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Journal Abstract Search

141 related items for PubMed ID: 15609677

  • 1. [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
    [Abstract] [Full Text] [Related]

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

  • 3. Treatment of symptomatic heterozygous aceruloplasminemia with oral zinc sulphate.
    Kuhn J, Bewermeyer H, Miyajima H, Takahashi Y, Kuhn KF, Hoogenraad TU.
    Brain Dev; 2007 Aug; 29(7):450-3. PubMed ID: 17307325
    [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
    [Abstract] [Full Text] [Related]

  • 5. [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
    [Abstract] [Full Text] [Related]

  • 6. The neurological presentation of ceruloplasmin gene mutations.
    McNeill A, Pandolfo M, Kuhn J, Shang H, Miyajima H.
    Eur Neurol; 2008 May; 60(4):200-5. PubMed ID: 18667828
    [Abstract] [Full Text] [Related]

  • 7. 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 15; 23(5):751-5. PubMed ID: 18200628
    [Abstract] [Full Text] [Related]

  • 8. Novel mutation in the ceruloplasmin gene causing a cognitive and movement disorder with diabetes mellitus.
    Shang HF, Jiang XF, Burgunder JM, Chen Q, Zhou D.
    Mov Disord; 2006 Dec 15; 21(12):2217-20. PubMed ID: 17013908
    [Abstract] [Full Text] [Related]

  • 9. 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 15; 9(3):267-72. PubMed ID: 7539672
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 42(9):1088-94. PubMed ID: 17710675
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 42(6):947-9. PubMed ID: 15885371
    [Abstract] [Full Text] [Related]

  • 12. [A case of hereditary ceruloplasmin deficiency with hemosiderosis].
    Nakane S, Shirabe S, Suenaga A, Yoshimura T, Nakamura T.
    Rinsho Shinkeigaku; 1999 Jun 15; 39(2-3):347-51. PubMed ID: 10391079
    [Abstract] [Full Text] [Related]

  • 13. [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 15; 43(7):398-402. PubMed ID: 14582365
    [Abstract] [Full Text] [Related]

  • 14. 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 15; 72(4):543-5. PubMed ID: 11909923
    [Abstract] [Full Text] [Related]

  • 15. Cerebellar ataxia associated with heteroallelic ceruloplasmin gene mutation.
    Miyajima H, Kono S, Takahashi Y, Sugimoto M, Sakamoto M, Sakai N.
    Neurology; 2001 Dec 26; 57(12):2205-10. PubMed ID: 11756598
    [Abstract] [Full Text] [Related]

  • 16. Aceruloplasminemia.
    Gitlin JD.
    Pediatr Res; 1998 Sep 26; 44(3):271-6. PubMed ID: 9727700
    [Abstract] [Full Text] [Related]

  • 17. Early onset insulin-dependent diabetes mellitus as an initial manifestation of aceruloplasminaemia.
    Muroi R, Yagyu H, Kobayashi H, Nagata M, Sato N, Ideno J, Fujita N, Ando A, Okada K, Takiyama Y, Nagasaka S, Miyajima H, Nakano I, Ishibashi S.
    Diabet Med; 2006 Oct 26; 23(10):1136-9. PubMed ID: 16978380
    [Abstract] [Full Text] [Related]

  • 18. Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus.
    Logan JI, Harveyson KB, Wisdom GB, Hughes AE, Archbold GP.
    QJM; 1994 Nov 26; 87(11):663-70. PubMed ID: 7820540
    [Abstract] [Full Text] [Related]

  • 19. 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 05; 217(1):89-95. PubMed ID: 8526944
    [Abstract] [Full Text] [Related]

  • 20. Aceruloplasminemia: molecular characterization of this disorder of iron metabolism.
    Harris ZL, Takahashi Y, Miyajima H, Serizawa M, MacGillivray RT, Gitlin JD.
    Proc Natl Acad Sci U S A; 1995 Mar 28; 92(7):2539-43. PubMed ID: 7708681
    [Abstract] [Full Text] [Related]

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