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 *

64 related articles for article (PubMed ID: 16586257)

  • 1. [Correlation of clinical aspects as well as genotype and phenotype in Wilson's disease on the basis of epidemiologic, clinical and cranial MRI findings].
    Hermann W; Günther P; Schneider JP; Villmann T; Kühn HJ; Eichelkraut S
    Fortschr Neurol Psychiatr; 2006 Oct; 74(10):558-66. PubMed ID: 16586257
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype correlation with fine motor symptoms in patients with Wilson's disease.
    Hermann W; Caca K; Eggers B; Villmann T; Clark D; Berr F; Wagner A
    Eur Neurol; 2002; 48(2):97-101. PubMed ID: 12186999
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characteristics of neurological Wilson's disease without Kayser-Fleischer ring.
    Youn J; Kim JS; Kim HT; Lee JY; Lee PH; Ki CS; Cho JW
    J Neurol Sci; 2012 Dec; 323(1-2):183-6. PubMed ID: 23043908
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The impact of apolipoprotein E genotypes on age at onset of symptoms and phenotypic expression in Wilson's disease.
    Schiefermeier M; Kollegger H; Madl C; Polli C; Oder W; Kühn H; Berr F; Ferenci P
    Brain; 2000 Mar; 123 Pt 3():585-90. PubMed ID: 10686180
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [The onset of psychiatric disorders and Wilson's disease].
    Benhamla T; Tirouche YD; Abaoub-Germain A; Theodore F
    Encephale; 2007 Dec; 33(6):924-32. PubMed ID: 18789784
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pseudo-dominant inheritance in Wilson’s disease.
    Neurol Sci; 2016 Jan; 37(1):7-8. PubMed ID: 26758994
    [No Abstract]   [Full Text] [Related]  

  • 7. Wilson's disease.
    Leggio L; Gasbarrini G; Addolorato G
    Lancet; 2007 Mar; 369(9565):902. PubMed ID: 17368142
    [No Abstract]   [Full Text] [Related]  

  • 8. Role of genotyping in Wilson's disease.
    Schmidt HH
    J Hepatol; 2009 Mar; 50(3):449-52. PubMed ID: 19118916
    [No Abstract]   [Full Text] [Related]  

  • 9. New mutation (T1232P) of the ATP-7B gene associated with neurologic and neuropsychiatric dominance onset of Wilson's disease in three unrelated Colombian kindred.
    Velez-Pardo C; Rio MJ; Moreno S; Ramírez-Gomez L; Correa G; Lopera F
    Neurosci Lett; 2004 Sep; 367(3):360-4. PubMed ID: 15337266
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Morphological and functional imaging in neurological and non-neurological Wilson's patients.
    Hermann W
    Ann N Y Acad Sci; 2014 May; 1315():24-9. PubMed ID: 24495036
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Monozygotic female twins discordant for phenotype of Wilson's disease.
    Członkowska A; Gromadzka G; Chabik G
    Mov Disord; 2009 May; 24(7):1066-9. PubMed ID: 19306278
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular pathology of Wilson's disease: a brief.
    Lalioti V; Sandoval I; Cassio D; Duclos-Vallée JC
    J Hepatol; 2010 Dec; 53(6):1151-3. PubMed ID: 20832891
    [No Abstract]   [Full Text] [Related]  

  • 13. Subclinical neurological involvement does not develop if Wilson's disease is treated early.
    Dubbioso R; Ranucci G; Esposito M; Di Dato F; Topa A; Quarantelli M; Matarazzo M; Santoro L; Manganelli F; Iorio R
    Parkinsonism Relat Disord; 2016 Mar; 24():15-9. PubMed ID: 26851839
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Wilson's disease].
    Ławniczak M; Raszeja-Wyszomirska J; Starzyńska T
    Pol Merkur Lekarski; 2010 Aug; 29(170):125-7. PubMed ID: 20842827
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neurological Wilson's disease lethal for the son, asymptomatic in the father.
    Denoyer Y; Woimant F; Bost M; Edan G; Drapier S
    Mov Disord; 2013 Mar; 28(3):402-3. PubMed ID: 23389864
    [No Abstract]   [Full Text] [Related]  

  • 16. Genotype-phenotype interactions in Wilson's disease: insight from an Icelandic mutation.
    Palsson R; Jonasson JG; Kristjansson M; Bodvarsson A; Goldin RD; Cox DW; Olafsson S
    Eur J Gastroenterol Hepatol; 2001 Apr; 13(4):433-6. PubMed ID: 11338076
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genotype-phenotype correlation in Italian children with Wilson's disease.
    Nicastro E; Loudianos G; Zancan L; D'Antiga L; Maggiore G; Marcellini M; Barbera C; Marazzi MG; Francavilla R; Pastore M; Vajro P; D'Ambrosi M; Vegnente A; Ranucci G; Iorio R
    J Hepatol; 2009 Mar; 50(3):555-61. PubMed ID: 19118915
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular modelling of the nucleotide-binding domain of Wilson's disease protein: location of the ATP-binding site, domain dynamics and potential effects of the major disease mutations.
    Efremov RG; Kosinsky YA; Nolde DE; Tsivkovskii R; Arseniev AS; Lutsenko S
    Biochem J; 2004 Aug; 382(Pt 1):293-305. PubMed ID: 15147237
    [TBL] [Abstract][Full Text] [Related]  

  • 19. R778L, H1069Q, and I1102T mutation study in neurologic Wilson disease.
    Kalita J; Somarajan BI; Misra UK; Mittal B
    Neurol India; 2010; 58(4):627-30. PubMed ID: 20739809
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 4.