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BMC Health Services Research|October 4, 2012
Exposure to second-hand smoke and direct healthcare costs in children - results from two German birth cohorts, GINIplus and LISAplusAriane Batscheider, Sylwia Zakrzewska, Joachim Heinrich, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|July 24, 2025
Prospective association between psychopathological symptoms in childhood and asthma in adolescence: Results from the GINIplus and LISA birth cohort studiesPia-Marie Keim, Ellen Greimel, Lisa Feldmann, et al.
Human Molecular Genetics|June 19, 2013
Genetic screening for Niemann-Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM studyPeter Bauer, David J Balding, Hans H Klünemann, et al.
European Journal of Human Genetics : EJHG|June 22, 2024
Facing the challenges to shorten the diagnostic odyssey: first Whole Genome Sequencing experience of a Colombian cohort with suspected rare diseasesHarvy Mauricio Velasco, Aida Bertoli-Avella, Carolina Jaramillo Jaramillo, et al.
European Journal of Human Genetics : EJHG|June 21, 2024
Limitations in next-generation sequencing-based genotyping of breast cancer polygenic risk score lociAlexandra Baumann, Christian Ruckert, Christoph Meier, et al.
European Journal of Anaesthesiology|May 23, 2015
Nonelective surgery at night and in-hospital mortality: Prospective observational data from the European Surgical Outcomes StudyBas van Zaane, Wilton A van Klei, Wolfgang F Buhre, et al.
Neurogenetics|May 4, 2012
A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genesClaudia Dufke, Nina Schlipf, Rebecca Schüle, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 12, 2018
Utility and implications of exome sequencing in early-onset Parkinson's diseaseJoanne Trinh, Katja Lohmann, Hauke Baumann, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
How many do we miss? - Evaluation of age at onset and family history as selection criteria for genetic testing in Parkinson's diseaseAlexander Balck, Eva-Juliane Vollstedt, Ana Westenberger, et al.
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