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European Journal of Pediatrics|December 5, 2024
Health and socio-demographic background of Ukrainian minors and their families in Germany - challenges for refugee medicine : A cross-sectional study from the German Network University Medicine (NUM)Anna Teresa Hoffmann, Robin Kobbe, Robin Denz, et al.European Journal of Pain (London, England)|November 10, 2020
The serotonin receptor 2A (HTR2A) rs6313 variant is associated with higher ongoing pain and signs of central sensitization in neuropathic pain patientsJuliane Sachau, Henrike Bruckmueller, Janne Gierthmühlen, et al.American Journal of Human Genetics|April 23, 2019
A Specific CNOT1 Mutation Results in a Novel Syndrome of Pancreatic Agenesis and Holoprosencephaly through Impaired Pancreatic and Neurological DevelopmentElisa De Franco, Rachel A Watson, Wolfgang J Weninger, et al.NPJ Parkinson'S Disease|August 1, 2025
Large-scale copy number variant analysis in genes linked to Parkinson´s diseaseZied Landoulsi, Katja Lohmann, Eva-Juliane Vollstedt, et al.Nature Communications|June 1, 2019
Publisher Correction: Transcriptomic alterations during ageing reflect the shift from cancer to degenerative diseases in the elderlyPeer Aramillo Irizar, Sascha Schäuble, Daniela Esser, et al.Nature Communications|February 1, 2018
Transcriptomic alterations during ageing reflect the shift from cancer to degenerative diseases in the elderlyPeer Aramillo Irizar, Sascha Schäuble, Daniela Esser, et al.American Journal of Human Genetics|December 7, 2014
Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndromeNadja Ehmke, Almuth Caliebe, Rainer Koenig, et al.Human Genetics|March 1, 2015
Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin-Siris and Nicolaides-Baraitser syndromesNuria C Bramswig, Hermann-Josef Lüdecke, Yasemin Alanay, et al.American Journal of Human Genetics|June 18, 2013
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathyAnne-Karin Arndt, Sebastian Schafer, Jorg-Detlef Drenckhahn, et al.European Journal of Human Genetics : EJHG|November 28, 2013
Structural genomic variation in childhood epilepsies with complex phenotypesIngo Helbig, Marielle E M Swinkels, Emmelien Aten, et al.Pageof 28