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Name
Manco, Licínio
 
Variants
Manco, L.
 
 
Email
lmanco@antrop.uc.pt
 
 
Scopus Author ID
 
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Status
UC Researcher
 

Publications
(All)

Refined By:
Author:  Ribeiro, Maria Letícia

Results 1-10 of 10 (Search time: 0.008 seconds).

Issue DateTitleAuthor(s)TypeAccess
12016Congenital dyserythropoietic anemia associated to a GATA1 mutation aggravated by pyruvate kinase deficiencyPereira, Janet ; Bento, Celeste ; Manco, Licinio ; Gonzalez, Ataulfo ; Vagace, Jose ; Ribeiro, Maria Letícia articleopenAccess
22016Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencingDel 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. articleopenAccess
32015Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese StudyFidalgo, Teresa ; Martinho, Patrícia ; Salvado, Ramon ; Manco, Licínio ; Oliveira, Ana C. ; Pinto, Catarina S. ; Gonçalves, Elsa ; Marques, Dalila ; Sevivas, Teresa ; Martins, Natália ; Ribeiro, Maria Letícia articleopenAccess
42016Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular studyManco, Licínio ; Bento, Celeste ; Victor, Bruno L. ; Pereira, Janet ; Relvas, Luís ; Brito, Rui M. ; Seabra, Carlos ; Maia, Tabita M. ; Ribeiro, M. Letícia articleopenAccess
5Jun-2015Intragenic haplotype analysis of common HFE mutations in the Portuguese populationToste, Sandra ; Relvas, Luís ; Pinto, Catarina ; Bento, Celeste ; Abade, Augusto ; Ribeiro, M. Letícia ; Manco, Licínio articleembargoedAccess
62006Molecular characterization of five Portuguese patients with pyrimidine 5’-nucleotidase deficient hemolytic anemia showing three new P5’N-I mutationsManco, Licínio ; Relvas, Luís ; Pinto, C. Silva ; Pereira, Janet ; Almeida, A. Bessa ; Ribeiro, M. Letícia articleopenAccess
72007Mutations and haplotype diversity in 70 Portuguese G6PD-deficient individuals: an overview on the origin and evolution of mutated allelesManco, Licínio ; Gonçalves, Paula ; Antunes, Patrícia ; Maduro, Filomena ; Abade, Augusto ; Ribeiro, M. Letícia articleopenAccess
82015Polymorphic variations influencing fetal hemoglobin levels: Association study in beta-thalassemia carriers and in normal individuals of Portuguese originPereira, Clara ; Relvas, Luís ; Bento, Celeste ; Abade, Augusto ; Ribeiro, M. Letícia ; Manco, Licínio articleopenAccess
92016Severe neonatal jaundice due to ade novoglucose-6-phosphate dehydrogenase deficient mutationDel 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. articleopenAccess
102005Two new glucose-6-phosphate dehydrogenase mutations causing chronic hemolysisManco, Licínio ; Gonçalves, Paula ; Macedo-Ribeiro, Sandra ; Seabra, Carlos ; Melo, Paula ; Ribeiro, Maria Letícia articleopenAccess