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Items: 1 to 20 of 304

1.

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.

2.

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.

4.

Hereditary nonspherocytic hemolytic anemia and hexokinase deficiency.

Beutler E, Dyment PG, Matsumoto F.

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

5.

Congenital nonspherocytic hemolytic anemia with an unstable hexokinase variant.

Board PG, Trueworthy R, Smith JE, Moore K.

Blood. 1978 Jan;51(1):111-8.

6.

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.

7.
8.

Human erythrocyte hexokinase deficiency: a new variant with abnormal kinetic properties.

Magnani M, Stocchi V, Canestrari F, Dachà M, Balestri P, Farnetani MA, Giorgi D, Fois A, Fornaini G.

Br J Haematol. 1985 Sep;61(1):41-50.

PMID:
4052330
9.

Red cell adenylate kinase deficiency associated with hereditary nonspherocytic hemolytic anemia: clinical and biochemical studies.

Miwa S, Fujii H, Tani K, Takahashi K, Takizawa T, Igarashi T.

Am J Hematol. 1983 Jun;14(4):325-33.

PMID:
6305188
11.
12.

Two cases of red cell aldolase deficiency associated with hereditary hemolytic anemia in a Japanese family.

Miwa S, Fujii H, Tani K, Takahashi K, Takegawa S, Fujinami N, Sakurai M, Kubo M, Tanimoto Y, Kato T, Matsumoto N.

Am J Hematol. 1981 Dec;11(4):425-37.

PMID:
7331996
13.

[New variant of glucose-6-phosphate dehydrogenase (G-6-PD "Kaluga") from erythrocytes of a patient with chronic nonspherocytic hemolytic anemia].

Shatskaia TL, Krasnopol'skaia KD, Idel'son LI.

Vopr Med Khim. 1976 Nov-Dec;22(6):764-8. Russian.

PMID:
17221
14.

Hexokinase mutations that produce nonspherocytic hemolytic anemia.

Bianchi M, Magnani M.

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

PMID:
7655856
15.

Non-spherocytic haemolytic anaemia in mother and son associated with hexokinase deficiency.

Newman P, Muir A, Parker AC.

Br J Haematol. 1980 Dec;46(4):537-47.

PMID:
7437332
16.

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.

17.

Compartmentation of hexokinase in human blood cells. Characterization of soluble and particulate enzymes.

Rijksen G, Staal GE, Beks PJ, Streefkerk M, Akkerman JW.

Biochim Biophys Acta. 1982 Dec 17;719(3):431-7.

PMID:
7150652
18.

Glucose-6-phosphate isomerase deficiency-Nahariya: extreme in vitro and in vivo lability of the mutant enzyme.

Rijksen G, Jansen G, Manaster J, Ezekiel E, Streichman S, Staal GE.

Isr J Med Sci. 1984 Jun;20(6):529-34.

PMID:
6469574
19.
20.

[Rare case of hereditary nonspherocytic anemia caused by glyceraldehydephosphate dehydrogenase deficiency in erythrocytes].

Reznik BIa, Soroka IuA.

Probl Gematol Pereliv Krovi. 1972 Aug;17(8):53-4. Russian. No abstract available.

PMID:
4265893

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