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 *

165 related articles for article (PubMed ID: 12130518)

  • 1. 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]  

  • 2. Severe-glucose-6-phosphate dehydrogenase (G6PD) deficiency associated with chronic hemolytic anemia, granulocyte dysfunction, and increased susceptibility to infections: description of a new molecular variant (G6PD Barcelona).
    Vives Corrons JL; Feliu E; Pujades MA; Cardellach F; Rozman C; Carreras A; Jou JM; Vallespí MT; Zuazu FJ
    Blood; 1982 Feb; 59(2):428-34. PubMed ID: 7055648
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Molecular basis and enzymatic properties of glucose 6-phosphate dehydrogenase volendam, leading to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections.
    Roos D; van Zwieten R; Wijnen JT; Gómez-Gallego F; de Boer M; Stevens D; Pronk-Admiraal CJ; de Rijk T; van Noorden CJ; Weening RS; Vulliamy TJ; Ploem JE; Mason PJ; Bautista JM; Khan PM; Beutler E
    Blood; 1999 Nov; 94(9):2955-62. PubMed ID: 10556177
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. [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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Three new electrophoretically normal glucose-6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: G6PD Ogikubo, Yokohama, and Akita.
    Miwa S; Fujii H; Nakashima K; Miura Y; Yamada K; Hagiwara T; Fukuda M
    Hum Genet; 1978 Nov; 45(1):11-7. PubMed ID: 730178
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Three new variants of glucose-6-phosphate dehydrogenase associated with chronic nonspherocytic hemolytic anemia: G-6-PD Lincoln Park, G-6-PD Arlington Heights, and G-6-PD West Town.
    Honig GR; Habacon E; Vida LN; Matsumoto F; Beutler E
    Am J Hematol; 1979; 6(4):353-60. PubMed ID: 532804
    [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 Beaumont: a new variant with severe enzyme deficiency and chronic nonspherocytic hemolytic anemia.
    Mamlok RJ; Mills GC; Goldblum RM; Daeschner CW
    Enzyme; 1985; 34(1):15-21. PubMed ID: 4085453
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Two new glucose 6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: GD(-) Tokushima and GD(-) Tokyo.
    Miwa S; Ono J; Nakashima K; Abe S; Kageoka T
    Am J Hematol; 1976; 1(4):433-42. PubMed ID: 1008056
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.