Page last updated: 2024-08-17

coenzyme a and Deficiency, Mental

coenzyme a has been researched along with Deficiency, Mental in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (100.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Hsia, YE; Lilljeqvist, AC; Rosenberg, LE	1

Other Studies

2 other study(ies) available for coenzyme a and Deficiency, Mental

Article	Year
Methylmalonic aciduria. An inborn error leading to metabolic acidosis, long-chain ketonuria and intermittent hyperglycinemia. The New England journal of medicine, 1968, Jun-13, Volume: 278, Issue:24 Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Chromatography, Thin Layer; Coenzyme A; Dietary Proteins; Glycine; Humans; Infant; Intellectual Disability; Isomerases; Ketone Bodies; Ligases; Male; Malonates; Vitamin B 12	1968
Importance of the single case. The New England journal of medicine, 1968, Jun-13, Volume: 278, Issue:24 Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Coenzyme A; Glycine; Humans; Infant; Intellectual Disability; Ketone Bodies; Male; Malonates; Vitamin B 12	1968

Article

Year

Methylmalonic aciduria. An inborn error leading to metabolic acidosis, long-chain ketonuria and intermittent hyperglycinemia.

The New England journal of medicine, 1968, Jun-13, Volume: 278, Issue:24

Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Chromatography, Thin Layer; Coenzyme A; Dietary Proteins; Glycine; Humans; Infant; Intellectual Disability; Isomerases; Ketone Bodies; Ligases; Male; Malonates; Vitamin B 12

1968

Importance of the single case.

The New England journal of medicine, 1968, Jun-13, Volume: 278, Issue:24

Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Coenzyme A; Glycine; Humans; Infant; Intellectual Disability; Ketone Bodies; Male; Malonates; Vitamin B 12

1968