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期刊名:Biomedica

缩写:BIOMEDICA

ISSN:0120-4157

e-ISSN:2590-7379

IF/分区:0.7/Q4

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共收录本刊相关文章索引1552
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Leticia Bequer,Tahiry Gómez,José Luis Molina et al. Leticia Bequer et al.
Introduction: The use of experimental models is essential to study the pathophysiological mechanisms of diabetes. Objectives: To compa...
José Enrique Velásquez-Hurtado,Yuleika Rodríguez,Marco Gonzáles et al. José Enrique Velásquez-Hurtado et al.
Introduction: Despite the reduction of poverty in Perú, the prevalence of anemia in the country remains high. Objective: To identify ...
John Fredy Nieto-Ríos,Lina Maria Serna-Higuita,Catalina Ocampo-Kohn et al. John Fredy Nieto-Ríos et al.
Introduction: Delayed graft function occurs in about 20 to 50 percent of kidney transplants. Objective: To describe the behavior of ur...
Yermis Carolina Rocha,Juan Álvaro López,Julio Cesar Orrego et al. Yermis Carolina Rocha et al.
Introduction: Chronic granulomatous disease is a primary immunodeficiency that results from mutations in proteins of the NADPH oxidase system that affect the microbicidal activity of phagocytes. Immune reconstitution by h...
Julián Alfredo Fernández-Niño,Eduardo Bustos-Vázquez Julián Alfredo Fernández-Niño
The growing number of patients with complex clinical profiles related to chronic diseases has contributed to the increasingly widespread use of the term 'multimorbidity'. A suitable measurement of this condition is essential to epidemiologi...
Carlos Andrés Ossa,Gustavo Molina,Alicia María Cock-Rada Carlos Andrés Ossa
The Li-Fraumeni syndrome is characterized clinically by the appearance of tumors in multiple organs generally at an early age. This hereditary condition is caused by germinal mutations in the TP53 gene, which codifies for the tumoural suppr...
Gerzaín Rodríguez,Elga Vargas,Claudia Abaúnza et al. Gerzaín Rodríguez et al.
Necrolytic migratory erythema is a rare paraneoplastic dermatosis that may be the first clinical manifestation of the glucagonoma syndrome, a disorder characterized by mucocutaneous rash, glucose intolerance, hypoaminoacidemia, hyperglucago...