sulfur has been researched along with CBS Deficiency in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (61.54) | 18.7374 |
| 1990's | 1 (7.69) | 18.2507 |
| 2000's | 1 (7.69) | 29.6817 |
| 2010's | 2 (15.38) | 24.3611 |
| 2020's | 1 (7.69) | 2.80 |
| Authors | Studies |
|---|---|
| Kožich, V; Stabler, S | 1 |
| Abman, SH; Allen, RH; Jiang, H; Maclean, KN; Stabler, SP | 1 |
| Hansen, S; MacDougall, L; Perry, TL; Warrington, PD | 1 |
| Brodehl, J; Byrd, DJ; Rödenbeck, D | 1 |
| Rozen, R | 1 |
| Mudd, SH | 1 |
| Cotton, RC; Danks, DM; Goldsmith, D; Patrick, MG | 1 |
| Conerly, EB; Edwards, WA; Mudd, SH; Poole, JR | 1 |
| Roe, DA | 1 |
| Frimpter, GW | 1 |
| Brown, DA; Turner, B; Wilcken, B | 1 |
| Coryell, ME; Findley, JK; Hall, WK; Hollowell, JG; Thevaos, TG | 1 |
| Ditrói, T; Ješina, P; Kožich, V; Krijt, J; Křížková, M; Nagy, P; Sokolová, J | 1 |
5 review(s) available for sulfur and CBS Deficiency
| Article | Year |
|---|---|
Lessons Learned from Inherited Metabolic Disorders of Sulfur-Containing Amino Acids Metabolism.
Topics: Amino Acids, Sulfur; Animals; Brain Diseases; Cysteine; Glutathione; Homocysteine; Homocystinuria; Humans; Hydrogen Sulfide; Liver; Metabolic Diseases; Metabolism, Inborn Errors; Methionine; Methionine Adenosyltransferase; Methylation; S-Adenosylmethionine; Sulfites; Sulfur; Sulfur Compounds | 2020 |
Genetic modulation of homocysteinemia.
Topics: Amino Acid Substitution; Cardiovascular Diseases; Cystathionine beta-Synthase; Cysteine; Folic Acid; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Homocysteine; Homocystinuria; Humans; Hyperhomocysteinemia; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Methyltransferases; Mutation, Missense; Oxidoreductases Acting on CH-NH Group Donors; Point Mutation; Polymorphism, Genetic; Sulfur; Tetrahydrofolates | 2000 |
Diseases of sulphur metabolism: implications for the methionine-homocysteine cycle, and vitamin responsiveness.
Topics: Adolescent; Cystathionine beta-Synthase; Homocysteine; Homocystinuria; Humans; Metabolism, Inborn Errors; Methionine; Methylation; Pyridoxine; Sulfur | 1979 |
Sulphur metabolism in relation to cutaneous disease.
Topics: Chondroitin; Dermatitis, Exfoliative; Glycosaminoglycans; Hair; Homocystinuria; Humans; Keratins; Methionine; Psoriasis; Skin Diseases; Sulfates; Sulfur | 1969 |
Aminoacidurias due to inherited disorders of metabolism (first of two parts).
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Child; Cystathionine; Cysteine; Cystine; Disulfides; Female; Homocystinuria; Humans; Infant, Newborn; Lactates; Male; Methionine; Oxidoreductases; Phenylalanine; Phenylketonurias; Pregnancy; Pyruvates; Sulfhydryl Compounds; Sulfites; Sulfur; Tyrosine | 1973 |
8 other study(ies) available for sulfur and CBS Deficiency
| Article | Year |
|---|---|
Altered hepatic sulfur metabolism in cystathionine β-synthase-deficient homocystinuria: regulatory role of taurine on competing cysteine oxidation pathways.
Topics: Animals; Blotting, Western; Carboxy-Lyases; Cystathionine beta-Synthase; Cysteine; Cysteine Dioxygenase; Dietary Supplements; Female; Homocystinuria; Humans; Liver; Male; Methionine; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Transgenic; Oxidation-Reduction; Real-Time Polymerase Chain Reaction; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Sulfur; Taurine | 2014 |
Sulfur-containing amino acids in the plasma and urine of homocystinurics.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Chromatography, Paper; Homocysteine; Homocystine; Homocystinuria; Humans; Infant; Infant, Newborn; Intellectual Disability; Iodoacetates; Methionine; Sulfoxides; Sulfur; Ultraviolet Rays | 1967 |
The plasma concentration and renal handling of taurine in healthy children and in pediatric patients with disturbed sulfur metabolism.
Topics: Adolescent; Child; Child, Preschool; Cystinosis; Cystinuria; Homocystinuria; Humans; Infant; Infant, Newborn; Kidney; Liver Cirrhosis; Sulfur; Taurine | 1994 |
A screening test for sulphur-containing metabolites in urine using auxotrophic mutants of Escherichia coli K12.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Biological Assay; Cystathionine; Cystinuria; Escherichia coli; Homocystinuria; Humans; Infant, Newborn; Methods; Mutation; S-Adenosylhomocysteine; S-Adenosylmethionine; Sulfur | 1975 |
Homocystinuria due to cystathionine synthase deficiency. Studies of nitrogen balance and sulfur excretion.
Topics: Adolescent; Adult; Amino Acids; Child; Cystathionine; Cystine; Diet; Female; Homocystinuria; Humans; Hydro-Lyases; Male; Methionine; Nitrogen; Pyridoxine; Sulfur | 1975 |
Detection of abnormal sulphur-containing amino acid excretion in a mass urine-screening programme.
Topics: Amino Acid Metabolism, Inborn Errors; Cystathionine; Female; Homocystinuria; Humans; Infant; Male; Mass Screening; Methionine; Renal Aminoacidurias; Sulfur | 1972 |
Homocystinuria as affected by pyridoxine, folic acid, and vitamin B12.
Topics: Adolescent; Child; Diet; Female; Folic Acid; Homocystinuria; Humans; Hydro-Lyases; Liver; Male; Methods; Pyridoxine; Sulfur; Vitamin B 12 | 1968 |
Metabolism of sulfur compounds in homocystinurias.
Topics: Adolescent; Adult; Child; Child, Preschool; Female; Homocystinuria; Humans; Infant; Male; Sulfur Compounds; Young Adult | 2019 |