E Bardou-Jacquet, ML Island, AM Jouanolle… - Blood Cells, Molecules, …, 2011 - Elsevier We report a patient with a similar phenotype due to two mutations in the SLC11A2 gene, the known p.Gly212Val (G212V) mutation and a novel one, p.Asn491Ser (N491S). To assess the expression of DMT1 in human liver, we studied the expression of the four DMT1 mRNA ...
E Urrechaga, L Borque… - American journal of clinical …, 2011 - 171.67.112.51 Cell counter–based formulas have been used in the differential diagnosis of microcytic anemia. The measurement of RBC subpopulations is now available on the Sysmex XE 5000 analyzer (Sysmex, Kobe, Japan). We describe the new formulas: % microcytic – % ... All 4 versions
CH Weng, JB Chen, J Wang, CC Wu, Y Yu… - Onkologie, 2011 - content.karger.com Background: Castleman's disease (CD) is a rare, benign lymphoproliferative disorder that can involve single lymph node stations or can be systemic. Unicentric CD in patients with microcytic anemia is rarely described in the English literature. Case Report: We describe the case of ... Cited by 1
[PDF] from niscair.res.inMW Akhtar, MY Siddiqui… - Indian Journal of …, 2011 - nopr.niscair.res.in Faqruddam ba Sabab-e-Qillat-e-Faulad (iron deficiency/ microcytic-hypochromic anemia) is responsible for greater morbidity and mortality than any other haematologic disorder, affecting about 25-50% population of developing countries. The incidence of anemia is highest ... Related articles
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