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Results: 14

Related Articles by Review for PubMed (Select 7151276)

1.

Pyruvate kinase deficiency: characterization of two new genetic variants.

Dente L, D'Urso M, Di Maio S, Brancaccio V, Luzzatto L.

Clin Chim Acta. 1982 Dec 9;126(2):143-54.

PMID:
7151276
2.

Red cell enzymopathies as a model of inborn errors of metabolism.

Miwa S, Kanno H, Hirono A, Fujii H.

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:112-9. Review.

PMID:
8629088
3.

Biochemical characterization of four new erythrocyte pyruvate kinase variants.

Tegos C, Anagnostoulis G.

Acta Haematol. 1994;92(2):91-6. Review.

PMID:
7817710
4.
5.

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
6.

Pyruvate kinase deficiency: the genotype-phenotype association.

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

Blood Rev. 2007 Jul;21(4):217-31. Epub 2007 Mar 13. Review.

PMID:
17360088
7.

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
8.

[Erythrocyte pyruvate kinase--an enzyme that may have an influence on oxygen transport to tissues].

Dabrowska A.

Postepy Hig Med Dosw. 1997;51(3):305-18. Review. Polish.

PMID:
9333782
9.

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
10.

Pyruvate kinase deficiency.

Miwa S.

Prog Clin Biol Res. 1990;344:843-52. Review.

PMID:
2203063
11.

Pyruvate kinase deficiency and other enzymopathies of the Embden--Meyerhof pathway.

Miwa S.

Clin Haematol. 1981 Feb;10(1):57-80. Review. No abstract available.

PMID:
6260408
12.

[Diagnosis of genetically determined diseases].

Jacobasch G, Kuckelkorn U, Gerth C, Megow D.

Z Med Lab Diagn. 1991;32(3-4):134-40. Review. German.

PMID:
1897289
13.

Hemochromatosis and pyruvate kinase deficiency. Report of a case and review of the literature.

De Braekeleer M, St-Pierre C, Vigneault A, Simard H, de Medicis E.

Ann Hematol. 1991 May;62(5):188-9. Review.

PMID:
2049467
14.

Mutations in pyruvate kinase.

Beutler E, Baronciani L.

Hum Mutat. 1996;7(1):1-6. Review.

PMID:
8664896
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