Page last updated: 2024-08-26

propionylcarnitine and Electron Transport Chain Deficiencies, Mitochondrial

propionylcarnitine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Ding, Y; Li, DX; Li, XY; Liu, YP; Qin, YP; Song, JQ; Wang, Q; Yang, YL; Zhang, Y	1

Other Studies

1 other study(ies) available for propionylcarnitine and Electron Transport Chain Deficiencies, Mitochondrial

Article	Year
[Clinical and laboratory studies on four Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduria]. Zhonghua er ke za zhi = Chinese journal of pediatrics, 2016, Volume: 54, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Asian People; Carnitine; Diagnosis, Differential; DNA Mutational Analysis; Humans; Infant; Infant, Newborn; Magnetic Resonance Imaging; Methylmalonic Acid; Mitochondrial Diseases; Mutation; Succinate-CoA Ligases	2016

Article

Year

[Clinical and laboratory studies on four Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduria].

Zhonghua er ke za zhi = Chinese journal of pediatrics, 2016, Volume: 54, Issue:5

Topics: Amino Acid Metabolism, Inborn Errors; Asian People; Carnitine; Diagnosis, Differential; DNA Mutational Analysis; Humans; Infant; Infant, Newborn; Magnetic Resonance Imaging; Methylmalonic Acid; Mitochondrial Diseases; Mutation; Succinate-CoA Ligases

2016