The role of the measurement of hepatic iron in the diagnosis of genetic hemochromatosis was studied, with particular reference to the differentiation of early hemochromatosis from alcoholic siderosis and the critical hepatic iron concentration associated with fibrosis in hemochromatosis. Hepatic iron was measured in 30 homozygous relatives of 17 hemochromatosis probands, 8 heterozygous relatives, 51 patients with alcoholic liver disease and 40 control subjects. Hepatic iron concentrations were greatly increased in the majority of homozygous hemochromatosis subjects, and there was little overlapwith the other groups. In the absence of alcoholism, fibrosis or cirrhosis in hemochromatosis was present only with hepatic iron concentrations above...
OBJECTIVES: Hepatic fibrosis is a complication of hereditary hemochromatosis. The aim of this study...
Hereditary haemochromatosis is a primary inherited disorder of iron metabolism leading to progressiv...
Haemochromatosis is most commonly due to the autosomal recessive inheritance of a C282Y substitution...
The biochemical hepatic iron index, defined as the ratio of hepatic iron concentration (expressed as...
The relationship of pretreatment serum ferritin and hepatic iron concentration to body iron removed ...
Liver iron concentrations were determined in 60 alcoholics with liver disease of varying severity, 1...
Genetic haemochromatosis is characterised by an inappropriately high rate of iron absorption by the ...
Iron abnormalities in chronic liver disease may be the result of genetic diseases or secondary facto...
SUMMARY The relationship between the serum ferritin concentration and total body iron stores was inv...
Primary, hereditary or genetic haemochromatosis is one of the most common inherited disorders in a C...
Hereditary hemochromatosis is a genetic disorder of iron metabolism leading to inappropriate iron ab...
Genetic hemochromatosis is one of the most common inherited disoders in Caucasian populations. The d...
SUMMARY Liver iron concentration has been determined chemically in 154 liver biopsies and the findin...
Several inherited forms of iron overload have been described. It is now accepted that HC, usually re...
242 members of 43 families with idiopathic hæmochromatosis were investigated for increased body-iron...
OBJECTIVES: Hepatic fibrosis is a complication of hereditary hemochromatosis. The aim of this study...
Hereditary haemochromatosis is a primary inherited disorder of iron metabolism leading to progressiv...
Haemochromatosis is most commonly due to the autosomal recessive inheritance of a C282Y substitution...
The biochemical hepatic iron index, defined as the ratio of hepatic iron concentration (expressed as...
The relationship of pretreatment serum ferritin and hepatic iron concentration to body iron removed ...
Liver iron concentrations were determined in 60 alcoholics with liver disease of varying severity, 1...
Genetic haemochromatosis is characterised by an inappropriately high rate of iron absorption by the ...
Iron abnormalities in chronic liver disease may be the result of genetic diseases or secondary facto...
SUMMARY The relationship between the serum ferritin concentration and total body iron stores was inv...
Primary, hereditary or genetic haemochromatosis is one of the most common inherited disorders in a C...
Hereditary hemochromatosis is a genetic disorder of iron metabolism leading to inappropriate iron ab...
Genetic hemochromatosis is one of the most common inherited disoders in Caucasian populations. The d...
SUMMARY Liver iron concentration has been determined chemically in 154 liver biopsies and the findin...
Several inherited forms of iron overload have been described. It is now accepted that HC, usually re...
242 members of 43 families with idiopathic hæmochromatosis were investigated for increased body-iron...
OBJECTIVES: Hepatic fibrosis is a complication of hereditary hemochromatosis. The aim of this study...
Hereditary haemochromatosis is a primary inherited disorder of iron metabolism leading to progressiv...
Haemochromatosis is most commonly due to the autosomal recessive inheritance of a C282Y substitution...