INTRODUCTION: HFE-associated haemochromatosis, the most common monogenic disorder amongst populations of northern European ancestry, is characterised by iron overload. Excess iron is stored in parenchymal tissues, leading to morbidity and mortality. Population screening programmes are likely to improve early diagnosis, thereby decreasing associated disease. Our aim was to develop and validate a health economics model of screening using utilities and costs from a haemochromatosis cohort. METHODS: A state-transition model was developed with Markov states based on disease severity. Australian males (aged 30 years) and females (aged 45 years) of northern European ancestry were the target populations. The screening strategy was the status quo ap...
Background: Hereditary hemochromatosis is the most common autosomal recessive disorder in population...
Background: Familial hypercholesterolemia (FH) imposes significant burden of premature coronary hear...
Objective: To evaluate DNA testing for detecting hereditary haemochromatosis (HHC) in subgroups of p...
Introduction: Amongst populations of northern European ancestry, HFE-associated haemochromatosis is ...
Haemochromatosis is one of the most common autosomal recessive disorders amongst populations of nort...
BACKGROUND: Hereditary hemochromatosis (HH) is a common autosomal recessive disorder amongst persons...
Abstract Hereditary haemochromatosis (HH) is an inherited disorder of iron absorption. It meets seve...
Genetic tests for hereditary hemochromatosis (HH) are currently included in the German ambulatory ca...
Background: Hereditary hemochromatosis (HH) is a common autosomal recessive disorder amongst persons...
Background: It is unclear whether screening of relatives of C282Y and H63D heterozygotes (other than...
Background: Hereditary haemochromatosis (HH) is a common genetic condition amongst people of norther...
Haemochromatosis associated with mutations in the HFE gene is the most common inherited disorder in ...
Haemochromatosis associated with mutations in the HFE gene is the most common inherited disorder in ...
Background: Haemochromatosis is a common genetic disease in populations of a northern European origi...
BACKGROUND: New techniques for diagnosing hereditary haemochromatosis (HHC) have become available al...
Background: Hereditary hemochromatosis is the most common autosomal recessive disorder in population...
Background: Familial hypercholesterolemia (FH) imposes significant burden of premature coronary hear...
Objective: To evaluate DNA testing for detecting hereditary haemochromatosis (HHC) in subgroups of p...
Introduction: Amongst populations of northern European ancestry, HFE-associated haemochromatosis is ...
Haemochromatosis is one of the most common autosomal recessive disorders amongst populations of nort...
BACKGROUND: Hereditary hemochromatosis (HH) is a common autosomal recessive disorder amongst persons...
Abstract Hereditary haemochromatosis (HH) is an inherited disorder of iron absorption. It meets seve...
Genetic tests for hereditary hemochromatosis (HH) are currently included in the German ambulatory ca...
Background: Hereditary hemochromatosis (HH) is a common autosomal recessive disorder amongst persons...
Background: It is unclear whether screening of relatives of C282Y and H63D heterozygotes (other than...
Background: Hereditary haemochromatosis (HH) is a common genetic condition amongst people of norther...
Haemochromatosis associated with mutations in the HFE gene is the most common inherited disorder in ...
Haemochromatosis associated with mutations in the HFE gene is the most common inherited disorder in ...
Background: Haemochromatosis is a common genetic disease in populations of a northern European origi...
BACKGROUND: New techniques for diagnosing hereditary haemochromatosis (HHC) have become available al...
Background: Hereditary hemochromatosis is the most common autosomal recessive disorder in population...
Background: Familial hypercholesterolemia (FH) imposes significant burden of premature coronary hear...
Objective: To evaluate DNA testing for detecting hereditary haemochromatosis (HHC) in subgroups of p...