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Andreas Hahn

Showing results (461-470 of 559) with videos related to

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Scientific Reports|October 3, 2024
Molecular composition of skeletal muscle in infants and adults: a comparative proteomic and transcriptomic studyAlexander Schaiter, Andreas Hentschel, Felix Kleefeld, et al.
Translational Psychiatry|February 1, 2023
Effects of bilateral sequential theta-burst stimulation on 5-HT<sub>1A</sub> receptors in the dorsolateral prefrontal cortex in treatment-resistant depression: a proof-of-concept trialMatej Murgaš, Jakob Unterholzner, Peter Stöhrmann, et al.
Molecular Genetics and Metabolism|June 6, 2022
Proteomic and morphological insights and clinical presentation of two young patients with novel mutations of BVES (POPDC1)Andrea Gangfuß, Andreas Hentschel, Lorena Heil, et al.
Acta Neuropathologica Communications|July 11, 2023
Correction: Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane traffickingAlexander H Swan, Roland F R Schindler, Marco Savarese, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 13, 2021
The phenotypic spectrum of PCDH12 associated disorders - Five new cases and review of the literatureWalid Fazeli, Daniel Bamborschke, Abubakar Moawia, et al.
The Lancet. Neurology|June 17, 2026
Safety and efficacy of levacetylleucine in ataxia-telangiectasia: a phase 3, randomised, double-blind, placebo-controlled crossover trialKyriakos Martakis, Tatiana Bremova-Ertl, Clare Bolton, et al.
Orphanet Journal of Rare Diseases|November 19, 2017
Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weaknessKatherine Johnson, Ana Töpf, Marta Bertoli, et al.
JIMD Reports|January 29, 2015
Outcome of patients with classical infantile pompe disease receiving enzyme replacement therapy in GermanyAndreas Hahn, Susanne Praetorius, Nesrin Karabul, et al.
EJNMMI Research|November 10, 2023
An update on the use of image-derived input functions for human PET studies: new hopes or old illusions?Tommaso Volpi, Lucia Maccioni, Maria Colpo, et al.
European Journal of Medical Genetics|November 14, 2018
Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11Karit Reinson, Reka Kovacs-Nagy, Eve Õiglane-Shlik, et al.
Pageof 56

Showing results (461-470 of 559) with videos related to

Sort By:
Pageof 56
Scientific Reports|October 3, 2024
Molecular composition of skeletal muscle in infants and adults: a comparative proteomic and transcriptomic studyAlexander Schaiter, Andreas Hentschel, Felix Kleefeld, et al.
Translational Psychiatry|February 1, 2023
Effects of bilateral sequential theta-burst stimulation on 5-HT<sub>1A</sub> receptors in the dorsolateral prefrontal cortex in treatment-resistant depression: a proof-of-concept trialMatej Murgaš, Jakob Unterholzner, Peter Stöhrmann, et al.
Molecular Genetics and Metabolism|June 6, 2022
Proteomic and morphological insights and clinical presentation of two young patients with novel mutations of BVES (POPDC1)Andrea Gangfuß, Andreas Hentschel, Lorena Heil, et al.
Acta Neuropathologica Communications|July 11, 2023
Correction: Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane traffickingAlexander H Swan, Roland F R Schindler, Marco Savarese, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 13, 2021
The phenotypic spectrum of PCDH12 associated disorders - Five new cases and review of the literatureWalid Fazeli, Daniel Bamborschke, Abubakar Moawia, et al.
The Lancet. Neurology|June 17, 2026
Safety and efficacy of levacetylleucine in ataxia-telangiectasia: a phase 3, randomised, double-blind, placebo-controlled crossover trialKyriakos Martakis, Tatiana Bremova-Ertl, Clare Bolton, et al.
Orphanet Journal of Rare Diseases|November 19, 2017
Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weaknessKatherine Johnson, Ana Töpf, Marta Bertoli, et al.
JIMD Reports|January 29, 2015
Outcome of patients with classical infantile pompe disease receiving enzyme replacement therapy in GermanyAndreas Hahn, Susanne Praetorius, Nesrin Karabul, et al.
EJNMMI Research|November 10, 2023
An update on the use of image-derived input functions for human PET studies: new hopes or old illusions?Tommaso Volpi, Lucia Maccioni, Maria Colpo, et al.
European Journal of Medical Genetics|November 14, 2018
Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11Karit Reinson, Reka Kovacs-Nagy, Eve Õiglane-Shlik, et al.
Pageof 56