Susana Maria Gouveia Fernandes
AuthID: R-000-K31
31
TITLE: Bruton Tyrosine Kinase (BTK) mutations in X-linked agammaglobulinaemia (XLA) Full Text
AUTHORS: Fernandes, S; Sousa, S; Faria, E; Marques, L; Victor, B; Martins, M; Vassal, H; Gusmao, R; Barros, A ;
PUBLISHED: 2008, SOURCE: 13th European-Soc-for-Immunodeficiencies/10th Int-Patient-Org-for-Primary-Immunodeficiencies/8th Int-Nursing-Group-for-Immunodeficiencies Meeting in CLINICAL AND EXPERIMENTAL IMMUNOLOGY, VOLUME: 154
AUTHORS: Fernandes, S; Sousa, S; Faria, E; Marques, L; Victor, B; Martins, M; Vassal, H; Gusmao, R; Barros, A ;
PUBLISHED: 2008, SOURCE: 13th European-Soc-for-Immunodeficiencies/10th Int-Patient-Org-for-Primary-Immunodeficiencies/8th Int-Nursing-Group-for-Immunodeficiencies Meeting in CLINICAL AND EXPERIMENTAL IMMUNOLOGY, VOLUME: 154
INDEXED IN: 
WOS
WOS32
TITLE: Identification of new breakpoints in AZFb and AZFc
AUTHORS: Paula Costa; Rita Goncalves; Cristina Ferras ; Susana Fernandes; Ana Teresa Fernandes; Marrio Sousa ; Alberto Barros ;
PUBLISHED: 2008, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 14, ISSUE: 4
AUTHORS: Paula Costa; Rita Goncalves; Cristina Ferras ; Susana Fernandes; Ana Teresa Fernandes; Marrio Sousa ; Alberto Barros ;
PUBLISHED: 2008, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 14, ISSUE: 4
33
TITLE: Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia
AUTHORS: Marques, CJ ; Costa, P; Vaz, B; Carvalho, F ; Fernandes, S; Barros, A ; Sousa, M ;
PUBLISHED: 2008, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 14, ISSUE: 2
AUTHORS: Marques, CJ ; Costa, P; Vaz, B; Carvalho, F ; Fernandes, S; Barros, A ; Sousa, M ;
PUBLISHED: 2008, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 14, ISSUE: 2
34
TITLE: Prevalence of structural autosomal abnormalities in 10248 infertile portuguese patients
AUTHORS: Lima, ; Doria, S ; Fernandes, S; Madureira, C; Almeida, C; Lemos, F; Reis, F; Pereira, S; Sousa, M; Barros, A ;
PUBLISHED: 2007, SOURCE: 6th European Cytogenetics Conference in CHROMOSOME RESEARCH, VOLUME: 15
AUTHORS: Lima, ; Doria, S ; Fernandes, S; Madureira, C; Almeida, C; Lemos, F; Reis, F; Pereira, S; Sousa, M; Barros, A ;
PUBLISHED: 2007, SOURCE: 6th European Cytogenetics Conference in CHROMOSOME RESEARCH, VOLUME: 15
INDEXED IN: WOS
WOS35
TITLE: DAZ gene copies: evidence of Y chromosome evolution
AUTHORS: Ana Teresa Fernandes; Susana Fernandes; Rita Goncalves; Rosalia S ; Paula Costa; Alexandra Rosa; Cristina Ferras ; Mario Sousa ; Antonio Brehm; Alberto Barros ;
PUBLISHED: 2006, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 12, ISSUE: 8
AUTHORS: Ana Teresa Fernandes; Susana Fernandes; Rita Goncalves; Rosalia S ; Paula Costa; Alexandra Rosa; Cristina Ferras ; Mario Sousa ; Antonio Brehm; Alberto Barros ;
PUBLISHED: 2006, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 12, ISSUE: 8
36
TITLE: Unique t(Y;1)(q12;q12) reciprocal translocation with loss of the heterochromatic region of chromosome 1 in a male with azoospermia due to meiotic arrest: a case report
AUTHORS: Pinho, MJ; Neves, R; Costa, P; Ferras, C ; Sousa, M ; Alves, C; Almeida, C ; Fernandes, S; Silva, J; Ferras, L ; Barros, A ;
PUBLISHED: 2005, SOURCE: HUMAN REPRODUCTION, VOLUME: 20, ISSUE: 3
AUTHORS: Pinho, MJ; Neves, R; Costa, P; Ferras, C ; Sousa, M ; Alves, C; Almeida, C ; Fernandes, S; Silva, J; Ferras, L ; Barros, A ;
PUBLISHED: 2005, SOURCE: HUMAN REPRODUCTION, VOLUME: 20, ISSUE: 3
37
TITLE: A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens
AUTHORS: Grangeia, A ; Carvalho, F ; Fernandes, S; Silva, J; Sousa, M ; Barros, A ;
PUBLISHED: 2005, SOURCE: FERTILITY AND STERILITY, VOLUME: 83, ISSUE: 2
AUTHORS: Grangeia, A ; Carvalho, F ; Fernandes, S; Silva, J; Sousa, M ; Barros, A ;
PUBLISHED: 2005, SOURCE: FERTILITY AND STERILITY, VOLUME: 83, ISSUE: 2
38
TITLE: Cytogenetic and molecular characterization of Y dicentric chromosomes
AUTHORS: Doria, S ; Fernandes, S; Alves, C; Lima, V; Almeida, C; Moreira, L; Pereira, S; Sousa, M; Barros, A ;
PUBLISHED: 2005, SOURCE: CHROMOSOME RESEARCH, VOLUME: 13
AUTHORS: Doria, S ; Fernandes, S; Alves, C; Lima, V; Almeida, C; Moreira, L; Pereira, S; Sousa, M; Barros, A ;
PUBLISHED: 2005, SOURCE: CHROMOSOME RESEARCH, VOLUME: 13
INDEXED IN: WOS
WOS39
TITLE: In-vitro cocultures of the normal human seminiferous epithelium
AUTHORS: Silva, J; Alves, C; Fernandes, MS; Cremades, N; Ferras, C; Carvalho, F ; Fernandes, S; Sousa, M ; Teixeira da Silva, JT; Barros, A ;
PUBLISHED: 2003, SOURCE: HUMAN REPRODUCTION, VOLUME: 18
AUTHORS: Silva, J; Alves, C; Fernandes, MS; Cremades, N; Ferras, C; Carvalho, F ; Fernandes, S; Sousa, M ; Teixeira da Silva, JT; Barros, A ;
PUBLISHED: 2003, SOURCE: HUMAN REPRODUCTION, VOLUME: 18
INDEXED IN: WOS
WOS40
TITLE: High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia
AUTHORS: Fernandes, S; Huellen, K; Goncalves, J ; Dukal, H; Zeisler, J; De MEyts, ER; Skakkebaek, NE; Habermann, B; Krause, W; Sousa, M ; Barros, A ; Vogt, PH;
PUBLISHED: 2002, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 8, ISSUE: 3
AUTHORS: Fernandes, S; Huellen, K; Goncalves, J ; Dukal, H; Zeisler, J; De MEyts, ER; Skakkebaek, NE; Habermann, B; Krause, W; Sousa, M ; Barros, A ; Vogt, PH;
PUBLISHED: 2002, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 8, ISSUE: 3
