91, ISSUE: 6
AUTHORS: David, D; Ventura, C; Moreira, I; Diniz, MJ; Antunes, M; Tavares, A; Araujo, F ; Morais, S; Campos, M; Lavinha, J; Kemball Cook, G;
PUBLISHED: 2006, SOURCE: HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, VOLUME: 91, ISSUE: 6
INDEXED IN: 
Scopus WOS
Scopus WOS15
TITLE: Molecular basis of inherited antithrombin deficiency in Portuguese families: Identification of genetic alterations and screening for additional thrombotic risk factors Full Text
AUTHORS: David, D; Ribeiro, S; Ferrao, L; Gago, T; Crespo, F;
PUBLISHED: 2004, SOURCE: AMERICAN JOURNAL OF HEMATOLOGY, VOLUME: 76, ISSUE: 2
AUTHORS: David, D; Ribeiro, S; Ferrao, L; Gago, T; Crespo, F;
PUBLISHED: 2004, SOURCE: AMERICAN JOURNAL OF HEMATOLOGY, VOLUME: 76, ISSUE: 2
16
TITLE: Molecular characterization of a familial translocation implicates disruption of HDAC9 and possible position effect on TGF beta 2 in the pathogenesis of Peters' anomaly Full Text
AUTHORS: David, D; Cardoso, J; Marques, B; Marques, R; Silva, ED ; Santos, H; Boavida, MG;
PUBLISHED: 2003, SOURCE: GENOMICS, VOLUME: 81, ISSUE: 5
AUTHORS: David, D; Cardoso, J; Marques, B; Marques, R; Silva, ED ; Santos, H; Boavida, MG;
PUBLISHED: 2003, SOURCE: GENOMICS, VOLUME: 81, ISSUE: 5
17
TITLE: Molecular characterization of a 7p15-21 homozygous deletion in a Wilms tumor Full Text
AUTHORS: Sossey Alaoui, K; Vieira, L; David, D; Boavida, MG; Cowell, JK;
PUBLISHED: 2003, SOURCE: GENES CHROMOSOMES & CANCER, VOLUME: 36, ISSUE: 1
AUTHORS: Sossey Alaoui, K; Vieira, L; David, D; Boavida, MG; Cowell, JK;
PUBLISHED: 2003, SOURCE: GENES CHROMOSOMES & CANCER, VOLUME: 36, ISSUE: 1
INDEXED IN: Scopus WOS
Scopus WOS18
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
19
TITLE: Analysis of the consequences of premature termination codons within factor VIII coding sequences. Premature termination codons within fviii coding sequences Full Text
AUTHORS: David, D; Santos, IMA; Johnson, K; Tuddenham, EGD; McVey, JH;
PUBLISHED: 2003, SOURCE: JOURNAL OF THROMBOSIS AND HAEMOSTASIS, VOLUME: 1, ISSUE: 1
AUTHORS: David, D; Santos, IMA; Johnson, K; Tuddenham, EGD; McVey, JH;
PUBLISHED: 2003, SOURCE: JOURNAL OF THROMBOSIS AND HAEMOSTASIS, VOLUME: 1, ISSUE: 1
20
TITLE: Molecular characterization of a 7p15-21 homozygous deletion in a Wilms tumor Full Text
AUTHORS: Khalid Sossey-Alaoui; Lu�s Vieira; Dezso David; Maria G Boavida; John K Cowell;
PUBLISHED: 2002, SOURCE: Genes Chromosom. Cancer - Genes, Chromosomes and Cancer, VOLUME: 36, ISSUE: 1
AUTHORS: Khalid Sossey-Alaoui; Lu�s Vieira; Dezso David; Maria G Boavida; John K Cowell;
PUBLISHED: 2002, SOURCE: Genes Chromosom. Cancer - Genes, Chromosomes and Cancer, VOLUME: 36, ISSUE: 1
