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Molecular analysis of chronic granulomatous disease caused by defects in gp91-phox
(Wiley-lissNew YorkEUA, 1999)
Caracterización clínico - molecular de la enfermedad granulomatosa crónica autosómica recesiva causada por déficit de p47-phox
(Sociedad Médica de Santiago, 2000)
Caracterización molecular en pacientes con enfermedad granulomatosa crónica por deficiencia en p47 phoxMolecular characterization in patients with chronic granulomatous disease due to p47 phox deficiency
(Universidad de Antioquia, Facultad de MedicinaInmunodeficiencias PrimariasMedellín, Colombia, 2021)
Hematologically important mutations: X-linked chronic granulomatous disease (third update)
(ACADEMIC PRESS INC ELSEVIER SCIENCE, 2010)
Chronic granulomatous disease (CGD) is an immunodeficiency disorder affecting about 1 in 250,000 individuals. The disease is caused by a lack of superoxide production by the leukocyte enzyme NADPH oxidase. Superoxide is ...
Estudo genetico-molecular da doença granulomatosa cronica
([s.n.], 2004)
POLYMORPHISM IN THE HMOX1 GENE IS ASSOCIATED WITH HIGH LEVELS OF FETAL HEMOGLOBIN IN BRAZILIAN PATIENTS WITH SICKLE CELL ANEMIA
(Informa HealthcareLondonInglaterra, 2013)
The use of reverse transcription-PCR for the diagnosis of X-linked chronic granulomatous disease
(Associação Brasileira de Divulgação Científica, 2004-05-01)
Chronic granulomatous disease (CGD) is an inherited disorder of the innate immune system characterized by a defective oxidative burst of phagocytes and subsequent impairment of their microbicidal activity. Mutations in one ...