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Martin Georg Häusler

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Multiple Sclerosis Journal - Experimental, Translational and Clinical|December 20, 2019
Evaluating the relationship between psychometric intelligence and cognitive functions in paediatric multiple sclerosisTugba Kapanci, Kevin Rostásy, Martin Georg Häusler, et al.
Frontiers in Neurology|November 16, 2020
Interval Timing in Pediatric Multiple Sclerosis: Impaired in the Subsecond Range but Unimpaired in the One-Second RangeStefan J Troche, Tugba Kapanci, Thomas H Rammsayer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 29, 2025
Characterization of children with early onset pediatric multiple sclerosisFranziska Kauth, Annikki Bertolini, Eva-Maria Wendel, et al.
Medrxiv : the Preprint Server for Health Sciences|September 15, 2025
Systematic analysis of snRNA genes reveals frequent <i>RNU2-2</i> variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.
Nature Genetics|March 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.
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Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Multiple Sclerosis Journal - Experimental, Translational and Clinical|December 20, 2019
Evaluating the relationship between psychometric intelligence and cognitive functions in paediatric multiple sclerosisTugba Kapanci, Kevin Rostásy, Martin Georg Häusler, et al.
Frontiers in Neurology|November 16, 2020
Interval Timing in Pediatric Multiple Sclerosis: Impaired in the Subsecond Range but Unimpaired in the One-Second RangeStefan J Troche, Tugba Kapanci, Thomas H Rammsayer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 29, 2025
Characterization of children with early onset pediatric multiple sclerosisFranziska Kauth, Annikki Bertolini, Eva-Maria Wendel, et al.
Medrxiv : the Preprint Server for Health Sciences|September 15, 2025
Systematic analysis of snRNA genes reveals frequent <i>RNU2-2</i> variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.
Nature Genetics|March 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.
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