Clinical haemochromatosis in HFE mutation carriers [4] (multiple letters)

Lancet

Volumn 360, Issue 9330, 2002, Pages 411-412

  Poullis, A ^a   Moodie, S J ^a   Maxwell, J D ^a   Cox, Timothy ^g   Rochette, Jacques ^g   Camaschella, Clara ^g   Walker, Ann ^g   Robson, Kathryn ^b   Allen, K J ^d   Warner, B ^c   Delatycki, M B ^c   Beutler, Ernest ^e   Felitti, Vincent ^f   Koziol, James A ^f   Gelbart, Terri ^f  

^a ST GEORGE S HOSPITAL   (United Kingdom)

^b JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^c MURDOCH CHILDREN'S RESEARCH INSTITUTE   (Australia)

^d ROYAL CHILDREN'S HOSPITAL   (Australia)

^e SCRIPPS RESEARCH INSTITUTE   (United States)

^f KAISER PERMANENTE   (United States)

^g NONE

Author keywords

[No Author keywords available]

Indexed keywords

ASPARTATE AMINOTRANSFERASE; FERRITIN; HFE PROTEIN;

AGE; ASPARTATE AMINOTRANSFERASE BLOOD LEVEL; CLINICAL FEATURE; DIABETES MELLITUS; DIAGNOSTIC VALUE; DISEASE COURSE; DISEASE SEVERITY; ENVIRONMENTAL FACTOR; ETHNIC GROUP; FERRITIN BLOOD LEVEL; GENE MUTATION; GENETIC PREDISPOSITION; GENETIC SCREENING; GENOTYPE; HEMOCHROMATOSIS; HEPATOMEGALY; HETEROZYGOTE; HOMOZYGOTE; HUMAN; IMMIGRATION; LETTER; LIVER BIOPSY; LIVER CIRRHOSIS; LIVER FIBROSIS; MASS SCREENING; ONSET AGE; PENETRANCE; PHENOTYPE; PREDICTION; PREVALENCE; PRIORITY JOURNAL; RELIABILITY; SCREENING TEST; SYMPTOM;

EID: 0037014884     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0140-6736(02)09581-8     Document Type: Letter

References (5)

1. E Beutler VJ Felitti JA Koziol NJ Ho T Gelbart Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA Lancet 359 2002 211 218
2. D Guyarder C Jacquelinet R Moirand Non-invasive prediction of fibrosis in C282Y homozygous haemochromatosis Gastroenterology 115 1998 929 936
3. P Adams P Brissot I.W. EASI international consensus conference on haemochromatosis J Hepatol 33 2000 485 504
4. A Poullis S Moodie L Ang CJ Finlayson JD Maxwell Identification of genetic haemochromatosis by routine transferrin saturation (TFS) testing of patients attending a liver clinic: St George's Hospital experience in applying the EASL guidelines Gut 49 suppl 3 2001 A2893
5. C Ellervik T Mandrup-Poulsen BG Nordestgaard Prevalence of hereditary haemochromatosis in late-onset type 1 diabetes mellitus: a retrospective study Lancet 358 2001 1405 1409