Found: 11
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Genetic polymorphisms and susceptibility to lung disease.
- Published in:
- Journal of Negative Results in Biomedicine, 2006, v. 5, p. 5, doi. 10.1186/1477-5751-5-5
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- Article
Intravenous Bevacizumab Therapy in a Patient with Hereditary Hemorrhagic Telangiectasia, ENG E137K, Alcoholic Cirrhosis, and Portal Hypertension.
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- Case Reports in Gastroenterology, 2017, v. 11, n. 2, p. 293, doi. 10.1159/000475748
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- Article
Sideroblastic anemia, iron overload, and ALAS2 R452S in African-American males: Phenotype and genotype features of five unrelated patients.
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- American Journal of Hematology, 2011, v. 86, n. 9, p. 787, doi. 10.1002/ajh.22088
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- Article
Iron overload and prolonged ingestion of iron supplements: Clinical features and mutation analysis of hemochromatosis‐associated genes in four cases.
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- American Journal of Hematology, 2006, v. 81, n. 10, p. 760, doi. 10.1002/ajh.20714
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- Article
Hemojuvelin (HJV) mutations in persons of European, African-American and Asian ancestry with adult onset haemochromatosis.
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- British Journal of Haematology, 2004, v. 127, n. 2, p. 224, doi. 10.1111/j.1365-2141.2004.05165.x
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- Article
Human transferrin G277S mutation: a risk factor for iron deficiency anaemia.
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- British Journal of Haematology, 2001, v. 115, n. 2, p. 329, doi. 10.1046/j.1365-2141.2001.03096.x
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- Article
Mild Iron Overload in an African American Man with SLC40A1 D270V.
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- Acta Haematologica, 2012, v. 128, n. 1, p. 28, doi. 10.1159/000337034
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- Article
Multi-Organ Iron Overload in an African-American Man with ALAS2 R452S and SLC40A1 R561G.
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- Acta Haematologica, 2009, v. 120, n. 3, p. 168, doi. 10.1159/000181183
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- Article
SLC40A1 c.1402G→A Results in Aberrant Splicing, Ferroportin Truncation after Glycine 330, and an Autosomal Dominant Hemochromatosis Phenotype.
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- Acta Haematologica, 2007, v. 118, n. 4, p. 237, doi. 10.1159/000112830
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- Article
Hemochromatosis and Severe Iron Overload Associated with Compound Heterozygosity for TFR2 R455Q and Two Novel Mutations TFR2 R396X and G792R.
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- Acta Haematologica, 2006, v. 115, n. 1/2, p. 102, doi. 10.1159/000089474
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- Article
Polymorphisms in iron-responsive binding protein 2 and lack of association with sporadic Parkinson's disease.
- Published in:
- Movement Disorders, 2002, v. 17, n. 6, p. 1302, doi. 10.1002/mds.10253
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- Article