نتایج جستجو برای: clinical laboratory techniques
تعداد نتایج: 1939517 فیلتر نتایج به سال:
Respiratory Distress Syndrome, which was previously known as Hyaline Membrane Disease (HMD), is among the most common cause of immature neonatal death. The present study has discussed the disease history, pathophysiology, clinical manifestations, laboratory findings, radiologic findings, and differential diagnosis. Meanwhile, recent progresses achieved in the field of treatment using surfactant...
abstract objective: homeostasis model assessment of insulin resistance (homa-ir) is a simple and practical method for estimation of insulin resistance (ir), but a reliable reference interval (ri) of homa-ir is needed to deduce the threshold level to define ir. this ri has been controversial in different populations and even more divergent when considering factors like age, gender and body mass ...
Background & Objective: Appropriate use of laboratory testing is essential for achieving safe and effective care to patient. Insufficient kno...
The history and origins of proficiency testing of clinical laboratories are reviewed. Since the introduction of proficiency testing in the late 1940s, dramatic improvement in laboratory performance has been demonstrated. Nonetheless, the poor performance found two decades earlier was summoned to support the passage of the Clinical Laboratory Improvement Act of 1967 (CLIA '67).
In planning the internal organization of central laboratories, the future needs for clinical chemistry in hospitals must be considered. For the next decade the medical laboratory will primarily be concerned with the interpretation of laboratory data and with organizational problems, such as sample identification, specimen splitting and especially the timing of its service. The consequences for ...
Hemophilia A is a worldwide disorder of coagulation system. It is a male disorder, yet females with hemophilia are rarely seen in communities with high rate of consanguineous marriages. The abnormalities in factor VIII gene transfer as an X-linked pattern in the family, affects as many as one-third of patients who had no family history of abnormality and thus the occurrence of a sporadic mutati...
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