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 *

149 related articles for article (PubMed ID: 8894739)

  • 61. Glial fibrillary acidic protein is greatly modified by oxidative stress in aceruloplasminemia brain.
    Kaneko K; Nakamura A; Yoshida K; Kametani F; Higuchi K; Ikeda S
    Free Radic Res; 2002 Mar; 36(3):303-6. PubMed ID: 12071349
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Hereditary ceruloplasmin deficiency increases advanced glycation end products in the brain.
    Tajima K; Kawanami T; Nagai R; Horiuchi S; Kato T
    Neurology; 1999 Aug; 53(3):619-22. PubMed ID: 10449130
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Hereditary ceruloplasmin deficiency--a new type of diabetes mellitus.
    Sasaki H; Yamatani K; Kato T; Kawanami T
    Intern Med; 1996 Aug; 35(8):596-7. PubMed ID: 8894730
    [No Abstract]   [Full Text] [Related]  

  • 64. 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]  

  • 65. Astrocytic deformity and globular structures are characteristic of the brains of patients with aceruloplasminemia.
    Kaneko K; Yoshida K; Arima K; Ohara S; Miyajima H; Kato T; Ohta M; Ikeda SI
    J Neuropathol Exp Neurol; 2002 Dec; 61(12):1069-77. PubMed ID: 12484569
    [TBL] [Abstract][Full Text] [Related]  

  • 66. 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]  

  • 67. [Ceruloplasmin deficiency or aceruloplasminemia].
    Shimizu N
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):176-7. PubMed ID: 9645036
    [No Abstract]   [Full Text] [Related]  

  • 68. Aceruloplasminemia in a Turkish adolescent with a novel mutation of ceruloplasmin gene: the first diagnosed case from Turkey.
    Meral Gunes A; Sezgin Evim M; Baytan B; Iwata A; Hida A; Avci R
    J Pediatr Hematol Oncol; 2014 Oct; 36(7):e423-5. PubMed ID: 25247888
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Increased oxysterols associated with iron accumulation in the brains and visceral organs of acaeruloplasminaemia patients.
    Miyajima H; Adachi J; Kohno S; Takahashi Y; Ueno Y; Naito T
    QJM; 2001 Aug; 94(8):417-22. PubMed ID: 11493718
    [TBL] [Abstract][Full Text] [Related]  

  • 70. [Pathological study on central nervous system of patients with hereditary ceruloplasmin deficiency].
    Kawanami T
    Nihon Naika Gakkai Zasshi; 2004 Aug; 93(8):1585-90. PubMed ID: 15384687
    [No Abstract]   [Full Text] [Related]  

  • 71. Age-dependent expression of hephaestin in the brain of ceruloplasmin-deficient mice.
    Cui R; Duan XL; Anderson GJ; Qiao YT; Yu P; Qian ZM; Yoshida K; Takeda S; Guo P; Yang ZL; Chang YZ
    J Trace Elem Med Biol; 2009; 23(4):290-9. PubMed ID: 19747625
    [TBL] [Abstract][Full Text] [Related]  

  • 72. [Hereditary ceruloplasmin deficiency and diabetes].
    Daimon M
    Nihon Naika Gakkai Zasshi; 2004 Aug; 93(8):1573-8. PubMed ID: 15384685
    [No Abstract]   [Full Text] [Related]  

  • 73. Quantification of different iron forms in the aceruloplasminemia brain to explore iron-related neurodegeneration.
    Vroegindeweij LHP; Bossoni L; Boon AJW; Wilson JHP; Bulk M; Labra-Muñoz J; Huber M; Webb A; van der Weerd L; Langendonk JG
    Neuroimage Clin; 2021; 30():102657. PubMed ID: 33839643
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Ectopic fat storage in the pancreas, liver, and abdominal fat depots: impact on β-cell function in individuals with impaired glucose metabolism.
    van der Zijl NJ; Goossens GH; Moors CC; van Raalte DH; Muskiet MH; Pouwels PJ; Blaak EE; Diamant M
    J Clin Endocrinol Metab; 2011 Feb; 96(2):459-67. PubMed ID: 21084401
    [TBL] [Abstract][Full Text] [Related]  

  • 75. [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]  

  • 76. Is aceruloplasminemia treatable? Combining iron chelation and fresh-frozen plasma treatment.
    Poli L; Alberici A; Buzzi P; Marchina E; Lanari A; Arosio C; Ciccone A; Semeraro F; Gasparotti R; Padovani A; Borroni B
    Neurol Sci; 2017 Feb; 38(2):357-360. PubMed ID: 27817091
    [TBL] [Abstract][Full Text] [Related]  

  • 77. [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]  

  • 78. Seizures in Hereditary Aceruloplasminemia.
    Marano M; Bove F; Ricci L; Rohani M; Di Lazzaro V; Assenza G; Fasano A
    Can J Neurol Sci; 2021 Jan; 48(1):144-147. PubMed ID: 32741407
    [No Abstract]   [Full Text] [Related]  

  • 79. Hormetic and regulatory effects of lipid peroxidation mediators in pancreatic beta cells.
    Maulucci G; Daniel B; Cohen O; Avrahami Y; Sasson S
    Mol Aspects Med; 2016 Jun; 49():49-77. PubMed ID: 27012748
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Evaluation of in vivo cerebral metabolism on proton magnetic resonance spectroscopy in patients with impaired glucose tolerance and type 2 diabetes mellitus.
    Sahin I; Alkan A; Keskin L; Cikim A; Karakas HM; Firat AK; Sigirci A
    J Diabetes Complications; 2008; 22(4):254-60. PubMed ID: 18413166
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.