المؤلفون: Licínio Manco, Paula Gonçalves, Patrícia Antunes, Filomena Maduro, Augusto Abade, M. Letícia Ribeiro

المصدر: Haematologica, Vol 92, Iss 12 (2007)

مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

العلاقة: https://haematologica.org/article/view/4678Test; https://doaj.org/toc/0390-6078Test; https://doaj.org/toc/1592-8721Test

الوصول الحر: https://doaj.org/article/85c8e1e969564530af486a580a05c8eaTest

المؤلفون: Álvaro M. Monge Calleja, Marina Lourenço, Marta Macedo, Rosa Ramos Gaspar, M. Letícia Ribeiro, Ana Luísa Santos

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::c4096e940e859e51a5d3442304c722d9Test
https://doi.org/10.21203/rs.3.rs-2591410/v1Test

المؤلفون: M. Letícia Ribeiro, Janet Pereira, Elisabete Cunha, Manuela Alvarez, Luís Relvas, Valeria Moreira, Tabita M. Maia, Licínio Manco, Celeste Bento

المصدر: Hemoglobin. 44:113-117

مصطلحات موضوعية: Adult, Male, Adolescent, Thalassemia, Quantitative Trait Loci, Clinical Biochemistry, Locus (genetics), Quantitative trait locus, Biology, Polymorphism, Single Nucleotide, Young Adult, Gene Frequency, medicine, Humans, Child, Fetal Hemoglobin, Genetics (clinical), Aged, Genetics, Portugal, beta-Thalassemia, Biochemistry (medical), Genetic variants, Genetic Variation, Hematology, Middle Aged, Locus Control Region, medicine.disease, language.human_language, Child, Preschool, language, Female, Portuguese

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18a84653ec7912af42978fb7bbfa21b5Test
https://doi.org/10.1080/03630269.2020.1753766Test

المؤلفون: Ana Bela Sarmento, M. Letícia Ribeiro, Catarina Silva, Teresa Fidalgo, Patrícia Martinho, Licínio Manco

المصدر: Blood Coagulation & Fibrinolysis. 29:528-532

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Adolescent, Genotype, Population sample, Single-nucleotide polymorphism, 030204 cardiovascular system & hematology, Polymorphism, Single Nucleotide, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Polymorphism (computer science), Internal medicine, ABO blood group system, medicine, Humans, Genetic Predisposition to Disease, cardiovascular diseases, Factor XI, Portugal, business.industry, Fibrinogen, Venous Thromboembolism, Hematology, General Medicine, Middle Aged, equipment and supplies, 030104 developmental biology, Genetic Loci, Female, Portuguese population, business, Venous thromboembolism

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e39d0adbcffa05250107199ad533e22Test
https://doi.org/10.1097/mbc.0000000000000753Test

المؤلفون: Ramune Reliene, Mariagabriella Mariani, Alberto Zanella, Walter H. Reinhart, M. Leticia Ribeiro, Emanuele Miraglia Del Giudice, Silverio Perrotta, Achille Iolascon, Stefan Eber, Hans U. Lutz, Red Cells Articles, Red Cells

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://bloodjournal.hematologylibrary.org/content/100/6/2208.full.pdfTest.

وصف الملف: application/pdf

العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.318.1981Test; http://bloodjournal.hematologylibrary.org/content/100/6/2208.full.pdfTest

الإتاحة: http://bloodjournal.hematologylibrary.org/content/100/6/2208.full.pdfTest

المؤلفون: Clara Pereira, Licínio Manco, Luís Relvas, Augusto Abade, M. Letícia Ribeiro, Celeste Bento

المصدر: Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP

مصطلحات موضوعية: Male, 0302 clinical medicine, hemic and lymphatic diseases, gamma-Globins, Child, Fetal Hemoglobin, Genetics, 0303 health sciences, Nuclear Proteins, Beta thalassemia, Hematology, Middle Aged, Child, Preschool, Molecular Medicine, Female, Adult, Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Adolescent, Kruppel-Like Transcription Factors, Single-nucleotide polymorphism, KLF1, Biology, Polymorphism, Single Nucleotide, HBG2, Proto-Oncogene Proteins c-myb, 03 medical and health sciences, GTP-Binding Proteins, Internal medicine, Fetal hemoglobin, medicine, Xmni polymorphism, Humans, HSP70 Heat-Shock Proteins, Genetic variability, Molecular Biology, Aged, 030304 developmental biology, Portugal, Genome, Human, beta-Thalassemia, Cell Biology, Peptide Elongation Factors, medicine.disease, Repressor Proteins, Endocrinology, Genetic Loci, Case-Control Studies, Mutation, Linear Models, Carrier Proteins, Genome-Wide Association Study, 030215 immunology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07cc1fe610b7fc2845f558dfcab1efeeTest
https://doi.org/10.1016/j.bcmd.2015.02.001Test

