119 related articles for article (PubMed ID: 9446671)
21. Serum iron, transferrin saturation, ferritin, and dietary data in age-related macular degeneration.
Richer S; Rudy D; Statkute L; Karofty K; Frankowski J
Am J Ther; 2002; 9(1):25-8. PubMed ID: 11782816
[TBL] [Abstract][Full Text] [Related]
22. Response to an iron fortification programme in relation to vitamin A status in 6-12-year-old school children.
van Stuijvenberg ME; Kruger M; Badenhorst CJ; Mansvelt EP; Laubscher JA
Int J Food Sci Nutr; 1997 Jan; 48(1):41-9. PubMed ID: 9093548
[TBL] [Abstract][Full Text] [Related]
23. Prevalence of abnormal iron studies in heterozygotes for hereditary hemochromatosis: an analysis of 255 heterozygotes.
Adams PC
Am J Hematol; 1994 Feb; 45(2):146-9. PubMed ID: 8141120
[TBL] [Abstract][Full Text] [Related]
24. The HLA linked iron loading gene in an Afrikaner population.
Meyer TE; Ballot D; Bothwell TH; Green A; Derman DP; Baynes RD; Jenkins T; Jooste PL; du Toit ED; Jacobs PJ
J Med Genet; 1987 Jun; 24(6):348-56. PubMed ID: 2886665
[TBL] [Abstract][Full Text] [Related]
25. Phenotypic expression of the HLA linked iron-loading gene in males over the age of 40 years: a population study using serial serum ferritin estimations.
Meyer T; Baynes R; Bothwell T; Jenkins T; Jooste P; Du Toit E; Martell R; Jacobs P
J Intern Med; 1990 Jun; 227(6):397-406. PubMed ID: 1972175
[TBL] [Abstract][Full Text] [Related]
26. African iron overload.
Kasvosve I; Gangaidzo IT; Gomo ZA; Gordeuk VR
Acta Clin Belg; 2000; 55(2):88-93. PubMed ID: 10881373
[TBL] [Abstract][Full Text] [Related]
27. A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation.
Gochee PA; Powell LW; Cullen DJ; Du Sart D; Rossi E; Olynyk JK
Gastroenterology; 2002 Mar; 122(3):646-51. PubMed ID: 11874997
[TBL] [Abstract][Full Text] [Related]
28. A Japanese family with ferroportin disease caused by a novel mutation of SLC40A1 gene: hyperferritinemia associated with a relatively low transferrin saturation of iron.
Koyama C; Wakusawa S; Hayashi H; Ueno T; Suzuki R; Yano M; Saito H; Okazaki T
Intern Med; 2005 Sep; 44(9):990-3. PubMed ID: 16258219
[TBL] [Abstract][Full Text] [Related]
29. Serum ferritin, iron status and plasma ascorbic acid in 40- to 49-year-old males in the Faroe Islands.
Milman N; Thomsen H; Mathiassen B
Scand J Clin Lab Invest; 1990 Sep; 50(5):559-64. PubMed ID: 2237268
[TBL] [Abstract][Full Text] [Related]
30. A study of serum ferritin in beta thalassemia. Iron deficiency and overload.
Saraya AK; Kumar R; Choudhry VP; Kailash S; Sehgal AK
Am J Clin Pathol; 1985 Jul; 84(1):103-7. PubMed ID: 4014070
[TBL] [Abstract][Full Text] [Related]
31. Relationship of body iron stores to levels of serum ferritin, serum iron, unsaturated iron binding capacity and transferrin saturation in patients with iron storage disease.
Beutler E; Felitti V; Ho NJ; Gelbart T
Acta Haematol; 2002; 107(3):145-9. PubMed ID: 11978935
[TBL] [Abstract][Full Text] [Related]
32. Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3).
Cazzola M; Cremonesi L; Papaioannou M; Soriani N; Kioumi A; Charalambidou A; Paroni R; Romtsou K; Levi S; Ferrari M; Arosio P; Christakis J
Br J Haematol; 2002 Nov; 119(2):539-46. PubMed ID: 12406098
[TBL] [Abstract][Full Text] [Related]
33. Relationship between genotype, assessed by HLA typing, and phenotypic expression of iron status markers in families of 29 probands with hereditary haemochromatosis.
Milman N; Fenger K; Graudal NA; Nielsen LS
Dan Med Bull; 1994 Jun; 41(3):366-70. PubMed ID: 7924465
[TBL] [Abstract][Full Text] [Related]
34. Screening for iron overload in the Turkish population.
Barut G; Balci H; Bozdayi M; Hatemi I; Ozcelik D; Senturk H
Dig Dis; 2003; 21(3):279-85. PubMed ID: 14571105
[TBL] [Abstract][Full Text] [Related]
35. Iron overload in sub-Saharan Africa involves a genetic component.
Nutr Rev; 1992 Aug; 50(8):238-9. PubMed ID: 1407756
[TBL] [Abstract][Full Text] [Related]
36. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
Gottschalk R; Seidl C; Schilling S; Braner A; Seifried E; Hoelzer D; Kaltwasser JP
Eur J Immunogenet; 2000 Jun; 27(3):129-34. PubMed ID: 10940080
[TBL] [Abstract][Full Text] [Related]
37. Diagnosis of hemochromatosis in young subjects: predictive accuracy of biochemical screening tests.
Bassett ML; Halliday JW; Ferris RA; Powell LW
Gastroenterology; 1984 Sep; 87(3):628-33. PubMed ID: 6745616
[TBL] [Abstract][Full Text] [Related]
38. Low serum aluminum values in dialysis patients with increased bone aluminum levels.
van Landeghem GF; D'Haese PC; Lamberts LV; Djukanovic L; Pejanovic S; Goodman WG; De Broe ME
Clin Nephrol; 1998 Aug; 50(2):69-76. PubMed ID: 9725776
[TBL] [Abstract][Full Text] [Related]
39. Survey and clinical application of serum iron, total iron binding capacity, transferrin saturation, and serum ferritin in captive black and white ruffed lemurs (Varecia variegata variegata).
Crawford GC; Andrews GA; Chavey PS; Dunker FH; Garner MM; Sargent EL
J Zoo Wildl Med; 2005 Dec; 36(4):653-60. PubMed ID: 17312723
[TBL] [Abstract][Full Text] [Related]
40. Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y.
Wallace DF; Walker AP; Pietrangelo A; Clare M; Bomford AB; Dixon JL; Powell LW; Subramaniam VN; Dooley JS
J Hepatol; 2002 Apr; 36(4):474-9. PubMed ID: 11943417
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]