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Frontiers in Public Health|January 23, 2023
Perspective: Lessons from COVID-19 of countries in the European region in light of findings from the health system response monitorFlorian Tille, Ewout Van Ginneken, Juliane Winkelmann, et al.Isotopes in Environmental and Health Studies|July 2, 2019
Sauna, sweat and science II - do we sweat what we drink?Michael Zech, Marianne Benesch, Johannes Hepp, et al.Isotopes in Environmental and Health Studies|July 10, 2015
Do n-alkane biomarkers in soils/sediments reflect the δ²H isotopic composition of precipitation? A case study from Mt. Kilimanjaro and implications for paleoaltimetry and paleoclimate researchMichael Zech, Roland Zech, Kazimierz Rozanski, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 23, 2020
Variability of clinical syndromes and cerebral glucose metabolism in symptomatic frontotemporal lobar degeneration associated with progranulin mutationsAbigail Licata, Timo Grimmer, Juliane Winkelmann, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 22, 2025
Generalized dystonia unraveled: Molecular mechanisms, diagnostic strategies, and treatment paradigmsFereshteh Yarahmadi, Ali Shoiebi, Mohammad Shariati, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 25, 2025
Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate SynthasePhilip Harrer, Magdalena Krygier, Martin Krenn, et al.Human Genome Variation|April 16, 2016
Excess of rare coding variants in PLD3 in late- but not early-onset Alzheimer's diseaseEva C Schulte, Alexander Kurz, Panagiotis Alexopoulos, et al.Biological Psychiatry|April 15, 2008
Heritability of sleep electroencephalogramUrte Ambrosius, Sonja Lietzenmaier, Renate Wehrle, et al.Stem Cell Research|September 9, 2023
Generation of two human iPSC lines, HMGUi004-A and FINCBi004-A, from fibroblasts of MPAN patients carrying pathogenic recessive mutations in the gene C19orf12Enrica Zanuttigh, Ejona Rusha, Camille Peron, et al.Sleep Medicine|November 15, 2016
Animal models of RLS phenotypesRichard P Allen, Nathan C Donelson, Byron C Jones, et al.Pageof 33