Page last updated: 2024-08-22

manganese and Cerebellar Diseases

manganese has been researched along with Cerebellar Diseases 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
Abou Jamra, R; Beaulieu, CL; Bezieau, S; Boycott, KM; Chudley, AE; Gálvez-Peralta, M; Gebril, OH; Hampson, S; Hegele, RA; Innes, AM; Kernohan, KD; Küry, S; Majewski, J; McLeod, DR; Mhanni, A; Nebert, DW; Parboosingh, JS; Puffenberger, EG; Qin, W; Ramaekers, VT; Redl, D; Reis, A; Schumacher, J; Scott, JN; Tetreault, M; Uebe, S	1

Other Studies

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

Article	Year
Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8. American journal of human genetics, 2015, Dec-03, Volume: 97, Issue:6 Topics: Adolescent; Cation Transport Proteins; Cations, Divalent; Cerebellar Diseases; Child; Dwarfism; Ethnicity; Exome; Female; Gene Expression; Genes, Recessive; High-Throughput Nucleotide Sequencing; Humans; Intellectual Disability; Ion Transport; Male; Manganese; White People; Young Adult; Zinc	2015

Article

Year

Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8.

American journal of human genetics, 2015, Dec-03, Volume: 97, Issue:6

Topics: Adolescent; Cation Transport Proteins; Cations, Divalent; Cerebellar Diseases; Child; Dwarfism; Ethnicity; Exome; Female; Gene Expression; Genes, Recessive; High-Throughput Nucleotide Sequencing; Humans; Intellectual Disability; Ion Transport; Male; Manganese; White People; Young Adult; Zinc

2015