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Items: 1 to 20 of 32

1.

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
2.
3.

[Hemolytic anemia due to abnormalities in erythrocyte nucleotide metabolism].

Masuda M, Mizoguchi H.

Nihon Rinsho. 1996 Sep;54(9):2473-7. Review. Japanese.

PMID:
8890581
4.

Introduction to discussion of regulation of erythrocyte glycolysis.

Valentine WN.

Exp Eye Res. 1971 May;11(3):273-9. Review. No abstract available.

PMID:
4941673
5.

Three cases of hereditary nonspherocytic hemolytic anemia associated with red blood cell glutathione deficiency.

Hirono A, Iyori H, Sekine I, Ueyama J, Chiba H, Kanno H, Fujii H, Miwa S.

Blood. 1996 Mar 1;87(5):2071-4. Review.

6.

[Pyrimidine 5'-nucleotidase deficiency as the congenital cause of nonspherocytic hemolytic anemia].

Pekrun A, Lakomek M, Eng W, Schröter W.

Dtsch Med Wochenschr. 1993 Sep 10;118(36):1276-80. Review. German.

PMID:
8375297
7.

Pyruvate kinase deficiency.

Miwa S, Fujii H.

Clin Biochem. 1990 Apr;23(2):155-7. Review.

PMID:
2197027
8.

Chronic non-spherocytic haemolytic anaemia due to congenital pyrimidine 5' nucleotidase deficiency: 25 years later.

Vives i Corrons JL.

Baillieres Best Pract Res Clin Haematol. 2000 Mar;13(1):103-18. Review.

PMID:
10916681
9.

Erythrocyte disorders of purine and pyrimidine metabolism.

Valentine WN, Paglia DE.

Hemoglobin. 1980;4(5-6):669-81. Review.

PMID:
6254919
10.

[Clinical significance and interpretation of red cell enzyme analyses].

Kanno H, Fujii H.

Rinsho Byori. 2001 Nov;Suppl 116:139-47. Review. Japanese.

PMID:
11797375
11.

[Pathophysiology and laboratory tests of hemolytic anemia: with special reference to erythroenzymopathies].

Fujii H, Miwa S.

Rinsho Byori. 1989 Dec;37(12):1331-43. Review. Japanese.

PMID:
2693773
12.

Red cell pyruvate kinase deficiency: molecular and clinical aspects.

Zanella A, Fermo E, Bianchi P, Valentini G.

Br J Haematol. 2005 Jul;130(1):11-25. Review.

PMID:
15982340
13.

Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinical and molecular studies.

Corrons JL, Alvarez R, Pujades A, Zarza R, Oliva E, Lasheras G, Callis M, Ribes A, Gelbart T, Beutler E.

Br J Haematol. 2001 Feb;112(2):475-82. Review.

PMID:
11167850
14.

Glucose-6-phosphate isomerase deficiency.

Kugler W, Lakomek M.

Baillieres Best Pract Res Clin Haematol. 2000 Mar;13(1):89-101. Review.

PMID:
10916680
15.
16.

The nonspherocytic congenital haemolytic anaemias.

de Gruchy GC, Grimes AJ.

Br J Haematol. 1972 Sep;23:Suppl:19-26. Review. No abstract available.

PMID:
4567191
17.

Erythrocyte enzyme disorders in children.

Sullivan DW, Glader BE.

Pediatr Clin North Am. 1980 May;27(2):449-62. Review.

PMID:
6247687
18.

Recent progress in the molecular genetic analysis of erythroenzymopathy.

Fujii H, Miwa S.

Am J Hematol. 1990 Aug;34(4):301-10. Review.

PMID:
2164322
19.

Rare hereditary red blood cell enzymopathies associated with hemolytic anemia - pathophysiology, clinical aspects, and laboratory diagnosis.

Koralkova P, van Solinge WW, van Wijk R.

Int J Lab Hematol. 2014 Jun;36(3):388-97. doi: 10.1111/ijlh.12223. Review.

PMID:
24750686
20.

Red cell pyruvate kinase deficiency: from genetics to clinical manifestations.

Zanella A, Bianchi P.

Baillieres Best Pract Res Clin Haematol. 2000 Mar;13(1):57-81. Review.

PMID:
10916678

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