The value of complete blood count parameters in the preoperative diagnosis of parathyroid tumor. [PDF]
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The diagnosis and clinical characterization of -α3.7/--SEA thalassemia patients: two cases report. [PDF]
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Hematological and mineral alterations associated with subclinical mastitis in dairy cattle following the foot-and-mouth disease outbreak in West Java, Indonesia. [PDF]
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Performance evaluation of the new Dymind automated hematology analyzer. [PDF]
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Although alpha thalassemia trait may be diagnosed in the neonate by the presence of hemoglobin Barts, no simple screeing test for this disorder is available. This study was performed to determine whether the mean corpucular volume (MCV) and mean corpuscular hemoglobin (MCH) could serve this purpose.
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Beta (β)-thalassemia is one of the most common hemoglobinopathies worldwide, creating major public health problems and social burdens in many regions. Screening for β-thalassemia carriers is crucial for controlling this condition. To investigate the effectiveness of mean corpuscular volume (MCV) and mean corpuscular hemoglobin (MCH) for screening β ...
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Mean corpuscular hemoglobin concentration in anoxic lung disease
Journal of Applied Physiology, 1961An analysis of patients suffering from polycythemia rubra vera, congenital heart disease, and anoxic lung disease is presented. The effect on the mean corpuscular hemoglobin concentration (MCHC) of anoxia and increased erythropoesis is compared. The results suggest that in chronic anoxic lung disease both desaturation and increased erythropoesis may ...
D, VEREL, D F, KERRIDGE
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