The evaluation of two genetic polymorphisms of paraoxonase 1 in patients with pulmonary embolism
Sign Up to like & getrecommendations! Published in 2018 at "Journal of Clinical Laboratory Analysis"
DOI: 10.1002/jcla.22455
Abstract: Pulmonary embolism (PE) is caused by some genetic factors for more than half patients. Paraoxonase 1 (PON1) has significant anti‐oxidative and anti‐inflammatory effects. According to our knowledge, there is no study researching the relation between… read more here.
Keywords: evaluation two; pulmonary embolism; genetic polymorphisms; two genetic ... See more keywords
The Coexistence of Two Genetic Astrocytopathies—Megalencephalic Leukoencephalopathy and Vanishing White Matter Disease—in an Indian Child
Sign Up to like & getrecommendations! Published in 2022 at "Neuropediatrics"
DOI: 10.1055/s-0042-1760367
Abstract: Abstract A 9-month-old male child, born of second-degree consanguinity, presented with a progressively enlarging head since early infancy. The child had normal early development, but further acquisition of milestones after 6 months was delayed. He… read more here.
Keywords: two genetic; genetic astrocytopathies; white matter; coexistence two ... See more keywords