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Items: 1 to 20 of 52

1.

A Case Report of Congenital Non-spherocytic Hemolytic Anemia in a Patient from India.

Sonaye R, Sombans S, Ramphul K.

Cureus. 2018 Apr 13;10(4):e2478. doi: 10.7759/cureus.2478.

2.

Allogeneic bone marrow transplantation for treatment of severe hemolytic anemia attributable to hexokinase deficiency.

Khazal S, Polishchuk V, Manwani D, Gallagher PG, Prinzing S, Mahadeo KM.

Blood. 2016 Aug 4;128(5):735-7. doi: 10.1182/blood-2016-03-702860. Epub 2016 Jun 13. No abstract available.

3.

Gene expression and biological significance of hexokinase in erythroid cells.

Murakami K, Kanno H, Tancabelic J, Fujii H.

Acta Haematol. 2002;108(4):204-9. Review.

PMID:
12432216
4.

HK Utrecht: missense mutation in the active site of human hexokinase associated with hexokinase deficiency and severe nonspherocytic hemolytic anemia.

van Wijk R, Rijksen G, Huizinga EG, Nieuwenhuis HK, van Solinge WW.

Blood. 2003 Jan 1;101(1):345-7. Epub 2002 Aug 8.

5.

Downeast anemia (dea), a new mouse model of severe nonspherocytic hemolytic anemia caused by hexokinase (HK(1)) deficiency.

Peters LL, Lane PW, Andersen SG, Gwynn B, Barker JE, Beutler E.

Blood Cells Mol Dis. 2001 Sep-Oct;27(5):850-60.

PMID:
11783948
6.

Hexokinase: gene structure and mutations.

Kanno H.

Baillieres Best Pract Res Clin Haematol. 2000 Mar;13(1):83-8. Review.

PMID:
10916679
7.

Deficiencies of glycolytic enzymes as a possible cause of hemolytic anemia.

Martinov MV, Plotnikov AG, Vitvitsky VM, Ataullakhanov FI.

Biochim Biophys Acta. 2000 Mar 6;1474(1):75-87.

PMID:
10699493
8.

The molecular basis of disorders of red cell enzymes.

McMullin MF.

J Clin Pathol. 1999 Apr;52(4):241-4. Review. No abstract available.

9.

[Hereditary hemolytic anemia due to abnormal enzymes of the glycolytic pathway].

Omine M.

Nihon Rinsho. 1996 Sep;54(9):2460-6. Review. Japanese.

PMID:
8890579
10.

Hemolytic anemias due to erythrocyte enzyme deficiencies.

Jacobasch G, Rapoport SM.

Mol Aspects Med. 1996 Apr;17(2):143-70.

PMID:
8813716
11.
12.

Hexokinase mutations that produce nonspherocytic hemolytic anemia.

Bianchi M, Magnani M.

Blood Cells Mol Dis. 1995;21(1):2-8.

PMID:
7655856
13.

The role of red cell aging in the diagnosis of glycolytic enzyme defects.

Staal GE, Rijksen G.

Adv Exp Med Biol. 1991;307:239-49. No abstract available.

PMID:
1805589
14.

Congenital non-spherocytic haemolytic anaemias.

Zanella A, Colombo MB, Rossi F, Merati G, Sirchia G.

Haematologica. 1989 Jul-Aug;74(4):387-96. Review.

PMID:
2551797
15.

Frequency of glucose-6-phosphate dehydrogenase, pyruvate kinase and hexokinase deficiency in the Saudi population.

el-Hazmi MA, Al-Swailem AR, Al-Faleh FZ, Warsy AS.

Hum Hered. 1986;36(1):45-9.

PMID:
3949360
16.

Hereditary nonspherocytic hemolytic anemia due to a new hexokinase variant with reduced stability.

Magnani M, Stocchi V, Cucchiarini L, Novelli G, Lodi S, Isa L, Fornaini G.

Blood. 1985 Sep;66(3):690-7.

17.

Hemolytic anemias and erythrocyte enzymopathies.

Valentine WN, Tanaka KR, Paglia DE.

Ann Intern Med. 1985 Aug;103(2):245-57. Review.

PMID:
2990276
18.

Molecular aspects of erythroenzymopathies associated with hereditary hemolytic anemia.

Miwa S, Fujii H.

Am J Hematol. 1985 Jul;19(3):293-305. Review.

PMID:
2990202
19.

Platelet functions and energy metabolism in a patient with hexokinase deficiency.

Akkerman JW, Rijksen G, Gorter G, Staal GE.

Blood. 1984 Jan;63(1):147-53.

20.

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