Add to ORKGBACKGROUND: HFEC282Y homozygotes have an increased risk for developing increased iron stores and related disorders. It is controversial whether dietary iron restrictions should be recommended to such individuals. OBJECTIVE: To determine whether dietary iron content influences iron stores in HFEC282Y homozygotes as assessed by serum ferritin concentration. DESIGN: Serum ferritin concentration was measured and a dietary iron questionnaire was completed as part of the evaluation of 213 HFE C282Yhomozygotes who were identified through screening of \u3e100,000 primary care patients at five HEmochromatosis and IRon Overload Screening (HEIRS) Study Field Centers in the United States and Canada. RESULTS: No significant relationships between serum f...
INTRODUCTION: HFE p.C282Y homozygosity is the most common cause of hereditary haemochromatosis. Ther...
Background: There is a marked difference in the degree of expression of the homozygous C282Y HFE gen...
Introduction: HFE p.C282Y homozygosity is the most common cause of hereditary haemochromatosis. Ther...
BACKGROUND: HFEC282Y homozygotes have an increased risk for developing increased iron...
BACKGROUND: HFEC282Y homozygotes have an increased risk for developing increased iron stores and rel...
Background: Public health policy to prevent iron deficiency through food fortification or other meas...
Item does not contain fulltextBACKGROUND: Hereditary hemochromatosis (HH) leads to iron loading beca...
Background: Hereditary hemochromatosis (HH) leads to iron loading because of a disturbance in the ne...
Background: Hereditary hemochromatosis (HH) leads to iron loading because of a disturbance in the ne...
BACKGROUND: Hereditary hemochromatosis (HH) leads to iron loading because of a disturbance in the ne...
Hemochromatosis gene (HFE)-associated hereditary hemochromatosis (HH) is a genetic predisposition to...
How often elevated serum ferritin in primary-care patients reflects increased iron stores (normally ...
Background: The suggestion that carriers of the HFE C282Y mutation absorb nonheme iron more efficien...
Background: Gene mutations associated with iron overload have been identified. How food and nutrien...
Contains fulltext : 81572.pdf (publisher's version ) (Closed access)BACKGROUND/AIM...
INTRODUCTION: HFE p.C282Y homozygosity is the most common cause of hereditary haemochromatosis. Ther...
Background: There is a marked difference in the degree of expression of the homozygous C282Y HFE gen...
Introduction: HFE p.C282Y homozygosity is the most common cause of hereditary haemochromatosis. Ther...
BACKGROUND: HFEC282Y homozygotes have an increased risk for developing increased iron...
BACKGROUND: HFEC282Y homozygotes have an increased risk for developing increased iron stores and rel...
Background: Public health policy to prevent iron deficiency through food fortification or other meas...
Item does not contain fulltextBACKGROUND: Hereditary hemochromatosis (HH) leads to iron loading beca...
Background: Hereditary hemochromatosis (HH) leads to iron loading because of a disturbance in the ne...
Background: Hereditary hemochromatosis (HH) leads to iron loading because of a disturbance in the ne...
BACKGROUND: Hereditary hemochromatosis (HH) leads to iron loading because of a disturbance in the ne...
Hemochromatosis gene (HFE)-associated hereditary hemochromatosis (HH) is a genetic predisposition to...
How often elevated serum ferritin in primary-care patients reflects increased iron stores (normally ...
Background: The suggestion that carriers of the HFE C282Y mutation absorb nonheme iron more efficien...
Background: Gene mutations associated with iron overload have been identified. How food and nutrien...
Contains fulltext : 81572.pdf (publisher's version ) (Closed access)BACKGROUND/AIM...
INTRODUCTION: HFE p.C282Y homozygosity is the most common cause of hereditary haemochromatosis. Ther...
Background: There is a marked difference in the degree of expression of the homozygous C282Y HFE gen...
Introduction: HFE p.C282Y homozygosity is the most common cause of hereditary haemochromatosis. Ther...