manganese has been researched along with Dystonic Disorders in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 4 (57.14) | 24.3611 |
| 2020's | 2 (28.57) | 2.80 |
| Authors | Studies |
|---|---|
| Guilarte, TR; Rodichkin, AN | 1 |
| Akbar, R; Arain, F; Chand, P; Padhani, ZA | 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 |
| Bonifati, V; Clayton, PT; Delnooz, CC; Mills, PB; Quadri, M; Steenbergen, EJ; Tuschl, K; van de Warrenburg, BP; Wevers, RA | 1 |
| Abdul-Sada, A; Bodamer, OA; Chong, WK; Clayton, PT; Coroleu-Lletget, W; Cuno, SM; Dadswell, C; Dale, RC; Eaton, S; Enns, CA; Gissen, P; Gregory, A; Hayflick, SJ; Houlden, H; Hung, CY; Jacques, TS; Kara, E; Kurian, MA; Maher, ER; Meyer, E; Mills, PB; Mohammad, SS; Pintos-Morell, G; Prokisch, H; Rihel, J; Sanford, L; Selim, LA; Simpson, MA; Spencer, J; Straatman-Iwanowska, A; Thomas, M; Tiranti, V; Tuschl, K; Valdivia, LE; Valletta, L; Wilson, SW; Woltjer, RL; Yoganathan, S; Younis, R; Zhao, N | 1 |
| Balint, B; Bhatia, KP | 1 |
| Fedoryshyn, L; Friedman, A; Jäger, HR; Komnatska, I; Krolicki, L; Kyrylchuk, M; Lees, A; Matviyenko, Y; Sanotsky, Y; Selikhova, M; Taylor, A | 1 |
1 review(s) available for manganese and Dystonic Disorders
| Article | Year |
|---|---|
Hereditary Disorders of Manganese Metabolism: Pathophysiology of Childhood-Onset Dystonia-Parkinsonism in
Topics: Animals; Cation Transport Proteins; Dystonia; Dystonic Disorders; Humans; Ions; Manganese; Mice; Models, Animal; Mutation; Parkinsonian Disorders; Zebrafish | 2022 |
6 other study(ies) available for manganese and Dystonic Disorders
| Article | Year |
|---|---|
Hypermanganesaemia with dystonia polycythemia and cirrhosis.
Topics: Adult; Cation Transport Proteins; Dystonia; Dystonic Disorders; Female; Humans; Liver Cirrhosis; Manganese; Metabolic Diseases; Mutation; Polycythemia; Young Adult | 2022 |
Novel founder intronic variant in SLC39A14 in two families causing Manganism and potential treatment strategies.
Topics: Cation Transport Proteins; Chelating Agents; Child; Child, Preschool; Dystonic Disorders; Female; Humans; Male; Manganese; Metal Metabolism, Inborn Errors; Mutation; Parkinsonian Disorders; Pedigree | 2018 |
Phenotypic variability in a dystonia family with mutations in the manganese transporter gene.
Topics: Brain; Cation Transport Proteins; Dystonic Disorders; Female; Humans; Manganese; Middle Aged; Mutation; Phenotype; Zinc Transporter 8 | 2013 |
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia.
Topics: Adolescent; Animals; Cation Transport Proteins; Child; Child, Preschool; Dystonic Disorders; Female; Genetic Predisposition to Disease; HEK293 Cells; Homeostasis; Humans; Male; Manganese; Mutation; Parkinsonian Disorders; Pedigree; Young Adult; Zebrafish | 2016 |
SLC39A14 mutations expand the spectrum of manganese transporter defects causing parkinsonism-dystonia.
Topics: Dystonia; Dystonic Disorders; Humans; Manganese; Mutation; Parkinsonian Disorders | 2016 |
Parkinsonism and dystonia caused by the illicit use of ephedrone--a longitudinal study.
Topics: Adolescent; Adult; Brain; Dystonic Disorders; Humans; Illicit Drugs; Longitudinal Studies; Magnetic Resonance Imaging; Male; Manganese; Middle Aged; Neurologic Examination; Parkinsonian Disorders; Propiophenones; Tomography, Emission-Computed, Single-Photon; Young Adult | 2008 |