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Items: 5

1.

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.

2.

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
3.

Generalized hexokinase deficiency in the blood cells of a patient with nonspherocytic hemolytic anemia.

Rijksen G, Akkerman JW, van den Wall Bake AW, Hofstede DP, Staal GE.

Blood. 1983 Jan;61(1):12-8.

4.

Hereditary nonspherocytic hemolytic anemia and hexokinase deficiency.

Beutler E, Dyment PG, Matsumoto F.

Blood. 1978 May;51(5):935-40.

5.

[Hereditary nonspherocytic hemolytic anemia caused by a deficiency in erythrocytic hexokinase associated with glycogenosis of muscles].

Badalian OL, Bondarenko ES, Ermil'chenko GV, Idel'son LI, Sitnikov VF, Kharit IO.

Klin Med (Mosk). 1970 Aug;48(8):156-63. Russian. No abstract available.

PMID:
5273487

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