ExLibris header image
SFX Logo
Title: Hereditary nonspherocytic hemolytic anemia and hexokinase deficiency
Source:

Blood [0006-4971] Beutler, E yr:1978


Collapse list of basic services Basic
Sorry, no full text available...
Please use the document delivery service (see below)  
Holding information
Holdings in library search engine ALBERT GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Rijksen, G. "Human erythrocyte hexokinase deficiency. Characterization of a mutant enzyme with abnormal regulatory properties." The Journal of clinical investigation 62.2 (1978): 294-301. Link to Full Text for this item Link to SFX for this item
2. Koralkova, P. "Molecular characterization of six new cases of red blood cell hexokinase deficiency yields four novel mutations in HK1." Blood cells, molecules, & diseases 59 (2016): 71-76. Link to SFX for this item
3. Beutler, E. "Downeast anemia (dea), a new mouse model of severe nonspherocytic hemolytic anemia caused by hexokinase (HKI) deficiency." Blood cells, molecules & diseases 27.5 (2001): 850-860. Link to Full Text for this item Link to SFX for this item
4. "Purification and physical properties of hexokinase from human erythrocytes." Biochimica et biophysica acta. 873.3: 335-339. Link to SFX for this item
5. Koralkova, P. "Rare hereditary red blood cell enzymopathies associated with hemolytic anemia - pathophysiology, clinical aspects, and laboratory diagnosis." International Journal of Laboratory Hematology 36.3 (2014): 388-397. Link to Full Text for this item Link to SFX for this item
6. "Hemolytic anemia and hexokinase deficiency associated with malformations." Journal of molecular medicine. 50.17: 849-851. Link to SFX for this item
7. Magnani, M. "Hereditary nonspherocytic hemolytic anemia due to a new hexokinase variant with reduced stability." Blood 66.3 (1985): 690-7. Link to SFX for this item
8. Mates, N. "Proteomic and functional consequences of hexokinase deficiency in glucose-repressible Kluyveromyces lactis." Molecular & cellular proteomics 13.3 (2014): 860-75. Link to Full Text for this item Link to SFX for this item
9. Bain, Barbara J. "A ghostly presence-G6PD deficiency." American journal of hematology 85.4 (2010): 271-271. Link to Full Text for this item Link to SFX for this item
10. de Vooght, K. "First mutation in the red blood cell-specific promoter of hexokinase combined with a novel missense mutation causes hexokinase deficiency and mild chronic hemolysis." Haematologica 94.9 (2009): 1203-1210. Link to Full Text for this item Link to SFX for this item
11. WILLIAMS, TN N. "Red blood cell defects and malaria." Molecular and biochemical parasitology 149.2 (2006): 121-127. Link to SFX for this item
12. Bianchi, M. "Expression, Purification, and Characterization of a Recombinant Erythroid-Specific Hexokinase Isozyme." Blood cells, molecules, & diseases 4.4 (1998): 401-411. Link to Full Text for this item Link to SFX for this item
13. Williams, Thomas N. "Human red blood cell polymorphisms and malaria." Current opinion in microbiology 9.4: 388-394. Link to SFX for this item
14. Kaplan, M. "Neonatal screening for glucose-6-phosphate dehydrogenase deficiency: biochemical versus genetic technologies." Seminars in perinatology 35.3 (2011): 155-161. Link to SFX for this item
15. Friedrich, M. J. J. "Advances reshaping sickle cell therapy." JAMA (Chicago, Ill.) 305.3 (2011): 239-40. Link to SFX for this item
16. Shah, A. "Thalassemia syndromes." Indian journal of medical sciences 58.10 (2004): 445-9. Link to SFX for this item
17. van Wijk, R. "The energy-less red blood cell is lost: erythrocyte enzyme abnormalities of glycolysis." Blood 106.13 (2006): 4034-42. Link to SFX for this item
18. Fermo, E. "Pyruvate kinase deficiency." Haematologica 92.6 (2007): 721-3. Link to SFX for this item
19. Williams, N. "Sickle Cell Trait and the Risk of Plasmodium falciparum Malaria and Other Childhood Diseases." The journal of infectious diseases 192.1 (2005): 178-186. Link to Full Text for this item Link to SFX for this item
20. Magnani, M. "Glucose metabolism in fibroblasts from patients with erythrocyte hexokinase deficiency." Journal of inherited metabolic disease 9.2: 129-139. Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced