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 *

132 related articles for article (PubMed ID: 26169058)

  • 21. 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]  

  • 22. 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]  

  • 23. 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]  

  • 24. Familial dysalbuminaemic hyperthyroxinaemia: a review.
    Jensen IW; Faber J
    J R Soc Med; 1988 Jan; 81(1):34-7. PubMed ID: 3278117
    [No Abstract]   [Full Text] [Related]  

  • 25. Detection of albumin binding abnormalities in sera of patients with familial dysalbuminaemic hyperthyroxinaemia using isoelectric focusing.
    Flechner I; Aranoff G; Reifen R; Landau H
    Endocr Res; 1992; 18(3):229-40. PubMed ID: 1446661
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Familial dysalbuminaemic hyperthyroxinaemia: studies of albumin binding and implications for hormone action.
    Barlow JW; Csicsmann JM; Meinhold H; Lim CF; Stockigt JR
    Clin Endocrinol (Oxf); 1986 Jan; 24(1):39-47. PubMed ID: 3708869
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Bisalbuminaemia due to novel mutation at a critical residue involved in recycling; Albumin Lyon (510His→Arg).
    Brennan SO; Potter HC; Hanss M
    Clin Biochem; 2016 May; 49(7-8):544-7. PubMed ID: 26774326
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Elevation of free thyroxine measurements in patients without thyrotoxicosis.
    Wood DF; Zalin AM; Ratcliffe WA; Sheppard MC
    Q J Med; 1987 Oct; 65(246):863-70. PubMed ID: 3449890
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. 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]  

  • 32. Familial dysalbuminaemic hyperthyroxinaemia and other causes of euthyroid hyperthyroxinaemia.
    Benvenga S
    J R Soc Med; 1988 Sep; 81(9):556-7. PubMed ID: 3184118
    [No Abstract]   [Full Text] [Related]  

  • 33. Inherited defects of thyroxine-binding proteins.
    Pappa T; Ferrara AM; Refetoff S
    Best Pract Res Clin Endocrinol Metab; 2015 Oct; 29(5):735-47. PubMed ID: 26522458
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Novel silent albumin variant (191Ala→Thr) detected by TOF MS of whole plasma.
    Brennan SO; Rollo C; Potter HC
    Clin Chim Acta; 2015 Feb; 440():40-3. PubMed ID: 25444746
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. Familial dysalbuminemic hyperthyroxinemia in a 12-year-old girl.
    Oda Y; Tamura M; Kitanaka S
    Pediatr Int; 2019 May; 61(5):520-522. PubMed ID: 31087584
    [No Abstract]   [Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.