"Hyperthyroxinemia, familial dysalbuminemic" AND Diagnosis/broad[filter] AND "english and humans"[filter] NOT comment[PTYP] NOT letter[PTYP] - Search Results

Year	Number of Results
2015	3
2016	2
2017	3
2019	1
2020	2
2021	1
2023	2
2024	1

1

Familial Dysalbuminemic Hyperthyroxinemia (FDH), Albumin Gene Variant (R218S), and Risk of Miscarriages in Offspring.

Lai S, Gopalakrishnan G, Li J, Liu X, Chen Y, Wen Y, Zhang S, Huang B, Phornphutkul C, Liu S, Kuang J. Lai S, et al. Am J Med Sci. 2020 Nov;360(5):566-574. doi: 10.1016/j.amjms.2020.05.035. Epub 2020 May 28. Am J Med Sci. 2020. PMID: 32665066 Free article.

2

Clinical characteristics of familial dysalbuminemic hyperthyroxinemia in Chinese patients and comparison of free thyroxine in three immunoassay methods.

Zhao L, Zhou Y, Huang F, He X, Mei G, Wang S, Zhao Y. Zhao L, et al. Front Endocrinol (Lausanne). 2023 Feb 14;14:1102777. doi: 10.3389/fendo.2023.1102777. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 36864842 Free PMC article.

3

Inherited defects of thyroxine-binding proteins.

Pappa T, Ferrara AM, Refetoff S. Pappa T, et al. Best Pract Res Clin Endocrinol Metab. 2015 Oct;29(5):735-47. doi: 10.1016/j.beem.2015.09.002. Epub 2015 Sep 30. Best Pract Res Clin Endocrinol Metab. 2015. PMID: 26522458 Free PMC article. Review.

4

Familial dysalbuminemic hyperthyroxinemia combined with Graves' disease: a rare case report.

Li Y, Chi Y, Chai X, Liu H, Li N, Lian X. Li Y, et al. BMC Endocr Disord. 2023 Oct 18;23(1):226. doi: 10.1186/s12902-023-01481-5. BMC Endocr Disord. 2023. PMID: 37853391 Free PMC article.

5

Familial dysalbuminemic hyperthyroxinemia (FDH) due to Arg242 His variant in ALB gene in Turkish children.

Turkkahraman D, Gullu M, Tekin S, Kalkan T. Turkkahraman D, et al. J Pediatr Endocrinol Metab. 2024 May 14;37(6):532-535. doi: 10.1515/jpem-2023-0506. Print 2024 Jun 25. J Pediatr Endocrinol Metab. 2024. PMID: 38736368

6

Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia.

Abali S, Yavas Abali Z, Yararbas K, Semiz S. Abali S, et al. J Pediatr Endocrinol Metab. 2021 Jun 18;34(9):1201-1205. doi: 10.1515/jpem-2021-0087. Print 2021 Sep 27. J Pediatr Endocrinol Metab. 2021. PMID: 34142517

7

SEVEN FAMILIAL DYSALBUMINEMIC HYPERTHYROXINEMIA CASES IN THREE UNRELATED JAPANESE FAMILIES AND HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY ANALYSIS OF THE THYROXINE BINDING PROFILE.

Nagano H, Nakagawa Y, Ishikawa N, Watanabe H, Miyabayashi Y, Nakayama A, Fujimoto M, Komai E, Shiga A, Tamura A, Kono T, Takiguchi T, Higuchi S, Sakuma I, Hashimoto N, Suzuki S, Koide H, Yokote K, Tanaka T. Nagano H, et al. Endocr Pract. 2017 Nov;23(11):1325-1332. doi: 10.4158/EP171964.OR. Epub 2017 Aug 17. Endocr Pract. 2017. PMID: 28816534

8

A case of familial dysalbuminemic hyperthyroxinemia (FDH) in Japan: FDH as a possible differential diagnosis of syndrome of inappropriate secretion of thyroid-stimulating hormone (SITSH).

Kobayashi S, Yoshimura Noh J, Shimizu T, Sato T, Kurihara I, Sugino K, Itoh H, Ito K. Kobayashi S, et al. Endocr J. 2017 Feb 27;64(2):207-212. doi: 10.1507/endocrj.EJ16-0135. Epub 2016 Nov 30. Endocr J. 2017. PMID: 27904073 Free article.

9

Familial dysalbuminemic hyperthyroxinemia in a 12-year-old girl.

Oda Y, Tamura M, Kitanaka S. Oda Y, et al. Pediatr Int. 2019 May;61(5):520-522. doi: 10.1111/ped.13839. Epub 2019 May 14. Pediatr Int. 2019. PMID: 31087584 No abstract available.

10

Familial dysalbuminemic hyperthyroxinemia in a 4-year-old girl with hyperactivity, palpitations and advanced dental age: how gold standard assays may be misleading.

Choudhary A, Sriphrapradang C, Refetoff S, Antal Z. Choudhary A, et al. J Pediatr Endocrinol Metab. 2015 Jan;28(1-2):241-5. doi: 10.1515/jpem-2014-0019. J Pediatr Endocrinol Metab. 2015. PMID: 25153218 Free PMC article.

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