Carreira, Isabel Marques
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Carreira, Isabel Marques
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Carreira, I.
Carreira, Isabel Marques
Carreira, Isabel Marques
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Results 1-25 of 25 (Search time: 0.01 seconds).
| Issue Date | Title | Author(s) | Type | Access | |
|---|---|---|---|---|---|
| 1 | 2012 | Beta thalassemia major due to acquired uniparental disomy in a previously healthy adolescent | Bento, C. ; Maia, T. M. ; Milosevic, J. D. ; Carreira, I. M. ; Kralovics, R. ; Ribeiro, M. L. | article | openAccess |
| 2 | May-2016 | BIRC3 alterations in chronic and B-cell acute lymphocytic leukemia patients | Alhourani, Eyad ; Othman, Moneeb A. K. ; Melo, Joana Barbosa ; Carreira, Isabel M. ; Grygalewicz, Beata; Vujić, Dragana; Zecević, Zeljko; Joksić, Gordana; Glaser, Anita ; Pohle, Beate; Schlie, Cordula; Hauke, Sven; Liehr, Thomas | article | openAccess |
| 3 | 2012 | Can Biofluids Metabolic Profiling Help to Improve Healthcare during Pregnancy? | Graça, Gonçalo ; Diaz, Sílvia O.; Pinto, Joana; Barros, António S.; Duarte, Iola F. ; Goodfellow, Brian J. ; Galhano, Eulália; Pita, Cristina; Almeida, Maria do Céu ; Carreira, Isabel M. ; Gil, Ana M. | article | openAccess |
| 4 | 2015 | Copy number variants prioritization after array-CGH analysis - a cohort of 1000 patients | Carreira, Isabel Marques ; Ferreira, Susana Isabel ; Matoso, Eunice ; Pires, Luís Miguel ; Ferrão, José ; Jardim, Ana ; Mascarenhas, Alexandra ; Pinto, Marta ; Lavoura, Nuno ; Pais, Claudia ; Paiva, Patrícia ; Simões, Lúcia ; Caramelo, Francisco ; Ramos, Lina ; Venâncio, Margarida ; Ramos, Fabiana; Beleza, Ana; Sá, Joaquim ; Saraiva, Jorge ; Melo, Joana Barbosa de | article | openAccess |
| 5 | 2-May-2012 | Critical region in 2q31.2q32.3 deletion syndrome: Report of two phenotypically distinct patients, one with an additional deletion in Alagille syndrome region | Ferreira, Susana Isabel ; Matoso, Eunice ; Venâncio, Margarida ; Saraiva, Jorge ; Melo, Joana B. ; Carreira, Isabel Marques | article | openAccess |
| 6 | 2015 | Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 gene | Melo, Joana B. ; Estevinho, Alexandra ; Saraiva, Jorge; Ramos, Lina ; Carreira, Isabel M. | article | openAccess |
| 7 | 23-Sep-2019 | Cytogenetics and Cytogenomics Evaluation in Cancer | Ribeiro, Ilda Patrícia ; Melo, Joana Barbosa ; Carreira, Isabel Marques | article | openAccess |
| 8 | 2016 | Early detection and personalized treatment in oral cancer: the impact of omics approaches | Ribeiro, Ilda Patrícia ; Barroso, Leonor ; Marques, Francisco ; Melo, Joana Barbosa ; Carreira, Isabel Marques | article | openAccess |
| 9 | 19-Dec-2017 | Effects of resistance exercise on endothelial progenitor cell mobilization in women | Ribeiro, Fernando; Ribeiro, Ilda P. ; Gonçalves, Ana C. ; Alves, Alberto J.; Melo, Elsa ; Fernandes, Raquel; Costa, Rui; Ribeiro, Ana B. Sarmento ; Duarte, José A.; Carreira, Isabel M. ; Witkowski, Sarah; Oliveira, José | article | openAccess |
| 10 | 22-Jun-2016 | Fibroblasts of Machado Joseph Disease patients reveal autophagy impairment | Onofre, Isabel ; Mendonça, Nuno ; Lopes, Sara ; Nobre, Rui J. ; Melo, Joana Barbosa ; Carreira, Isabel Marques ; Januário, Cristina ; Gonçalves, António Freire ; Almeida, Luís Pereira de | article | openAccess |
| 11 | May-2018 | Generation and characterization of a human iPS cell line from a patient-related control to study disease mechanisms associated with DAND5 p.R152H alteration | Pars, Selin; Cristo, Fernando; Inácio, José M.; Rosas, Graça; Carreira, Isabel Marques ; Melo, Joana Barbosa ; Mendes, Patrícia; Martins, Duarte Saraiva; Almeida, Luís Pereira de ; Maio, José; Anjos, Rui ; Belo, José A. | article | openAccess |
| 12 | 2017 | Generation of human iPSC line from a patient with laterality defects and associated congenital heart anomalies carrying a DAND5 missense alteration | Cristo, Fernando; Inácio, José M; Rosas, Graça; Carreira, Isabel Marques ; Melo, Joana Barbosa ; Almeida, Luís Pereira de ; Mendes, Patrícia; Martins, Duarte Saraiva; Maio, José; Anjos, Rui ; Belo, José A. | article | openAccess |
