Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 136

Similar articles for PubMed (Select 728372)

1.

Hereditary pyruvate kinase deficiency: role of the abnormal enzyme in red cell pathophysiology.

Zanella A, Rebulla P, Vullo C, Izzo C, Tedesco F, Sirchia G.

Br J Haematol. 1978 Dec;40(4):551-62.

PMID:
728372
2.

Four new pyruvate kinase (PK) variants and a classical PK deficiency.

Miwa S, Nakashima K, Ariyoshi K, Shinohara K, Oda E.

Br J Haematol. 1975 Jan;29(1):157-69.

PMID:
1201198
3.

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
4.

Erythrocytic pyruvate kinase deficiency and hemolytic anemia inherited as a dominant trait.

Etiemble J, Picat C, Dhermy D, Buc HA, Morin M, Boivin P.

Am J Hematol. 1984 Oct;17(3):251-60.

PMID:
6475936
5.

Pyruvate kinase Greensboro. A four-generation study of a high K0.5s (phosphoenolpyruvate) variant.

Valentine WN, Herring WB, Paglia DE, Steuterman MC, Brockway RA, Nakatani M.

Blood. 1988 Sep;72(3):1054-9. Erratum in: Blood 1988 Dec;72(6):2082.

7.
9.

Erythrocyte pyruvate kinase deficiency: characterization of a new variant (PK "Aarau").

Lakomek M, Winkler H, Scharnetzky M, Tillmann W, Laier G, Marti HR, Schröter W.

Blut. 1984 Mar;48(3):123-9.

PMID:
6697002
10.

Determination of erythrocyte pyruvate kinase deficiency in Basenjis with chronic hemolytic anemia.

Giger U, Noble NA.

J Am Vet Med Assoc. 1991 May 15;198(10):1755-61.

PMID:
2071475
11.
12.

A red cell pyruvate kinase mutant with normal L-type PK in the liver.

Etiemble J, Picat C, Boivin P.

Hum Genet. 1982;61(3):256-8.

PMID:
7173870
13.

Simultaneous inheritance of mutant isoenzymes of erythrocyte pyruvate kinase associated with chronic haemolytic anaemia.

Pagila DE, Gray GR, Growe GH, Valentine WN.

Br J Haematol. 1976 Sep;34(1):61-8.

PMID:
952770
14.

Concomitance of an active and an inactive mutant of red cell pyruvate kinase (PK).

Zanella A, Rebulla P, Izzo C, Zanuso F, Sirchia G.

Scand J Haematol. 1979 Feb;22(2):145-53.

PMID:
432551
15.

Haemolytic anaemia with hereditary pyruvate kinase instability developing acute leukaemia.

Goebel KM, Goebel FD, Janzen R, Kaffarnik H.

Scand J Haematol. 1975 May;14(4):249-57.

PMID:
1057238
16.
17.

Identification of an erythrocyte pyruvate kinase variant in a family from Latium with non-spherocytic congenital haemolytic anaemia.

Papa G, De Laurenzi A, Isacchi GC, Bonifazi G, Parziale L, Salvati AM.

Acta Haematol. 1979;61(5):288-94.

PMID:
111457
18.
19.

Seven pyruvate kinase variants characterized by the ICSH recommended methods.

Miwa S, Fujii H, Takegawa S, Nakatsuji T, Yamato K, Ishida Y, Ninomiya N.

Br J Haematol. 1980 Aug;45(4):575-83.

PMID:
7426438
20.

Transgenic rescue of hemolytic anemia due to red blood cell pyruvate kinase deficiency.

Kanno H, Utsugisawa T, Aizawa S, Koizumi T, Aisaki K, Hamada T, Ogura H, Fujii H.

Haematologica. 2007 Jun;92(6):731-7.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk