(Q48468324)

11 February 2018

title

Lack of clinical manifestation of hereditary haemochromatosis in South African patients with multiple sclerosis (English)

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11 February 2018

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3

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11 February 2018

author name string

Maritha J Kotze

1

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J Nico P de Villiers

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Stephen Schmidt

4

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Jonathan Carr

5

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Erna Mansvelt

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Elba Fourie

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11 February 2018

Susan J van Rensburg

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11 February 2018

publication date

19 July 2006

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11 February 2018

published in

Metabolic Brain Disease

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11 February 2018

volume

21

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11 February 2018

issue

2-3

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11 February 2018

page(s)

109-120

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11 February 2018

https://scigraph.springernature.com/pub.10.1007/s11011-006-9015-4

exact match

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cites work

Imaging iron stores in the brain using magnetic resonance imaging

1 reference

12 December 2020

Idiopathic hemochromatosis, an interim report.

1 reference

12 December 2020

Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.

1 reference

12 December 2020

Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12.

1 reference

12 December 2020

Iron, transferrin, and ferritin in the rat brain during development and aging

1 reference

12 December 2020

Mutations in the hemochromatosis gene (HFE) and multiple sclerosis.

1 reference

12 December 2020

Identification of three mutations and associated haplotypes in the protoporphyrinogen oxidase gene in South African families with variegate porphyria

1 reference

12 December 2020

Alterations in levels of iron, ferritin, and other trace metals in neurodegenerative diseases affecting the basal ganglia. The Royal Kings and Queens Parkinson's Disease Research Group

1 reference

12 December 2020

High incidence and prevalence of multiple sclerosis in south east Scotland: evidence of a genetic predisposition

1 reference

12 December 2020

Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group

1 reference

12 December 2020

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

1 reference

12 December 2020

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

12 December 2020

The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

1 reference

12 December 2020

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

1 reference

12 December 2020

Hereditary coproporphyria: an imitator of multiple sclerosis

1 reference

12 December 2020

Immunological patterns identifying disease course and evolution in multiple sclerosis patients

1 reference

12 December 2020

Homozygosity for the predominant Cys282Tyr mutation and absence of disease expression in hereditary haemochromatosis

1 reference

12 December 2020

Effect of manipulation of iron storage, transport, or availability on myelin composition and brain iron content in three different animal models.

1 reference

12 December 2020

Spectrum of mutations in the HFE gene implicated in haemochromatosis and porphyria.

1 reference

12 December 2020

Distribution of transferrin and ferritin binding in normal and multiple sclerotic human brains

1 reference

12 December 2020

Analysis of the NRAMP1 gene implicated in iron transport: association with multiple sclerosis and age effects

1 reference

12 December 2020

Porphyria cutanea tarda: the etiological importance of mutations in the HFE gene and viral infection is population-dependent

1 reference

12 December 2020

The major histocompatibility complex-encoded class I-like HFE abrogates endocytosis of transferrin receptor by inducing receptor phosphorylation

1 reference

12 December 2020

Iron uptake in blood-brain barrier endothelial cells cultured in iron-depleted and iron-enriched media.

1 reference

12 December 2020

Biochemical model for inflammation of the brain: the effect of iron and transferrin on monocytes and lipid peroxidation

1 reference

12 December 2020

Abnormalities in iron metabolism in multiple sclerosis

1 reference

12 December 2020

Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis

1 reference

12 December 2020

Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis

1 reference

12 December 2020

High prevalence of the Cys282Tyr HFE mutation facilitates an improved diagnostic service for hereditary haemochromatosis in South Africa

1 reference

12 December 2020

Multiple sclerosis, porphyria-like symptoms, and a history of iron deficiency anemia in a family of Scottish descent

1 reference

12 December 2020

Significance of linkage disequilibrium between mutation C282Y and a MseI polymorphism in population screening and DNA diagnosis of hemochromatosis

1 reference

12 December 2020

A R59W mutation in human protoporphyrinogen oxidase results in decreased enzyme activity and is prevalent in South Africans with variegate porphyria

1 reference

12 December 2020

Molecular analysis reveals a high mutation frequency in the first untranslated exon of the PPOX gene and largely excludes variegate porphyria in a subset of clinically affected Afrikaner families

1 reference

12 December 2020

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group

1 reference

12 December 2020

Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda

1 reference

12 December 2020

Fatigue syndromes: new thoughts and reinterpretation of previous data

1 reference

12 December 2020

The anaemia of chronic disease

1 reference

12 December 2020

A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group

1 reference

12 December 2020

Tissue-specific regulation of iron metabolism and heme synthesis: distinct control mechanisms in erythroid cells.

1 reference

12 December 2020

10.1007/S11011-006-9015-4

Identifiers

DOI

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11 February 2018

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11 February 2018