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 *

141 related articles for article (PubMed ID: 574811)

  • 1. Heterozygote detection in glucose-6-phosphate dehydrogenase deficiency: limitation of hair follicle analysis.
    Vermorken AJ; Spierenburg GT; van Bennekom CA; de Bruyn CH; Oei TL; Staal GE; Geerdink RA
    Clin Genet; 1979 Nov; 16(5):353-6. PubMed ID: 574811
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Family investigations of erythrocyte glucose-6-phosphate dehydrogenase in favism.
    Rozynkowa D; Gebala A; Zagórski Z
    Pol Med J; 1970; 9(5):1093-9. PubMed ID: 5510280
    [No Abstract]   [Full Text] [Related]  

  • 3. Glucose-6-phosphate dehydrogenase deficiency: biochemical and histochemical studies on hair roots for carrier detection.
    Vermorken AJ; Wirtz P; Spierenburg GT; van Bennekom CA; de Bruyn CH; Oei TL
    J Clin Chem Clin Biochem; 1979 May; 17(5):325-9. PubMed ID: 469470
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Favism in a Portuguese family due to a deficient glucose-phosphate dehydrogenase variant (Canton) or (cpanton-like) type.
    Kahn A; Marie J; Desbois JC; Boivin P
    Acta Haematol; 1976; 56(1):58-64. PubMed ID: 822676
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Favism in GdMediterranean heterozygous females.
    Sanna G; De Virgiliis S; Palmas C; Argiolu F; Frau F; Cao A
    Pediatr Res; 1979 Jul; 13(7):812-6. PubMed ID: 481952
    [No Abstract]   [Full Text] [Related]  

  • 6. [Favism - a familial enzymatic defect of the red blood cells in a 7-year-old girl].
    Pohorecka J; Jabłońska-Skwiecińska E; Powiertowska-Ryszka G
    Pediatr Pol; 1982; 57(9):731-4. PubMed ID: 7170153
    [No Abstract]   [Full Text] [Related]  

  • 7. Glucose-6 phosphate dehydrogenase deficiency: an easy and sensitive quantitative assay for the detection of female heterozygotes in red blood cells.
    Solem E
    Clin Chim Acta; 1984 Sep; 142(2):153-60. PubMed ID: 6499202
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Population screening for glucose-6-phosphate dehydrogenase deficiency on the Baleares.
    Miguel A; Ramon M; Petitpierre E; Goos CM; Vermeesch-Markslag AM; Vermorken AJ
    Hum Genet; 1983; 64(2):176-9. PubMed ID: 6885055
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Human hair follicles may be used for population screening of heterozygotes of glucose-6-phosphate dehydrogenase deficiency.
    Vermorken AJ; Markslag AM; Goos CM; Miguel A; Ramon M; Petitpierre E
    Clin Genet; 1982 Aug; 22(2):57-61. PubMed ID: 7172478
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Glucose-6 phosphate dehydrogenase mosaicism: utilization as a tracer in the study of the development of hair root cells.
    Gartler SM; Gandini E; Angioni G; Argiolas N
    Ann Hum Genet; 1969 Oct; 33(2):171-6. PubMed ID: 5383983
    [No Abstract]   [Full Text] [Related]  

  • 11. The suitability of saliva for detection of glucose-6-phosphate dehydrogenase deficiency.
    Beamont AH; Miguel A; Goos CM; Vermeesch-Markslag AM; Hermans A; Vermorken AJ
    Mol Biol Rep; 1988; 13(2):73-8. PubMed ID: 3221843
    [TBL] [Abstract][Full Text] [Related]  

  • 12. G6PD Aures: a new mutation (48 Ile-->Thr) causing mild G6PD deficiency is associated with favism.
    Nafa K; Reghis A; Osmani N; Baghli L; Benabadji M; Kaplan JC; Vulliamy TJ; Luzzatto L
    Hum Mol Genet; 1993 Jan; 2(1):81-2. PubMed ID: 8490627
    [No Abstract]   [Full Text] [Related]  

  • 13. [Favism in Polish families].
    Jabłońska-Skwiecińska E; Pogłód R; Skrobowska A
    Pol Tyg Lek; 1990 Sep 17-24; 45(38-39):778-81. PubMed ID: 2095545
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Polish variant of glucose-6-phosphate dehydrogenase (G-6-PD Lublin).
    Pawlak AL; Zagórski Z; Rozynkowa D; Horst A
    Humangenetik; 1970; 10(4):340-3. PubMed ID: 5493238
    [No Abstract]   [Full Text] [Related]  

  • 15. Erythrocyte glucose-6-phosphate dehydrogenase (1.1.1.49) deficiency in Antalya province, Turkey: an epidemiologic and biochemical study.
    Aksu TA; Esen F; Dolunay MS; Alicigüzel Y; Yücel G; Cali S; Baykal Y
    Am J Epidemiol; 1990 Jun; 131(6):1094-7. PubMed ID: 2343862
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Combined erythrocyte phosphohexose isomerase and glucose-6-phosphate dehydrogenase deficiency.
    Sanpitak N; Supalert Y; Chayutimonkul L; Flatz G
    Hum Hered; 1973; 23(1):83-7. PubMed ID: 4742044
    [No Abstract]   [Full Text] [Related]  

  • 17. Heterogeneity of "Mediterranean type" glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain and description of two new variants associated with favism.
    Vives Corrons JL; Pujades A
    Hum Genet; 1982; 60(3):216-21. PubMed ID: 7106752
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Double heterozygosity for glucose-6-phosphate dehydrogenase deficiency.
    Chan TK; Lai MC
    J Med Genet; 1971 Jun; 8(2):149-52. PubMed ID: 5096537
    [No Abstract]   [Full Text] [Related]  

  • 19. [Electrophoretic and kinetic properties of erythrocyte glucose-6-phosphate dehydrogenase (Gd) in hereditary enzyme deficiency. A new variant of glucose-6-phosphate dehydrogenase : Gd Kremenchug].
    Tokarev YN; Chernyak NB; Batishchev AI; Lamzina NV; Alexeyev GA
    Nouv Rev Fr Hematol (1978); 1978; 20(4):557-64. PubMed ID: 752149
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Family studies of erythrocyte glucose-6-phosphate dehydrogenase in favism].
    Rozynkowa D; Gebala A; Zagórski Z
    Pol Tyg Lek; 1970 Feb; 25(6):201-4. PubMed ID: 5436736
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.