OBJECTIVE: To analyze the clinical characteristics and genetic background associated with the presence of hand arthropathy, as determined by radiological findings, in Italian patients with hereditary hemochromatosis (HHC). METHODS: In 88 consecutive unselected patients with phenotypically expressed HHC, joint involvement was systematically evaluated in plain radiographs of hands, wrists, lumbar spine, pelvis, and knees. Risk factors considered were age, sex, body mass index, alcohol abuse, organ involvement at other sites, and indices of iron overload, including ferritin, transferrin saturation, and iron removed to reach depletion. HFE genotype was also considered. The independent role of risk factors was tested by logistic regression anal...
AIMS OF THE STUDY Hereditary haemochromatosis is a genetic disease characterised by progressive a...
Genetic haemochromatosis is an autosomal recessive disorder, mostly due to HFE gene mutation, leadin...
AIMS OF THE STUDY Hereditary haemochromatosis is a genetic disease characterised by progressive a...
OBJECTIVE: To analyze the clinical characteristics and genetic background associated with the presen...
Objective: To determine the frequency and character of arthropathy in hereditary haemochromatosis (H...
OBJECTIVE: To determine the frequency and character of arthropathy in hereditary hemochromatosis (H...
OBJECTIVE: Arthropathy that mimics osteoarthritis (OA) and osteoporosis (OP) is considered a complic...
OBJECTIVE: To determine if there is an association between radiographic osteoarthritis (OA) of the h...
Hereditary hemochromatosis (HH) is a common inherited metabolic disorder characterized by systemic i...
Arthropathy that mimics osteoarthritis (OA) and osteoporosis (OP) is considered a complication of he...
Idiopathic hemochromatosis is a recessive autosomal disorder of iron metabolism manifested by a tiss...
AIMS OF THE STUDY Hereditary haemochromatosis is a genetic disease characterised by progr...
Background and Aim: Mutations in the hemochromatosis (HFE) gene are carried by one in three individ...
OBJECTIVE: To determine the effects of iron depletion on serum levels of joint biomarkers and on joi...
Genetic hemochromatosis is not a rare disease and represents a frequently underestimated cause of ar...
AIMS OF THE STUDY Hereditary haemochromatosis is a genetic disease characterised by progressive a...
Genetic haemochromatosis is an autosomal recessive disorder, mostly due to HFE gene mutation, leadin...
AIMS OF THE STUDY Hereditary haemochromatosis is a genetic disease characterised by progressive a...
OBJECTIVE: To analyze the clinical characteristics and genetic background associated with the presen...
Objective: To determine the frequency and character of arthropathy in hereditary haemochromatosis (H...
OBJECTIVE: To determine the frequency and character of arthropathy in hereditary hemochromatosis (H...
OBJECTIVE: Arthropathy that mimics osteoarthritis (OA) and osteoporosis (OP) is considered a complic...
OBJECTIVE: To determine if there is an association between radiographic osteoarthritis (OA) of the h...
Hereditary hemochromatosis (HH) is a common inherited metabolic disorder characterized by systemic i...
Arthropathy that mimics osteoarthritis (OA) and osteoporosis (OP) is considered a complication of he...
Idiopathic hemochromatosis is a recessive autosomal disorder of iron metabolism manifested by a tiss...
AIMS OF THE STUDY Hereditary haemochromatosis is a genetic disease characterised by progr...
Background and Aim: Mutations in the hemochromatosis (HFE) gene are carried by one in three individ...
OBJECTIVE: To determine the effects of iron depletion on serum levels of joint biomarkers and on joi...
Genetic hemochromatosis is not a rare disease and represents a frequently underestimated cause of ar...
AIMS OF THE STUDY Hereditary haemochromatosis is a genetic disease characterised by progressive a...
Genetic haemochromatosis is an autosomal recessive disorder, mostly due to HFE gene mutation, leadin...
AIMS OF THE STUDY Hereditary haemochromatosis is a genetic disease characterised by progressive a...