BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 10391079)

  • 1. [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]  

  • 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. 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]  

  • 5. Hereditary ceruloplasmin deficiency with hemosiderosis.
    Okamoto N; Wada S; Oga T; Kawabata Y; Baba Y; Habu D; Takeda Z; Wada Y
    Hum Genet; 1996 Jun; 97(6):755-8. PubMed ID: 8641692
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [An autopsy case of multiple system atrophy with a heteroallelic ceruloplasmin gene mutation].
    Yomono H; Kurisaki H; Murayama S; Hebisawa A; Miyajima H; Takahashi Y
    Rinsho Shinkeigaku; 2003 Jul; 43(7):398-402. PubMed ID: 14582365
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family.
    Morita H; Ikeda S; Yamamoto K; Morita S; Yoshida K; Nomoto S; Kato M; Yanagisawa N
    Ann Neurol; 1995 May; 37(5):646-56. PubMed ID: 7755360
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis.
    Yazaki M; Yoshida K; Nakamura A; Furihata K; Yonekawa M; Okabe T; Yamashita N; Ohta M; Ikeda S
    J Neurol Sci; 1998; 156(1):30-4. PubMed ID: 9559983
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

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

  • 11. A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans.
    Yoshida K; Furihata K; Takeda S; Nakamura A; Yamamoto K; Morita H; Hiyamuta S; Ikeda S; Shimizu N; Yanagisawa N
    Nat Genet; 1995 Mar; 9(3):267-72. PubMed ID: 7539672
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. Cerebellar ataxia associated with heteroallelic ceruloplasmin gene mutation.
    Miyajima H; Kono S; Takahashi Y; Sugimoto M; Sakamoto M; Sakai N
    Neurology; 2001 Dec; 57(12):2205-10. PubMed ID: 11756598
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [A case of cerebellar degeneration with schizophrenia-like psychosis, severe iron deficiency, hypoceruloplasminemia and abnormal electroretinography: a new syndrome?].
    Kimura A; Yoshino H; Yuasa T
    Rinsho Shinkeigaku; 2001 Aug; 41(8):507-11. PubMed ID: 11889836
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A case of aceruloplasminaemia: abnormal serum ceruloplasmin protein without ferroxidase activity.
    Takeuchi Y; Yoshikawa M; Tsujino T; Kohno S; Tsukamoto N; Shiroi A; Kikuchi E; Fukui H; Miyajima H
    J Neurol Neurosurg Psychiatry; 2002 Apr; 72(4):543-5. PubMed ID: 11909923
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. A case of IgA nephropathy and renal hemosiderosis associated with primary hemochromatosis.
    Nakayama M; Kaizu Y; Uesugi N; Nakashita S; Suehiro T
    Ren Fail; 2008; 30(8):813-7. PubMed ID: 18791957
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hepatic iron overload or cirrhosis may occur in acquired copper deficiency and is likely mediated by hypoceruloplasminemia.
    Thackeray EW; Sanderson SO; Fox JC; Kumar N
    J Clin Gastroenterol; 2011 Feb; 45(2):153-8. PubMed ID: 20502350
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.