BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 35695473)

  • 1. A case of G6PD Utrecht associated with β-thalassemia responding to splenectomy.
    Yang K; Liu X; Chen K; Luo S; Kong W; Huang W; Xiao J
    Pediatr Blood Cancer; 2022 Sep; 69(9):e29837. PubMed ID: 35695473
    [TBL] [Abstract][Full Text] [Related]  

  • 2. G6Pd Kanazawa: a new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
    Kitao T; Ito K; Hattori K; Matsuki T; Yoneyama Y
    Acta Haematol; 1982; 68(2):131-5. PubMed ID: 6812368
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new glucose-6-phosphate dehydrogenase variant with congenital nonspherocytic hemolytic anemia (G6PD Genova). Biochemical characterization and mosaicism expression in the heterozygote.
    Gaetani GF; Galiano S; Melani C; Miglino M; Forni GL; Napoli G; Perrone L; Ferraris AM
    Hum Genet; 1990 Mar; 84(4):337-40. PubMed ID: 2307454
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP). Molecular study of a new variant (G6PD Clinic) with markedly acidic pH optimum.
    Vives-Corrons JL; Pujades MA; Petit J; Colomer D; Corbella M; Aguilar i Bascompte JL; Merino A
    Hum Genet; 1989 Jan; 81(2):161-4. PubMed ID: 2912886
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chronic nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency: report of two families with novel mutations causing G6PD Bangkok and G6PD Bangkok Noi.
    Tanphaichitr VS; Hirono A; Pung-amritt P; Treesucon A; Wanachiwanawin W
    Ann Hematol; 2011 Jul; 90(7):769-75. PubMed ID: 21302115
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian child.
    Gangarossa S; Romano V; Miraglia del Giudice E; Perrotta S; Iolascon A; Schiliro G
    Acta Haematol; 1995; 93(1):36-9. PubMed ID: 7725848
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. G6PD (Dublin): chronic non-spherocytic haemolytic anaemia resulting from glucose-6-phosphate dehydrogenase deficiency in an Irish kindred.
    McCann SR; Smithwick AM; Temperley IJ; Tipton K
    J Med Genet; 1980 Jun; 17(3):191-3. PubMed ID: 7401130
    [TBL] [Abstract][Full Text] [Related]  

  • 9. G6PD-Puerto Limón: a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
    Elizondo J; Sáenz GF; Páez CA; Ramón M; García M; Gutiérrez A; Estrada M
    Hum Genet; 1982; 62(2):110-2. PubMed ID: 7160841
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chronic non-spherocytic haemolytic disorders associated with glucose-6-phosphate dehydrogenase variants.
    Fiorelli G; Martinez di Montemuros F; Cappellini MD
    Baillieres Best Pract Res Clin Haematol; 2000 Mar; 13(1):39-55. PubMed ID: 10916677
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Distinct phenotypic expression of two de novo missense mutations affecting the dimer interface of glucose-6-phosphate dehydrogenase.
    van Wijk R; Huizinga EG; Prins I; Kors A; Rijksen G; Bierings M; van Solinge WW
    Blood Cells Mol Dis; 2004; 32(1):112-7. PubMed ID: 14757424
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Deletion of leucine 61 in glucose-6-phosphate dehydrogenase leads to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections.
    van Bruggen R; Bautista JM; Petropoulou T; de Boer M; van Zwieten R; Gómez-Gallego F; Belohradsky BH; Hartwig NG; Stevens D; Mason PJ; Roos D
    Blood; 2002 Aug; 100(3):1026-30. PubMed ID: 12130518
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gd(-) Rennes, a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia found in France.
    Picat C; Etiemble J; Boivin P; Le Prise PY
    Hum Genet; 1980; 55(1):125-7. PubMed ID: 7450748
    [TBL] [Abstract][Full Text] [Related]  

  • 14. G6PD deficiency with hemolytic anemia due to a rare gene deletion--a report of the first case in Malaysia.
    Ainoon O; Boo NY; Yu YH; Cheong SK; Hamidah HN
    Hematology; 2006 Apr; 11(2):113-8. PubMed ID: 16753852
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular basis of chronic non-spherocytic haemolytic anaemia: a new G6PD variant (393 Arg----His) with abnormal KmG6P and marked in vivo instability.
    Filosa S; Calabrò V; Vallone D; Poggi V; Mason P; Pagnini D; Alfinito F; Rotoli B; Martini G; Luzzatto L
    Br J Haematol; 1992 Jan; 80(1):111-6. PubMed ID: 1536798
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [The C1155G mutation of the red blood cell glucose-6-phosphate dehydrogenase gene in a subject with severe hereditary chronic nonspherocytic anaemia].
    Burzyńska B; Adamowicz-Salach A; Płochocka D; Gołaszewska E; Witos I
    Med Wieku Rozwoj; 2009; 13(2):136-9. PubMed ID: 19837994
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A family of new glucose 6-phosphate dehydrogenase (G 6 PD) variant associated with chronic nonspherocytic hemolytic anemia: G 6 PD Kurume (author's transl)].
    Kaneto A; Motokawa M; Koga T; Shimokawa Y; Tanikawa K; Fujii H; Miwa S
    Rinsho Ketsueki; 1979 Jan; 20(1):82-9. PubMed ID: 423378
    [No Abstract]   [Full Text] [Related]  

  • 18. Glucose-6-phosphate dehydrogenase Guadalajara--a case of chronic non-spherocytic haemolytic anaemia responding to splenectomy and the role of splenectomy in this disorder.
    Hamilton JW; Jones FG; McMullin MF
    Hematology; 2004 Aug; 9(4):307-9. PubMed ID: 15621740
    [TBL] [Abstract][Full Text] [Related]  

  • 19. G6PD Varadero. A new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
    Estrada M; García M; Gutiérrez A; Quintero I; González R
    Vox Sang; 1982; 43(2):102-4. PubMed ID: 7123903
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Direct detection for G6PD Bangkok and G6PD Bangkok Noi mutations in the families with chronic nonspherocytic hemolytic anemia (CNSHA).
    Glomglao W; Chansing K; Treesucon A; Siraprapapat P; Thongnoppakhun W; Sanpakit K; Tanphaichitr VS
    Int J Lab Hematol; 2015 Apr; 37(2):e21-4. PubMed ID: 24923766
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.