Search Results - "Collazo Abal, Cristina"
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Identification of a new mutation in the human xanthine dehydrogenase responsible for xanthinuria type I
Published in Advances in laboratory medicine (01-12-2021)“…Hereditary xanthinuria is a rare, autosomal and recessive disorder characterized by severe hypouricemia and increased xanthine excretion, caused by a…”
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Identificación de una nueva mutación en el gen humano xantina causante de la xantinuria tipo I
Published in Advances in laboratory medicine (01-12-2021)“…La xantinuria es una enfermedad rara, de herencia autosómica recesiva caracterizada por la presencia de hipouricemia y elevada excreción de xantina, provocada…”
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Identificación de una nueva mutación en el gen humano xantina causante de la xantinuria tipo I
Published in Advances in laboratory medicine (01-12-2021)Get full text
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Pseudothrombocytopenia by ethylenediaminetetraacetic acid can jeopardize patient safety - report
Published in EJIFCC (20-03-2020)“…Pseudothrombocytopenia by ethylenediaminetetraacetic acid (EDTA) is an infrequent phenomenon of platelet agglutination due to the presence of antiplatelet…”
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Pseudothrombocytopenia by ethylenediaminetetraacetic acid can jeopardize patient safety - report
Published in EJIFCC (01-03-2020)Get full text
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