methylmalonic acid has been researched along with Infant, Newborn, Diseases in 15 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.
Infant, Newborn, Diseases: Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (86.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (13.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lubrano, R | 2 |
| Perez, B | 1 |
| Elli, M | 1 |
| Schroder, TH | 1 |
| Mattman, A | 1 |
| Sinclair, G | 1 |
| Vallance, HD | 1 |
| Lamers, Y | 1 |
| Giardini, O | 1 |
| Marzetti, G | 1 |
| Laurenti, F | 1 |
| Martino, F | 1 |
| Mannarino, O | 1 |
| D'Eufemia, P | 1 |
| Ruberto, U | 1 |
| Kuhara, T | 1 |
| Matsumoto, I | 1 |
| Palmer, T | 1 |
| Oberholzer, VG | 1 |
| Burgess, EA | 1 |
| Mantagos, S | 1 |
| Krieger, IE | 1 |
| Nigro, M | 1 |
| Sarnaik, A | 1 |
| Taqi, Q | 1 |
| Haney, ML | 1 |
| Jeffrey, CP | 1 |
| Cavanagh, HD | 1 |
| Packman, S | 1 |
| Mahoney, MJ | 1 |
| Tanaka, K | 1 |
| Hsia, YE | 1 |
| Morrow, G | 1 |
| Revsin, B | 1 |
| Clark, R | 1 |
| Lebowitz, J | 1 |
| Whelan, DT | 1 |
| Goodman, SI | 1 |
| McCabe, ER | 1 |
| Fennessey, PV | 1 |
| Miles, BS | 1 |
| Mace, JW | 1 |
| Jellum, E | 1 |
| Snyderman, SE | 1 |
| Baumgartner, ER | 1 |
| Bachmann, C | 1 |
| Brechbühler, T | 1 |
| Wick, H | 1 |
| Barness, LA | 1 |
| Shih, VE | 1 |
| Coulombe, JT | 1 |
| Maties, M | 1 |
| Levy, HL | 1 |
| Mills, GA | 1 |
| Walker, V | 1 |
| Clench, MR | 1 |
| Parr, VC | 1 |
1 review available for methylmalonic acid and Infant, Newborn, Diseases
| Article | Year |
|---|---|
The dietary therapy of inherited metabolic disease.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child; C | 1975 |
14 other studies available for methylmalonic acid and Infant, Newborn, Diseases
| Article | Year |
|---|---|
Methylmalonic acidemia and kidney transplantation.
Topics: Female; Heart Defects, Congenital; Heart Failure; Humans; Infant, Newborn, Diseases; Kidney Diseases | 2013 |
Reference interval of methylmalonic acid concentrations in dried blood spots of healthy, term newborns to facilitate neonatal screening of vitamin B12 deficiency.
Topics: Humans; Infant, Newborn; Infant, Newborn, Diseases; Methylmalonic Acid; Neonatal Screening; Referenc | 2016 |
[The neonatal acute form of methylmalonic acidemia. Report of 2 clinical cases].
Topics: Acidosis; Acute Disease; Amino Acid Metabolism, Inborn Errors; Female; Humans; Hyperglycemia; Infant | 1980 |
Studies on the urinary acidic metabolites from three patients with methylmalonic aciduria.
Topics: Carboxylic Acids; Female; Gas Chromatography-Mass Spectrometry; Humans; Infant; Infant, Newborn; Inf | 1980 |
Three instances of neonatal death with hyperammonaemia, each resulting from a different cause.
Topics: Amino Acids; Ammonia; Autopsy; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Lactates; | 1980 |
Screening of high risk infants for metabolic disease in a metropolitan hospital.
Topics: Amino Acids; Ammonia; Carboxylic Acids; Humans; Infant, Newborn; Infant, Newborn, Diseases; Lactates | 1981 |
Corneal involvement in methylmalonic aciduria.
Topics: Amino Acid Metabolism, Inborn Errors; Cornea; Corneal Ulcer; Epithelium; Female; Humans; Infant, New | 1981 |
Severe hyperammonemia in a newborn infant with methylmalonyl-CoA mutase deficiency.
Topics: Ammonia; Humans; Infant, Newborn; Infant, Newborn, Diseases; Isomerases; Liver; Male; Methylmalonic | 1978 |
A new variant of methylmalonic acidemia-defective coenzyme-apoenzyme binding in cultured fibroblasts.
Topics: Amino Acid Metabolism, Inborn Errors; Cells, Cultured; Coenzymes; Female; Fibroblasts; Humans; Infan | 1978 |
Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, Gas; Humans; Hydroxy Acids; Infant, Newborn; I | 1978 |
Acute neonatal nonketotic hyperglycinemia: normal propionate and methylmalonate metabolism.
Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Coenzyme A; Female; Fi | 1975 |
Organic acidosis in infants.
Topics: Acidosis; Adult; Child; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Lactates; Methyl | 1977 |
Methylmalonic aciduria in the newborn.
Topics: Breast Feeding; Follow-Up Studies; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Malon | 1976 |
Analysis of urinary organic acids by Plasmaspray liquid chromatography/mass spectrometry.
Topics: Acidosis; Acids; Chromatography, High Pressure Liquid; Humans; Infant, Newborn; Infant, Newborn, Dis | 1988 |