Literature DB >> 8937333

Hereditary deficiency of ferroxidase (aka caeruloplasmin)

J I Logan.   

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Year:  1996        PMID： 8937333      PMCID： PMC1074035          DOI： 10.1136/jnnp.61.5.431

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  18 in total

Review 1.  Hereditary caeruloplasmin deficiency: clinicopathological study of a patient.

Authors:  T Kawanami; T Kato; M Daimon; M Tominaga; H Sasaki; K Maeda; S Arai; Y Shikama; T Katagiri
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-11       Impact factor: 10.154

Review 2.  The blue oxidases, ascorbate oxidase, laccase and ceruloplasmin. Modelling and structural relationships.

Authors:  A Messerschmidt; R Huber
Journal:  Eur J Biochem       Date:  1990-01-26

3.  A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans.

Authors:  K Yoshida; K Furihata; S Takeda; A Nakamura; K Yamamoto; H Morita; S Hiyamuta; S Ikeda; N Shimizu; N Yanagisawa
Journal:  Nat Genet       Date:  1995-03       Impact factor: 38.330

4.  The possible significance of the ferrous oxidase activity of ceruloplasmin in normal human serum.

Authors:  S Osaki; D A Johnson; E Frieden
Journal:  J Biol Chem       Date:  1966-06-25       Impact factor: 5.157

5.  Factors influencing serum ceruloplasmin levels in normal individuals.

Authors:  D W Cox
Journal:  J Lab Clin Med       Date:  1966-12

6.  The FET3 gene of S. cerevisiae encodes a multicopper oxidase required for ferrous iron uptake.

Authors:  C Askwith; D Eide; A Van Ho; P S Bernard; L Li; S Davis-Kaplan; D M Sipe; J Kaplan
Journal:  Cell       Date:  1994-01-28       Impact factor: 41.582

7.  Caeruloplasmin: a multi-functional metalloprotein of vertebrate plasma.

Authors:  E Frieden
Journal:  Ciba Found Symp       Date:  1980

8.  The role of ceruloplasmin in iron metabolism.

Authors:  H P Roeser; G R Lee; S Nacht; G E Cartwright
Journal:  J Clin Invest       Date:  1970-12       Impact factor: 14.808

9.  Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus.

Authors:  J I Logan; K B Harveyson; G B Wisdom; A E Hughes; G P Archbold
Journal:  QJM       Date:  1994-11

10.  Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration.

Authors:  H Miyajima; Y Nishimura; K Mizoguchi; M Sakamoto; T Shimizu; N Honda
Journal:  Neurology       Date:  1987-05       Impact factor: 9.910
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