methylmalonic acid has been researched along with Proteinuria in 6 studies
Methylmalonic Acid: A malonic acid derivative which is a vital intermediate in the metabolism of fat and protein. Abnormalities in methylmalonic acid metabolism lead to methylmalonic aciduria. This metabolic disease is attributed to a block in the enzymatic conversion of methylmalonyl CoA to succinyl CoA.
methylmalonic acid : A dicarboxylic acid that is malonic acid in which one of the methylene hydrogens is substituted by a methyl group.
Proteinuria: The presence of proteins in the urine, an indicator of KIDNEY DISEASES.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Proteinuria were a primary presenting symptom, followed by anemia and neurologic symptoms (frequent convulsions and unstable walking, respectively)." | 5.56 | Proteinuria as a presenting sign of combined methylmalonic acidemia and homocysteinemia: case report. ( Chen, LQ; Chen, RY; Chen, XQ; Li, XZ; Lin, Q; Shen, YY; Wu, HY; Xu, QY; Zhu, XM; Zhu, Y, 2020) |
| "A 7-month-old boy presented with vomiting and failure to thrive associated with proteinuria, methylmalonic aciduria and macrocytosis, but without anaemia." | 3.67 | Selective vitamin B12 malabsorption without anaemia but with profound failure to thrive. ( Auchterlonie, IA; Campbell, AG; Thom, H, 1985) |
| "Proteinuria were a primary presenting symptom, followed by anemia and neurologic symptoms (frequent convulsions and unstable walking, respectively)." | 1.56 | Proteinuria as a presenting sign of combined methylmalonic acidemia and homocysteinemia: case report. ( Chen, LQ; Chen, RY; Chen, XQ; Li, XZ; Lin, Q; Shen, YY; Wu, HY; Xu, QY; Zhu, XM; Zhu, Y, 2020) |
| " Increasing the dosage of hydroxycobalamin from 1 to 2." | 1.31 | Cobalamin disorder Cbl-C presenting with late-onset thrombotic microangiopathy. ( Arnout, J; Baumgartner, ER; Fowler, B; Fryns, JP; Grünewald, S; Peters, H; Van Damme, B; Van Damme-Lombaerts, R; Van Hove, JL; Wevers, R, 2002) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 3 (50.00) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, RY | 1 |
| Li, XZ | 1 |
| Lin, Q | 1 |
| Zhu, Y | 1 |
| Shen, YY | 1 |
| Xu, QY | 1 |
| Zhu, XM | 1 |
| Chen, LQ | 1 |
| Wu, HY | 1 |
| Chen, XQ | 1 |
| Kook, PH | 2 |
| Reusch, CE | 1 |
| Hersberger, M | 2 |
| Watkins, D | 1 |
| Rosenblatt, DS | 1 |
| Van Hove, JL | 1 |
| Van Damme-Lombaerts, R | 1 |
| Grünewald, S | 1 |
| Peters, H | 1 |
| Van Damme, B | 1 |
| Fryns, JP | 1 |
| Arnout, J | 1 |
| Wevers, R | 1 |
| Baumgartner, ER | 1 |
| Fowler, B | 1 |
| Auchterlonie, IA | 1 |
| Thom, H | 1 |
| Campbell, AG | 1 |
6 other studies available for methylmalonic acid and Proteinuria
| Article | Year |
|---|---|
Proteinuria as a presenting sign of combined methylmalonic acidemia and homocysteinemia: case report.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Base Sequence; Carnitine; Child, Pres | 2020 |
Prospective long-term evaluation of parenteral hydroxocobalamin supplementation in juvenile beagles with selective intestinal cobalamin malabsorption (Imerslund-Gräsbeck syndrome).
Topics: Anemia, Megaloblastic; Animals; Creatinine; Dog Diseases; Dogs; Drug Administration Schedule; Female | 2018 |
Daily oral cyanocobalamin supplementation in Beagles with hereditary cobalamin malabsorption (Imerslund-Gräsbeck syndrome) maintains normal clinical and cellular cobalamin status.
Topics: Administration, Oral; Anemia, Megaloblastic; Animals; Dog Diseases; Dogs; Female; Malabsorption Synd | 2019 |
Inborn errors of cobalamin absorption and metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Megaloblastic; Cobamides; Homocysteine; Humans; Hyperh | 2011 |
Cobalamin disorder Cbl-C presenting with late-onset thrombotic microangiopathy.
Topics: Age of Onset; Child; Child, Preschool; Female; Hematinics; Hematuria; Hemolysis; Hemolytic-Uremic Sy | 2002 |
Selective vitamin B12 malabsorption without anaemia but with profound failure to thrive.
Topics: Child, Preschool; Dietary Proteins; Humans; Infant; Malabsorption Syndromes; Male; Methylmalonic Aci | 1985 |