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Results: 1 to 20 of 140

1.

Hereditary pyruvate kinase abnormalities associated with erythrocytosis.

Rosa R, Max-Audit I, Izrael V, Beuzard Y, Thillet J, Rosa J.

Am J Hematol. 1981;10(1):47-55.

PMID:
7258181
[PubMed - indexed for MEDLINE]
2.

Study of a kindred with partial deficiency of red cell 2,3-diphosphoglycerate mutase (2,3-DPGM) and compensated hemolysis.

Travis SF, Martinez J, Garvin J Jr, Atwater J, Gillmer P.

Blood. 1978 Jun;51(6):1107-16.

PMID:
148301
[PubMed - indexed for MEDLINE]
Free Article
3.

[Diphosphoglyceromutase deficiency: new cases associated with erythrocytosis].

Galacteros F, Rosa R, Prehu MO, Najean Y, Calvin MC.

Nouv Rev Fr Hematol. 1984;26(2):69-74. French.

PMID:
6326048
[PubMed - indexed for MEDLINE]
4.

Pyruvate kinase hyperactivity genetically determined metabolic consequences and molecular characterization.

Max-Audit I, Rosa R, Marie J.

Blood. 1980 Nov;56(5):902-9.

PMID:
7426754
[PubMed - indexed for MEDLINE]
Free Article
5.

Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose-6-phosphate dehydrogenase (G-6-PD) deficiency.

Hoyer JD, Allen SL, Beutler E, Kubik K, West C, Fairbanks VF.

Am J Hematol. 2004 Apr;75(4):205-8.

PMID:
15054810
[PubMed - indexed for MEDLINE]
6.

[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
[PubMed - indexed for MEDLINE]
7.

Erythrocyte pyruvate kinase deficiency. The influence of physiologically important metabolites on the function of normal and defective enzymes.

Lakomek M, Winkler H, Pekrun A, Krüger N, Sander M, Huppke P, Schröter W.

Enzyme Protein. 1994-1995;48(3):149-63.

PMID:
8589802
[PubMed - indexed for MEDLINE]
8.

Autosomal Dominant familial erythrocytosis due to autonomous erythropoietin production.

Distelhorst CW, Wagner DS, Goldwasser E, Adamson JW.

Blood. 1981 Dec;58(6):1155-8.

PMID:
7306703
[PubMed - indexed for MEDLINE]
Free Article
9.

[Idiopathic familial erythrocytosis. Report on a family with autosomal dominant inheritance].

Queisser W, Heim ME, Schmitz JM, Worst P.

Dtsch Med Wochenschr. 1988 May 27;113(21):851-6. German.

PMID:
3371213
[PubMed - indexed for MEDLINE]
10.

Characterization of the pyruvate kinase which induces the low 2,3-DPG level of fetal rabbit red cells.

Franzke R, Jelkmann W.

Pflugers Arch. 1982 Jul;394(1):21-5.

PMID:
7122212
[PubMed - indexed for MEDLINE]
11.

Hereditary erythrocyte pyruvate-kinase (PK) deficiency and chronic hemolytic anemia: clinical, genetic and molecular studies in six new Spanish patients.

Vives-Corrons JL, Marie J, Pujades MA, Kahn A.

Hum Genet. 1980;53(3):401-8.

PMID:
7372343
[PubMed - indexed for MEDLINE]
12.

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
[PubMed - indexed for MEDLINE]
13.

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.

PMID:
17550844
[PubMed - indexed for MEDLINE]
Free Article
14.

Erythrocyte enzyme activities in myelodysplastic syndromes: elevated pyruvate kinase activity.

Tani K, Fujii H, Takahashi K, Kodo H, Asano S, Takaku F, Miwa S.

Am J Hematol. 1989 Feb;30(2):97-103.

PMID:
2913762
[PubMed - indexed for MEDLINE]
15.

Novel type of red blood cell pyruvate kinase hyperactivity predicts a remote regulatory locus involved in PKLR gene expression.

van Oirschot BA, Francois JJ, van Solinge WW, van Wesel AC, Rijksen G, van Amstel HK, van Wijk R.

Am J Hematol. 2014 Apr;89(4):380-4. doi: 10.1002/ajh.23647. Epub 2014 Mar 3.

PMID:
24375447
[PubMed - indexed for MEDLINE]
16.

Increased adsorption of cytoplasmic proteins to the erythrocyte membrane in ATP-depleted normal and pyruvate kinase-deficient mature cells and reticulocytes.

Allen DW, Groat JD, Finkel B, Rank BH, Wood PA, Eaton JW.

Am J Hematol. 1983 Feb;14(1):11-25.

PMID:
6837565
[PubMed - indexed for MEDLINE]
17.

2,3-DPG levels in relation to red cell enzyme activities in rat fetuses and hypoxic newborns.

Jelkmann W, Bauer C.

Pflugers Arch. 1980 Dec;389(1):61-8.

PMID:
6451226
[PubMed - indexed for MEDLINE]
18.

Pyruvate kinase deficiency hemolytic anemia: enzymatic characterization studies in twelve patients.

Shinohara K, Tanaka KR.

Hemoglobin. 1980;4(5-6):611-25.

PMID:
7440218
[PubMed - indexed for MEDLINE]
19.

Red cell pyruvate kinase deficiency in neonatal jaundice cases in India.

Kedar PS, Warang P, Colah RB, Mohanty D.

Indian J Pediatr. 2006 Nov;73(11):985-8.

PMID:
17127778
[PubMed - indexed for MEDLINE]
20.

Hereditary high-adenosine triphosphate syndrome: study of a new variant.

Bapat JP, Baxi AJ.

Biochem Genet. 1981 Oct;19(9-10):1017-22.

PMID:
6460500
[PubMed - indexed for MEDLINE]

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