Page last updated: 2024-08-22

manganese and Genetic Diseases

manganese has been researched along with Genetic Diseases in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Alfadhel, M; Umair, M	1
Applegarth, D; McLeod, DR; Merante, F; Pitkanen, S; Robinson, BH; Tong, T	1

Reviews

1 review(s) available for manganese and Genetic Diseases

Article	Year
Genetic Disorders Associated with Metal Metabolism. Cells, 2019, 12-09, Volume: 8, Issue:12 Topics: Animals; Copper; Genetic Diseases, Inborn; Humans; Iron; Manganese; Selenium; Zinc	2019

Other Studies

1 other study(ies) available for manganese and Genetic Diseases

Article	Year
Familial cardiomyopathy with cataracts and lactic acidosis: a defect in complex I (NADH-dehydrogenase) of the mitochondria respiratory chain. Pediatric research, 1996, Volume: 39, Issue:3 Topics: Acidosis, Lactic; Blotting, Northern; Blotting, Southern; Blotting, Western; Cardiomyopathies; Cataract; Cells, Cultured; Electron Transport; Female; Fibroblasts; Genetic Diseases, Inborn; Humans; Male; Manganese; Mitochondria; Muscle, Skeletal; Myocardium; NAD(P)H Dehydrogenase (Quinone); Pedigree; Pregnancy; Skin; Superoxide Dismutase	1996

Article

Year

Familial cardiomyopathy with cataracts and lactic acidosis: a defect in complex I (NADH-dehydrogenase) of the mitochondria respiratory chain.

Pediatric research, 1996, Volume: 39, Issue:3

Topics: Acidosis, Lactic; Blotting, Northern; Blotting, Southern; Blotting, Western; Cardiomyopathies; Cataract; Cells, Cultured; Electron Transport; Female; Fibroblasts; Genetic Diseases, Inborn; Humans; Male; Manganese; Mitochondria; Muscle, Skeletal; Myocardium; NAD(P)H Dehydrogenase (Quinone); Pedigree; Pregnancy; Skin; Superoxide Dismutase

1996