(Q36834658)

16 August 2017

1 reference

title

Hereditary caeruloplasmin deficiency: clinicopathological study of a patient (English)

1 reference

16 August 2017

Kawanami T

1

1 reference

16 August 2017

Kato T

2

1 reference

16 August 2017

Daimon M

3

1 reference

16 August 2017

Tominaga M

4

1 reference

16 August 2017

Sasaki H

5

1 reference

16 August 2017

Maeda K

6

1 reference

16 August 2017

Arai S

7

1 reference

16 August 2017

Shikama Y

8

1 reference

16 August 2017

Katagiri T

9

1 reference

16 August 2017

language of work or name

English

0 references

publication date

1 November 1996

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

16 August 2017

1 reference

16 August 2017

61

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16 August 2017

5

1 reference

16 August 2017

506-509

1 reference

Aceruloplasminemia: molecular characterization of this disorder of iron metabolism

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074049

Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074049

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074049

Hallervorden-Spatz disease: cysteine accumulation and cysteine dioxygenase deficiency in the globus pallidus

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074049

Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074049

Hallervorden-Spatz Syndrome and Brain Iron Metabolism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074049

Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074049

Observations on the pathogenesis, complications and treatment of diabetes in 115 cases of haemochromatosis

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074049

Hereditary hypoceruloplasminemia

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074049

Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074049

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

5 September 2018

1 reference

12 December 2020

A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus

1 reference

12 December 2020

The Mobilization of Iron from the Perfused Mammalian Liver by a Serum Copper Enzyme, Ferroxidase I

1 reference

12 December 2020

Cloning the Wilson disease gene

1 reference

12 December 2020

Factors influencing serum ceruloplasmin levels in normal individuals

1 reference

12 December 2020

Identifiers

DOI

10.1136/JNNP.61.5.506

1 reference

16 August 2017

1 reference

16 August 2017

PubMed publication ID

8937346

1 reference