manganese has been researched along with Dystonia in 15 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (6.67) | 18.7374 |
| 1990's | 2 (13.33) | 18.2507 |
| 2000's | 1 (6.67) | 29.6817 |
| 2010's | 7 (46.67) | 24.3611 |
| 2020's | 4 (26.67) | 2.80 |
| Authors | Studies |
|---|---|
| Bianco, IH; Busch-Nentwich, EM; Dadswell, C; González-Méndez, R; Houart, C; Neuhauss, SCF; Niklaus, S; Rihel, J; Sealy, IM; Trivedi, C; Tuschl, K; Valdivia, LE; White, RJ; Wilson, SW | 1 |
| Edler, MK; Guilarte, TR; McGlothan, JL; Rodichkin, AN | 1 |
| Guilarte, TR; Rodichkin, AN | 1 |
| Akbar, R; Arain, F; Chand, P; Padhani, ZA | 1 |
| Aquino, L; Artuch, R; Baide, H; Batllori, M; Darling, A; Dueñas, P; Kurian, MA; Macaya, A; Marti-Sanchez, L; Molero-Luis, M; Muchart, J; Ortigoza-Escobar, JD; Vanegas, MI; Villaronga, M | 1 |
| Abugrara, A; Kabuka, M; Zeglam, A | 1 |
| Anagianni, S; Tuschl, K | 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 |
| Balint, B; Bhatia, KP | 1 |
| Walter, U | 1 |
| Bhatia, KP; Burroughs, AK; Chong, WK; Clayton, PT; Mills, PB; Stamelou, M; Tuschl, K | 1 |
| Chu, NS | 1 |
| Barron, TF; Devenyi, AG; Mamourian, AC | 1 |
| Becker, G; Berg, D; Lange, HK; Rausch, WD; Reiners, K; Riederer, P | 1 |
| Adlmici, G; Callea, L; Di Monda, V; Fazzari, G | 1 |
3 review(s) available for manganese and Dystonia
| 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 |
Genetic Disorders of Manganese Metabolism.
Topics: Biological Transport; Cation Transport Proteins; Child; Dystonia; Homeostasis; Humans; Magnetic Resonance Imaging; Manganese; Mutation | 2019 |
Transcranial sonography in brain disorders with trace metal accumulation.
Topics: Copper; Dystonia; Hepatolenticular Degeneration; Humans; Iron; Manganese; Metals; Parkinson Disease; Trace Elements; Ultrasonography | 2010 |
12 other study(ies) available for manganese and Dystonia
| Article | Year |
|---|---|
Loss of slc39a14 causes simultaneous manganese hypersensitivity and deficiency in zebrafish.
Topics: Animals; Calcium; Cation Transport Proteins; Dystonia; Ions; Manganese; Zebrafish | 2022 |
Pathophysiological studies of aging Slc39a14 knockout mice to assess the progression of manganese-induced dystonia-parkinsonism.
Topics: Aging; Animals; Cation Transport Proteins; Dystonia; Humans; Manganese; Mice; Mice, Knockout; Parkinsonian Disorders; Substantia Nigra | 2022 |
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 |
Hypermanganesemia due to mutations in SLC39A14: further insights into Mn deposition in the central nervous system.
Topics: Cation Transport Proteins; Central Nervous System; Dystonia; Female; Globus Pallidus; Humans; Magnetic Resonance Imaging; Male; Manganese; Metabolic Diseases; Mutation; Zinc Transporter 8 | 2018 |
Autosomal-recessive iron deficiency anemia, dystonia and hypermanganesemia caused by new variant mutation of the manganese transporter gene SLC39A14.
Topics: Anemia, Iron-Deficiency; Cation Transport Proteins; Child, Preschool; Consanguinity; Dystonia; Female; Humans; Manganese; Metabolism, Inborn Errors; Mutation, Missense | 2019 |
Manganese transport disorder: novel SLC30A10 mutations and early phenotypes.
Topics: Adolescent; Cation Transport Proteins; Child, Preschool; Consanguinity; Dystonia; Female; Humans; Male; Manganese; Metal Metabolism, Inborn Errors; Mutation; Pedigree; Phenotype; Zinc Transporter 8 | 2015 |
SLC39A14 mutations expand the spectrum of manganese transporter defects causing parkinsonism-dystonia.
Topics: Dystonia; Dystonic Disorders; Humans; Manganese; Mutation; Parkinsonian Disorders | 2016 |
Dystonia with brain manganese accumulation resulting from SLC30A10 mutations: a new treatable disorder.
Topics: Brain; Cation Transport Proteins; Chelating Agents; Dystonia; Female; Humans; Longitudinal Studies; Magnetic Resonance Imaging; Manganese; Mutation; Pentetic Acid; Young Adult; Zinc Transporter 8 | 2012 |
Effect of levodopa treatment for parkinsonism in welders: a double-blind study.
Topics: Age of Onset; Brain; Clinical Trials as Topic; Diagnosis, Differential; Diagnostic Errors; Dopamine Agents; Double-Blind Method; Dystonia; Gait Disorders, Neurologic; Humans; Levodopa; Manganese; Manganese Poisoning; Occupational Exposure; Parkinson Disease, Secondary; Tremor; Welding | 2004 |
Dystonia, hyperintense basal ganglia, and high whole blood manganese levels in Alagille's syndrome.
Topics: Alagille Syndrome; Basal Ganglia; Child; Dystonia; Female; Humans; Liver Transplantation; Magnetic Resonance Imaging; Manganese; Neurotoxins | 1994 |
Increased tissue copper and manganese content in the lentiform nucleus in primary adult-onset dystonia.
Topics: Age of Onset; Aged; Brain Chemistry; Calcium; Copper; Dystonia; Humans; Manganese; Middle Aged; Zinc | 1999 |
[On a muscular dystony case from manganism. Therapeutic clinic considerations (author's transl)].
Topics: Benserazide; Diazepam; Dystonia; Haloperidol; Humans; Hydrazines; Levodopa; Male; Manganese; Middle Aged | 1979 |