Deficiency of ceruloplasmin in patients with hepat...[Science. 1952]

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1: Science. 1952 Oct 31;116(3018):484-5. Links

Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease).

PMID: 12994898 [PubMed - indexed for MEDLINE]

Molecular studies of ceruloplasmin deficiency in Wilson's disease.
J Clin Invest. 1987 Oct; 80(4):1200-4.

[J Clin Invest. 1987]
Relation of ceruloplasmin and plasma copper to hepatolenticular degeneration (Wilson's disease).
Prog Neurobiol. 1956; 1:52-63.

[Prog Neurobiol. 1956]
[The onset of psychiatric disorders and Wilson's disease]
Encephale. 2007 Dec; 33(6):924-32. Epub 2007 Sep 5.

[Encephale. 2007]
ReviewWilson's disease: a patient undiagnosed for 18 years.
Hong Kong Med J. 2006 Apr; 12(2):154-8.

[Hong Kong Med J. 2006]
Review[Wilson's disease]
Acta Med Croatica. 2003; 57(3):227-35.

[Acta Med Croatica. 2003]
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Placental expression of ceruloplasmin in pregnancies complicated by severe preeclampsia.
Guller S, Buhimschi CS, Ma YY, Huang ST, Yang L, Kuczynski E, Zambrano E, Lockwood CJ, Buhimschi IA. Lab Invest. 2008 Oct; 88(10):1057-67. Epub 2008 Aug 4.

[Lab Invest. 2008]
A family study of the biochemical defects in Wilson's disease.
Soothill JF, Blainey JD, Neale FC, Fischer-Williams M, Melnick SC. J Clin Pathol. 1961 May; 14(3):264-70.

[J Clin Pathol. 1961]
DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.
Sternlier I, Morell AG, Bauer CD, Combes B, De Bobes-Sternberg S, Schein-Berg IH. J Clin Invest. 1961 Apr; 40(4):707-15.

[J Clin Invest. 1961]
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