Publications by authors named "Li-Qin Ling"

β-Thalassemia (β-thal) is caused by mutations on the β-globin genes, causing reduced (β) or absent (β) synthesis of the β chains of hemoglobin (Hb). In this report, a 28-year-old male patient with anemia and jaundice, was diagnosed with triple-heterozygous β-thal [an IVS-II-654 (C>T) mutation, a Hb Zürich-Langstrasse (: c.151A>T) mutation and a Hb G-Siriraj (: c.

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Article Synopsis
  • - This study investigates how normalizing clotting times for lupus anticoagulant (LA) tests can improve diagnostic performance and reduce variability across different reagent batches by using various denominators.
  • - Results showed that normalization effectively eliminated significant differences between reagent batches and yielded comparable diagnostic efficacy across different reference intervals (RIs), with a specific focus on a more sensitive LA test when normalized.
  • - The findings suggest that normalizing test results can minimize the need for new RIs with each reagent batch and demonstrate that day-to-day variations in clotting times do not compromise the effectiveness of normalization methods.
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Background: Acute pancreatitis (AP) is associated with high complications. Early, reliable prediction of mortality may improve patient management.

Methods: We retrospectively reviewed medical records of 1,599 patients with AP treated at a single large hospital in southwest China.

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Hemoglobin H (Hb H) disease is usually characterized by the existence of Hb H, which influences the degree of functional anemia. We here report a patient with a rare Hb H disease genotype (-/-α), who was observed to paradoxically have no detectable Hb H fraction on electrophoresis. To date, the reason why the quantity of Hb H component and the clinical presentation in Hb H disease vary widely is still incompletely understood.

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Objective: To explore a better method to adjust platelet counts for light transmission aggregometry (LTA).

Methods: Blood samples from 36 healthy participants aged from 18 to 50 yr. were collected.

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Objectives: To study the effects of Danqi Capsule on platelet function in healthy people.

Methods: Sixteen healthy volunteer were divided into low dose (4 capsules/time, 3 times/d) and high dose group (6 capsules/time, 3 times/d), and received Danqi Capsule by orally administration for 2 weeks. The venous blood were collect at 3 time points: one week before taking Danqi Capsule (control), one week after taking Danqi Capsule (1 week), two week after taking Danqi Capsule (2 weeks).

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Light transmission aggregometry (LTA) is the "gold standard" for platelet function assessment, but it is time-consuming and labor intensive. Recently, an automated platelet aggregation method has been developed on a routine coagulation analyzer (Sysmex CS-2100i). In this study, the performances of CS-2100i including repeatability, correlation with a reference aggregometer (Chrono-log Model 700), and the threshold limitation of platelet counts in platelet-rich plasma (PRP) were evaluated for clinical use.

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Aim: Imperialine is an effective compound in the traditional Chinese medicine chuanbeimu (Bulbus Fritillariae Cirrhosae) that has been used as antitussive/expectorant in a clinical setting. In this study we investigated the absorption characteristics of imperialine in intestinal segments based on an evaluation of its physicochemical properties.

Methods: Caco-2 cells were used to examine uptake and transport of imperialine in vitro, and a rat in situ intestinal perfusion model was used to characterize the absorption of imperialine.

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