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Hyperthyroxinemia, Familial Dysalbuminemic

Known as: Hyperthyroxinemia, Familial Dysalbuminemic [Disease/Finding], EUTHYROID HYPERTHYROXINEMIA 1, FDAH 
An inherited autosomal dominant trait characterized by abnormally elevated levels of total serum THYROXINE; (T4) in euthyroid patients with abnormal… 
National Institutes of Health

Papers overview

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2009
2009
This paper gives a new application of DEA to evaluate the scheduling solutions of parallel processing. It evaluates the… 
Review
2007
Review
2007
Enzymes have become important tools in several industries due to their ability to produce chirally pure and complex molecules… 
2007
2007
Wild-type cmFDH contains no cystines, hence it is a good candidate to test the hypothesis that thermostability can be achieved by… 
2004
2004
Photochemical and enzymatic synthesis of formic acid was investigated from HCO 3 - with formate dehydrogenase (FDH) from… 
Highly Cited
2002
Highly Cited
2002
The CO2 fixation system, that is formic acid production from CO2 with FDH from Saccharomyces cerevisiae and reduced Methyl… 
1995
1995
In this study a protein expression system was used to synthesize recombinant human serum albumin containing a mutation that has… 
1993
1993
Familial dysalbuminemic hyperthyroxinemia (FDH) is an autosomal dominant syndrome in which clinically euthyroid patients have… 
1987
1987
SummaryTwo classes of mutants defective in benzyl viologen-linked formate dehydrogenase (FDH-BV) activity were isolated from… 
1983
1983
Resistance to thyroid hormone associated with a defect in hormone transport across the plasma membrane occurred in a 74-year-old… 
1972
1972
Cell-free extracts of mixed rumen microorganisms were incubated in vitro in order to determine the existence and nature of…