All individuals with variants in gene HMOX1

5 entries on 1 page. Showing entries 1 - 5.
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00057173 - PubMed: Gil 2013, Journal: Gil 2013 111 controls compared with 107 sickle cell anemia patients - - Brazil - - - - - anemia, sickle cell, HBFQTL significantly higher HbF levels compared to AA and AT genotypes (P 0.0131) 1 30 Johan den Dunnen
00057175 - {PMID:Yachie:1999:9884342} 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Japan - >06y - - regular transfusions of erythrocytes HMOX1D see paper; severe growth retardation, persistent hemolytic anemia characterized by marked erythrocyte fragmentation and intravascular hemolysis, with paradoxical increase serum haptoglobin and low bilirubin, abnormal coagulation/fibrinolysis system, associated with elevated thrombomodulin and von Willebrand factor, indicated severe, persistent endothelial damage; electron microscopy renal glomeruli revealed endothelium detachment, with subendothelial deposition of unidentified material; iron deposition renal/hepatic tissue, ... 2 1 Johan den Dunnen
00057176 - PubMed: Yamada 2000 comparison 101 smokers with/100 without chronic pulmonary emphysema F;M - Japan - - - - - COPD - 1 159 Johan den Dunnen
00057177 - PubMed: Yamada 2000 comparison 101 smokers with/100 without chronic pulmonary emphysema F;M - Japan - - - - - COPD - 1 181 Johan den Dunnen
00057178 - PubMed: Yamada 2000 comparison 101 smokers with/100 without chronic pulmonary emphysema F;M - Japan - - - - - COPD - 1 62 Johan den Dunnen
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