Browsing by Author Ribeiro, Letícia
Results 15 to 28 of 28
previous
| Issue Date | Title | Author(s) | Type | Access |
|---|---|---|---|---|
| Jun-2011 | Kawasaki Disease and Human Bocavirus – potential association? | Santos, R. A. ; Nogueira, C. S. ; Baptista, J. B ; Granja, S. ; Ribeiro, M. L. ; Rocha, M. G. | article | openAccess |
| 2006 | Molecular characterization of five Portuguese patients with pyrimidine 5’-nucleotidase deficient hemolytic anemia showing three new P5’N-I mutations | Manco, Licínio ; Relvas, Luís ; Pinto, C. Silva ; Pereira, Janet ; Almeida, A. Bessa ; Ribeiro, M. Letícia | article | openAccess |
| 2013 | Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?) | Bento, Celeste ; Almeida, Helena ; Maia, Tabita M. ; Relvas, Luís ; Oliveira, Ana C. ; Rossi, Cédric ; Girodon, François ; Fernandez-Lago, Carlos ; Aguado-Diaz, Ascension ; Fraga, Cristina ; Costa, Ricardo M. ; Araújo, Ana L. ; Silva, João ; Vitória, Helena ; Miguel, Natalina ; Silveira, Maria Pedro ; Martin-Nuñez, Guillermo ; Ribeiro, Maria Letícia | article | openAccess |
| 2007 | Mutations and haplotype diversity in 70 Portuguese G6PD-deficient individuals: an overview on the origin and evolution of mutated alleles | Manco, Licínio ; Gonçalves, Paula ; Antunes, Patrícia ; Maduro, Filomena ; Abade, Augusto ; Ribeiro, M. Letícia | article | openAccess |
| 2010 | Percentagem de plaquetas reticuladas : um parâmetro útil no diagnóstico da Púrpura Trombocitopénica Imune Primária | Pinheiro, Ana Cristina da Costa Abrantes | masterThesis | openAccess |
| 2015 | Polymorphic variations influencing fetal hemoglobin levels: Association study in beta-thalassemia carriers and in normal individuals of Portuguese origin | Pereira, Clara ; Relvas, Luís ; Bento, Celeste ; Abade, Augusto ; Ribeiro, M. Letícia ; Manco, Licínio | article | openAccess |
| 2013 | Primary familial congenital erythrocytosis: two novel EPOR mutations found in Spain | Bento, C. ; Almeida, H. ; Fernandez-Lago, C. ; Ribeiro, M. L. | article | openAccess |
| 2010 | Prothrombotic status in Myeloproliferative neoplasms : the role of JAK2V617F allele burden and platelets/leukocytes activation | Coucelo, Margarida Carreira Revez Pereira | masterThesis | openAccess |
| 2012 | Pyruvate kinase deficiency in sub-Saharan Africa: identification of a highly frequent missense mutation (G829A;Glu277Lys) and association with malaria | Machado, Patrícia ; Manco, Licínio ; Gomes, Cláudia; Mendes, Cristina ; Fernandes, Natércia; Salomé, Graça; Sitoe, Luis; Chibute, Sérgio; Langa, José; Ribeiro, Letícia ; Miranda, Juliana ; Cano, Jorge ; Pinto, João; Amorim, António ; do Rosário, Virgílio E; Arez, Ana Paula | article | openAccess |
| 2008 | Risk markers for progression of mild nonproliferative retinopathy to clinically significant macular edema in type 2 diabetic patients | Pereira, I. ; Nunes, S. ; Ribeiro, M. L. ; Bernardes, R. ; Cunha-Vaz, J. | article | openAccess |
| 2016 | Severe neonatal jaundice due to ade novoglucose-6-phosphate dehydrogenase deficient mutation | Del Orbe Barreto, R. ; Arrizabalaga, B. ; de la Hoz, A. B ; Aragües, P. ; Garcia-Ruiz, J. C. ; Arrieta, A. ; Adán, R. ; Manco, L. ; Macedo-Ribeiro, S. ; Bento, C. ; Ribeiro, M. L. | article | openAccess |
| 2013 | Transient Neonatal Cyanosis Associated With a New Hb F Variant | Bento, Celeste ; Magalhães Maia, Tabita ; Carvalhais, Ines ; Moita, Filipa ; Abreu, Gabriela ; Relvas, Luís ; Pereira, Alexandra ; Farela Neves, José ; Ribeiro, Maria L. | article | openAccess |
| 2005 | Two new glucose-6-phosphate dehydrogenase mutations causing chronic hemolysis | Manco, Licínio ; Gonçalves, Paula ; Macedo-Ribeiro, Sandra ; Seabra, Carlos ; Melo, Paula ; Ribeiro, Maria Letícia | article | openAccess |
| 10-Jul-2017 | Von Willebrand factor and ADAMTS13 : Duality in hemorrhagic and thrombotic disease | Fidalgo, Teresa de Jesus Semedo | doctoralThesis | openAccess |