Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Patricia N. Konrad"'
Autor:
Patricia N. Konrad, Anthony Shaw
Publikováno v:
Current Problems in Cancer. 8:1-44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e7604ac2abd34a7e8edc5a9f563f297
https://doi.org/10.1016/s0147-0272(84)80014-8
https://doi.org/10.1016/s0147-0272(84)80014-8
Publikováno v:
Clinica Chimica Acta. 73:395-405
A mutant erythrocyte isozyme of pyruvate kinase (PK) (ATP:pyruvate phosphotransferase, EC 2.7.1.40) has been found in association with chronic hemolytic anemia in two siblings who were doubly heterozygous for the isozyme and for quantitative PK defic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4438893a9c50a8f88f7fa3a4b722bca5
https://doi.org/10.1016/0009-8981(76)90140-6
https://doi.org/10.1016/0009-8981(76)90140-6
Autor:
Dennis J. McCarthy, Patricia N. Konrad, William N. Valentine, Donlad E. Paglia, Alvin M. Mauer
Publikováno v:
The Journal of Pediatrics. 82:456-460
Two brothers with congenital nonspherocytic hemolytic anemia and neurologic disease were found to have erythrocyte and leukocyte phosphoglycerate kinase deficiency. Elevated levels of red cell dihydroxyacetone phosphate and 2,3-diphosphoglycerate wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34446224c548fc529f4d16e474fd941f
https://doi.org/10.1016/s0022-3476(73)80120-9
https://doi.org/10.1016/s0022-3476(73)80120-9
Publikováno v:
Blood. 36:797-808
Hereditary hydroxyacl-glutathione hydrolase (Glyoxalase II) deficiency was demonstrated in both homozygous and heterozygous form in kindred in which hereditary elliptocytosis was inherited independently. Homozygotes and heterozygotes for the enzyme d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2504d187da8c0ea6fbe22842bb6138dd
https://doi.org/10.1182/blood.v36.6.797.797
https://doi.org/10.1182/blood.v36.6.797.797
Publikováno v:
Blood. 41:857-875
Twenty-one enzymatic activities and red cell glutathione content are compared in cord blood, dyserythropoietic disorders, normal subjects, and subjects with hemolytic syndromes and reticulocytosis approximating that of the newborn. The dyserythropoie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::674842c151194a577f827d7e6780a1a7
https://doi.org/10.1182/blood.v41.6.857.857
https://doi.org/10.1182/blood.v41.6.857.857
Publikováno v:
British Journal of Haematology. 23:107-112
Summary. In one type of hereditary dyserythropoietic anaemia, HEMPAS (hereditary erythroblastic multinuclearity with a positive acidified-serum test) striking increases in the activity of some, but not all, erythrocyte enzymes have been detected in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab2a9c54f4d1d063f7693010a0061977
https://doi.org/10.1111/j.1365-2141.1972.tb03464.x
https://doi.org/10.1111/j.1365-2141.1972.tb03464.x
Autor:
Helen M. Anderson, Susan R. Harris, Patricia N. Konrad, William N. Valentine, Klaus K. Kürschner, Donald E. Paglia, Ernst R. Jaffé
Publikováno v:
Blood. 39:674-684
A 29-yr-old black woman was found to have a long-standing, nonspherocytic hemolytic disorder associated with a marked reduction in the activity of erythrocyte ribosephosphate pyrophosphokinase (RPK, PRPP synthetase, E.C. 2.7.6.1). Although the patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::971d52b8c330b3af03ebf1cae8136900
https://doi.org/10.1182/blood.v39.5.674.674
https://doi.org/10.1182/blood.v39.5.674.674
Publikováno v:
The Journal of Pediatrics. 82:80-82
7. Holland, N. H., Jurichs, R., and Clemons, G.: Detection of asymptomatic urinary tract infection in girls, J. Ky. Med, Assoc. 67: 662, 1969. 8. Dodge, W. F., West, E. F., Fras, P. A., and Travis, L. B.: Detection of bacteriuria in children, J. PEDI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e953be87103be0982475e6af273399d1
https://doi.org/10.1016/s0022-3476(73)80016-2
https://doi.org/10.1016/s0022-3476(73)80016-2
Publikováno v:
American journal of clinical pathology. 68(2)
A mutant isozyme of erythrocyte pyruvate kinase was found in a family of French-Canadian ancestry in association with hemolytic anemia. The isozyme was characterized by normal maximal activity, p H optimum, heat stability, and fructosediphosphate act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cdadadf9f741234b6c8f948e5bc1c22
https://pubmed.ncbi.nlm.nih.gov/18004
https://pubmed.ncbi.nlm.nih.gov/18004
Publikováno v:
The New England journal of medicine. 286(11)
In some families with hemolytic anemia and a low level of reduced glutathione in erythrocytes, the disorder is associated with a deficiency of glutathione synthetase, the second of two enz...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::738b46b9e0be868439d42cd2dfe14c98
https://pubmed.ncbi.nlm.nih.gov/5058793
https://pubmed.ncbi.nlm.nih.gov/5058793