Showing results (1331-1340 of 1,757) with videos related to
Sort By:
Pageof 176
Neurology|April 23, 2003
The phenotype of limb-girdle muscular dystrophy type 2IM Poppe, L Cree, J Bourke, et al.Transfusion|September 5, 2019
Analyses of sphingosine-1-phosphate in the context of transfusion: how much is in stored blood products and in patient blood?Annika Poppe, Eileen Moritz, Maria Geffken, et al.Micromachines|October 5, 2019
Liver-on-a-Chip‒Magnetic Nanoparticle Bound Synthetic Metalloporphyrin-Catalyzed Biomimetic Oxidation of a Drug in a Magnechip ReactorBalázs Decsi, Réka Krammer, Kristóf Hegedűs, et al.Die Pharmazie|December 1, 1985
[Antiarrhythmic effectiveness of 3-carbalkoxyamino-5-(omega-aminoacyl)-10,11-dihydro-5H-dibenz-[b,f]- azepines]N V Kaverina, Z P Senova, V V Lyskovzev, et al.Journal of Pediatric Gastroenterology and Nutrition|August 27, 2019
Relationships Between Early Neonatal Nutrition and Neurodevelopment at School Age in Children Born Very PretermAnna C Tottman, Jane M Alsweiler, Frank H Bloomfield, et al.International Journal of Cardiology|December 8, 2009
Understanding differences in results from literature-based and individual patient meta-analyses: an example from meta-analyses of observational dataKatrina K Poppe, Robert N Doughty, Cheuk-Man Yu, et al.Neurosurgical Review|January 1, 2024
Craniocervical instability in patients with Ehlers-Danlos syndromes: outcomes analysis following occipito-cervical fusionFraser C Henderson, Jane R Schubart, Malini V Narayanan, et al.Frontiers in Allergy|April 7, 2022
Corrigendum: Patients Unmet Needs in Chronic Rhinosinusitis With Nasal Polyps Care: A Patient Advisory Board Statement of EUFOREAN Claeys, M T Teeling, P Legrand, et al.Breast Cancer Research and Treatment|May 10, 2011
Prevalence of BRCA1/2 mutations in sporadic breast/ovarian cancer patients and identification of a novel de novo BRCA1 mutation in a patient diagnosed with late onset breast and ovarian cancer: implications for genetic testingKim De Leeneer, Ilse Coene, Brecht Crombez, et al.Neuromolecular Medicine|May 2, 2013
Variant ataxia telangiectasia: clinical and molecular findings and evaluation of radiosensitive phenotypes in a patient and relativesKathleen Claes, Julie Depuydt, A Malcolm R Taylor, et al.Pageof 176