methionine has been researched along with Bronze Diabetes in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Brown, RE; Hale, AT; Hudson, BH; Luka, Z; Matta, P; Williams, CS; York, JD | 1 |
| Bratkovic, D; Couper, R; Davidson, GP; Fahy, R; Fletcher, JM; Mackay, RJ; Ranieri, E | 1 |
| Deprez, M; Fridman, V; Gosseye, S; Hubert, AF; Lambert, Y; Lombet, J; Rigo, J; Sokal, E; Verloes, A | 1 |
3 other study(ies) available for methionine and Bronze Diabetes
| Article | Year |
|---|---|
Modulation of sulfur assimilation metabolic toxicity overcomes anemia and hemochromatosis in mice.
Topics: Anemia, Iron-Deficiency; Animals; Basic Helix-Loop-Helix Transcription Factors; Diet; Disease Models, Animal; Female; Gene Expression Regulation; Hemochromatosis; Hemochromatosis Protein; Homeostasis; Homozygote; Humans; Intestinal Mucosa; Iron; Liver; Male; Methionine; Mice; Mice, Knockout; Mutation; Nucleotidases; Organoids; Signal Transduction; Sulfur | 2020 |
Detection of treatable neonatal liver disease by expanded newborn screening.
Topics: alpha-Fetoproteins; Amino Acid Metabolism, Inborn Errors; Antioxidants; Biomarkers; Blood Coagulation Disorders; Diagnosis, Differential; Ferritins; Hemochromatosis; Humans; Hypoalbuminemia; Infant, Newborn; Iron; Iron Chelating Agents; Liver; Male; Methionine; Neonatal Screening; Predictive Value of Tests; Tandem Mass Spectrometry; Treatment Outcome; Tyrosine | 2008 |
Tricho-hepato-enteric syndrome: further delineation of a distinct syndrome with neonatal hemochromatosis phenotype, intractable diarrhea, and hair anomalies.
Topics: Amino Acid Metabolism, Inborn Errors; Diarrhea; Face; Female; Hair; Hemochromatosis; Humans; Infant; Infant, Newborn; Liver; Lung; Male; Methionine; Pregnancy; Syndrome | 1997 |