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Journal Abstract Search
147 related items for PubMed ID: 8721620
1. Increased plasma lipid peroxidation in patients with aceruloplasminemia. Miyajima H, Takahashi Y, Serizawa M, Kaneko E, Gitlin JD. Free Radic Biol Med; 1996; 20(5):757-60. PubMed ID: 8721620 [Abstract] [Full Text] [Related]
2. 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]
3. Late onset diabetes mellitus in patients with hereditary aceruloplasminemia. Miyajima H, Takahashi Y, Shimizu H, Sakai N, Kamata T, Kaneko E. Intern Med; 1996 Aug 28; 35(8):641-5. PubMed ID: 8894739 [Abstract] [Full Text] [Related]
4. Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis. Harris ZL, Klomp LW, Gitlin JD. Am J Clin Nutr; 1998 May 28; 67(5 Suppl):972S-977S. PubMed ID: 9587138 [Abstract] [Full Text] [Related]
5. Aceruloplasminemia. Kono S. Curr Drug Targets; 2012 Aug 28; 13(9):1190-9. PubMed ID: 22515740 [Abstract] [Full Text] [Related]
6. Increased very long-chain fatty acids in erythrocyte membranes of patients with aceruloplasminemia. Miyajima H, Adachi J, Tatsuno Y, Takahashi Y, Fujimoto M, Kaneko E, Gitlin JD. Neurology; 1998 Jan 28; 50(1):130-6. PubMed ID: 9443469 [Abstract] [Full Text] [Related]
7. Aceruloplasminemia, an inherited disorder of iron metabolism. Miyajima H, Takahashi Y, Kono S. Biometals; 2003 Mar 28; 16(1):205-13. PubMed ID: 12572680 [Abstract] [Full Text] [Related]
8. Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis. Xu X, Pin S, Gathinji M, Fuchs R, Harris ZL. Ann N Y Acad Sci; 2004 Mar 28; 1012():299-305. PubMed ID: 15105274 [Abstract] [Full Text] [Related]
9. [Aceruloplasminemia]. Miyajima H. Rinsho Shinkeigaku; 2000 Dec 28; 40(12):1290-2. PubMed ID: 11464482 [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 28; 42(9):1088-94. PubMed ID: 17710675 [Abstract] [Full Text] [Related]
17. CSF abnormalities in patients with aceruloplasminemia. Miyajima H, Fujimoto M, Kohno S, Kaneko E, Gitlin JD. Neurology; 1998 Oct 28; 51(4):1188-90. PubMed ID: 9781556 [Abstract] [Full Text] [Related]
18. Genetic and Clinical Heterogeneity in Thirteen New Cases with Aceruloplasminemia. Atypical Anemia as a Clue for an Early Diagnosis. Vila Cuenca M, Marchi G, Barqué A, Esteban-Jurado C, Marchetto A, Giorgetti A, Chelban V, Houlden H, Wood NW, Piubelli C, Dorigatti Borges M, Martins de Albuquerque D, Yotsumoto Fertrin K, Jové-Buxeda E, Sanchez-Delgado J, Baena-Díez N, Burnyte B, Utkus A, Busti F, Kaubrys G, Suku E, Kowalczyk K, Karaszewski B, Porter JB, Pollard S, Eleftheriou P, Bignell P, Girelli D, Sanchez M. Int J Mol Sci; 2020 Mar 30; 21(7):. PubMed ID: 32235485 [Abstract] [Full Text] [Related]
19. Aceruloplasminemia, an iron metabolic disorder. Miyajima H. Neuropathology; 2003 Dec 30; 23(4):345-50. PubMed ID: 14719552 [Abstract] [Full Text] [Related]
20. Clinical relevance of heterozygosis for aceruloplasminemia. Borges MD, de Albuquerque DM, Lanaro C, Costa FF, Fertrin KY. Am J Med Genet B Neuropsychiatr Genet; 2019 Jun 30; 180(4):266-271. PubMed ID: 30901137 [Abstract] [Full Text] [Related] Page: [Next] [New Search]