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Luís Relvas

Showing results (11-20 of 23) with videos related to

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Journal of Genetics|July 16, 2015
Intragenic haplotype analysis of common HFE mutations in the Portuguese populationSandra Toste, Luís Relvas, Catarina Pinto, et al.
Haematologica|February 8, 2006
Molecular characterization of five Portuguese patients with pyrimidine 5'-nucleotidase deficient hemolytic anemia showing three new P5'N-I mutationsLicínio Manco, Luís Relvas, C Silva Pinto, et al.
European Journal of Haematology|September 18, 2009
Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell diseaseLicínio Manco, José Manuel Vagace, Luís Relvas, et al.
BMC Public Health|March 20, 2024
Sickle cell trait in São Tomé e Príncipe: a population-based prevalence study in women of reproductive ageGuilherme Queiroz, Celdidy Monteiro, Licínio Manco, et al.
Blood Cells, Molecules & Diseases|March 15, 2011
Chronic hemolytic anemia is associated with a new glucose-6-phosphate dehydrogenase in-frame deletion in an older womanLicínio Manco, Janet Pereira, Luís Relvas, et al.
Frontiers in Bioscience (Scholar Edition)|July 4, 2025
Genetic Modifiers of HbF in HbAA and HbAS Women From São Tomé e Príncipe: An Association Study of Common Genetic Variants in <i>BCL11A</i>, <i>MYB</i>, <i>HBG2</i>, and <i>BGLT3</i>Licínio Manco, Afonso Marques Morais, Sara Miguel Almeida, et al.
Hemoglobin|May 31, 2022
Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene ClusterLicínio Manco, Raquel Santos, Catarina Rocha, et al.
Hemoglobin|April 23, 2020
Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia CarriersLicínio Manco, Celeste Bento, Luís Relvas, et al.
Ejhaem|September 2, 2022
Variants in the new E1' cryptic exon of the <i>VHL</i> gene associated with congenital erythrocytosis-Description of three casesCatarina Dantas Rodrigues, Rita Pombal, Janet Pereira, et al.
Blood Cells, Molecules & Diseases|August 14, 2016
Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular studyLicínio Manco, Celeste Bento, Bruno L Victor, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Journal of Genetics|July 16, 2015
Intragenic haplotype analysis of common HFE mutations in the Portuguese populationSandra Toste, Luís Relvas, Catarina Pinto, et al.
Haematologica|February 8, 2006
Molecular characterization of five Portuguese patients with pyrimidine 5'-nucleotidase deficient hemolytic anemia showing three new P5'N-I mutationsLicínio Manco, Luís Relvas, C Silva Pinto, et al.
European Journal of Haematology|September 18, 2009
Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell diseaseLicínio Manco, José Manuel Vagace, Luís Relvas, et al.
BMC Public Health|March 20, 2024
Sickle cell trait in São Tomé e Príncipe: a population-based prevalence study in women of reproductive ageGuilherme Queiroz, Celdidy Monteiro, Licínio Manco, et al.
Blood Cells, Molecules & Diseases|March 15, 2011
Chronic hemolytic anemia is associated with a new glucose-6-phosphate dehydrogenase in-frame deletion in an older womanLicínio Manco, Janet Pereira, Luís Relvas, et al.
Frontiers in Bioscience (Scholar Edition)|July 4, 2025
Genetic Modifiers of HbF in HbAA and HbAS Women From São Tomé e Príncipe: An Association Study of Common Genetic Variants in <i>BCL11A</i>, <i>MYB</i>, <i>HBG2</i>, and <i>BGLT3</i>Licínio Manco, Afonso Marques Morais, Sara Miguel Almeida, et al.
Hemoglobin|May 31, 2022
Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene ClusterLicínio Manco, Raquel Santos, Catarina Rocha, et al.
Hemoglobin|April 23, 2020
Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia CarriersLicínio Manco, Celeste Bento, Luís Relvas, et al.
Ejhaem|September 2, 2022
Variants in the new E1' cryptic exon of the <i>VHL</i> gene associated with congenital erythrocytosis-Description of three casesCatarina Dantas Rodrigues, Rita Pombal, Janet Pereira, et al.
Blood Cells, Molecules & Diseases|August 14, 2016
Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular studyLicínio Manco, Celeste Bento, Bruno L Victor, et al.
Pageof 3