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 *

86 related articles for article (PubMed ID: 26286547)

  • 1. Wilson disease: a most unusual patient.
    Walshe JM
    QJM; 2016 Feb; 109(2):117-8. PubMed ID: 26286547
    [No Abstract]   [Full Text] [Related]  

  • 2. [The importance of confirmative diagnosis of presymptomatic patients with Wilson's disease].
    Qiu ZQ
    Zhonghua Er Ke Za Zhi; 2013 Jun; 51(6):406-7. PubMed ID: 24120054
    [No Abstract]   [Full Text] [Related]  

  • 3. [Wilson disease].
    Shimizu N
    Nihon Rinsho; 2004 Jan; 62 Suppl():399-403. PubMed ID: 15011394
    [No Abstract]   [Full Text] [Related]  

  • 4. A tale of two sisters with liver disease.
    Hanouneh MA; Garber A; Tavill AS; Zein NN; Hanouneh IA
    Cleve Clin J Med; 2016 Feb; 83(2):109-15. PubMed ID: 26871387
    [No Abstract]   [Full Text] [Related]  

  • 5. Early and severe liver disease associated with homozygosity for an exon 7 mutation, G691R, in Wilson's disease.
    Barada K; Nemer G; ElHajj II; Touma J; Cortas N; Boustany RM; Usta J
    Clin Genet; 2007 Sep; 72(3):264-7. PubMed ID: 17718866
    [No Abstract]   [Full Text] [Related]  

  • 6. Early diagnosis of Wilson Disease in a six-year-old child.
    Lo Curto AG; Marchi A; Grasso M; Arbustini E; Loudianos G; Brega A
    J Pediatr; 2006 Jan; 148(1):141. PubMed ID: 16423616
    [No Abstract]   [Full Text] [Related]  

  • 7. Diagnosis and treatment of Wilson disease: an update.
    Roberts EA; Schilsky ML;
    Hepatology; 2008 Jun; 47(6):2089-111. PubMed ID: 18506894
    [No Abstract]   [Full Text] [Related]  

  • 8. Simple and effective strategies for detection of allele dropout in PCR-based diagnosis of Wilson disease.
    Gupta A; Nasipuri P; Das SK; Ray K
    Clin Chem; 2006 Aug; 52(8):1611-2. PubMed ID: 16873303
    [No Abstract]   [Full Text] [Related]  

  • 9. Wilson disease: lessons from an island population.
    Tanner S
    J Pediatr Gastroenterol Nutr; 2012 Jan; 54(1):6-7. PubMed ID: 21832954
    [No Abstract]   [Full Text] [Related]  

  • 10. Genotype-phenotype correlation in Wilson disease.
    Horslen S; Hahn SH
    J Clin Gastroenterol; 2010 Jul; 44(6):387-8. PubMed ID: 20421802
    [No Abstract]   [Full Text] [Related]  

  • 11. Wilson disease in children: analysis of 57 cases.
    Manolaki N; Nikolopoulou G; Daikos GL; Panagiotakaki E; Tzetis M; Roma E; Kanavakis E; Syriopoulou VP
    J Pediatr Gastroenterol Nutr; 2009 Jan; 48(1):72-7. PubMed ID: 19172127
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Retrospective determination of ceruloplasmin in newborn screening blood spots of patients with Wilson disease.
    Kroll CA; Ferber MJ; Dawson BD; Jacobson RM; Mensink KA; Lorey F; Sherwin J; Cunningham G; Rinaldo P; Matern D; Hahn SH
    Mol Genet Metab; 2006; 89(1-2):134-8. PubMed ID: 16644258
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [CME laboratory tests. Non-cirrhotic portal hypertension with nearly lethal consequences. Wilson disease]].
    Jaeger A
    Praxis (Bern 1994); 2013 May; 102(11):692-5. PubMed ID: 23692912
    [No Abstract]   [Full Text] [Related]  

  • 14. Muddying the water: Wilson's disease challenges will not soon disappear.
    Dufour JF; Kaplan MM
    Gastroenterology; 1997 Jul; 113(1):348-50. PubMed ID: 9207298
    [No Abstract]   [Full Text] [Related]  

  • 15. New knowledge of genetic pathogenesis of hemochromatosis and Wilson's disease.
    Bacon BR; Schilsky ML
    Adv Intern Med; 1999; 44():91-116. PubMed ID: 9929706
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Alagille syndrome and Wilson disease in siblings: a diagnostic conundrum.
    Amson M; Lamoureux E; Hilzenrat N; Tischkowitz M
    Can J Gastroenterol; 2012 Jun; 26(6):330-2. PubMed ID: 22720273
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Strokelike presentation of Wilson disease with homozygosity for a novel T766R mutation.
    Pendlebury ST; Rothwell PM; Dalton A; Burton EA
    Neurology; 2004 Nov; 63(10):1982-3. PubMed ID: 15557537
    [No Abstract]   [Full Text] [Related]  

  • 18. Overcoming obstacles to the diagnosis of Wilson's disease.
    Schilsky ML; Sternlieb I
    Gastroenterology; 1997 Jul; 113(1):350-3. PubMed ID: 9207299
    [No Abstract]   [Full Text] [Related]  

  • 19. Acute Gallbladder Hydrops and Arthritis: unusual initial manifestations of Wilson's Disease (WD): Case Report.
    Gucev ZS; Pop-Jordanova N; Calovska V; Tasic V; Slavevska N; Laban N; Noli MC; Lepori MB; Loudianos G
    Prilozi; 2011; 32(2):307-15. PubMed ID: 22286624
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diagnostic accuracy of serum ceruloplasmin in Wilson disease: determination of sensitivity and specificity by ROC curve analysis among ATP7B-genotyped subjects.
    Mak CM; Lam CW; Tam S
    Clin Chem; 2008 Aug; 54(8):1356-62. PubMed ID: 18556333
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.