Ana Maria Figueiredo Tavares Fortuna
AuthID: R-00H-H5G
31
TITLE: Genes, children and paediatricians
AUTHORS: Gabriela Soares; Isabel Pimentel; Cristina Dias; Jorge Pinto Basto; Márcia Martins; Ana Fortuna; Margarida Reis Lima;
PUBLISHED: 2004, SOURCE: Nascer e Crescer, VOLUME: 13, ISSUE: 4
AUTHORS: Gabriela Soares; Isabel Pimentel; Cristina Dias; Jorge Pinto Basto; Márcia Martins; Ana Fortuna; Margarida Reis Lima;
PUBLISHED: 2004, SOURCE: Nascer e Crescer, VOLUME: 13, ISSUE: 4
INDEXED IN: 
Scopus
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ORCID
ORCID32
TITLE: Cervical aortic arch and 22q11 deletion - The role of MRI in diagnosis [Associação de arco aórtico cervical a delecção 22q11 - Papel da RMN no diagnóstico]
AUTHORS: Almeida, R; Alvares, S; Fortuna, A; Moreira, J; Vieira, A;
PUBLISHED: 2003, SOURCE: Revista Portuguesa de Cardiologia, VOLUME: 22, ISSUE: 10
AUTHORS: Almeida, R; Alvares, S; Fortuna, A; Moreira, J; Vieira, A;
PUBLISHED: 2003, SOURCE: Revista Portuguesa de Cardiologia, VOLUME: 22, ISSUE: 10
INDEXED IN: Scopus
Scopus IN MY: ORCID
ORCID33
TITLE: FG syndrome
AUTHORS: Sameiro Barreirinho; Lina Ramos; Albina Silva; Márcia Martins; Céu Mota; Ana Fortuna; Margarida Reis Lima;
PUBLISHED: 2002, SOURCE: Arquivos de Medicina, VOLUME: 16, ISSUE: 1
AUTHORS: Sameiro Barreirinho; Lina Ramos; Albina Silva; Márcia Martins; Céu Mota; Ana Fortuna; Margarida Reis Lima;
PUBLISHED: 2002, SOURCE: Arquivos de Medicina, VOLUME: 16, ISSUE: 1
INDEXED IN: Scopus
Scopus IN MY: ORCID
ORCID34
TITLE: Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B Full Text
AUTHORS: Oldridge, M; Fortuna, AM; Maringa, M; Propping, P; Mansour, S; Pollitt, C; DeChiara, TM; Kimble, RB; Valenzuela, DM; Yancopoulos, GD; Wilkie, AOM;
PUBLISHED: 2000, SOURCE: NATURE GENETICS, VOLUME: 24, ISSUE: 3
AUTHORS: Oldridge, M; Fortuna, AM; Maringa, M; Propping, P; Mansour, S; Pollitt, C; DeChiara, TM; Kimble, RB; Valenzuela, DM; Yancopoulos, GD; Wilkie, AOM;
PUBLISHED: 2000, SOURCE: NATURE GENETICS, VOLUME: 24, ISSUE: 3
35
TITLE: T cell numbers relate to bone involvement in Gaucher disease Full Text
AUTHORS: Lacerda, L; Arosa, FA ; Lacerda, R; Cabeda, JM ; Porto, G ; Amaral, O; Fortuna, A; Pinto, R; Oliveira, P ; McLaren, CE; Miranda, CS; de Sousa, M ;
PUBLISHED: 1999, SOURCE: BLOOD CELLS MOLECULES AND DISEASES, VOLUME: 25, ISSUE: 8
AUTHORS: Lacerda, L; Arosa, FA ; Lacerda, R; Cabeda, JM ; Porto, G ; Amaral, O; Fortuna, A; Pinto, R; Oliveira, P ; McLaren, CE; Miranda, CS; de Sousa, M ;
PUBLISHED: 1999, SOURCE: BLOOD CELLS MOLECULES AND DISEASES, VOLUME: 25, ISSUE: 8
36
TITLE: Otological and audiological abnormalities in oculo-auriculo-vertebral spectrum [Alteracoes otologicas e audiologicas no complexo oculo-auriculo- vertebral (Goldenhar)]
AUTHORS: Coutinho, MB; Mota, CR; Fortuna, A; Lima, MR;
PUBLISHED: 1999, SOURCE: Nascer e Crescer, VOLUME: 8, ISSUE: 2
AUTHORS: Coutinho, MB; Mota, CR; Fortuna, A; Lima, MR;
PUBLISHED: 1999, SOURCE: Nascer e Crescer, VOLUME: 8, ISSUE: 2
INDEXED IN: Scopus
Scopus IN MY: ORCID
ORCID37
TITLE: Obesity and polidactily
AUTHORS: Martins M.; Ramos L.; Mota C.R.; Fortuna A.; Lima M.R.;
PUBLISHED: 1999, SOURCE: Nascer e Crescer, VOLUME: 8, ISSUE: 2
AUTHORS: Martins M.; Ramos L.; Mota C.R.; Fortuna A.; Lima M.R.;
PUBLISHED: 1999, SOURCE: Nascer e Crescer, VOLUME: 8, ISSUE: 2
INDEXED IN: Scopus
Scopus IN MY: ORCID
ORCID38
TITLE: Cardiac anomalies in Williams Syndrome [Avaliacao cardiaca na Sindrome de Williams]
AUTHORS: Figueiredo, AC; Proenca, E; Mota, C; Fortuna, A; Criado, B; Lima, MR; Alvares, S;
PUBLISHED: 1998, SOURCE: Nascer e Crescer, VOLUME: 7, ISSUE: 4
AUTHORS: Figueiredo, AC; Proenca, E; Mota, C; Fortuna, A; Criado, B; Lima, MR; Alvares, S;
PUBLISHED: 1998, SOURCE: Nascer e Crescer, VOLUME: 7, ISSUE: 4
INDEXED IN: Scopus
Scopus IN MY: ORCID
ORCID39
TITLE: Prenatal diagnosis of Machado-Joseph disease by direct mutation analysis Full Text
AUTHORS: Sequeiros, J ; Maciel, P ; Taborda, F; Ledo, S ; Rocha, JC; Lopes, A; Reto, F; Fortuna, AM; Rousseau, M; Fleming, M; Coutinho, P ; Rouleau, GA; Jorge, CS;
PUBLISHED: 1998, SOURCE: Prenatal Diagnosis, VOLUME: 18, ISSUE: 6
AUTHORS: Sequeiros, J ; Maciel, P ; Taborda, F; Ledo, S ; Rocha, JC; Lopes, A; Reto, F; Fortuna, AM; Rousseau, M; Fleming, M; Coutinho, P ; Rouleau, GA; Jorge, CS;
PUBLISHED: 1998, SOURCE: Prenatal Diagnosis, VOLUME: 18, ISSUE: 6
40
TITLE: Prenatal diagnosis in Portugal
AUTHORS: Pinto, MR; Fortuna, AMT;
PUBLISHED: 1997, SOURCE: Proceedings of an EUCROMIC Workshop on Prenatal Diagnosis in Europe in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 5, ISSUE: SUPPL. 1
AUTHORS: Pinto, MR; Fortuna, AMT;
PUBLISHED: 1997, SOURCE: Proceedings of an EUCROMIC Workshop on Prenatal Diagnosis in Europe in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 5, ISSUE: SUPPL. 1
INDEXED IN: Scopus 
WOS
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