Contains fulltext : 88397.pdf (publisher's version ) (Closed access)BACKGROUND: The C282Y mutation of the hemochromatosis (HFE)-gene increases body iron status. Among Caucasians, the carrier frequency of this mutation is 8-9%. C282Y carriers may be more susceptible to iron-induced atherosclerosis due to higher iron levels. It has also been postulated that the C282Y mutation could alter aspects of iron metabolism. We examined the relationship between the C282Y mutation, iron status, and carotid intima-media thickness (IMT) as a marker of atherosclerosis. METHODS AND RESULTS: The present study comprised 764 Dutch men and post-menopausal women aged 50-70 years. Mean and maximum carotid IMT were assessed by B-mode ultrasonogra...
Purpose: Hereditary haemochromatosis (HH) is a genetic disease with autosomal recessive trait. Recen...
Background & Aims: There are few longitudinal studies of serum ferritin (SF) and transferrin saturat...
Background: Increased iron stores and haemochromatosis gene mutations may be risk factors for corona...
BACKGROUND: The C282Y mutation of the hemochromatosis (HFE)-gene increases body iron status. Among C...
Background The C282Y mutation of the hemochromatosis (HFE)-gene increases body iron status. Among Ca...
textabstractBACKGROUND AND PURPOSE: Increased serum iron is found to be a risk factor for stroke. Ca...
Contains fulltext : 50101.pdf (publisher's version ) (Closed access)BACKGROUND: Al...
Contains fulltext : 153230.pdf (publisher's version ) (Open Access)BACKGROUND: Pre...
Contains fulltext : 53320.pdf (publisher's version ) (Open Access)Homozygosity for...
The C282Y and H63D mutations in the HFE gene are important causes of hemochromatosis. In the elderly...
Contains fulltext : 81572.pdf (publisher's version ) (Closed access)BACKGROUND/AIM...
Contains fulltext : 69186.pdf (publisher's version ) (Closed access)We describe a ...
Background: HFE gene mutations have been shown to be responsible for hereditary hemochromatosis. The...
Absorption, transport and storage of iron are tightly regulated, as expected for an element, which i...
Background & Aims: Two major mutations are defined within the hemochromatosis gene, HFE. Although th...
Purpose: Hereditary haemochromatosis (HH) is a genetic disease with autosomal recessive trait. Recen...
Background & Aims: There are few longitudinal studies of serum ferritin (SF) and transferrin saturat...
Background: Increased iron stores and haemochromatosis gene mutations may be risk factors for corona...
BACKGROUND: The C282Y mutation of the hemochromatosis (HFE)-gene increases body iron status. Among C...
Background The C282Y mutation of the hemochromatosis (HFE)-gene increases body iron status. Among Ca...
textabstractBACKGROUND AND PURPOSE: Increased serum iron is found to be a risk factor for stroke. Ca...
Contains fulltext : 50101.pdf (publisher's version ) (Closed access)BACKGROUND: Al...
Contains fulltext : 153230.pdf (publisher's version ) (Open Access)BACKGROUND: Pre...
Contains fulltext : 53320.pdf (publisher's version ) (Open Access)Homozygosity for...
The C282Y and H63D mutations in the HFE gene are important causes of hemochromatosis. In the elderly...
Contains fulltext : 81572.pdf (publisher's version ) (Closed access)BACKGROUND/AIM...
Contains fulltext : 69186.pdf (publisher's version ) (Closed access)We describe a ...
Background: HFE gene mutations have been shown to be responsible for hereditary hemochromatosis. The...
Absorption, transport and storage of iron are tightly regulated, as expected for an element, which i...
Background & Aims: Two major mutations are defined within the hemochromatosis gene, HFE. Although th...
Purpose: Hereditary haemochromatosis (HH) is a genetic disease with autosomal recessive trait. Recen...
Background & Aims: There are few longitudinal studies of serum ferritin (SF) and transferrin saturat...
Background: Increased iron stores and haemochromatosis gene mutations may be risk factors for corona...