Page last updated: 2024-08-22

manganese and Spasms, Infantile

manganese has been researched along with Spasms, Infantile 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
Beaulieu, CL; Biskup, S; Boycott, KM; DuChesne, I; Fiedler, B; Gleixner, EM; Grüneberg, M; Hogrebe, M; Hörtnagel, K; Innes, AM; Kurlemann, G; Marquardt, T; Mhanni, AA; Nebert, DW; Omran, H; Park, JH; Reunert, J; Rust, S; Rutsch, F; Santer, R; Schlingmann, KP; Tsiakas, K; von der Heiden, AL; Wada, Y	1

Other Studies

1 other study(ies) available for manganese and Spasms, Infantile

Article	Year
SLC39A8 Deficiency: A Disorder of Manganese Transport and Glycosylation. American journal of human genetics, 2015, Dec-03, Volume: 97, Issue:6 Topics: Amino Acid Sequence; Carbohydrate Sequence; Cation Transport Proteins; Cations, Divalent; Congenital Disorders of Glycosylation; Dwarfism; Female; Galactose; Gene Expression; High-Throughput Nucleotide Sequencing; Humans; Infant; Ion Transport; Manganese; Molecular Sequence Data; Mutation; Pedigree; Sequence Alignment; Spasms, Infantile	2015

Article

Year

SLC39A8 Deficiency: A Disorder of Manganese Transport and Glycosylation.

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

Topics: Amino Acid Sequence; Carbohydrate Sequence; Cation Transport Proteins; Cations, Divalent; Congenital Disorders of Glycosylation; Dwarfism; Female; Galactose; Gene Expression; High-Throughput Nucleotide Sequencing; Humans; Infant; Ion Transport; Manganese; Molecular Sequence Data; Mutation; Pedigree; Sequence Alignment; Spasms, Infantile

2015