These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 24494774)

  • 1. A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extraction.
    Greenberg SM; Ferrara AM; Nicholas ES; Dumitrescu AM; Cody V; Weiss RE; Refetoff S
    Thyroid; 2014 Jun; 24(6):945-50. PubMed ID: 24494774
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    Endocr Pract; 2017 Nov; 23(11):1325-1332. PubMed ID: 28816534
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    Front Endocrinol (Lausanne); 2023; 14():1102777. PubMed ID: 36864842
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    Am J Med Sci; 2020 Nov; 360(5):566-574. PubMed ID: 32665066
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial dysalbuminemic hyperthyroxinemia: a rare example of albumin polymorphism and its rapid molecular diagnosis.
    AvRuskin TW; Juan CS; Weiss RE
    J Pediatr Endocrinol Metab; 2002 Jun; 15(6):801-7. PubMed ID: 12099390
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine.
    Pannain S; Feldman M; Eiholzer U; Weiss RE; Scherberg NH; Refetoff S
    J Clin Endocrinol Metab; 2000 Aug; 85(8):2786-92. PubMed ID: 10946882
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Artifactually elevated serum-free thyroxine levels measured by equilibrium dialysis in a pregnant woman with familial dysalbuminemic hyperthyroxinemia.
    Hoshikawa S; Mori K; Kaise N; Nakagawa Y; Ito S; Yoshida K
    Thyroid; 2004 Feb; 14(2):155-60. PubMed ID: 15068631
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.
    Wada N; Chiba H; Shimizu C; Kijima H; Kubo M; Koike T
    J Clin Endocrinol Metab; 1997 Oct; 82(10):3246-50. PubMed ID: 9329347
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inhibition of serum protein binding of thyroxine in a hypothyroid patient with familial dysalbuminemic hyperthyroxinemia.
    Premachandra BN; Wortsman J; Williams IK
    Clin Biochem; 1996 Feb; 29(1):85-8. PubMed ID: 8929830
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial dysalbuminemic hyperthyroxinemia: cumulative experience in 29 consecutive patients.
    Heufelder AE; Klee GG; Wynne AG; Gharib H
    Endocr Pract; 1995; 1(1):4-8. PubMed ID: 15251607
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial Dysalbuminemic Hyperthyroxinemia in a Japanese Man Caused by a Point Albumin Gene Mutation (R218P).
    Osaki Y; Hayashi Y; Nakagawa Y; Yoshida K; Ozaki H; Fukazawa H
    Jpn Clin Med; 2016; 7():9-13. PubMed ID: 27081329
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Linkage of familial dysalbuminemic hyperthyroxinemia to the albumin gene in a large Amish kindred.
    Weiss RE; Sunthornthepvarakul T; Angkeow P; Marcus-Bagley D; Cox N; Alper CA; Refetoff S
    J Clin Endocrinol Metab; 1995 Jan; 80(1):116-21. PubMed ID: 7829599
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    Endocr J; 2017 Feb; 64(2):207-212. PubMed ID: 27904073
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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.
    Liu H; Ran J; Chen C; Chen G; Zhu P; Tan R; Liu Y
    Int J Endocrinol; 2019; 2019():5947415. PubMed ID: 31582975
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families.
    Sunthornthepvarakul T; Angkeow P; Weiss RE; Hayashi Y; Refetoff S
    Biochem Biophys Res Commun; 1994 Jul; 202(2):781-7. PubMed ID: 8048949
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Homozygous Mutation in Human Serum Albumin and Its Implication on Thyroid Tests.
    Mimoto MS; Karaca A; Scherberg N; Dumitrescu AM; Refetoff S
    Thyroid; 2018 Jun; 28(6):811-814. PubMed ID: 29676214
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hyperthyroxinemia and Hypercortisolemia due to Familial Dysalbuminemia.
    Moran C; Seger C; Taylor K; Oddy S; Burling K; Rajanayagam O; Fairall L; McGowan A; Lyons G; Halsall D; Gurnell M; Schwabe J; Chatterjee K; Strey C
    Thyroid; 2020 Nov; 30(11):1681-1684. PubMed ID: 32669045
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A family with familial dysalbuminaemic hyperthyroxinaemia].
    Dai WX; Liu ZY; Guo ZS; Liu ZX; Dou YL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):40-3. PubMed ID: 15696477
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rapid molecular diagnosis of
    Abali S; Yavas Abali Z; Yararbas K; Semiz S
    J Pediatr Endocrinol Metab; 2021 Sep; 34(9):1201-1205. PubMed ID: 34142517
    [TBL] [Abstract][Full Text] [Related]  

  • 20. First Report of Familial Dysalbuminemic Hyperthyroxinemia With an ALB Variant.
    Cho YY; Song JS; Park HD; Kim YN; Kim HI; Kim TH; Chung JH; Ki CS; Kim SW
    Ann Lab Med; 2017 Jan; 37(1):63-65. PubMed ID: 27834068
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.