References in periodicals archive ?
Two transthyretin mutations associated with euthyroid hyperthyroxinemia.
Individuals with one of these conditions causing euthyroid hyperthyroxinemia (3) and/or hypertriiodothyroninemia may be misdiagnosed and even treated as having thyrotoxicosis (4,5).
7) first described familial euthyroid hyperthyroxinemia attributable to a mutant TTR with increased [T.
An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families.
Identification of a human serum albumin species associated with familial dysalbuminemic hyperthyroxinemia.
Prevalence of familial dysalbuminemic hyperthyroxinemia in serum samples received for thyroid testing.
Free thyroxine measured by the Ciba Corning ACS-180 on samples from patients with familial dysalbuminemic hyperthyroxinemia [Letter].
4], free thyroxine; FDH, familial dysalbuminemic hyperthyroxinemia.
Familial dysalbuminemic hyperthyroxinemia (FDH) is an autosomal dominant condition with a prevalence of 0.
Stockigt JR: Hyperthyroxinemia secondary to drugs and acute illness.
Euthyroid hyperthyroxinemia, the situation when the total [T.
Increased thyroid-binding globulin Familial dysalbuminemic hyperthyroxinemia Peripheral resistance to thyroid hormone Acute psychiatric illness Amiodarone Ipodate Propranolol