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Martin Krenn

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Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 2025
Reduced Penetrance in Interferonopathy-Associated Dystonia: Hope for Clues to Mechanism?Martin Krenn, Michael Zech
Journal of the Neurological Sciences|July 31, 2022
Spinal muscular atrophy presenting with mild limb-girdle weakness in adulthood: Diagnostic pitfalls in the era of disease-modifying therapiesMartin Krenn, Suren Jengojan, Wolfgang Grisold
BMJ Case Reports|April 12, 2014
CANOMAD responding to weekly treatment with intravenous immunoglobulin (IVIg)Martin Krenn, Geoff Keir, Udo Carl Wieshmann
Movement Disorders : Official Journal of the Movement Disorder Society|October 23, 2022
GNAO1 Haploinsufficiency Associated with a Mild Delayed-Onset Dystonia PhenotypeMartin Krenn, Rudolf Sommer, Thomas Sycha, et al.
Eneurologicalsci|January 13, 2025
Bilateral foot drop as presenting feature of facioscapulohumeral muscular dystrophy type 1Martin Krenn, Veronika Vetchy, Gregor Kasprian, et al.
Seizure|August 27, 2025
ADAM23 haploinsufficiency as a putative oligogenic contributor in an individual with focal epilepsyMartin Krenn, Karl-Heinz Nenning, Susanne Aull-Watschinger, et al.
Scientific Reports|September 28, 2021
Real-world treatment of adult patients with Guillain-Barré syndrome over the last two decadesJakob Rath, Gudrun Zulehner, Bernadette Schober, et al.
Frontiers in Molecular Neuroscience|September 14, 2020
Pathomechanisms and Clinical Implications of Myasthenic Syndromes Exacerbated and Induced by Medical TreatmentsMartin Krenn, Anna Grisold, Philipp Wohlfarth, et al.
International Journal of Molecular Sciences|September 20, 2019
Rare Human Missense Variants can affect the Function of Disease-Relevant Proteins by Loss and Gain of Peroxisomal Targeting MotifsCheng-Shoong Chong, Markus Kunze, Bernhard Hochreiter, et al.
Neurology. Genetics|August 13, 2019
Adult-onset variant ataxia-telangiectasia diagnosed by exome and cDNA sequencingMartin Krenn, Ivan Milenkovic, Gertrud Eckstein, et al.
Pageof 7

Showing results (1-10 of 64) with videos related to

Sort By:
Pageof 7
Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 2025
Reduced Penetrance in Interferonopathy-Associated Dystonia: Hope for Clues to Mechanism?Martin Krenn, Michael Zech
Journal of the Neurological Sciences|July 31, 2022
Spinal muscular atrophy presenting with mild limb-girdle weakness in adulthood: Diagnostic pitfalls in the era of disease-modifying therapiesMartin Krenn, Suren Jengojan, Wolfgang Grisold
BMJ Case Reports|April 12, 2014
CANOMAD responding to weekly treatment with intravenous immunoglobulin (IVIg)Martin Krenn, Geoff Keir, Udo Carl Wieshmann
Movement Disorders : Official Journal of the Movement Disorder Society|October 23, 2022
GNAO1 Haploinsufficiency Associated with a Mild Delayed-Onset Dystonia PhenotypeMartin Krenn, Rudolf Sommer, Thomas Sycha, et al.
Eneurologicalsci|January 13, 2025
Bilateral foot drop as presenting feature of facioscapulohumeral muscular dystrophy type 1Martin Krenn, Veronika Vetchy, Gregor Kasprian, et al.
Seizure|August 27, 2025
ADAM23 haploinsufficiency as a putative oligogenic contributor in an individual with focal epilepsyMartin Krenn, Karl-Heinz Nenning, Susanne Aull-Watschinger, et al.
Scientific Reports|September 28, 2021
Real-world treatment of adult patients with Guillain-Barré syndrome over the last two decadesJakob Rath, Gudrun Zulehner, Bernadette Schober, et al.
Frontiers in Molecular Neuroscience|September 14, 2020
Pathomechanisms and Clinical Implications of Myasthenic Syndromes Exacerbated and Induced by Medical TreatmentsMartin Krenn, Anna Grisold, Philipp Wohlfarth, et al.
International Journal of Molecular Sciences|September 20, 2019
Rare Human Missense Variants can affect the Function of Disease-Relevant Proteins by Loss and Gain of Peroxisomal Targeting MotifsCheng-Shoong Chong, Markus Kunze, Bernhard Hochreiter, et al.
Neurology. Genetics|August 13, 2019
Adult-onset variant ataxia-telangiectasia diagnosed by exome and cDNA sequencingMartin Krenn, Ivan Milenkovic, Gertrud Eckstein, et al.
Pageof 7