메뉴 건너뛰기




Volumn 61, Issue 5, 1996, Pages 506-509

Hereditary caeruloplasmin deficiency: Clinicopathological study of a patient

Author keywords

Dementia; Diabetes mellitus; Hereditary caeruloplasmin deficiency; Iron deposition

Indexed keywords

CERULOPLASMIN;

EID: 0029850401     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.61.5.506     Document Type: Article
Times cited : (39)

References (18)
  • 1
    • 0023240051 scopus 로고
    • Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration
    • Miyajima H, Nishimura Y, Mizoguchi K, Sakamoto M, Shimizu T, Honda N. Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration. Neurology 1987;37:761-7.
    • (1987) Neurology , vol.37 , pp. 761-767
    • Miyajima, H.1    Nishimura, Y.2    Mizoguchi, K.3    Sakamoto, M.4    Shimizu, T.5    Honda, N.6
  • 3
    • 0029007765 scopus 로고
    • Hereditary ceruloplasmin deficiency with hemosiderosis: A clinicopathological study of a Japanese family
    • Monta H, Ikeda S, Yamamoto K, et al. Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family. Ann Neurol 1995;37: 640-56.
    • (1995) Ann Neurol , vol.37 , pp. 640-656
    • Monta, H.1    Ikeda, S.2    Yamamoto, K.3
  • 4
    • 0028895749 scopus 로고
    • A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans
    • Yoshida K, Furihata K, Takeda S, et al. A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans. Nature Genetics 1995;9:267-72.
    • (1995) Nature Genetics , vol.9 , pp. 267-272
    • Yoshida, K.1    Furihata, K.2    Takeda, S.3
  • 6
    • 0027376466 scopus 로고
    • Cloning the Wilson disease gene
    • Chelly J, Monaco AP. Cloning the Wilson disease gene. Nature Genetics 1993;5:317-8.
    • (1993) Nature Genetics , vol.5 , pp. 317-318
    • Chelly, J.1    Monaco, A.P.2
  • 7
    • 0012330650 scopus 로고
    • Hemochromatosis and other iron storage disorders
    • Lee GR, Bithell TC, Foerster J, Athers JW, Lukens JN, eds. Philadelphia: Lea and Febiger
    • Edwards CQ. Hemochromatosis and other iron storage disorders. In: Lee GR, Bithell TC, Foerster J, Athers JW, Lukens JN, eds. Witnrobe's clinical hematology, 9th ed. Philadelphia: Lea and Febiger, 1993:872-84.
    • (1993) Witnrobe's Clinical Hematology, 9th Ed. , pp. 872-884
    • Edwards, C.Q.1
  • 8
    • 0029086742 scopus 로고
    • Hereditary haemochromatosis: A case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome
    • Nielsen JE, Jensen NL, Krabbe K. Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome. J Neurol Neurosurg Psychiatry 1995;59:318-21.
    • (1995) J Neurol Neurosurg Psychiatry , vol.59 , pp. 318-321
    • Nielsen, J.E.1    Jensen, N.L.2    Krabbe, K.3
  • 9
    • 0029618814 scopus 로고
    • A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus
    • Daimon M, Kato T, Kawanami T, et al. A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus. Biochem Biophys Res Commun 1995;217:89-95.
    • (1995) Biochem Biophys Res Commun , vol.217 , pp. 89-95
    • Daimon, M.1    Kato, T.2    Kawanami, T.3
  • 10
    • 0026317374 scopus 로고
    • Hallervorden-Spatz syndrome and brain iron metabolism
    • Swaiman KF. Hallervorden-Spatz syndrome and brain iron metabolism. Arch Neurol 1991;48:1285-93.
    • (1991) Arch Neurol , vol.48 , pp. 1285-1293
    • Swaiman, K.F.1
  • 11
    • 0002840628 scopus 로고
    • Nutritional deficiencies and metabolic disorders
    • Adams JH, Duchen LW, eds. London: Edward Arnold
    • Duchen LW, Jacobs JM. Nutritional deficiencies and metabolic disorders. In: Adams JH, Duchen LW, eds. Greenfield's neuropathology. 5th ed. London: Edward Arnold, 1992:811-80.
    • (1992) Greenfield's Neuropathology. 5th Ed. , pp. 811-880
    • Duchen, L.W.1    Jacobs, J.M.2
  • 12
    • 0013977884 scopus 로고
    • Factors influencing ceruloplasmin levels in normal individuals
    • Cox DW. Factors influencing ceruloplasmin levels in normal individuals. J Lab Clin Med 1966;68:893-904.
    • (1966) J Lab Clin Med , vol.68 , pp. 893-904
    • Cox, D.W.1
  • 14
    • 0015217690 scopus 로고
    • The mobilization of iron from the perfused mammalian liver by a serum copper enzyme, ferroxidase I
    • Osaki S, Johnson DA, Frieden E. The mobilization of iron from the perfused mammalian liver by a serum copper enzyme, ferroxidase I. J Biol Chem 1971;246:3018-23.
    • (1971) J Biol Chem , vol.246 , pp. 3018-3023
    • Osaki, S.1    Johnson, D.A.2    Frieden, E.3
  • 15
    • 0014027719 scopus 로고
    • The possible significance of the ferrous oxidase activity of ceruloplasmin in normal human serum
    • Osaki S, Johnson DA, Frieden E. The possible significance of the ferrous oxidase activity of ceruloplasmin in normal human serum. J Biol Chem 1966;241:2746-51.
    • (1966) J Biol Chem , vol.241 , pp. 2746-2751
    • Osaki, S.1    Johnson, D.A.2    Frieden, E.3
  • 16
    • 0015295917 scopus 로고
    • Observations on the pathogenesis, complications, and treatment of diabetes in 115 cases of hemochromatosis
    • Dymock IW, Cassaar J, Pyke DA, Oakley WG, Williams R. Observations on the pathogenesis, complications, and treatment of diabetes in 115 cases of hemochromatosis. Am J Med 1972;52:203-10.
    • (1972) Am J Med , vol.52 , pp. 203-210
    • Dymock, I.W.1    Cassaar, J.2    Pyke, D.A.3    Oakley, W.G.4    Williams, R.5
  • 18
    • 0022381482 scopus 로고
    • Hallervorden-Spatz disease: Cysteine accumulation and cysteine dioxygenase deficiency in the globus pallidus
    • Perry TL, Norman MG, Yong VW, et al. Hallervorden-Spatz disease: cysteine accumulation and cysteine dioxygenase deficiency in the globus pallidus. Ann Neurol 1985;18:482-9.
    • (1985) Ann Neurol , vol.18 , pp. 482-489
    • Perry, T.L.1    Norman, M.G.2    Yong, V.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.