Page last updated: 2024-09-02

zinc coproporphyrin iii and Hepatic Porphyria

zinc coproporphyrin iii has been researched along with Hepatic Porphyria in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (33.33)	18.2507
2000's	2 (66.67)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Daimon, M; Kato, T; Kondo, M; Sasaki, H; Susa, S; Yamamori, I; Yamatani, K	1
Daimon, M; Kondo, M; Susa, S; Takeuchi, H; Togari, H; Uemura, O; Ueoka, K	1
Deybach, JC; Doss, MO; Gross, U; Jacob, K; Kühnel, A; Martasek, P; Meissauer, U; Nordmann, Y; Puy, H	1

Reviews

1 review(s) available for zinc coproporphyrin iii and Hepatic Porphyria

Article	Year
Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria. Cellular and molecular biology (Noisy-le-Grand, France), 2002, Volume: 48, Issue:1 Topics: Adult; Coproporphyrinogen Oxidase; Coproporphyrins; DNA Mutational Analysis; Family Health; Female; Heterozygote; Humans; Pedigree; Porphyria Cutanea Tarda; Porphyrias, Hepatic	2002

Article

Year

Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.

Cellular and molecular biology (Noisy-le-Grand, France), 2002, Volume: 48, Issue:1

Topics: Adult; Coproporphyrinogen Oxidase; Coproporphyrins; DNA Mutational Analysis; Family Health; Female; Heterozygote; Humans; Pedigree; Porphyria Cutanea Tarda; Porphyrias, Hepatic

2002

Other Studies

2 other study(ies) available for zinc coproporphyrin iii and Hepatic Porphyria

Article	Year
A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family. Journal of human genetics, 1998, Volume: 43, Issue:3 Topics: Coproporphyrinogen Oxidase; Coproporphyrins; Feces; Female; Humans; Japan; Male; Mutation; Polymorphism, Single-Stranded Conformational; Porphyrias, Hepatic	1998
Neonatal-onset hereditary coproporphyria with male pseudohermaphrodism. Blood, 2001, Dec-15, Volume: 98, Issue:13 Topics: Adrenal Insufficiency; Adrenocorticotropic Hormone; Base Sequence; Chorionic Gonadotropin; Coproporphyrins; Deoxyribonuclease HpaII; Disorders of Sex Development; DNA; Exons; Feces; Heterozygote; Humans; Hydrocortisone; Infant, Newborn; Karyotyping; Male; Molecular Sequence Data; Mutation; Pedigree; Polymerase Chain Reaction; Porphyrias, Hepatic; Sequence Analysis, DNA; Testosterone	2001

Article

Year

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

Journal of human genetics, 1998, Volume: 43, Issue:3

Topics: Coproporphyrinogen Oxidase; Coproporphyrins; Feces; Female; Humans; Japan; Male; Mutation; Polymorphism, Single-Stranded Conformational; Porphyrias, Hepatic

1998

Neonatal-onset hereditary coproporphyria with male pseudohermaphrodism.

Blood, 2001, Dec-15, Volume: 98, Issue:13

Topics: Adrenal Insufficiency; Adrenocorticotropic Hormone; Base Sequence; Chorionic Gonadotropin; Coproporphyrins; Deoxyribonuclease HpaII; Disorders of Sex Development; DNA; Exons; Feces; Heterozygote; Humans; Hydrocortisone; Infant, Newborn; Karyotyping; Male; Molecular Sequence Data; Mutation; Pedigree; Polymerase Chain Reaction; Porphyrias, Hepatic; Sequence Analysis, DNA; Testosterone

2001