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methylmalonic acid and MS (Multiple Sclerosis)

methylmalonic acid has been researched along with MS (Multiple Sclerosis) in 3 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.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's1 (33.33)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Vrethem, M1
Mattsson, E1
Hebelka, H1
Leerbeck, K1
Osterberg, A1
Landtblom, AM1
Balla, B1
Nilsson, H1
Hultgren, M1
Brattström, L1
Kågedal, B1
Goodkin, DE1
Jacobsen, DW1
Galvez, N1
Daughtry, M1
Secic, M1
Green, R1
Carmel, R1
Watkins, D1
Goodman, SI1
Rosenblatt, DS1

Other Studies

3 other studies available for methylmalonic acid and MS (Multiple Sclerosis)

ArticleYear
Increased plasma homocysteine levels without signs of vitamin B12 deficiency in patients with multiple sclerosis assessed by blood and cerebrospinal fluid homocysteine and methylmalonic acid.
    Multiple sclerosis (Houndmills, Basingstoke, England), 2003, Volume: 9, Issue:3

    Topics: Adult; Aged; Aged, 80 and over; Female; Homocysteine; Humans; Male; Methylmalonic Acid; Middle Aged;

2003
Serum cobalamin deficiency is uncommon in multiple sclerosis.
    Archives of neurology, 1994, Volume: 51, Issue:11

    Topics: Adult; Homocysteine; Humans; Methylmalonic Acid; Middle Aged; Multiple Sclerosis; Muscular Diseases;

1994
Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood.
    The New England journal of medicine, 1988, Jun-30, Volume: 318, Issue:26

    Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adult; Diagnosis, Differential; Female; H

1988