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First published 1987-12

Familial Dysalbuminaemic Hyperthyroxinaemia and Other Causes of Euthyroid Hyperthyroxinaemia

C Farror, M L Wellby, C Beng

Journal of the Royal Society of Medicine

Free access

Research article

First published 2016-7

Familial dysalbuminaemic hyperthyroxinaemia: a rapid and novel mass spectrometry approach to diagnosis

Joshua B Ryan, Stephen O Brennan, Howard Potter [...]

Annals of Clinical Biochemistry: International Journal of Laboratory Medicine

Free access

Other

First published 1988-1

Familial Dysalbuminaemic Hyperthyroxinaemia: A Review

I W Jensen, J Faber

Journal of the Royal Society of Medicine

Free access

In brief

First published 1987-12

Euthyroid Hyperthyroxinaemia in Acute Psychiatric Admissions

T. J. R. Lambert, R. Davidson, G. H. McLellan

Australian & New Zealand Journal of Psychiatry

Free access

Letter

First published 1988-9

Familial Dysalbuminaemic Hyperthyroxinaemia and other Causes of Euthyroid Hyperthyroxinaemia

S Benvenga

Journal of the Royal Society of Medicine

Free access

Research article

First published 1986-1

Thyroid Function Tests in Patients with Familial Dysalbuminaemic Hyperthyroxinaemia (FDH)

M Felicity Stewart, Wendy A Ratcliffe, Ian Roberts

Annals of Clinical Biochemistry: International Journal of Laboratory Medicine

Open access

Research article

First published 2020-11

Hyperthyroxinemia and Hypercortisolemia due to Familial Dysalbuminemia

Carla Moran, Christoph Seger, Kevin Taylor [...]

Thyroid®

Free access

Case report

First published 1992-1

Familial Non-Toxic Hyperthyroxinaemia: Receptor or 5′-Deiodinase Defect or Deficiency

D C Crothers, T C Harvey, J Faber [...]

Annals of Clinical Biochemistry: International Journal of Laboratory Medicine

Retricted access

Letter

First published 2008-09

Marked Hyperthyroxinemia During Amiodarone Treatment Revealing Thyroid Hormone Resistance Syndrome

Bernard Goichot, Frédérique Savagner, Rémy Sapin [...]

Thyroid®

Open access

Case report

First published 2016

Familial Dysalbuminemic Hyperthyroxinemia in a Japanese Man Caused by a Point Albumin Gene Mutation (R218P)

Yoshinori Osaki, Yoshitaka Hayashi, Yoshinori Nakagawa [...]

Japanese Clinical Medicine

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