Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 10

1.

Five unknown mutations in the LR pyruvate kinase gene associated with severe hereditary nonspherocytic haemolytic anaemia in France.

Rouger H, Valentin C, Craescu CT, Galactéros F, Cohen-Solal M.

Br J Haematol. 1996 Mar;92(4):825-30.

PMID:
8616073
2.
3.

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
4.

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
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.

Mutations in pyruvate kinase.

Beutler E, Baronciani L.

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

PMID:
8664896
7.

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
8.

[Screening methods in genetic diagnosis of hereditary protein C deficiency].

Dávid M, Losonczy H, Nagy A, Kutscher G, Meyer M.

Orv Hetil. 1999 Jan 17;140(3):125-32. Review. Hungarian.

PMID:
9990817
9.

Biochemical characterization of four new erythrocyte pyruvate kinase variants.

Tegos C, Anagnostoulis G.

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

PMID:
7817710
10.

Red blood cell PK deficiency: An update of PK-LR gene mutation database.

Canu G, De Bonis M, Minucci A, Capoluongo E.

Blood Cells Mol Dis. 2016 Mar;57:100-9. doi: 10.1016/j.bcmd.2015.12.009. Epub 2016 Jan 12. Review.

PMID:
26832193
Items per page

Supplemental Content

Write to the Help Desk