المؤلفون: M. Letícia Ribeiro, Luís Relvas, Tabita M. Maia, Janet Pereira, Licínio Manco, Rui M. M. Brito, Bruno L. Victor, Celeste Bento, Carlos Seabra

المصدر: Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
CIÊNCIAVITAE

مصطلحات موضوعية: Models, Molecular, 0301 basic medicine, Hemolytic anemia, Protein Conformation, Reticulocytosis, Mutation, Missense, Biology, Compound heterozygosity, medicine.disease_cause, Frameshift mutation, 03 medical and health sciences, Exon, 0302 clinical medicine, Catalytic Domain, medicine, Humans, Missense mutation, Frameshift Mutation, Molecular Biology, Genetics, Mutation, Portugal, Glucose-6-Phosphate Isomerase, Anemia, Hemolytic, Congenital Nonspherocytic, Sequence Analysis, DNA, Cell Biology, Hematology, medicine.disease, Molecular biology, Null allele, 3. Good health, 030104 developmental biology, 030220 oncology & carcinogenesis, Molecular Medicine, medicine.symptom

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d733a77f38d3e174d9b940fa8e4e6f1cTest

المؤلفون: Nadiene Alves Martins, E. D. Gonçalves, C. Silva Pinto, M. Letícia Ribeiro, A. Markoff, Patrícia Martinho, Dânia Sofia Marques, Ramon Salvado, Teresa Fidalgo

المصدر: Haemophilia. 18:129-138

مصطلحات موضوعية: Genetics, Mutation, Haemophilia A, Prenatal diagnosis, Hematology, General Medicine, Biology, medicine.disease_cause, Haemophilia, medicine.disease, Bioinformatics, Phenotype, Genotype, medicine, Missense mutation, Multiplex ligation-dependent probe amplification, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::d283597c329e3453fb86523b95a04318Test
https://doi.org/10.1111/j.1365-2516.2011.02570.xTest

المؤلفون: M. Letícia Ribeiro, Licínio Manco, Janet Pereira, Umbelina Rebelo, Luís Relvas, Ana Isabel Crisóstomo, Celeste Bento

المصدر: CIÊNCIAVITAE

مصطلحات موضوعية: Anemia, Hemolytic, Heterozygote, Reading Frames, Anemia, Glucosephosphate Dehydrogenase, Biology, X-inactivation, Glucosefosfato Desidrogenase, Loss of heterozygosity, chemistry.chemical_compound, Reticulocyte, X Chromosome Inactivation, hemic and lymphatic diseases, Anemia Hemolítica, medicine, Humans, Glucose-6-phosphate dehydrogenase, Allele, Molecular Biology, Aged, Sequence Deletion, Delecção de Sequência, Heterozygote advantage, Cell Biology, Hematology, medicine.disease, medicine.anatomical_structure, chemistry, Hemizygote, Chronic Disease, Immunology, Molecular Medicine, Female, Granulocytes

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7448a454ac5a675ce9365ced118ac20aTest
https://doi.org/10.1016/j.bcmd.2011.02.001Test

المؤلفون: Maria Jesus Trovoada, Luís Varandas, Luís Relvas, Manuela Alvarez, Licínio Manco, M. Letícia Ribeiro, Kovana M. Loua, Ana Paula Arez, Tamba S. Millimono, David Albuquerque, Dinora Lopes, Fátima Nogueira, Silvia L. Rath

المصدر: Annals of Human Biology. 38:378-381

مصطلحات موضوعية: Aging, Physiology, Epidemiology, Population, Ferroportin, Black People, Exon, Gene Frequency, Genetics, Chromosomes, Human, Humans, education, Cation Transport Proteins, Gene, Allele frequency, Africa South of the Sahara, education.field_of_study, biology, Haplotype, Public Health, Environmental and Occupational Health, Molecular biology, Transmembrane protein, Amino Acid Substitution, Haplotypes, Mutation, Mutation (genetic algorithm), biology.protein

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f9a0ad851c90c79189954481a04e0b4Test
https://doi.org/10.3109/03014460.2010.541496Test