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Scientific Reports
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October 3, 2024
Molecular composition of skeletal muscle in infants and adults: a comparative proteomic and transcriptomic study
Alexander 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 trial
Matej 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 trafficking
Alexander 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 literature
Walid 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 trial
Kyriakos 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 weakness
Katherine 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 Germany
Andreas 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 NDUFB11
Karit Reinson, Reka Kovacs-Nagy, Eve Õiglane-Shlik, et al.
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of 56
Search research articles
Search
Showing results (461-470 of 559) with videos related to
Sort By:
Page
of 56
Scientific Reports
|
October 3, 2024
Molecular composition of skeletal muscle in infants and adults: a comparative proteomic and transcriptomic study
Alexander 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 trial
Matej 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 trafficking
Alexander 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 literature
Walid 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 trial
Kyriakos 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 weakness
Katherine 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 Germany
Andreas 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 NDUFB11
Karit Reinson, Reka Kovacs-Nagy, Eve Õiglane-Shlik, et al.
Page
of 56