Bento, Celeste
Claim profile
Loading...
2
0
20
0
false
Credit Name
Bento, Celeste
Name
Bento, Celeste
Variants
Bento, C.
Unidade de I&D
Scopus Author ID
Status
UC Researcher
Loading...
3
0
20
0
false
Publications
(All)
Results 1-8 of 8 (Search time: 0.004 seconds).
| Issue Date | Title | Author(s) | Type | Access | |
|---|---|---|---|---|---|
| 1 | 2016 | A novel haemoglobin variant mimicking cyanotic congenital heart disease | Abecasis, Francisco ; Marques, Inês ; Bento, Celeste ; Ferrão, Anabela | article | embargoedAccess |
| 2 | 2016 | Congenital dyserythropoietic anemia associated to a GATA1 mutation aggravated by pyruvate kinase deficiency | Pereira, Janet ; Bento, Celeste ; Manco, Licinio ; Gonzalez, Ataulfo ; Vagace, Jose ; Ribeiro, Maria Letícia | article | openAccess |
| 3 | 2016 | Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing | Del Orbe Barreto, R. ; Arrizabalaga, B. ; De la Hoz, A. B. ; García-Orad, Á. ; Tejada, M. I. ; Garcia-Ruiz, J. C. ; Fidalgo, T. ; Bento, C. ; Manco, L. ; Ribeiro, M. L. | article | openAccess |
| 4 | 2016 | Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations | Camps, Carme ; Petousi, Nayia ; Bento, Celeste ; Cario, Holger ; Copley, Richard R. ; McMullin, Mary Frances ; van Wijk, Richard ; Ratcliffe, Peter J. ; Robbins, Peter A. ; Taylor, Jenny C. | article | openAccess |
| 5 | 2016 | Haemoglobin kenitra identified in a Portuguese man with type 2 diabetes and pheochromocytoma | Cabral, V. ; Silva Nunes, J. ; Bento, C. ; Sobreira, R. ; Rodrigues, I. ; Shvets, R. ; Silvestre, M. J. ; Barros, R. | article | openAccess |
| 6 | 2016 | Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study | Manco, Licínio ; Bento, Celeste ; Victor, Bruno L. ; Pereira, Janet ; Relvas, Luís ; Brito, Rui M. ; Seabra, Carlos ; Maia, Tabita M. ; Ribeiro, M. Letícia | article | openAccess |
| 7 | 2016 | Hereditary xerocytosis, a misleading anemia | Del Orbe Barreto, R. ; Arrizabalaga, B. ; De la Hoz Rastrollo, A. B. ; García-Orad, A. ; Gonzalez Vallejo, I. ; Bento, C. ; Villegas, A. ; García-Ruiz, J. C. | article | openAccess |
| 8 | 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 |