False Hypercortisolemia Due to Abnormal Albumin-Cortisol Binding in a Patient with Familial Dysalbuminemic Hyperthyroxinemia-Reference-Cited by-同舟云学术

False Hypercortisolemia Due to Abnormal Albumin-Cortisol Binding in a Patient with Familial Dysalbuminemic Hyperthyroxinemia

Published:2021-11-23 Issue: Volume: Page:
ISSN:1050-7256
Container-title:Thyroid
language:en
Short-container-title:Thyroid

Author:

Chiba Koki¹^ORCID,Kameda Hiraku¹^ORCID,Miya Aika¹,Nomoto Hiroshi¹,Cho Kyu Yong¹,Nakamura Akinobu¹,Jin Shigeki²,Matoba Kotaro²,Miyoshi Hideaki¹³,Atsumi Tatsuya¹

Affiliation:

1. Department of Rheumatology, Endocrinology and Nephrology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

2. Department of Forensic Medicine, Graduate School of Medicine, Sapporo, Hokkaido University, Japan.

3. Division of Diabetes and Obesity, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.liebertpub.com/doi/pdf/10.1089/thy.2021.0460

Reference5 articles.

1. Hyperthyroxinemia and Hypercortisolemia due to Familial Dysalbuminemia

2. Familial Dysalbuminemic Hyperthyroxinemia in a Swiss Family Caused by a Mutant Albumin (R218P) Shows an Apparent Discrepancy between Serum Concentration and Affinity for Thyroxine

3. A Novel Missense Mutation in Codon 218 of the Albumin Gene in a Distinct Phenotype of Familial Dysalbuminemic Hyperthyroxinemia in a Japanese Kindred

4. Artifactually Elevated Serum-Free Thyroxine Levels Measured by Equilibrium Dialysis in a Pregnant Woman with Familial Dysalbuminemic Hyperthyroxinemia

5. Structural basis of albumin-thyroxine interactions and familial dysalbuminemic hyperthyroxinemia

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