| 13 | 2017 | Genetic and epigenetic characterization of the tumors in a patient with a tongue primary tumor, a recurrence and a pharyngoesophageal second primary tumor | Ribeiro, Ilda Patrícia ; Marques, Francisco ; Barroso, Leonor ; Miguéis, Jorge ; Caramelo, Francisco ; Santos, André ; Julião, Maria J.; Melo, Joana B. ; Carreira, Isabel M. | article | openAccess |
| 14 | 2018 | Genomic and epigenetic signatures associated with survival rate in oral squamous cell carcinoma patients | Ribeiro, Ilda Patrícia ; Caramelo, Francisco ; Esteves, Luísa ; Oliveira, Camila ; Marques, Francisco ; Barroso, Leonor ; Melo, Joana Barbosa ; Carreira, Isabel Marques | article | openAccess |
| 15 | 24-Oct-2017 | Genomic predictive model for recurrence and metastasis development in head and neck squamous cell carcinoma patients | Ribeiro, Ilda Patrícia ; Caramelo, Francisco ; Esteves, Luísa ; Menoita, Joana ; Marques, Francisco ; Barroso, Leonor ; Miguéis, Jorge ; Melo, Joana Barbosa ; Carreira, Isabel Marques | article | openAccess |
| 16 | 2019 | Head and neck cancer: searching for genomic and epigenetic biomarkers in body fluids - the state of art | Ribeiro, Ilda Patrícia ; Melo, Joana Barbosa de ; Carreira, Isabel Marques | article | openAccess |
| 17 | 2015 | High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia | Othman, Moneeb A. K. ; Melo, Joana B. ; Carreira, Isabel M. ; Rincic, Martina ; Glaser, Anita ; Grygalewicz, Beata; Gruhn, Bernd; Wilhelm, Kathleen; Rittscher, Katharina; Meyer, Britta; Silva, Maria Luiza Macedo; de Jesus Marques Salles, Terezinha; Liehr, Thomas | article | openAccess |
| 18 | 19-Mar-2012 | High resolution melting: improvements in the genetic diagnosis of hypertrophic cardiomyopathy in a Portuguese cohort | Santos, Susana; Marques, Vanda; Pires, Marina Joana Dias ; Silveira, Leonor; Oliveira, Helena; Lança, Vasco; Brito, Dulce; Madeira, Hugo; Esteves, J Fonseca; Freitas, António; Carreira, Isabel M. ; Gaspar, Isabel M.; Monteiro, Carolino; Fernandes, Alexandra R. | article | openAccess |
| 19 | 2015 | Isochromosome 17q in Chronic Lymphocytic Leukemia | Alhourani, Eyad ; Rincic, Martina ; Melo, Joana B. ; Carreira, Isabel M. ; Glaser, Anita ; Pohle, Beate; Schlie, Cordula; Liehr, Thomas | article | openAccess |
| 20 | 2017 | MLPA analysis in a cohort of patients with autism | Peixoto, Sara ; Melo, Joana B. ; Ferrão, José ; Pires, Luís M. ; Lavoura, Nuno ; Pinto, Marta ; Oliveira, Guiomar ; Carreira, Isabel M. | article | openAccess |
| 21 | 2014 | A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic Leukemia | Othman, Moneeb A. K. ; Rincic, Martina ; Melo, Joana B. ; Carreira, Isabel M. ; Alhourani, Eyad ; Hunstig, Friederike ; Glaser, Anita ; Liehr, Thomas | article | openAccess |
| 22 | 2014 | Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the Sao Miguel Island, Azores, revealed the second patient with a triplication | Pires, Renato ; Pires, Luís M. ; Vaz, Sara O. ; Maciel, Paula ; Anjos, Rui ; Moniz, Raquel ; Branco, Claudia C. ; Cabral, Rita ; Carreira, Isabel M. ; Mota-Vieira, Luisa | article | openAccess |
| 23 | 1-Aug-2018 | Stroma-derived IL-6, G-CSF and Activin-A mediated dedifferentiation of lung carcinoma cells into cancer stem cells | Rodrigues, Carlos F. D. ; Serrano, Eurico ; Patrício, Maria I.; Val, Mariana; Albuquerque, Patrícia; Fonseca, João ; Gomes, Célia M. F. ; Abrunhosa, Antero ; Paiva, Artur ; Carvalho, Lina ; Botelho, Maria F. ; Almeida, Luís ; Carreira, Isabel M. ; Alpoim, Maria Carmen | article | openAccess |
| 24 | 22-Aug-2015 | A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases | Vaz, Sara O. ; Pires, Renato ; Pires, Luís M. ; Carreira, Isabel M. ; Anjos, Rui ; Maciel, Paula ; Mota-Vieira, Luisa | article | openAccess |
| 25 | 20-Jul-2010 | X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation | Ferreira, Susana I. ; Matoso, Eunice ; Pinto, Marta ; Almeida, Joana ; Liehr, Thomas ; Melo, Joana B. ; Carreira, Isabel M. | article | openAccess |