Page last updated: 2024-08-25

uroporphyrin i and Congenital Erythropoietic Porphyria

uroporphyrin i has been researched along with Congenital Erythropoietic Porphyria in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Azuero-Dajud, R; Bragazzi Cunha, J; Elenbaas, JS; Ferguson, AC; Griffin, MS; Kuo, N; Lentz, SI; Maitra, D; Omary, MB; Shavit, JA1
Costet, P; Daniel, JY; de Verneuil, H; Dubus, P; Ged, C; Lalanne, M; Lamrissi-Garcia, I; Mazurier, F; Mendez, M; Moreau-Gaudry, F; Robert, E1
Calvas, P; Colombies, P; De Verneuil, H; Ged, C; Hombrados, I; Moreau-Gaudry, F; Taine, L1

Other Studies

3 other study(ies) available for uroporphyrin i and Congenital Erythropoietic Porphyria

ArticleYear
Acitretin mitigates uroporphyrin-induced bone defects in congenital erythropoietic porphyria models.
    Scientific reports, 2021, 05-05, Volume: 11, Issue:1

    Topics: Acitretin; Animals; Bone and Bones; Bone Development; Cell Line; Disease Models, Animal; Porphyria, Erythropoietic; Uroporphyrins; Zebrafish

2021
A knock-in mouse model of congenital erythropoietic porphyria.
    Genomics, 2006, Volume: 87, Issue:1

    Topics: Amino Acid Substitution; Animals; Bone Marrow Transplantation; Disease Models, Animal; Genetic Therapy; Mice; Mice, Transgenic; Mutation, Missense; Porphyria, Erythropoietic; Uroporphyrinogen III Synthetase; Uroporphyrins

2006
Prenatal diagnosis in congenital erythropoietic porphyria by metabolic measurement and DNA mutation analysis.
    Prenatal diagnosis, 1996, Volume: 16, Issue:1

    Topics: Amniotic Fluid; DNA Mutational Analysis; Female; Fetal Diseases; Homozygote; Humans; Mutation; Porphyria, Erythropoietic; Pregnancy; Prenatal Diagnosis; Uroporphyrinogen III Synthetase; Uroporphyrins

1996