Filipa Abreu Gomes de Carvalho


AuthID: R-000-K35

Confirmed Publications: 121



81
TITLE: A complex case at prenatal diagnosis
AUTHORS: Pinto Leite; Souto, M; Carvalho, B; Marques, B; Carvalho, F ; Ribeiro, E;
PUBLISHED: 2007, SOURCE: 6th European Cytogenetics Conference in CHROMOSOME RESEARCH, VOLUME: 15
INDEXED IN: WOS
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
82
TITLE: Analysis of H19 and MEST/PEG1 and Line 1 transposon methylation patterns in oligozoospermia
AUTHORS: Carvalho, F ; Marques, CJ ; Costa, P; Vaz, B; Fernandes, S; Arnaud, P; 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: ORCID | ResearcherID | CIÊNCIAVITAE
83
TITLE: Evidence for selective low leukocyte enzyme activity levels associated with the G1170C > T 5 ' untranslated polymorphism of the alpha-galactosidase A gene  Full Text
AUTHORS: Ferreira, S; Barcelo, J; Carvalho, F ; Mansson, JE; Oliveira, JP ;
PUBLISHED: 2007, SOURCE: 7th Annual European Round Table on Fabry Disease in CLINICAL THERAPEUTICS, VOLUME: 29
INDEXED IN: WOS CrossRef
IN MY: ORCID | CIÊNCIAVITAE
84
TITLE: Frequency of 5 ' untranslated region single nucleotide polymorphisms of the alpha-Galactosidase A gene in the Portuguese population
AUTHORS: Ferreira, S; Barcelo, J; Carvalho, F ; Oliveira, JP ;
PUBLISHED: 2007, SOURCE: 7th Annual European Round Table on Fabry Disease in CLINICAL THERAPEUTICS, VOLUME: 29
INDEXED IN: WOS
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
85
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: ORCID | ResearcherID | CIÊNCIAVITAE
86
87
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: ORCID | ResearcherID | CIÊNCIAVITAE
88
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: 26
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
89
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: ORCID | ResearcherID | CIÊNCIAVITAE
90
Page 9 of 13. Total results: 121.

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