heme has been researched along with Coproporphyria, Hereditary in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (55.56) | 29.6817 |
| 2010's | 4 (44.44) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Brown, FC; Conway, AJ; Curtis, DJ; Fullinfaw, RO; Jane, SM; Kile, BT | 1 |
| Cuny, JF | 1 |
| Bonkovsky, HL; Dixon, N; Dozier, S; Faust, D; Li, T; Marion, B; Molina, A; Rudnick, S | 1 |
| Ma, E; Mar, V; Nicoll, A; Ross, G; Varigos, G | 1 |
| Allen, KR; Barth, JH; Degg, TJ; Whatley, SD | 1 |
| Beaumont, C; Boileau, C; Camadro, JM; Da Silva, V; Deybach, JC; Flamme, M; Gouya, L; Grandchamp, B; Lamoril, J; Lyoumi, S; Malonova, E; Puy, H; Rose, C; Schmitt, C | 1 |
| Florkowski, C; George, P; Potter, H; Sies, C | 1 |
| Bonkovsky, HL | 1 |
| Sassa, S | 1 |
3 review(s) available for heme and Coproporphyria, Hereditary
| Article | Year |
|---|---|
[The cutaneous porphyrias].
Topics: Biopsy; Coproporphyria, Hereditary; Diagnosis, Differential; Heme; Humans; Photosensitivity Disorders; Porphyria Cutanea Tarda; Porphyria, Erythropoietic; Porphyrias; Protoporphyria, Erythropoietic; Skin; Skin Diseases, Metabolic | 2019 |
Clinical indications for the investigation of porphyria: case examples and evolving laboratory approaches to its diagnosis in New Zealand.
Topics: Adult; Aged, 80 and over; Biomarkers; Child, Preschool; Clinical Laboratory Techniques; Coproporphyria, Hereditary; Female; Heme; Humans; Male; Middle Aged; Porphyria Cutanea Tarda; Porphyria, Acute Intermittent; Porphyria, Erythropoietic; Porphyria, Variegate; Porphyrias; Porphyrins; Protoporphyria, Erythropoietic | 2005 |
Modern diagnosis and management of the porphyrias.
Topics: Acute Disease; Chronic Disease; Coproporphyria, Hereditary; Heme; Humans; Porphobilinogen Synthase; Porphyria Cutanea Tarda; Porphyria, Erythropoietic; Porphyria, Hepatoerythropoietic; Porphyria, Variegate; Porphyrias; Porphyrias, Hepatic; Protoporphyria, Erythropoietic | 2006 |
6 other study(ies) available for heme and Coproporphyria, Hereditary
| Article | Year |
|---|---|
A mouse model of hereditary coproporphyria identified in an ENU mutagenesis screen.
Topics: Anemia, Hypochromic; Animals; Base Sequence; Biosynthetic Pathways; Coproporphyria, Hereditary; Coproporphyrinogen Oxidase; Disease Models, Animal; Ethylnitrosourea; Fasting; Feces; Female; Heme; Male; Mice, Mutant Strains; Mutagenesis; Mutation; Phenobarbital; Phenotype; Pregnancy | 2017 |
Pilot study of mitochondrial bioenergetics in subjects with acute porphyrias.
Topics: Adenosine Triphosphate; Adult; Aged; Aged, 80 and over; Blood Platelets; Coproporphyria, Hereditary; Electron Transport; Energy Metabolism; Female; Heme; Humans; Infant; Leukocytes, Mononuclear; Male; Middle Aged; Mitochondria; Oxygen; Pilot Projects; Porphyria, Acute Intermittent | 2019 |
Haem arginate as effective maintenance therapy for hereditary coproporphyria.
Topics: Abdominal Pain; Adult; Arginine; Coproporphyria, Hereditary; Female; Heme; Humans; Photosensitivity Disorders; Porphobilinogen; Severity of Illness Index; Treatment Outcome | 2011 |
Hereditary coproporphyria: comparison of molecular and biochemical investigations in a large family.
Topics: Adolescent; Adult; Aged; Child; Coproporphyria, Hereditary; DNA Mutational Analysis; Family Health; Feces; Female; Frameshift Mutation; Heme; Humans; Infant, Newborn; Male; Middle Aged; Mutation; Pedigree; Porphyrins; Sequence Analysis, DNA | 2005 |
Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria.
Topics: Amino Acid Sequence; Coproporphyria, Hereditary; Coproporphyrinogen Oxidase; Exons; Gene Expression; Heme; Humans; Iron Overload; Molecular Sequence Data; Mutation; Mutation, Missense; Pedigree; Porphyrias, Hepatic; Protein Structure, Secondary; Sequence Homology | 2005 |
Neurovisceral porphyrias: what a hematologist needs to know.
Topics: Coproporphyria, Hereditary; Erythrocytes; Heme; Humans; Porphobilinogen Synthase; Porphyria, Acute Intermittent; Porphyrias | 2005 |