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The New England Journal of Medicine|July 29, 2011
A mosaic activating mutation in AKT1 associated with the Proteus syndromeMarjorie J Lindhurst, Julie C Sapp, Jamie K Teer, et al.
Journal of Neurology|February 14, 2024
The comorbidity profiles and medication issues of patients with multiple system atrophy: a systematic cross-sectional analysisLan Ye, Stephan Greten, Florian Wegner, et al.
The Lancet. Neurology|March 28, 2016
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association dataKin Y Mok, Una Sheerin, Javier Simón-Sánchez, et al.
Journal of Clinical Medicine|September 9, 2022
Retinal Vascular Occlusion after COVID-19 Vaccination: More Coincidence than Causal Relationship? Data from a Retrospective Multicentre StudyNicolas Feltgen, Thomas Ach, Focke Ziemssen, et al.
Nature Genetics|August 20, 2008
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasiaBirgit S Budde, Yasmin Namavar, Peter G Barth, et al.
Annals of Surgery|September 5, 2020
mTOR Inhibition Is Most Beneficial After Liver Transplantation for Hepatocellular Carcinoma in Patients With Active TumorsAndreas A Schnitzbauer, Natalie Filmann, René Adam, et al.
Sensors (Basel, Switzerland)|October 19, 2019
An Ocean-Colour Time Series for Use in Climate Studies: The Experience of the Ocean-Colour Climate Change Initiative (OC-CCI)Shubha Sathyendranath, Robert J W Brewin, Carsten Brockmann, et al.
Movement Disorders Clinical Practice|January 27, 2025
A Short Cognitive and Neuropsychiatric Assessment Scale for Progressive Supranuclear PalsySonja Porsche, Martin Klietz, Stephan Greten, et al.
NPJ Parkinson'S Disease|March 30, 2024
Genotype-phenotype correlation in PRKN-associated Parkinson's diseasePoornima Jayadev Menon, Sara Sambin, Baptiste Criniere-Boizet, et al.
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