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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

181 related items for PubMed ID: 8596313

  • 21. Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome.
    Monaghan G, Ryan M, Seddon R, Hume R, Burchell B.
    Lancet; 1996 Mar 02; 347(9001):578-81. PubMed ID: 8596320
    [Abstract] [Full Text] [Related]

  • 22. Genetic inheritance of Gilbert's syndrome.
    Bosma P, Chowdhury JR, Jansen PH.
    Lancet; 1995 Jul 29; 346(8970):314-5. PubMed ID: 7630272
    [No Abstract] [Full Text] [Related]

  • 23. Familial unconjugated hyperbilirubinemia syndromes.
    Reichen J.
    Semin Liver Dis; 1983 Feb 29; 3(1):24-35. PubMed ID: 6836332
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Kernicterus in an adult who is heterozygous for Crigler-Najjar syndrome and homozygous for Gilbert-type genetic defect.
    Chalasani N, Chowdhury NR, Chowdhury JR, Boyer TD.
    Gastroenterology; 1997 Jun 29; 112(6):2099-103. PubMed ID: 9178703
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Inherited disorders of bilirubin metabolism.
    Bosma PJ.
    J Hepatol; 2003 Jan 29; 38(1):107-17. PubMed ID: 12480568
    [No Abstract] [Full Text] [Related]

  • 29. [Gilbert disease and type I and II Crigler-Najjar syndrome due to mutations in the same UGT1A1 gene locus].
    Kraemer D, Scheurlen M.
    Med Klin (Munich); 2002 Sep 15; 97(9):528-32. PubMed ID: 12371080
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. The genetic basis of Gilbert's syndrome.
    Mathew P.
    N Engl J Med; 1996 Mar 21; 334(12):802-3. PubMed ID: 8592567
    [No Abstract] [Full Text] [Related]

  • 32. A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome.
    Nakagawa T, Mure T, Yusoff S, Ono E, Kusuma Harahap IS, Morikawa S, Morioka I, Takeshima Y, Nishio H, Matsuo M.
    Kobe J Med Sci; 2011 Jul 20; 57(1):E26-31. PubMed ID: 22169899
    [Abstract] [Full Text] [Related]

  • 33. [Crigler-Najjar syndrome].
    Torres M, Bruguera M.
    Gastroenterol Hepatol; 2005 Dec 20; 28(10):637-40. PubMed ID: 16373016
    [No Abstract] [Full Text] [Related]

  • 34. The relationship between UGT1A1 gene & various diseases and prevention strategies.
    Liu D, Yu Q, Ning Q, Liu Z, Song J.
    Drug Metab Rev; 2022 Feb 20; 54(1):1-21. PubMed ID: 34807779
    [Abstract] [Full Text] [Related]

  • 35. Analysis of the UDP-glucuronosyltransferase gene in Portuguese patients with a clinical diagnosis of Gilbert and Crigler-Najjar syndromes.
    Costa E, Vieira E, Martins M, Saraiva J, Cancela E, Costa M, Bauerle R, Freitas T, Carvalho JR, Santos-Silva E, Barbot J, Dos Santos R.
    Blood Cells Mol Dis; 2006 Feb 20; 36(1):91-7. PubMed ID: 16269258
    [Abstract] [Full Text] [Related]

  • 36. Influence of mutations associated with Gilbert and Crigler-Najjar type II syndromes on the glucuronidation kinetics of bilirubin and other UDP-glucuronosyltransferase 1A substrates.
    Udomuksorn W, Elliot DJ, Lewis BC, Mackenzie PI, Yoovathaworn K, Miners JO.
    Pharmacogenet Genomics; 2007 Dec 20; 17(12):1017-29. PubMed ID: 18004206
    [Abstract] [Full Text] [Related]

  • 37. Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome.
    Iolascon A, Faienza MF, Giordani L, Perrotta S, Ruggiu G, Meloni GF, del Giudice EM.
    Eur J Haematol; 1999 May 20; 62(5):307-10. PubMed ID: 10359058
    [Abstract] [Full Text] [Related]

  • 38. Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn.
    Monaghan G, McLellan A, McGeehan A, Li Volti S, Mollica F, Salemi I, Din Z, Cassidy A, Hume R, Burchell B.
    J Pediatr; 1999 Apr 20; 134(4):441-6. PubMed ID: 10190918
    [Abstract] [Full Text] [Related]

  • 39. Crigler-Najjar Syndrome Type II Diagnosed in a Patient with Jaundice Since Birth.
    Liaqat A, Shahid A, Attiq H, Ameer A, Imran M.
    J Coll Physicians Surg Pak; 2018 Oct 20; 28(10):806-808. PubMed ID: 30266131
    [Abstract] [Full Text] [Related]

  • 40. Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter.
    Hsieh TY, Shiu TY, Huang SM, Lin HH, Lee TC, Chen PJ, Chu HC, Chang WK, Jeng KS, Lai MM, Chao YC.
    Pharmacogenet Genomics; 2007 Apr 20; 17(4):229-36. PubMed ID: 17496722
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 10.