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

178 related items for PubMed ID: 33421605

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II.
    Sun L, Li M, Zhang L, Teng X, Chen X, Zhou X, Ma Z, Qi L, Wang P.
    Medicine (Baltimore); 2017 Nov; 96(45):e8620. PubMed ID: 29137095
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [From gene to disease; unconjugated hyperbilirubinemia: Gilbert's syndrome and Crigler-Najjar types I and II].
    Drenth JP, Peters WH, Jansen JB.
    Ned Tijdschr Geneeskd; 2002 Aug 10; 146(32):1488-90. PubMed ID: 12198827
    [Abstract] [Full Text] [Related]

  • 8. Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome.
    Gailite L, Rots D, Pukite I, Cernevska G, Kreile M.
    BMC Pediatr; 2018 Oct 03; 18(1):317. PubMed ID: 30285761
    [Abstract] [Full Text] [Related]

  • 9. Co-occurrence of three different mutations in the bilirubin UDP-glucuronosyltransferase gene in a Chinese family with Crigler-Najjar syndrome type I and Gilbert's syndrome.
    Maruo Y, Poon KK, Ito M, Iwai M, Takahashi H, Mori A, Sato H, Takeuchi Y.
    Clin Genet; 2003 Nov 03; 64(5):420-3. PubMed ID: 14616765
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis.
    Zheng B, Hu G, Yu J, Liu Z.
    BMC Pediatr; 2014 Oct 15; 14():267. PubMed ID: 25319636
    [Abstract] [Full Text] [Related]

  • 13. UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias.
    Khan S, Irfan M, Sher G, Zubaida B, Alvi MA, Yasinzai M, Naeem M.
    Ann Hum Genet; 2013 Nov 15; 77(6):482-7. PubMed ID: 23992562
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes.
    Sampietro M, Iolascon A.
    Haematologica; 1999 Feb 15; 84(2):150-7. PubMed ID: 10091414
    [Abstract] [Full Text] [Related]

  • 17. Gilbert and Crigler Najjar syndromes: an update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database.
    Canu G, Minucci A, Zuppi C, Capoluongo E.
    Blood Cells Mol Dis; 2013 Apr 15; 50(4):273-80. PubMed ID: 23403257
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Analysis of UGT1A1 genotype-phenotype correlation in Chinese patients with gilbert and crigler-Najjar II syndrome.
    Wu L, Li Z, Song Y, Li Y, Zhang W, Zhong X, Wang X, Huang J, Ou X.
    Eur J Med Genet; 2024 Oct 15; 71():104962. PubMed ID: 39069255
    [Abstract] [Full Text] [Related]

  • 20. Compound heterozygosity of a novel exon 3 frameshift (p.R357P fs*24) mutation and Y486D mutation in exon 5 of the UGT1A1 gene in a Thai infant with Crigler-Najjar syndrome type 2.
    Tesapirat L, Nilyanimit P, Wanlapakorn N, Poovorawan Y.
    Genet Mol Res; 2015 Apr 13; 14(2):3293-9. PubMed ID: 25966095
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.