methylmalonic acid and leucine

methylmalonic acid has been researched along with leucine in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19904 (50.00)18.7374
1990's3 (37.50)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (12.50)2.80

Authors

AuthorsStudies
Mahoney, MJ1
Amédée-Manesme, O; Besson-Leaud, M; Charpentier, C; Checouri, A; Coude, FX; Ferre, P; Lavaud, J; Leraillez, J; Mselati, JC; Ogier, H; Saudubray, JM1
Porath, U; Schreier, K1
Carter, RJ; Parsons, HG; Snyder, FF; Unrath, M1
Halliday, D; Leonard, JV; Thompson, GN; Walter, JH1
Bartlett, K; Halliday, D; Leonard, JV; Thompson, GN; Walter, JH1
De Meirleir, L; De Raeve, L; Gerlo, E; Ramet, J; Vandenplas, Y1
Haijes, HA; Jans, JJM; van der Ham, M; van Hasselt, PM; Verhoeven-Duif, NM1

Reviews

2 review(s) available for methylmalonic acid and leucine

ArticleYear
Organic acidemias.
    Clinics in perinatology, 1976, Volume: 3, Issue:1

    Topics: Acidosis, Renal Tubular; Acids; Amino Acid Metabolism, Inborn Errors; Amino Acids, Essential; Ammonia; Child; Diagnosis, Differential; Glutarates; Humans; Hydrogen-Ion Concentration; Infant; Infant, Newborn; Leucine; Ligases; Methylmalonic Acid; Prenatal Diagnosis; Propionates; Pyruvates; Urea; Valerates

1976
[Congenital metabolic acidosis in the postnatal period].
    Deutsche medizinische Wochenschrift (1946), 1978, Jun-02, Volume: 103, Issue:22

    Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Fructose-1,6-Diphosphatase Deficiency; Glutarates; Glycogen Storage Disease Type I; Humans; Hyperglycemia; Infant, Newborn; Isoleucine; Ketosis; Lactates; Leucine; Leukoencephalitis, Acute Hemorrhagic; Methylmalonic Acid; Propionates; Syndrome; Thiamine; Valerates; Valine

1978

Other Studies

6 other study(ies) available for methylmalonic acid and leucine

ArticleYear
[Emergency treatment of inborn amino errors of amino acid metabolism detected in the neonatal period].
    Archives francaises de pediatrie, 1979, Volume: 36, Issue:10

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Diuretics, Osmotic; Emergencies; Enteral Nutrition; Exchange Transfusion, Whole Blood; Humans; Infant, Newborn; Leucine; Methylmalonic Acid; Peritoneal Dialysis; Propionates; Valerates

1979
Evaluation of branched-chain amino acid intake in children with maple syrup urine disease and methylmalonic aciduria.
    Journal of inherited metabolic disease, 1990, Volume: 13, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Branched-Chain; Ammonia; Body Weight; Child, Preschool; Creatinine; Dietary Proteins; Female; Food, Formulated; Growth; Humans; Infant; Infant, Newborn; Isoleucine; Leucine; Male; Malonates; Maple Syrup Urine Disease; Methylmalonic Acid; Nutritional Requirements; Valine

1990
In vivo enzyme activity in inborn errors of metabolism.
    Metabolism: clinical and experimental, 1990, Volume: 39, Issue:8

    Topics: Adult; Bicarbonates; Carbon Isotopes; Child; Child, Preschool; Deuterium; Female; Humans; Hydroxylation; Isotope Labeling; Leucine; Male; Malonates; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Methylmalonic Acid; Oxidation-Reduction; Phenylalanine; Phenylketonurias; Propionates; Radioisotope Dilution Technique; Reference Values; Tyrosine

1990
Contribution of aminoacid catabolism to propionate production in methylmalonic acidaemia.
    Lancet (London, England), 1989, Jun-10, Volume: 1, Issue:8650

    Topics: Acyl Coenzyme A; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Humans; Isoleucine; Kinetics; Leucine; Malonates; Methionine; Methylmalonic Acid; Phenylalanine; Threonine; Time Factors; Valine

1989
Acrodermatitis enteropathica-like cutaneous lesions in organic aciduria.
    The Journal of pediatrics, 1994, Volume: 124, Issue:3

    Topics: Acrodermatitis; Amino Acid Metabolism, Inborn Errors; Female; Humans; Infant; Infant, Newborn; Isoleucine; Leucine; Male; Methylmalonic Acid; Microscopy, Electron; Propionates; Skin; Valine

1994
Understanding acute metabolic decompensation in propionic and methylmalonic acidemias: a deep metabolic phenotyping approach.
    Orphanet journal of rare diseases, 2020, 03-06, Volume: 15, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Biochemical Phenomena; Humans; Leucine; Methylmalonic Acid; Propionic Acidemia; Retrospective Studies

2020