Hereditary coproporphyria in Germany: clinical-biochemical studies in 53 patients (Q31555522)

2 July 2017

Hereditary coproporphyria in Germany: clinical-biochemical studies in 53 patients (English)

1 reference

hereditary coproporphyria

2 July 2017

0 references

1 reference

Kühnel A

1

1 reference

PubMed ID

11074238

2 July 2017

Gross U

series ordinal

2

1 reference

PubMed ID

11074238

2 July 2017

Doss MO

series ordinal

3

1 reference

2 July 2017

1 August 2000

1 reference

2 July 2017

Clinical Biochemistry

1 reference

2 July 2017

33

1 reference

2 July 2017

6

1 reference

2 July 2017

465-473

1 reference

Coproporphyrinogen-oxidase deficiency in hereditary coproporphyria

2 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Characterization and expression of cDNA encoding coproporphyrinogen oxidase from a patient with hereditary coproporphyria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphisms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Hormonal oral contraceptives, urinary porphyrin excretion and porphyrias.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

A novel missense mutation in exon 4 of the human coproporphyrinogen oxidase gene in two patients with hereditary coproporphyria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Drug treatment in acute porphyria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Biochemical differentiation of the porphyrias.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Biochemistry of porphyria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Studies on coproporphyrin isomers in urine and feces in the porphyrias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Treatment of the porphyrias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Early administration of heme arginate for acute porphyric attacks

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Relation between uroporphyrin excretion, acute attacks of hereditary coproporphyria and successful treatment with haem arginate

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Compound heterozygous hereditary coproporphyria with fluorescing teeth

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Enzyme assays and the porphyrias: which tissues and when indicated

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Coexistence of hereditary coproporphyria and epilepsy: Coproporphyrinogen oxidase deficiency in liver and kidney

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

[Hereditary coproporphyria (author's transl)]

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Advances in understanding and treating 'the little imitator,' acute porphyria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

The prooxidant effect of 5-aminolevulinic acid in the brain tissue of rats: implications in neuropsychiatric manifestations in porphyrias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

The biochemistry of heme synthesis in porphyria and in the porphyrinurias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Motor neuropathy in porphobilinogen deaminase-deficient mice imitates the peripheral neuropathy of human acute porphyria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Acute porphyrias: pathogenesis of neurological manifestations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyria.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Coproporphyrinogen oxidase: gene organization and description of a mutation leading to exon 6 skipping

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Hereditary coproporphyria: exon screening by heteroduplex analysis detects three novel mutations in the coproporphyrinogen oxidase gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Identification of a novel mutation of the CPO gene in a Japanese hereditary coproporphyria family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Hereditary coproporphyria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Harderoporphyrin coproporphyria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Harderoporphyria: a variant hereditary coproporphyria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

Hereditary coproporphyria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-9120%2800%2900159-4

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0009-9120(00)00159-4

1 reference

2 July 2017

1 reference

PubMed ID

11074238