Page last updated: 2024-10-17

methylmalonic acid and Atrophy

methylmalonic acid has been researched along with Atrophy 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.

Atrophy: Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes.

Research Excerpts

ExcerptRelevanceReference
"The Cobalamin C deficiency (cblC), characterized with elevated methylmalonic acidemia and homocystinuria in plasma, is an inborn error of cobalamin metabolism."3.88Late-onset cobalamin C deficiency Chinese sibling patients with neuropsychiatric presentations. ( Liu, YM; Wang, SJ; Yan, CZ; Zhao, YY, 2018)
"Mental retardation was identified in most of the cases."1.31Cobalamin (Cbl) C/D deficiency: clinical, neurophysiological and neuroradiologic findings in 14 cases. ( Biancheri, R; Caruso, U; Cerone, R; Gatti, R; Perrone, MV; Rossi, A; Schiaffino, MC; Veneselli, E, 2001)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's2 (33.33)18.2507
2000's2 (33.33)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Wang, SJ1
Yan, CZ1
Liu, YM1
Zhao, YY1
Björkegren, K1
Svärdsudd, K1
Lindgren, A2
Kilander, A1
Bagge, E2
Nexø, E1
Cederblad, A1
Nilsson, O1
Persson, H1
Kilander, AF1
Biancheri, R1
Cerone, R1
Schiaffino, MC1
Caruso, U1
Veneselli, E1
Perrone, MV1
Rossi, A1
Gatti, R1
Heidenreich, R1
Natowicz, M1
Hainline, BE1
Berman, P1
Kelley, RI1
Hillman, RE1
Berry, GT1

Other Studies

6 other studies available for methylmalonic acid and Atrophy

ArticleYear
Late-onset cobalamin C deficiency Chinese sibling patients with neuropsychiatric presentations.
    Metabolic brain disease, 2018, Volume: 33, Issue:3

    Topics: Adolescent; Adult; Asian People; Atrophy; Brain; Brain Diseases; Carrier Proteins; Child; Child, Pre

2018
Reported symptoms and clinical findings in relation to serum cobalamin, folate, methylmalonic acid and total homocysteine among elderly Swedes: a population-based study.
    Journal of internal medicine, 2003, Volume: 254, Issue:4

    Topics: Aged; Atrophy; Cohort Studies; Female; Folic Acid; Health Surveys; Homocysteine; Humans; Male; Methy

2003
Holotranscobalamin - a sensitive marker of cobalamin malabsorption.
    European journal of clinical investigation, 1999, Volume: 29, Issue:4

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Atrophy; Female; Gastric Mucosa; Homocysteine; Humans; I

1999
Schilling and protein-bound cobalamin absorption tests are poor instruments for diagnosing cobalamin malabsorption.
    Journal of internal medicine, 1997, Volume: 241, Issue:6

    Topics: Adult; Atrophy; Duodenum; Female; Homocysteine; Humans; Intestinal Absorption; Male; Methylmalonic A

1997
Cobalamin (Cbl) C/D deficiency: clinical, neurophysiological and neuroradiologic findings in 14 cases.
    Neuropediatrics, 2001, Volume: 32, Issue:1

    Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Atrophy; Brain; Brain Diseases, Metabolic

2001
Acute extrapyramidal syndrome in methylmalonic acidemia: "metabolic stroke" involving the globus pallidus.
    The Journal of pediatrics, 1988, Volume: 113, Issue:6

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Atrophy; Basal Ganglia Diseases; Brain Diseases, M

1988