Found: 11
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A case of hemoglobin Hiroshima (β146 histidine to aspartic acid) with compensatory erythremia and undetectable HbA₁c.
- Published in:
- 2012
- By:
- Publication type:
- journal article
A case of hemoglobin Hiroshima (β146 histidine to aspartic acid) with compensatory erythremia and undetectable HbA.
- Published in:
- 2012
- By:
- Publication type:
- Report
High Incidence of α-Thalassemia, Hemoglobin E, and Glucose-6-Phosphate Dehydrogenase Deficiency in Populations of Malaria-Endemic Southern Shan State, Myanmar.
- Published in:
- International Journal of Hematology, 2005, v. 82, n. 2, p. 119, doi. 10.1532/IJH97.05028
- By:
- Publication type:
- Article
Hb Nishinomiya [Leu-Gly-inserted between codons 69(E13) and 70(E14) of beta]: a novel unstable hemoglobin with reduced oxygen affinity found in a patient with spherocytic hemolysis.
- Published in:
- 2002
- By:
- Publication type:
- journal article
A Case of Alpha-Thalassemia-2 Associated with Pulmonary Infarction.
- Published in:
- Lung, 2006, v. 184, n. 4, p. 223, doi. 10.1007/s00408-005-2587-7
- By:
- Publication type:
- Article
Japanese β°-thalassemia: Molecular characterization of a novel insertion causing a stop codon.
- Published in:
- American Journal of Hematology, 1996, v. 52, n. 1, p. 39, doi. 10.1002/(SICI)1096-8652(199605)52:1<39::AID-AJH6>3.0.CO;2-7
- By:
- Publication type:
- Article
A wider molecular spectrum of β-thalassaemia in Myanmar.
- Published in:
- British Journal of Haematology, 2002, v. 117, n. 4, p. 988, doi. 10.1046/j.1365-2141.2002.03539.x
- By:
- Publication type:
- Article
The COL4A5 gene in Japanese Alport syndrome patients: spectrum of mutations of all exons. The Japanese Alport Network.
- Published in:
- 1996
- By:
- Publication type:
- journal article
A splicing mutation in the α5(IV) collagen gene of a family with Alport's syndrome.
- Published in:
- Kidney International, 1993, v. 43, n. 5, p. 1116, doi. 10.1038/ki.1993.157
- By:
- Publication type:
- Article
Band 4.2 Shiga: 317 CGC → TGC in compound heterozygotes with 142 GCT → ACT results in band 4.2 deficiency and microspherocytosis.
- Published in:
- British Journal of Haematology, 1995, v. 91, n. 2, p. 333, doi. 10.1111/j.1365-2141.1995.tb05299.x
- By:
- Publication type:
- Article
A 6-year-old Girl With Hemoglobin H Disease.
- Published in:
- 2011
- By:
- Publication type:
- Case Study