Page last updated: 2024-10-16

carnitine and Asymptomatic Conditions

carnitine has been researched along with Asymptomatic Conditions in 4 studies

Research Excerpts

ExcerptRelevanceReference
"Carnitine transport was significantly reduced in fibroblasts obtained from all patients with primary carnitine deficiency, but was significantly higher in the asymptomatic women's than in the symptomatic patients' fibroblasts (P < 0."1.38Genotype-phenotype correlation in primary carnitine deficiency. ( Ardon, O; di San Filippo, CA; Longo, N; Ndukwe Erlingsson, UC; Pasquali, M; Rose, EC, 2012)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (75.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Ng, TKS1
Kovalik, JP1
Ching, J1
Chan, AW1
Matchar, DB1
Han, L1
Wu, S1
Ye, J1
Qiu, W1
Zhang, H1
Gao, X1
Wang, Y1
Gong, Z1
Jin, J1
Gu, X1
Couce, ML1
Aldamiz-Echevarría, L1
Bueno, MA1
Barros, P1
Belanger-Quintana, A1
Blasco, J1
García-Silva, MT1
Márquez-Armenteros, AM1
Vitoria, I1
Vives, I1
Navarrete, R1
Fernández-Marmiesse, A1
Pérez, B1
Pérez-Cerdá, C1
Rose, EC1
di San Filippo, CA1
Ndukwe Erlingsson, UC1
Ardon, O1
Pasquali, M1
Longo, N1

Other Studies

4 other studies available for carnitine and Asymptomatic Conditions

ArticleYear
Novel metabolomics markers are associated with pre-clinical decline in hand grip strength in community-dwelling older adults.
    Mechanisms of ageing and development, 2021, Volume: 193

    Topics: Aged; Aging; Asymptomatic Diseases; Biomarkers; Carnitine; Energy Metabolism; Fatty Acids; Female; F

2021
Biochemical, molecular and outcome analysis of eight chinese asymptomatic individuals with methyl malonic acidemia detected through newborn screening.
    American journal of medical genetics. Part A, 2015, Volume: 167A, Issue:10

    Topics: Acetylcarnitine; Acidosis; Asian People; Asymptomatic Diseases; Carboxy-Lyases; Carnitine; Carrier P

2015
Genotype and phenotype characterization in a Spanish cohort with isovaleric acidemia.
    Journal of human genetics, 2017, Volume: 62, Issue:3

    Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Asymptomatic Diseases; Carnitine; Child; Child,

2017
Genotype-phenotype correlation in primary carnitine deficiency.
    Human mutation, 2012, Volume: 33, Issue:1

    Topics: Adult; Animals; Asymptomatic Diseases; Biological Transport; Cardiomyopathies; Carnitine; Child; Chi

2012