BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 7820540)

  • 1. Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus.
    Logan JI; Harveyson KB; Wisdom GB; Hughes AE; Archbold GP
    QJM; 1994 Nov; 87(11):663-70. PubMed ID: 7820540
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [A case of ceruloplasmin deficiency which showed dementia, ataxia and iron deposition in the brain].
    Morita H; Inoue A; Yanagisawa N
    Rinsho Shinkeigaku; 1992 May; 32(5):483-7. PubMed ID: 1458725
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Cerebral hemosiderosis related to hereditary ceruloplasmin deficiency. Clinical familial case study].
    Servan J; Elghozi D; Gaynot S; Duclos H
    Rev Neurol (Paris); 1998 Feb; 154(2):158-62. PubMed ID: 9773037
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hepatic iron overload associated with a decreased serum ceruloplasmin level in a novel clinical type of aceruloplasminemia.
    Kono S; Suzuki H; Takahashi K; Takahashi Y; Shirakawa K; Murakawa Y; Yamaguchi S; Miyajima H
    Gastroenterology; 2006 Jul; 131(1):240-5. PubMed ID: 16831606
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Aceruloplasminemia].
    Miyajima H
    Rinsho Shinkeigaku; 2000 Dec; 40(12):1290-2. PubMed ID: 11464482
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary caeruloplasmin deficiency: clinicopathological study of a patient.
    Kawanami T; Kato T; Daimon M; Tominaga M; Sasaki H; Maeda K; Arai S; Shikama Y; Katagiri T
    J Neurol Neurosurg Psychiatry; 1996 Nov; 61(5):506-9. PubMed ID: 8937346
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [A case of hereditary ceruloplasmin deficiency with hemosiderosis].
    Nakane S; Shirabe S; Suenaga A; Yoshimura T; Nakamura T
    Rinsho Shinkeigaku; 1999; 39(2-3):347-51. PubMed ID: 10391079
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. Identification and in silico characterization of a novel compound heterozygosity associated with hereditary aceruloplasminemia.
    Hofmann WP; Welsch C; Takahashi Y; Miyajima H; Mihm U; Krick C; Zeuzem S; Sarrazin C
    Scand J Gastroenterol; 2007 Sep; 42(9):1088-94. PubMed ID: 17710675
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A case of hereditary ceruloplasmin deficiency with iron deposition in the brain associated with chorea, dementia, diabetes mellitus and retinal pigmentation: administration of fresh-frozen human plasma.
    Yonekawa M; Okabe T; Asamoto Y; Ohta M
    Eur Neurol; 1999; 42(3):157-62. PubMed ID: 10529542
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Aceruloplasminemia: a novel mutation in a family with marked phenotypic variability.
    Fasano A; Colosimo C; Miyajima H; Tonali PA; Re TJ; Bentivoglio AR
    Mov Disord; 2008 Apr; 23(5):751-5. PubMed ID: 18200628
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus.
    Daimon M; Kato T; Kawanami T; Tominaga M; Igarashi M; Yamatani K; Sasaki H
    Biochem Biophys Res Commun; 1995 Dec; 217(1):89-95. PubMed ID: 8526944
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A case of aceruloplasminemia presenting as cerebellar ataxia with homozygous mutation nt2602 delG].
    Nagata M; Takiyama Y; Shimazaki H; Nakano I; Miyajima H
    No To Shinkei; 2004 Oct; 56(10):885-9. PubMed ID: 15609677
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Serum antioxidant activity in diabetes mellitus.
    Jones AF; Winkles JW; Jennings PE; Florkowski CM; Lunec J; Barnett AH
    Diabetes Res; 1988 Feb; 7(2):89-92. PubMed ID: 3396268
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Wilson's disease: the importance of measuring serum caeruloplasmin non-immunologically.
    Walshe JM;
    Ann Clin Biochem; 2003 Mar; 40(Pt 2):115-21. PubMed ID: 12662398
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Aceruloplasminemia in an asymptomatic patient with a new mutation. Diagnosis and family genetic analysis.
    Pérez-Aguilar F; Burguera JA; Benlloch S; Berenguer M; Rayón JM
    J Hepatol; 2005 Jun; 42(6):947-9. PubMed ID: 15885371
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Central nervous system involvement in a rare genetic iron overload disorder.
    Bethlehem C; van Harten B; Hoogendoorn M
    Neth J Med; 2010 Oct; 68(10):316-8. PubMed ID: 21071777
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Aceruloplasminemia (hereditary ceruloplasmin deficiency) and diabetes mellitus].
    Momoki T; Terauchi Y
    Nihon Rinsho; 2006 Sep; Suppl 3():100-4. PubMed ID: 17022509
    [No Abstract]   [Full Text] [Related]  

  • 19. Iron accumulation in the liver of male patients with Wilson's disease.
    Shiono Y; Wakusawa S; Hayashi H; Takikawa T; Yano M; Okada T; Mabuchi H; Kono S; Miyajima H
    Am J Gastroenterol; 2001 Nov; 96(11):3147-51. PubMed ID: 11721763
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Use of the stable isotope 65Cu test for the screening of Wilson's disease in a family with two affected members.
    Merli M; Patriarca M; Loudianos G; Valente C; Riggio O; De Felice G; Petrucci F; Caroli S; Attili AF
    Ital J Gastroenterol Hepatol; 1998 Jun; 30(3):270-5. PubMed ID: 9759594
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.