Page last updated: 2024-08-22

manganese and Metal Metabolism, Inborn Errors

manganese has been researched along with Metal Metabolism, Inborn Errors in 6 studies

Research

Studies (6)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (33.33)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	4 (66.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Mukhopadhyay, S; Zogzas, CE	1
Agrawal, PB; Al-Jasmi, F; Berry, GT; Cao, S; D'Gama, AM; Gropman, A; Hauptman, M; Hayflick, SJ; Hertecant, J; Qualls, AE; Rodan, LH; Tuschl, K; Wessling-Resnick, M; Woolf, AD; Yang, ET	1
Aneja, S; Bonifati, V; Breedveld, GJ; Goel, M; Graafland, J; Gulati, P; Hattiholi, V; Jain, P; Kamate, M; Kori, I; Kumar, A; Olgiati, S; Quadri, M; Sharma, S; Talukdar, B	1
Bartnikas, TB	1
Bell, LT; Hurley, LS	1
Field, AC; Wiener, G	1

Reviews

2 review(s) available for manganese and Metal Metabolism, Inborn Errors

Article	Year
Inherited Disorders of Manganese Metabolism. Advances in neurobiology, 2017, Volume: 18 Topics: Cation Transport Proteins; Deficiency Diseases; Humans; Manganese; Manganese Poisoning; Metal Metabolism, Inborn Errors; Zinc; Zinc Transporter 8	2017
Known and potential roles of transferrin in iron biology. Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine, 2012, Volume: 25, Issue:4 Topics: Anemia; Animals; Antimicrobial Cationic Peptides; Hepcidins; Humans; Iron; Manganese; Metal Metabolism, Inborn Errors; Mice; Transferrin	2012

Other Studies

4 other study(ies) available for manganese and Metal Metabolism, Inborn Errors

Article	Year
Novel founder intronic variant in SLC39A14 in two families causing Manganism and potential treatment strategies. Molecular genetics and metabolism, 2018, Volume: 124, Issue:2 Topics: Cation Transport Proteins; Chelating Agents; Child; Child, Preschool; Dystonic Disorders; Female; Humans; Male; Manganese; Metal Metabolism, Inborn Errors; Mutation; Parkinsonian Disorders; Pedigree	2018
Manganese transport disorder: novel SLC30A10 mutations and early phenotypes. Movement disorders : official journal of the Movement Disorder Society, 2015, Volume: 30, Issue:7 Topics: Adolescent; Cation Transport Proteins; Child, Preschool; Consanguinity; Dystonia; Female; Humans; Male; Manganese; Metal Metabolism, Inborn Errors; Mutation; Pedigree; Phenotype; Zinc Transporter 8	2015
Genetic influence on response to dietary manganese deficiency in mice. The Journal of nutrition, 1974, Volume: 104, Issue:1 Topics: Animal Nutritional Physiological Phenomena; Animals; Birth Weight; Deficiency Diseases; Dose-Response Relationship, Drug; Ear, Inner; Female; Genes; Genetics; Hybridization, Genetic; Manganese; Maternal-Fetal Exchange; Metal Metabolism, Inborn Errors; Mice; Mice, Inbred Strains; Mutation; Nutritional Requirements; Pigmentation Disorders; Placenta Diseases; Pregnancy; Pregnancy Complications; Reproduction; Species Specificity	1974
Genetic variation in mineral metabolism of ruminants. The Proceedings of the Nutrition Society, 1971, Volume: 30, Issue:1 Topics: Animals; Calcium; Cattle; Cattle Diseases; Copper; Deficiency Diseases; Female; Liver; Magnesium; Manganese; Metal Metabolism, Inborn Errors; Milk; Phosphates; Potassium; Pregnancy; Sheep; Sheep Diseases; Swayback; Tetany	1971