Alberto Manuel Barros da Silva


AuthID: R-000-KE6

Confirmed Publications: 266



181
TITLE: Genetic expression of mammalian stem cell markers in the human male germ line
AUTHORS: Sa, R; Carvalho, F ; Leite, C; Barros, A ; Sousa, M;
PUBLISHED: 2007, SOURCE: 23rd Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology in HUMAN REPRODUCTION, VOLUME: 22
INDEXED IN: WOS
IN MY: ResearcherID
182
TITLE: Heritable genomic imprinting defects in infertile patients with oligozoospermia and azoospermia [Alteração transmissível do imprinting genómico em pacientes inférteis por oligozoospermia e azoospermia]
AUTHORS: Marques, CJ ; Vaz, B; Costa, P; Sousa, S; Carvalho, F ; Fernandes, S; Silva, J; Sousa, M ; Barros, A ;
PUBLISHED: 2007, SOURCE: Arquivos de Medicina, VOLUME: 21, ISSUE: 2
INDEXED IN: Scopus
IN MY: ORCID
183
TITLE: Increased rates of phosphatidylserine translocation on spermatid and spermatozoa from men with azoospermia [Aumento das taxas de translocação da fosfatidilserina nos espermatídeos e espermatozóides de homens com azoospermia]
AUTHORS: Almeida, C ; Sousa, M ; Viana, P; Goncalves, A; Silva, J; Ferras, L ; Barros, A ;
PUBLISHED: 2007, SOURCE: Revista Iberoamericana de Fertilidad y Reproduccion Humana, VOLUME: 24, ISSUE: 2
INDEXED IN: Scopus
IN MY: ORCID
184
TITLE: Molecular characterisation of the cystic fibrosis transmembrane conductance regulator gene in congenital absence of the vas deferens
AUTHORS: Grangeia, A ; Sa, R; Carvalho, F ; Martin, J; Girodon, E; Ferraz, L; Barros, A ; Sousa, M;
PUBLISHED: 2007, SOURCE: 23rd Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology in HUMAN REPRODUCTION, VOLUME: 22
INDEXED IN: WOS
IN MY: ResearcherID
185
TITLE: Molecular characterization of the cystic fibrosis transmembrane conductance regulator gene in congenital absence of the vas deferens
AUTHORS: Ana Grangeia ; Rosalia Sa ; Filipa Carvalho ; Josiane Martin; Emmanuelle Girodon; Joaquina Silva; Luis Ferraz; Alberto Barros ; Mario Sousa ;
PUBLISHED: 2007, SOURCE: GENETICS IN MEDICINE, VOLUME: 9, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 25
IN MY: ORCID | ResearcherID
186
TITLE: Prevalence of sex chromosome abnormalities in 13630 karyotyped portuguese patients
AUTHORS: Doria, ; Lima, V; Fernandes, S; Madureira, C; Moreira, L; Pinho, MJ; Pereira, S; Sousa, M; Barros, A ;
PUBLISHED: 2007, SOURCE: 6th European Cytogenetics Conference in CHROMOSOME RESEARCH, VOLUME: 15
INDEXED IN: WOS
IN MY: ResearcherID
187
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
INDEXED IN: WOS
IN MY: ResearcherID
188
TITLE: Prevalence, characterization and distribution of sex chromosome abnormalities in 9,448 Portuguese infertile patients
AUTHORS: Cunha, M ; Doria, S ; Lima, V; Pinho, MJ; Almeida, C; Oliveira, C; Goncalves, A; Sousa, M; Barros, A ;
PUBLISHED: 2007, SOURCE: 23rd Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology in HUMAN REPRODUCTION, VOLUME: 22
INDEXED IN: WOS
IN MY: ResearcherID
189
TITLE: Role of tissue growth factor beta-1 polymorphisms in congenital bilateral absence of the vas deferens
AUTHORS: Havasi, V; Rowe, SM; Kolettis, P; Grangeia, A; Carvalho, F ; Barros, A ; Sousa, M ; Dayangac, D; Casals, T; Pierucci Alves, F; Schultz, B; Sorscher, EJ;
PUBLISHED: 2007, SOURCE: PEDIATRIC PULMONOLOGY
INDEXED IN: WOS
IN MY: ResearcherID
190
TITLE: Stereological ultrastructural characterization of human oocytes at prophase I
AUTHORS: Luis, A; Rocha, E; Oliveira, E; Silva, J; Barros, A ; Sousa, M;
PUBLISHED: 2007, SOURCE: 23rd Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology in HUMAN REPRODUCTION, VOLUME: 22
INDEXED IN: WOS
IN MY: ResearcherID
Página 19 de 27. Total de resultados: 266.

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