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: 24646103)

  • 1. A novel albumin gene mutation (R222I) in familial dysalbuminemic hyperthyroxinemia.
    Schoenmakers N; Moran C; Campi I; Agostini M; Bacon O; Rajanayagam O; Schwabe J; Bradbury S; Barrett T; Geoghegan F; Druce M; Beck-Peccoz P; O'Toole A; Clark P; Bignell M; Lyons G; Halsall D; Gurnell M; Chatterjee K
    J Clin Endocrinol Metab; 2014 Jul; 99(7):E1381-6. PubMed ID: 24646103
    [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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Hyperthyroxinemia due to the coexistence of two raised affinity thyroxine-binding proteins (albumin and prealbumin) in one family.
    Lalloz MR; Byfield PG; Goel KM; Loudon MM; Thomson JA; Himsworth RL
    J Clin Endocrinol Metab; 1987 Feb; 64(2):346-52. PubMed ID: 3098776
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Free Thyroxine Concentrations in Sera of Individuals with Familial Dysalbuminemic Hyperthyroxinemia: A Comparison of Three Methods of Measurement.
    Refetoff S; Scherberg NH; Yuan C; Wu W; Wu Z; McPhaul MJ
    Thyroid; 2020 Jan; 30(1):37-41. PubMed ID: 31822224
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Clinical, Genetic, and Protein Structural Aspects of Familial Dysalbuminemic Hyperthyroxinemia and Hypertriiodothyroninemia.
    Kragh-Hansen U; Galliano M; Minchiotti L
    Front Endocrinol (Lausanne); 2017; 8():297. PubMed ID: 29163366
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial dysalbuminemic hyperthyroxinemia confounding management of coexistent autoimmune thyroid disease.
    Khoo S; Lyons G; Solomon A; Oddy S; Halsall D; Chatterjee K; Moran C
    Endocrinol Diabetes Metab Case Rep; 2020 Feb; 2020():. PubMed ID: 32101523
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Familial dysalbuminemic hyperthyroxinemia (FDH) due to Arg242 His variant in
    Turkkahraman D; Gullu M; Tekin S; Kalkan T
    J Pediatr Endocrinol Metab; 2024 Jun; 37(6):532-535. PubMed ID: 38736368
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial Dysalbuminemic Hyperthyroxinemia as a Cause for Discordant Thyroid Function Tests.
    Ting MJM; Zhang R; Lim EM; Ward BK; Wilson SG; Walsh JP
    J Endocr Soc; 2021 Apr; 5(4):bvab012. PubMed ID: 33728390
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.