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Karin Tuschl

Showing results (1-10 of 31) with videos related to

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Movement Disorders Clinical Practice|January 24, 2020
Hypermanganesemia with Dystonia 1: A Novel Mutation and Response to Iron SupplementationZuhal Yapici, Karin Tuschl, Mefkure Eraksoy
International Review of Neurobiology|November 12, 2013
Manganese and the brainKarin Tuschl, Philippa B Mills, Peter T Clayton
Brain & Development|April 28, 2016
Hypermanganesemia with Dystonia, Polycythemia and Cirrhosis (HMDPC) due to mutation in the SLC30A10 geneKhairunnisa Mukhtiar, Shahnaz Ibrahim, Karin Tuschl, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 27, 2004
Rapid analysis of total plasma homocysteine by tandem mass spectrometryKarin Tuschl, Olaf A Bodamer, Wolfgang Erwa, et al.
JIMD Reports|January 13, 2023
Hyperphosphatasia with mental retardation syndrome 3: Cerebrospinal fluid abnormalities and correction with pyridoxine and Folinic acidMartina Messina, Emanuela Manea, Thomas Cullup, et al.
Pediatric Neurology|March 31, 2005
Mucopolysaccharidosis type II in females: case report and review of literatureKarin Tuschl, Andreas Gal, Eduard Paschke, et al.
Journal of Inherited Metabolic Disease|November 2, 2025
Removal of Toxic Metabolites-Chelation: Manganese DisordersHendrik Vogt, George E Kostakis, Rupert Purchase, et al.
American Journal of Medical Genetics. Part A|August 7, 2007
Trisomy 1q42.3-qter and monosomy 21q22.3-qter associated with ear anomaly, facial dysmorphology, psychomotor retardation, and epilepsy: delineation of a new syndromeKarin Tuschl, Barbara Fritz, Marion Herle, et al.
Cell Discovery|June 16, 2026
Manganese: biology, physiology and role in diseaseZhidan Xia, Xinran Li, Rui Liu, et al.
Journal of Inherited Metabolic Disease|April 9, 2008
Hepatic cirrhosis, dystonia, polycythaemia and hypermanganesaemia--a new metabolic disorderKarin Tuschl, Philippa B Mills, Howard Parsons, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Movement Disorders Clinical Practice|January 24, 2020
Hypermanganesemia with Dystonia 1: A Novel Mutation and Response to Iron SupplementationZuhal Yapici, Karin Tuschl, Mefkure Eraksoy
International Review of Neurobiology|November 12, 2013
Manganese and the brainKarin Tuschl, Philippa B Mills, Peter T Clayton
Brain & Development|April 28, 2016
Hypermanganesemia with Dystonia, Polycythemia and Cirrhosis (HMDPC) due to mutation in the SLC30A10 geneKhairunnisa Mukhtiar, Shahnaz Ibrahim, Karin Tuschl, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 27, 2004
Rapid analysis of total plasma homocysteine by tandem mass spectrometryKarin Tuschl, Olaf A Bodamer, Wolfgang Erwa, et al.
JIMD Reports|January 13, 2023
Hyperphosphatasia with mental retardation syndrome 3: Cerebrospinal fluid abnormalities and correction with pyridoxine and Folinic acidMartina Messina, Emanuela Manea, Thomas Cullup, et al.
Pediatric Neurology|March 31, 2005
Mucopolysaccharidosis type II in females: case report and review of literatureKarin Tuschl, Andreas Gal, Eduard Paschke, et al.
Journal of Inherited Metabolic Disease|November 2, 2025
Removal of Toxic Metabolites-Chelation: Manganese DisordersHendrik Vogt, George E Kostakis, Rupert Purchase, et al.
American Journal of Medical Genetics. Part A|August 7, 2007
Trisomy 1q42.3-qter and monosomy 21q22.3-qter associated with ear anomaly, facial dysmorphology, psychomotor retardation, and epilepsy: delineation of a new syndromeKarin Tuschl, Barbara Fritz, Marion Herle, et al.
Cell Discovery|June 16, 2026
Manganese: biology, physiology and role in diseaseZhidan Xia, Xinran Li, Rui Liu, et al.
Journal of Inherited Metabolic Disease|April 9, 2008
Hepatic cirrhosis, dystonia, polycythaemia and hypermanganesaemia--a new metabolic disorderKarin Tuschl, Philippa B Mills, Howard Parsons, et al.
Pageof 4