These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 6025012)

  • 21. A case of haemolytic anaemia due to pyruvate kinase deficiency.
    Hanel HK; Harvald B; Mor G; Christensen N; Deckert T
    Scand J Haematol; 1967; 4(1):53-60. PubMed ID: 6031894
    [No Abstract]   [Full Text] [Related]  

  • 22. Three cases in two families with congenital nonspherocytic hemolytic anemia due to defective glucosephosphate isomerase: GPI Matsumoto.
    Miwa S; Nakashima K; Tajiri M; Ono J; Abe S
    Nihon Ketsueki Gakkai Zasshi; 1975 Jun; 38(3):238-47. PubMed ID: 1243218
    [No Abstract]   [Full Text] [Related]  

  • 23. [Enzymatic erythropathies in children].
    Kovalev IuR; Osipov AI
    Pediatriia; 1966 Aug; 45(8):69-76. PubMed ID: 6004020
    [No Abstract]   [Full Text] [Related]  

  • 24. [Intra-erythrocyte enzymes; analysis of 200 cases].
    Vovan L; Perrimond H; Orsini A
    Mars Med; 1971; 108(2):91-7. PubMed ID: 5548386
    [No Abstract]   [Full Text] [Related]  

  • 25. Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell disease.
    Manco L; Vagace JM; Relvas L; Rebelo U; Bento C; Villegas A; Letícia Ribeiro M
    Eur J Haematol; 2010 Jan; 84(1):89-90. PubMed ID: 19758413
    [No Abstract]   [Full Text] [Related]  

  • 26. [Erythrocytic pyruvate kinase. II. Enzymatic heterogeneity of deficiencies. Studies concerning 28 cases with congenital hemolytic anemia].
    Boivin P; Galand C; Demartial MC
    Nouv Rev Fr Hematol; 1972; 12(5):569-94. PubMed ID: 4266429
    [No Abstract]   [Full Text] [Related]  

  • 27. [Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia].
    Shalev O; Leibowitz G; Brok-Simoni F
    Harefuah; 1994 Jun; 126(12):699-702, 764, 763. PubMed ID: 7927011
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [From gene to disease; hereditary non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency].
    de Vooght KM; van Wijk R; Nieuwenhuis HK; Ploos van Amstel JK; Rijksen G; van Solinge WW
    Ned Tijdschr Geneeskd; 2002 Sep; 146(39):1828-31. PubMed ID: 12382367
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Hereditary high-adenosine triphosphate syndrome: study of a new variant.
    Bapat JP; Baxi AJ
    Biochem Genet; 1981 Oct; 19(9-10):1017-22. PubMed ID: 6460500
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel missense mutation in glucose-6-phosphate dehydrogenase gene causing chronic nonspherocytic hemolytic anemia in an Indian family.
    Edison ES; Melinkeri SR; Chandy M
    Ann Hematol; 2006 Dec; 85(12):879-80. PubMed ID: 16944148
    [No Abstract]   [Full Text] [Related]  

  • 31. Glucose 6-phosphate dehydrogenase Palermo R257M: a novel variant associated with chronic non-spherocytic haemolytic anaemia.
    Rigano P; Fabiano C; Pojero F; Niceta M; Pecoraro A; Maggio A; Sammarco P
    Br J Haematol; 2010 Apr; 149(2):296-7. PubMed ID: 20085579
    [No Abstract]   [Full Text] [Related]  

  • 32. [Congenital non-spherocytic anemias].
    Vacca G
    Minerva Med; 1968 Nov; 59(88):4727-30. PubMed ID: 5697156
    [No Abstract]   [Full Text] [Related]  

  • 33. [Hexokinase activity of erythrocytes in cancer patients].
    Sensini A; Braussi M; Spadoni M; Giacchi R
    Quad Sclavo Diagn; 1981 Dec; 17(4):431-7. PubMed ID: 7347823
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Problems of erythrocyte metabolism in anemias with pyruvate kinase deficiency].
    Busch D
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1965; 83(4):395-406. PubMed ID: 4160310
    [No Abstract]   [Full Text] [Related]  

  • 35. [6 cases of inherited nonspherocytic hemolytic anemia associated with a deficit of 6-phosphogluconate dehydrogenase in the erythrocytes].
    Idel'son LI; Ermil'chenko GV
    Probl Gematol Pereliv Krovi; 1970 Mar; 15(3):32-40. PubMed ID: 5449823
    [No Abstract]   [Full Text] [Related]  

  • 36. [Effect of oxyfedrine on the enzymatic activity and on energy rich phosphates of isolated ischemic guinea pig heart].
    Moser K; Lujf A
    Arzneimittelforschung; 1969 Mar; 19(3):305-8. PubMed ID: 5818777
    [No Abstract]   [Full Text] [Related]  

  • 37. [Congenital non spherocytic hemolytic anemia due to lack of glucose-6-phosphate dehydrogenase (G-6-PD)].
    Brunetti P; Nenci GG; Parma A; Berardi G; Migliorini E
    Haematologica; 1965; 50(5):359-401. PubMed ID: 4954293
    [No Abstract]   [Full Text] [Related]  

  • 38. Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism.
    Jablonska-Skwiecinska E; Lewandowska I; Plochocka D; Topczewski J; Zimowski JG; Klopocka J; Burzynska B
    Hum Mutat; 1999; 14(6):477-84. PubMed ID: 10571945
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Congenital hemolytic anemias with glutatione metabolism disorders (excluding glucose-6-phosphate dehydrogenase deficiency)].
    Boivin P
    Minerva Pediatr; 1968 Dec; 20(51):2659-66. PubMed ID: 4309730
    [No Abstract]   [Full Text] [Related]  

  • 40. Haemoglobin Köln in a Jewish family.
    Hällén J; Charlesworth D; Lehmann H
    Acta Med Scand; 1972 Mar; 191(3):177-80. PubMed ID: 5033708
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.