Page last updated: 2024-08-23

heme and Metabolism, Inborn Errors

heme has been researched along with Metabolism, Inborn Errors in 13 studies

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-199010 (76.92)18.7374
1990's0 (0.00)18.2507
2000's2 (15.38)29.6817
2010's1 (7.69)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Balwani, M; Desnick, RJ1
Hoffmann, F; Lindberg, RL; Meyer, RP; Meyer, UA1
Koizumi, S1
Hindmarsh, JT1
Gross, R; Kübler, W; Schneider, W1
Meuer, UA1
Lathe, GH1
Winterhalter, KH1
Arias, IM; Wolkoff, AW1
Cline, MJ; Lehrer, RI; Salmon, SE; Schultz, J1
Ota, H; Tanaka, M1
Smith, JC1
Chatterjea, JB; Chatterji, AK1

Reviews

4 review(s) available for heme and Metabolism, Inborn Errors

ArticleYear
The porphyrias: advances in diagnosis and treatment.
    Hematology. American Society of Hematology. Education Program, 2012, Volume: 2012

    Topics: 5-Aminolevulinate Synthetase; DNA; Erythrocytes; Genes, Recessive; Genetic Therapy; Hematology; Heme; Homozygote; Humans; Metabolism, Inborn Errors; Models, Biological; Mutation; Phlebotomy; Porphyria Cutanea Tarda; Porphyria, Erythropoietic; Porphyrias; Skin; Stem Cells

2012
Human heme oxygenase-1 deficiency: a lesson on serendipity in the discovery of the novel disease.
    Pediatrics international : official journal of the Japan Pediatric Society, 2007, Volume: 49, Issue:2

    Topics: Animals; Bilirubin; Biomedical Research; Biosynthetic Pathways; Heme; Heme Oxygenase-1; Humans; Infant, Newborn; Male; Metabolism, Inborn Errors; Mice; Mice, Knockout

2007
Clinical disorders of porphyrin metabolism.
    Clinical biochemistry, 1983, Volume: 16, Issue:4

    Topics: Adult; Child; Erythropoiesis; Feces; Female; Heme; Humans; Jaundice, Chronic Idiopathic; Male; Metabolism, Inborn Errors; Models, Chemical; Pedigree; Porphyrins; Protoporphyrins; Skin Diseases

1983
The degradation of haem by mammals and its excretion as conjugated bilirubin.
    Essays in biochemistry, 1972, Volume: 8

    Topics: Animals; Apoproteins; Bile Pigments; Bilirubin; Carrier Proteins; Chemical Phenomena; Chemistry; Cholestasis; Glucosyltransferases; Glucuronates; Haptoglobins; Heme; Hemopexin; Humans; Hyperbilirubinemia, Hereditary; Infant, Newborn; Jaundice, Neonatal; Kernicterus; Ligands; Liver; Metabolism, Inborn Errors; Serum Albumin; Uridine Diphosphate Sugars

1972

Other Studies

9 other study(ies) available for heme and Metabolism, Inborn Errors

ArticleYear
Cytosolic persistence of mouse brain CYP1A1 in chronic heme deficiency.
    Biological chemistry, 2005, Volume: 386, Issue:11

    Topics: Animals; beta-Naphthoflavone; Brain; Chronic Disease; Cytochrome P-450 CYP1A1; Cytosol; Disease Models, Animal; Enzyme Inhibitors; Female; Genotype; Heme; Hydroxymethylbilane Synthase; Liver; Metabolism, Inborn Errors; Mice; Molecular Sequence Data; RNA, Messenger; Subcellular Fractions

2005
[On a simultaneous occurrence of a glutathione reductase deficiency, a heme synthesis disorder and an Hb-F increase in the erythrocytes].
    Folia haematologica (Leipzig, Germany : 1928), 1969, Volume: 91, Issue:1

    Topics: Adenine Nucleotides; Adult; Erythrocytes; Female; Fetal Hemoglobin; Glutathione Reductase; Heinz Bodies; Heme; Humans; Lactates; Male; Metabolism, Inborn Errors; Middle Aged; Pyruvates

1969
[Intermittent acuteporphyria. Clinical significance of reduced activity of uroporphyrinogen-I-synthetase].
    Schweizerische medizinische Wochenschrift, 1974, Dec-14, Volume: 104, Issue:50

    Topics: 5-Aminolevulinate Synthetase; Acute Disease; Animals; Chlorides; Enzyme Induction; Heme; Lead; Liver; Lyases; Metabolism, Inborn Errors; Porphyrias; Rats

1974
Structure and synthesis of heme and references to globin synthesis.
    Hamatologie und Bluttransfusion, 1972, Volume: 10

    Topics: 5-Aminolevulinate Synthetase; Globins; Heme; Iron; Levulinic Acids; Metabolism, Inborn Errors; Peptide Chain Initiation, Translational; Porphobilinogen; Porphobilinogen Synthase; Porphyrias; Porphyrins; Protein Conformation

1972
Coproporphyrin excretion in amniotic fluid and urine from premature infants: a possible maturation defect.
    Pediatric research, 1974, Volume: 8, Issue:5

    Topics: Ammonia-Lyases; Amniotic Fluid; Chromatography, Thin Layer; Creatinine; Female; Heme; Humans; Infant, Newborn; Infant, Premature; Jaundice, Chronic Idiopathic; Male; Metabolism, Inborn Errors; Porphyrins

1974
Myeloperoxidase deficiency. Immunologic study of a genetic leukocyte defect.
    The New England journal of medicine, 1970, Jan-29, Volume: 282, Issue:5

    Topics: Candidiasis; Eosinophils; Fluorescent Antibody Technique; Genes, Recessive; Heme; Homozygote; Humans; Immunodiffusion; Immunoelectrophoresis; Leukocytes; Metabolism, Inborn Errors; Monocytes; Neutrophils; Peroxidases; Precipitin Tests; Spectrophotometry

1970
A case of primary acquired sideroblastic anemia with deficient -aminolevulinic acid synthetase activity in bone marrow erythroblasts.
    The Tohoku journal of experimental medicine, 1972, Volume: 106, Issue:2

    Topics: 5-Aminolevulinate Synthetase; Acyltransferases; Aged; Anemia, Sideroblastic; Bone Marrow; Bone Marrow Cells; Carbon Isotopes; Erythrocytes; Female; Hematopoietic Stem Cells; Heme; Humans; Iron; Metabolism, Inborn Errors; Myelography; Porphyrins

1972
Heme pigment metabolism: a clinicopathologic spectrum.
    The Medical annals of the District of Columbia, 1968, Volume: 37, Issue:7

    Topics: Heme; Humans; Indicators and Reagents; Infant; Metabolism, Inborn Errors

1968
Porphyrins and porphyrias: new horizons.
    Bulletin of the Calcutta School of Tropical Medicine, 1969, Volume: 17, Issue:3

    Topics: Anemia, Sideroblastic; Heme; India; Metabolic Diseases; Metabolism, Inborn Errors; Porphyrias; Porphyrins; Pyrroles

1969