Literature DB >> 21149501

Spuriously high free thyroxine values in familial dysalbuminemic hyperthyroxinemia.

H Alec Ross, Yolanda B de Rijke, Fred C G J Sweep.   

Abstract

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Year:  2010        PMID： 21149501     DOI： 10.1373/clinchem.2010.158170

Source DB:  PubMed          Journal:  Clin Chem        ISSN： 0009-9147            Impact factor:   8.327


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  10 in total

Review 1.  Clinical recognition and evaluation of patients with inherited serum thyroid hormone-binding protein mutations.

Authors:  M S Mimoto; S Refetoff
Journal:  J Endocrinol Invest       Date:  2019-07-27       Impact factor: 4.256

2.  A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extraction.

Authors:  Solomon Maximo Greenberg; Alfonso Massimiliano Ferrara; Everton S Nicholas; Alexandra M Dumitrescu; Vivian Cody; Roy E Weiss; Samuel Refetoff
Journal:  Thyroid       Date:  2014-03-21       Impact factor: 6.568

Review 3.  Inherited defects of thyroxine-binding proteins.

Authors:  Theodora Pappa; Alfonso Massimiliano Ferrara; Samuel Refetoff
Journal:  Best Pract Res Clin Endocrinol Metab       Date:  2015-09-30       Impact factor: 4.690

4.  Free Thyroxine Concentrations in Sera of Individuals with Familial Dysalbuminemic Hyperthyroxinemia: A Comparison of Three Methods of Measurement.

Authors:  Samuel Refetoff; Neal H Scherberg; Chao Yuan; William Wu; Zengru Wu; Michael J McPhaul
Journal:  Thyroid       Date:  2020-01       Impact factor: 6.568

5.  First Report of Familial Dysalbuminemic Hyperthyroxinemia With an ALB Variant.

Authors:  Yoon Young Cho; Ju Sun Song; Hyung Doo Park; Young Nam Kim; Hye In Kim; Tae Hyuk Kim; Jae Hoon Chung; Chang Seok Ki; Sun Wook Kim
Journal:  Ann Lab Med       Date:  2017-01       Impact factor: 3.464

Review 6.  Clinical, Genetic, and Protein Structural Aspects of Familial Dysalbuminemic Hyperthyroxinemia and Hypertriiodothyroninemia.

Authors:  Ulrich Kragh-Hansen; Monica Galliano; Lorenzo Minchiotti
Journal:  Front Endocrinol (Lausanne)       Date:  2017-11-01       Impact factor: 5.555

7.  A Chinese Family with Familial Dysalbuminemic Hyperthyroxinemia (FDH) due to R242H Mutation on Human Albumin Gene: Reevaluating the Role of FDH in Patients with Asymptomatic Hyperthyroxinemia.

Authors:  Hongbing Liu; Jianmin Ran; Chuping Chen; Guangshu Chen; Ping Zhu; Rongshao Tan; Yan Liu
Journal:  Int J Endocrinol       Date:  2019-09-09       Impact factor: 3.257

8.  Familial dysalbuminaemic hyperthyroxinaemia interferes with current free thyroid hormone immunoassay methods.

Authors:  Serena Khoo; Greta Lyons; Anne McGowan; Mark Gurnell; Susan Oddy; W Edward Visser; Sjoerd van den Berg; David Halsall; Kevin Taylor; Krishna Chatterjee; Carla Moran
Journal:  Eur J Endocrinol       Date:  2020-06       Impact factor: 6.664

Review 9.  Hormone Immunoassay Interference: A 2021 Update.

Authors:  Khaldoun Ghazal; Severine Brabant; Dominique Prie; Marie-Liesse Piketty
Journal:  Ann Lab Med       Date:  2022-01-01       Impact factor: 3.464

10.  A novel albumin gene mutation (R222I) in familial dysalbuminemic hyperthyroxinemia.

Authors:  Nadia Schoenmakers; Carla Moran; Irene Campi; Maura Agostini; Olivia Bacon; Odelia Rajanayagam; John Schwabe; Sonia Bradbury; Timothy Barrett; Frank Geoghegan; Maralyn Druce; Paolo Beck-Peccoz; Angela O'Toole; Penelope Clark; Michelle Bignell; Greta Lyons; David Halsall; Mark Gurnell; Krishna Chatterjee
Journal:  J Clin Endocrinol Metab       Date:  2014-03-19       Impact factor: 5.958
  10 in total

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