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 *

108 related articles for article (PubMed ID: 9738861)

  • 1. Crigler-Najjar syndrome in Saudi Arabia.
    Nazer H; Al-Mehaidib A; Shabib S; Ali MA
    Am J Med Genet; 1998 Aug; 79(1):12-5. PubMed ID: 9738861
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Living-related liver transplantation for Crigler-Najjar syndrome in Saudi Arabia.
    Al Shurafa H; Wali S; Chehab MS; Al Shahed M; Jawdat M; Djurberg H; Bassas A
    Clin Transplant; 2002 Jun; 16(3):222-6. PubMed ID: 12010148
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Orthotopic liver transplantation for type I Crigler-Najjar syndrome.
    Kaufman SS; Wood RP; Shaw BW; Markin RS; Rosenthal P; Gridelli B; Vanderhoof JA
    Hepatology; 1986; 6(6):1259-62. PubMed ID: 3098664
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Type I Crigler Najjar syndrome in Tunisia: a study of 30 cases].
    Aloulou H; Ben Thabet A; Khanfir S; Ben Mansour L; Chabchoub I; Labrune P; Kammoun T; Hachicha M
    Tunis Med; 2010 Oct; 88(10):707-9. PubMed ID: 20890816
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lack of deafness in Crigler-Najjar syndrome type 1: a patient survey.
    Suresh G; Lucey JF
    Pediatrics; 1997 Nov; 100(5):E9. PubMed ID: 9347003
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Crigler-Najjar Type 1 syndrome: absence of hepatic bilirubin UDP-glucuronyl transferase activity and therapeutic responses to light.
    Farrell GC; Gollan JL; Stevens SM; Grierson JM
    Aust N Z J Med; 1982 Aug; 12(4):280-5. PubMed ID: 6814411
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [A case of Crigler-Najjar syndrome type I: long survival with bilirubin adsorption and liver transplantation].
    Shimizu N; Mizutani M; Aoki T
    No To Hattatsu; 2005 Jul; 37(4):337-41. PubMed ID: 16026101
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Removal of protein-bound and unbound unconjugated bilirubin by perfusion of plasma through an anion-exchange resin in a case of Crigler-Najjar syndrome type I.
    Ihara H; Shino Y; Hashizume N; Shimizu N; Aoki T; Yoshida M
    Ann Clin Biochem; 2003 Sep; 40(Pt 5):528-33. PubMed ID: 14503990
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two Different UGT1A1 Mutations causing Crigler-Najjar Syndrome types I and II in an Iranian Family.
    Maruo Y; Behnam M; Ikushiro S; Nakahara S; Nouri N; Salehi M
    J Gastrointestin Liver Dis; 2015 Dec; 24(4):523-6. PubMed ID: 26697581
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.
    Kadakol A; Ghosh SS; Sappal BS; Sharma G; Chowdhury JR; Chowdhury NR
    Hum Mutat; 2000 Oct; 16(4):297-306. PubMed ID: 11013440
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Liver Fibrosis Associated With Crigler-Najjar Syndrome in a Compound Heterozygote: A Case Report.
    Fata CR; Gillis LA; Pacheco MC
    Pediatr Dev Pathol; 2017; 20(6):522-525. PubMed ID: 28590786
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Crigler-Najjar syndrome: diagnosis and treatment].
    Lodoso Torrecilla B; Palomo Atance E; Camarena Grande C; Díaz Fernández MC; Hierro Llanillo L; De la Vega Bueno A; Frauca Remacha E; Muñoz Bartolo G; Jara Vega P
    An Pediatr (Barc); 2006 Jul; 65(1):73-8. PubMed ID: 16945293
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Investigation of the molecular basis of the genetic deficiency of UDP-glucuronosyltransferase in Crigler-Najjar syndrome.
    Robertson KJ; Clarke D; Sutherland L; Wooster R; Coughtrie MW; Burchell B
    J Inherit Metab Dis; 1991; 14(4):563-79. PubMed ID: 1749222
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Unconjugated bilirubin and an increased proportion of bilirubin monoconjugates in the bile of patients with Gilbert's syndrome and Crigler-Najjar disease.
    Fevery J; Blanckaert N; Heirwegh KP; Préaux AM; Berthelot P
    J Clin Invest; 1977 Nov; 60(5):970-9. PubMed ID: 409736
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Crigler-Najjar type 1 in children].
    Bach Knudsen K; Ebbesen F
    Ugeskr Laeger; 2013 Oct; 175(42):2489-91. PubMed ID: 24629116
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new type of defect in the gene for bilirubin uridine 5'-diphosphate-glucuronosyltransferase in a patient with Crigler-Najjar syndrome type I.
    Aono S; Yamada Y; Keino H; Sasaoka Y; Nakagawa T; Onishi S; Mimura S; Koiwai O; Sato H
    Pediatr Res; 1994 Jun; 35(6):629-32. PubMed ID: 7936809
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia.
    Zmetáková I; Ferák V; Minárik G; Ficek A; Poláková H; Feráková E; Kádasi L
    Gen Physiol Biophys; 2007 Dec; 26(4):306-10. PubMed ID: 18281749
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 28(10):806-808. PubMed ID: 30266131
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Crigler-Najjar syndrome: treatment at home with phototherapy.
    O'Reilly C; Dixon R
    Scott Med J; 1988 Oct; 33(5):335-6. PubMed ID: 3227337
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Retrovirus-mediated expression of HUG Br1 in Crigler-Najjar syndrome type I human fibroblasts and correction of the genetic defect in Gunn rat hepatocytes.
    Askari F; Hitomi E; Thiney M; Wilson JM
    Gene Ther; 1995 May; 2(3):203-8. PubMed ID: 7614251
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.